Chemical Diversity in Species Belonging to Soft Coral Genus Sacrophyton and Its Impact on Biological Activity: A Review

Abstract

One of the most widely distributed soft coral species, found especially in shallow waters of the Indo-Pacific region, Red Sea, Mediterranean Sea, and also the Arctic, is genus Sacrophyton. The total number of species belonging to it was estimated to be 40. Sarcophyton species are considered to be a reservoir of bioactive natural metabolites. Secondary metabolites isolated from members belonging to this genus show great chemical diversity. They are rich in terpenoids, in particular, cembranoids diterpenes, tetratepenoids, triterpenoids, and ceramide, in addition to steroids, sesquiterpenes, and fatty acids. They showed a broad range of potent biological activities, such as antitumor, neuroprotective, antimicrobial, antiviral, antidiabetic, antifouling, and anti-inflammatory activity. This review presents all isolated secondary metabolites from species of genera Sacrophyton, as well as their reported biological activities covering a period of about two decades (1998–2019). It deals with 481 metabolites, including 323 diterpenes, 39 biscembranoids, 11 sesquiterpenes, 53 polyoxygenated sterols, and 55 miscellaneous and their pharmacological activities.

1. Introduction

Classification of alcyonacean corals, subclass Octocorallia implies the existence of polyps with eight tentacles, which differentiates them from hexacorallian Scleractinia corals. Alcyonaceans are sessile large invertebrate with distinct stalk and a smooth, mushroom-shaped top known as capitulum, and their tissue comprises sclerites, which give support to the colony [1,2]. Traditionally, identification and classification of most soft coral have been carried out by sclerite classification. Sarcophyton covers 35 species, and another six species of Sarcophyton were described [3,4,5,6,7,8]. Later, [9] reported that, within Sarcophyton samples, Sarcophyton glaucum contains six different genetic clades, signifying that this morphologically heterogeneous species was mysterious [10]. Studies revealed that Sarcophyton were mostly seen in shallow water of the Indo-Pacific region [11,12], Red Sea [13], Mediterranean Sea [14], and also the Arctic area [10,15]. However, to our knowledge, nothing was reported from North and South of America (Figure 1). Sarcophyton sp. synonyms include Toadstool Mushroom Leather, Toadstool Leather Coral, Umbrella Coral, Toadstool Mushroom Coral, Mushroom Leather Coral, Sarcophyton Coral, and Mushroom Coral. Sarcophyton sp. were considered a reservoir of bioactive natural metabolites such as diterpenes, steroids, sesquiterpenes, and fatty acids [16,17]. These metabolites, mainly macrocyclic cembranes and their byproducts, represented an important natural bioactive product, with significant biological activities, including anticancer [18,19], antimicrobial [20], anti-inflammatory [21], anti-osteoporotic, antimetastatic, antiangiogenic, and neuroprotective [22]. One metabolite, sarcophytol A 15, isolated from Sarcophyton obtained from Ishigaki Island, Okinawa, Southern Japan, was studied and highlighted because of its important anticancer activity [23]. Some recent articles had partially covered the chemistry and pharmacology of secondary metabolites from Sarcophyton sp. [24,25,26]. This review concentrates on marine bioactive metabolites isolated from Sarcophyton species, their biological properties, and studies of the biosynthesis of marine metabolites. In this review, we reported all metabolites isolated from Sarcophyton species and their reported biological activities stated in the literature over the years from 1998 to 2019. Different online databases were utilized through this review, including Scifinder, Marinlit, and Web of Science. The present review aims to present the progress made in the last two decades regarding the potential application of biomolecules (481 compounds) isolated from Sacrophyton soft corals, to complete the previously published papers (Figure 2 and Figure 3) on the interesting subject of Sacrophyton. It deals with the chemistry, as well as the biological activity of secondary metabolites, including terpenoids, in particular diterpenes, sesquiterpenes, biscembranoids, and polyhydroxysterols, in addition to a number of miscellaneous compounds. The percentage of different chemical classes is represented in (Figure 2), and Figure 3 shows a diagram of isolated classes from each Sarcophyton sp.

Figure 1. Worldwide distribution of chemically studied Sarcophyton soft coral.

Figure 2. Pie chart showing the percentage of each class of metabolites identified in Sarcophyton sp.

Figure 3. A diagram of isolated classes from each Sarcophyton sp.

2. Classes of Secondary Metabolites

2.1. Diterpenes

Sarcophyton ehrenbergi dichloromethane extract yielded sarcophytol T 1, (1E,3E,7E,11R*12R*)-15-(acetoxymethyl)cembra-11,12-epoxy-1,3,7-triene 2, and (11S*,12S*)-15-(acetoxymethyl) cembra-3,4:11,12-diepoxy-1,7-diene 3, together with known isoneocembrene A 4, an isomer to neocembrane A 5, and (2S*,11R*,12R*)-isosarcophytoxide 6. Compound 2 was found to possess several structural similarities with the former two isolates in conjugated diene system (C-1 and C-4) and Δ^7,8 double bond and 11,12-epoxy functional group [27].

Another three cembrenolide diterpenes identified as crassolide 7, sarcocrassolide A 8, and 13-acetoxysarcocrassolide 9, alongside known cembrenolide denticulatolide 10, were reported from S. crassocaule [28].

From S. trocheliophorum, the isolation of 7,8-epoxy-1(E),3(E),11(E)cembratrien-15-ol 11, 7,8-epoxy1(E),3(E),11(E)-cembratriene 12, and sarcophin 13 was reported, and the absolute configuration of sarcophin 13 was investigated through modified Mosher’s assay [29].

Using chromatographic techniques, cembrane alcohol identified as acutanol 14 beside sarcophytol A 15 and sarcophytol A acetate 16 were isolated from S. acutangulum extract. The absolute configuration of sarcophytol A 15 was assessed with the use of many chiral anisotropic reagents, as 1-naphthylmethoxyacetic acid [30].

Four cembranes, (1S,2E,4R,6E,8S,11S,12S)-11,12-Epoxy-2,6-cembrane-4,8-diol 17, (1S,2E,4R,6E,8R,11S,12S)-11,12-Epoxy-2,6-cembrane-4,8-diol 18, (1S,2E,4R,7S)-11,12-Epoxy-2,8(19)-cembradiene-4,7-diol 19, and (1S,2E,4R,7R)-11,12-Epoxy-2,8(19)-cembradiene-4,7-diol 20, were isolated from Sarcophyton sp. It is worth noticing that these metabolites were not previously found in nature. Their absolute configurations were validated with X-ray analysis [31].

The hydroperoxide cembrane diterpenoid, sarcophycrassolide A 21, together with sacophyocrassolide B 22 and compound 8, was reported from S. crassocaule. Identification of compound 21 was resolved by using X-ray diffraction and spectral analysis [32].

Three furano-cembranoids and two seco-cembranoid acetates, which were identified as 13-dehydroxysarcoglaucol 23, 13-dehydroxysarcoglaucol-16-one 24 and sarcoglaucol-16-one 25, (3E)-7-hydroxy-4,8,15,15-tetramethyl-1-[(E)-12-methyl-10-oxo-12-pentenyl]-3,8-decadienyl acetate 26, (3E)-7-hydroxy-4,8,15,15-tetramethyl-1-[(Z)-12-methyl-10-oxo-12-pentenyl]-3,8-decadienyl acetate 27 beside sarcoglaucol 28, and decaryiol 29, were isolated form S. cherbonnieri. Spectral data showed that compound 25 was a 16-keto derivative of compound 28 and the 13-hydroxy derivative of compound 24 [33]. The absolute configuration of compound 25 was investigated similarly to compound 13 by using the modified Mosher’s method [34]. Another two bicyclic cembranolides metabolites, with infrequent structures in marine literature, having a 12Z double bond, identified as (4Z,8S,9S,12Z,14E)-9-Hydroxy-1-isopropyl-8,12-dimethyl-oxabicyclo [9.3.2]-hexadeca-4,12,14-trien-18-one 30, and (4Z,12Z,14E)-sarcophytolide 31, in addition to sarcophytolide 32, (4Z,8S,9R,12E,14E)-9-Hydroxy-1-isopropyl-8,12-dimethyloxabicyclo[9.3.2]-hexadeca-4,12,14-trien-18-one 33 and (4Z,8S,9R,12E,14E)-1-Isopropyl-8,12-dimethyl-18-oxo-oxabicyclo[9.3.2]-hexadeca-4,12,14-trien-2-yl acetate 34, were reported from Sarcophyton new sp. Additionally, the authors presented biosynthetic pathways for all isolated compounds which resulted from the common acyclic precursor (all-E)-geranylgeranyl pyrophosphate (GGPP), by converting geranylgeranyl-PP [GGPP] into geranylneryl-PP [GNPP], using diterpene synthase, followed by cyclization to cembranoid ring with a 12Z double bond [35]. Three diterpenes, sarcophytolol 35, sarcophytolide B 36, and sarcophytolide C 37, were reported from S. glaucum [34].

Sarcophytonolides A–D 38–41, four cembranolides were isolated from S. tortuosum. Sarcophytonolide B 39 was found to be the 12-(methoxycarbonyl) derivative of compound 38, in which it exhibited αβ-unsaturated methyl ester instead of the methyl group. Sarcophytonolide D 41 was similar in structure to compound 40, while, compound 41 possessed an extra trisubstituted C=C and acetoxy group [36]. Four more sarcophytonolides E-H 42–45 from S. latum were isolated. All isolated compounds were related in structure to compound 40, with an α, β-unsaturated butanolide group. Sarcophytonolide G 44 was found to be the epimer of Sarcophytonolide F 43 at C-6, while sarcophytonolide H 45 was 14-acetoxy methoxycarbonyl derivative of compound 43. The absolute configuration was investigated by using the modified Mosher’s assay as they all possessed secondary alcohol at C-6. It is worth noting that the structural configuration supporting all cembrane diterpenes stated, in the order alcyonacea, with the identified absolute configuration at C-1, belonged to α-series [37]. Moreover, sarcophytonolides I–L 46–49 were isolated from S. latum. All compounds were related in structure to the previously isolated compounds 38–45; all possessed α, β-unsaturated butenolactone group. The absolute configuration of compounds 38–45 still need further determination. Considering the fact that these compounds were structurally related to previously isolated sarcophytonolide, the structure of sarcophytonolide I 46 differs from sarcophytonolide D 41, in the olefinic C₇=C₈ bond and absence of C=O group at C6 [38]. Another five cembranolide, sarcophytonolides N–R 50–54, ketoemblide 55, and (E,E,E)-1-isopropenyl-4,8,12-trimethylcyclotetradeca-3,7,11-tiene 56 were isolated from S. trocheliophorum Marenzeller. A detailed spectroscopic analysis was done, in which sarcophytonolides N–R 50–54 were found to be either mono- or bicyclic cembranoids possessing oxidized methyl groups and three/four double bonds [39]. The absolute configuration of another six metabolites isolated from S. trocheliophorum, sarcophytonolides S–U 57–59 and sartrolides H–J; α,β-unsaturated ε-lactone 60–62, along with seven known analogues, were carried out through different techniques [40]. Chemical determination of S. trocheliophorum yielded seven cembranolides, sartrolides A–G 63–69 and bissartrolide dimer 70; a third member of this scarce class of cembrane dimers [41]. Yalongenes A and B 71 and 72 another two cembranoids, isolated from S. trocheliophorum [42], and another two cembranoids, trochelioids A and B 73 and 74, and 16-oxosarcophytonin E 75 were isolated [43].

Five diterpenes cembrane type, sarcrassins A–E 76–80, beside emblide 81 isolated from S. crassocaule were identified based on 1D and 2D NMR. Sarcrassins B and C 77 and 78, cyclic diterpenes, derivatives of sarcrassin A 76 in which the double bond in sarcrassin A 76 was replaced by an epoxy ring in sarcrassin B 77. However, in sarcrassin C 78 the epoxy ring in sarcrassin A 76 was replaced by a hydroxyl and methoxy group. As for sarcrassin D 79, its bicyclic diterpene structure was confirmed through spectral data [44], and its absolute configuration, as well as that of emblide 81, was determined by X-ray analysis [41,45].

Investigation of ethyl acetate extract of S. crassocaule yielded six polyoxygenated cembrane-diterpenoids with a trans-fused α-methylene-γ-lactone, identified as crassocolides A–F 82–87 alongside lobophytolide 88. Absolute configuration for crassocolide A 82 was resolved by using modified Mosher’s method [46]. Another seven polyoxygenated cembranoids with α-methylene-γ-lactone group identified as crassocolides G–M 89–95, were reported. The structures of all compounds were determined through a full spectral data analysis, and the absolute configuration of crassocolide G 89 was investigated by modified reaction of Mosher’s assay [47]. Other crassocolides N–P 96–98 were isolated from S. crassocaule [48]. The CHCl₃/MeOH extract of S. flexuosum yielded three cembranes, identified through spectral data as flexusines A, B, and epimukulol 99–101 [49].

From ethyl acetate extract of S. stolidotum, seven cembranes, sarcostolides A–G 102–108, alongside isosarcophin 109, were reported, and their structures were elucidated through spectral data. The authors also proposed a reasonable biogenetic pathway for all isolates, in which cyclization of GPP with lactonization and oxidation may lead to the production of sarcostolide C 104. Sarcostolides A and B 102 and 103 and D–G 105–108 were converted from sacostolide C 104 through migration and isomerization of double bonds [50].

Sarcophyton mililatensis methanol extract yielded cembranoid diterpenes identified as (−)-7β-hydroxy-8α-methoxy-deepoxy-sarcophytoxide 110, (−)-7β,8β-dihydroxy-deepoxy-sarcophytoxide 111, (−)-17-hydroxysarcophytonin A 112, sarcophytol V 113, and sarcophytoxide 114 [51].

Two cembrane diterpenes known as 17-hydroxysarcophytoxide 115 and 7β-acetoxy-8α-hydroxydeepoxysarcophine 116, along with 7β,8α, dihydroxydeepoxysarcophine 117, sarcophytonin A 118, and (−)-β-elemene 119 reported from Sarcophyton sp., were isolated from S. glaucum [52]. Investigation of S. glaucum extract led to the isolation of two cembranoids, (7R,8S)-dihydroxydeepoxy-ent-sarcophine 120 and secosarcophinolide 121, in addition to, ent-sarcophin 122. Structural elucidation of the isolates was established by their spectral data and chemical correlation, as (7R,8S)-dihydroxydeepoxy-ent-sarcophine 120 was found to be the enantiomer of (7S,8R)-dihydroxydeepoxysarcophine 123 and compound 121 has a unique butyl ester group at C-16 [53].

Seven cembranoids were isolated from Sarcophyton sp., 5-epi-sinuleptolide 124, lobohedleolide 125, (7Z)-lobohedleolide 126, and two uncommon cembranoids, sarcofuranocembrenolide A 127; with a unique carbon skeleton of 8,19-bisnorfuranocembrenolide, and sarcofuranocembrenolide B 128; a furanocembrenolide [54]. Sarcophytonins F and G 129 and 130, another two dihydrofuranocembranoids, were reported from Sarcophyton sp. [55]. Nineteen compounds from Sarcophyton sp., of which five cembrane diterpenoids were isolated and identified as 7-acetyl-8-epi- sinumaximol G 131, 8-epi- sinumaximol G 132, 12-acetyl-7,12-epi- sinumaximol G 133, 12-hydroxysarcoph-10-ene 134, and 8-hydroxy-epi-sarcophinone 135, together with sinumaximol G 136, were reported [56].

Five isolated cembranoids, sarcocrassocolides A–E 137–141, together with sinularolide 142, were isolated from S. crassocaule. Structural elucidation of the compounds was determined through spectral analysis, and the absolute configuration of sarcocrassocolide A 137 was investigated by modified Mosher’s method. It is worth mentioning that sarcocrassocolides A–D 137–140 possessed a tetrahydrofuran group with a seldomly found 4,7-ether bond, which was discovered previously in Eunicea mammosa soft coral [57,58]. Another seven cembranoids with α-methylene-γ-lactonic group and rare trans 6,7-disubstituted double bond, uncovered earlier only in soft coral Eunicea pinta, identified as sarcocrassocolides F–L 143–149, were isolated from S. crassocaule [59]. Besides the abovementioned sarcocrassocolides, another three sarcocrassocolides, M–O 150–152, from S. crassocaule, were identified. Through structural analysis, sarcocrassocolide N 151 was found to have the same relative configuration of sarcocrassocolide M 150, while sarcocrassocolide O 152 was found to be the 13-deacetoxy derivative of sarcocrassocolide M 150 [60]. Three more cembranoids, sarcocrassocolides P–R 153–155, were identified, and their structures were investigated by an extensive spectral study [61].

Investigation of n-hexane fraction for S. ehrenbergi led to the isolation of (+)-7,8-epoxy-7,8-dihydrocembrene C 156, in which its optical rotation indicated that it was (+)- (7S,8S)-7,8-epoxy-7,8-dihydrocembrene C 156, not (−)-7,8-Epoxy-7,8-dihydrocembrene C, which was reported previously from S. crassocaule [62].

Six cembranoids, (+)-12-carboxy-11Z-sarcophytoxide 157, (+)-12-methoxycarbonyl-11Z-sarcophine 158, ehrenberoxides A–C 159–161 and lobophynin C 162 were isolated from S. ehrenbergi. Compound 157 has a 2,5-dihydrofuran ring attached to a 14 membered ring at carbon-1 and carbon-2, a carboxylic acid at carbon-12 and an epoxide moiety at carbon-7 and carbon-8. Moreover, the authors mentioned that both ehrenberoxides B and C 160–161 raised from the exact precursor with a 7,8-epoxide through a transannular cleavage of the 7,8-epoxide by both ends of an 11,12-diol, while compound 160 has a unique oxepane ring, which was not detected previously in cembranoid [63] and from S. infundibuliforme diterpenoids cembrene C 163, sarcophytol B 164, sarcophytol E 165, and sarcophytol H 166, (−)-marasol 167 were reported [64].

A cembrane diterpene identified as 2R,7R,8R-dihydroxydeepoxysarcophine 168 was isolated from S. glaucum [65], and three compounds were reported from its ethyl acetate fraction, of which two were peroxide diterpenes identified as 11(S)-hydroperoxylsarcoph-12(20)-ene 169, 12(S)-hydroperoxylsarcoph-10-ene 170, and 8-epi-sarcophinone 171. All structures were investigated by spectral data, and their relative configuration was assigned by X-ray diffraction [66].

Methyl sarcotroates A and B 172 and 173 two diterpenes, along with sarcophytonolide M 174, a precursor for the former two compounds, were isolated from S. trocheliophorum, and their biogenetic pathways were proposed, in which isomaration, cycloaddition followed by oxidation of compound 174 led to the formation of both compounds 172 and 173. The authors also studied the absolute configuration of methyl sarcotroate B 173 through TDDFT ECD calculations, helping in determining the absolute configurations for methyl sarcotroate A 172 and sarcophytonolide M 174 by a biogenetic relationship and ECD comparison, respectively [67].

Cembranoid diterpene, identified as (1S,2E,4R,6E,8S,11R,12S)-8,11-epoxy-4,12-epoxy- 2,6-cembradiene 175, (1S,2E,4R,6E,8R,11S,12R)-8,12-epoxy-2,6-cembradiene-4,11-diol 176, and (1S,4R,13S)-cembra-2E,7E,11E-trien-4,13-diol 177, were reported from nature for the first time, from S. glaucum [68].

From an acetone extract of S. ehrenbergi, three cembranoids were isolated. Through full NMR data, the existence of α, β unsaturated ethyl ester and α, β unsaturated methyl ester of both (+)-12-ethoxycarbonyl-11Z-sarcophine; ehrenbergol A and B 178–180 were confirmed. Ehrenbergol B 179 showed a trisubstituted epoxide and two trisubstituted olefins. [69].

Fifteen cembrane-type diterpenoids were isolated from S. elegans, sarcophyolides B–E 181–184, along with sarcophytol L 185, 13α-hydroxysarcophytol L 186, sarcophyolide A 187, sarcophinone 188, 7α-hydroxy-Δ8(19)-deepoxysarcophine 189, 4β-hydroxy-Δ2(3)-sarcophine 190, 1,15β-epoxy-2-epi-16-deoxysarcophine 191, sarcophytol Q 192, and lobocrasol 193. A detailed structural elucidation was determined by spectral data and reported data. The absolute configurations of sarcophyolides B–E 181–184 were approved by single-crystal X-ray diffraction assay, using Flack’s assay [22], and the structure of lobocrasol 193 was further studied [70].

From the ethyl acetate extract of S. ehrenbergi two diterpenes were isolated, acetyl ehrenberoxide B 194 and ehrenbergol C 195. Ehrenbergol C 195 shared a structure similar to lobocrasol 193, isolated from Lobophytum crassum [71]. Yet, relative stereochemistry of carbon-7 and carbon-8 in ehrenbergol C 195 differed from lobocrasol 193 in hydroxy group and a conjugated enone evidenced by the IR spectrum at 3444 and 1696 cm⁻¹, respectively [72].

An oxygenated cembranoid diterpene, sarcophytol W 196, together with (2E,7E)-4,1l-dihydroxy-1,12-oxidocembra-2,7-dien 197, were isolated before from S. infundibuliforme and S. glaucum, (+)-11,12-epoxy-11,12-dihydrocembrene-C 198, (+)-11,12-epoxysarcophytol A 199 and sarcolactone A 200, previously known, were reported from Sarcophyton sp. Structures were determined through spectral data and comparing the reported data. The absolute configuration of sarcophytol W 196 was elucidated based on the modified Mosher’s assay [73].

Two diterpenes were isolated from S. tortuosum, identified as tortuosenes A and B 201 and 202. Structural elucidation of compounds 201 and 202 were investigated by spectral data. The absolute configuration of tortuosene A 201 was investigated using TDDFT ECD method. Moreover, the authors proposed a biosynthetic pathway for tortuosenes A and B 201 and 202 from the assumed cembranoidal precursor; (1Z, 3Z, 7E, 11E)-4-isopropyl-1,7,11-trimethylcyclotetradeca-1,3,7,11-tertaene, by oxidation of carbon-20 and the carbon-7/carbon-8 double bond was epoxidize, forming aldehydocembrane, a structure related to emblide 81. The resulting aldehydocembrane additionally formed a cycle from carbon-2 to carbon-20 by acid-catalyzed affecting the carbon-1/carbon-2 double bond of the carbonyl moiety [74].

2-epi-sarcophine 203 and (1R,2E,4S,6E,8R,11R,12R)-2,6-cembradiene-4,8,11,12-tetrol 204, two diterpenes were isolated from S. auritum [75]. An extensive chemical investigation of Sarcophyton sp. extract yielded four cembranoids, sarcophytons A–D 205–208, along with cembranoids, 2-[(E,E,E)-7′,8′-epoxy-4′,8′,12′-trimethylcyclotetradeca-1′,3′,11-trienyl]propan-2-ol 209, (1E,3E,7R*,8R*,11E)-1-(2-methoxy-propan-2-yl)-4,8,12-trimethyloxabicyclo[12.1.0]-pentadeca-1,3,11-triene 210, crassumol C 211, and laevigatol A 212. [76]. Two unique pyrane-based cembranoids, sarcotrocheliol acetate and sarcotrocheliol 213 and 214 were isolated from S. trocheliophorum [77]. Investigation of S. glaucum organic extract resulted in the isolation of sarcophinediol 215, previously processed semi-syntheticaly [78].

Cembranoid diterpenes, 7-keto-8α-hydroxy-deepoxysarcophine 216 similar to compound 13, in which the carbon at carbon-3 and carbon-11 were presumed to be in E configuration established on compound 13 derivatives; this was established through spectral data. 7β-chloro-8α-hydroxy-12acetoxy-deepoxysarcophine 217 was close to 7-keto-8α-hydroxy-deepoxysarcophine 216 except for the disappearance of ketone signal at C-7 which co-exists with the presence of an up fielded signal at δ62.9 (C-7), a downfield of C-20 and the presence of carbonyl and methyl group at 170 and 22.2, respectively, were isolated from S. ehrenbergi. [79].

From S. trocheliophorum, sarsolenane diterpenes and capnosane diterpenes were obtained. Sarsolenane diterpenes are uncommon in nature, symbolized only by sarsolenone isolated from S. solidum. Two sarsolenane diterpenes, dihydrosarsolenone 218, methyl dihydrosarsolenoneate 219, and two capnosane diterpenes, sarsolilides B and C 220 and 221, together with sarsolilide A 222 were isolated. Dihydrosarsolenone 218 resulting from sarsolenone 223 by terminal double bond Δ¹⁵ reduction followed by the oxidation of C-18 gave methyl dihydrosarsolenoneate 219. Capnosane diterpenes were first isolated from S. solidum and S. trocheliphorum. The only example reported with α, β-unsaturated ε-lactone subunit was sarsolilide A 222, from S. solidum, in which, the hydration of the exomethylene group provided carbon-10 epimers, sarsolilides B and C 220 and 221 [80]

Ethyl acetate extract of S. trocheliophorum yielded twenty-three isolates, of which nineteen were cembranoids with unique capnosane skeleton identified as trocheliophols A–S 224–242 and two analogues, 4-epi-sarcophytol L 243 and sarcophyolide C 182. The structures were investigated by a full spectral data, and their absolute configurations were established through modified Mosher’s assay, CD and X-ray diffraction. Trocheliophols C 226, E 228, F 229, and M 236 all possessed a structure similar to sarcophytolide C 176, while, trocheliophol Q 240 was identified as the C-8 methoxylated model of trocheliophol F 229. However, trocheliophol R 241 possessed a similar structure to trocheliophol F 229 but it differed in the presence of the methoxy group [81].

Chemical determination of S. elegans CH₂Cl₂/MeOH extract resulted in isolation of four cembranoids identified as sarcophelegans A–D 244–247. Sarcophelegan A 244 was found to be the 11,12-epoxy derivative of sarcophelegan C 246. Through X-ray crystallographic examination using anomalous scattering of Cu Kα radiation, sarcophelegan A 244 structure was verified. Moreover, sarcophelegan C 246 was found to be the 7-hydrogenated derivative of sarcophelegan B 245 [18].

Five polyoxygenated cembranoids were identified as polyoxygenated cembranoids, (+)-1,15-epoxy-2-methoxy-12methoxycarbonyl-11E-sarcophytoxide 248, (+)-2-epi-12-methoxycarbonyl-11E-sarcophine 249, 3,4-epoxyehrenberoxide A 250, ehrenbergol D 251 and ehrenbergol E 252 in S. ehrenbergi. The authors proposed that (+)-1,15-epoxy-2-methoxy-12methoxycarbonyl-11E-sarcophytoxide 248 was the 1,15 epoxy-2-methoxylated equivalent of lobophynin C 162. Through investigating the spectral data and X-ray crystallization of (+)-2-epi-12-methoxycarbonyl-11E-sarcophine 249 it was found that it differed in the alignment of the α,β-unsaturated γ-lactone ring attached to C-2 of the 14-membered ring [63]. 3,4-epoxyehrenberoxide A 250; an analogue to ehrenberoxide A 159 where the epoxide in ehrenberoxide A 159 was substituted by a double bond at C3 and C4 [82].

Eight metabolites were isolated from S. solidum, three sarsolenanes, 7-deacetyl-sarsolenone 253, sarsolenone 223, and methyl dihydro-sarsolenoneate 219 together with, sarsolilide B 220. All 7-deacetyl-sarsolenone 253, sarsolenone 223, sarsolilide B 220, could be used as a chemotaxonomic marker for this species [83].

Three isolates; trocheliane 254, tetracyclic biscembrane and two cembranoid diterpenes, sarcotrocheldiols A and B 255 and 256, were isolated from S. trocheliophorum. Their relative configuration and structure of the isolates were investigated by spectral data [84].

From Sarcophyton sp., one cembrane diterpene, 16-hydroxycembra-1,3,7,11-tetraene 257, besides, 15-hydroxycembra-1,3,7,11-tetraene 258 were reported. Structures were investigated by spectral data [85].

Three cembranoids from S. trocheliophorum, sarcophytrols D–F 259–261 highly oxidative compounds, besides, 11,12-epoxy-1(E),3(E), 7(E)-cembratrien-15-ol 262 and sinugibberol 263 were isolated. All structures were investigated by a full spectral data and by comparing with previous stated data [86]. Another six cembranoids, sarcophytrols G–L 264–269 together with crassumol A 270, were isolated from S. trocheliophorum [87]. Additionally, another nine cembranoids, sarcophytrols M–U 271–279, were also reported. Their structures were interpreted with extensive spectral analysis and chemical conversion and the absolute configuration for sarcophytrols M–S 271–277 were investigated by the modified Mosher’s assay. Sarcophytrols R and S 276 and 277 revealed a unique decaryiol skeleton with an uncommon C12/C15 cyclization [88]. Another cembranoid, trocheliolide B 280 from S. trocheliophorum was isolated [89]. Chemical determination of S. trocheliophorum organic extract, yielded pyrane-based diterpene, 9-Hydroxy-10,11-dehydro-sarcotrocheliol 281 [90].

From S. ehrenbergi eight cembranoids, sarcophytonoxides A–E 282–286 were identified. Sarcophytonoxide A 282, a cembrane diterpene with epoxide, dihydrofuran, acetyl group and three olefin bonds were confirmed by spectral data analysis while sarcophytonoxide D 285 was the deacetylated form of sarcophytonoxide C 284 which has a structure similar to sarcophytonoxide A 282. However, sarcophytonoxide C 283 differed in the chemical shift of C-19, C-6, C-7, and C-9 because of the 7,8-double bond configuration or chiral center of C-6. However, sarcophytonoxide E 286 differed in the position of acetyl group and the exocyclic double bond. [91]. From S. trocheliophorum a sarsolenane diterpene, secodihydrosarsolenone 287 was identified [92].

The chemical investigation of both diethyl ether and dichloromethane extracts of S. stellatum yielded the isolation of three cembranoid diterpenes and enantiomer, (+)-(1E,3E,11E)-7,8-epoxycembra-1,3,11,15-tetraene 288, (+)-(7R,8R,14S,1Z,3E,11E)-14-acetoxy-7,8-epoxycembra-1,3,11-triene 289 [93].

Five isoprenoids from S. glaucum, 3,4,8,16-tetra-epi-lobocrasol, 1,15β-epoxy-deoxysarcophine, 3,4-dihydro-4α,7β,8α-trihydroxy-∆²-sarcophine, ent-sarcophyolide E 290–293, together with, 3,4-dihydro-4α-hydroxy-∆²-sarcophine, 3,4-dihydro-4β-hydroxy-∆²-sarcophine 294 and 295 and klyflaccicembranol F 296 were reported and their structures were elucidated by spectral data. [70]. Moreover, five cembranoids, sarelengans C–G 297–301 from S. elegans were also stated. Isolates structures were established by spectral data, and absolute configuration of sarelengans D–F 298–300 were investigated through single crystal X-ray diffraction [94].

Isolation of seven diterpenes were reported from S. ehrenbergi and identified as sarcoehrenbergilids A–C 302–304 together with sinulolides A and B 305 and 306. The absolute configuration of sarcoehrenbergilid A 301 was investigated by scattering of CaKα radiation with the flack parameter [95]. Moreover, sarcoehrenbergilid D–F 307–309, diterpenes isolated from S. ehrenbergi were isolated and their absolute configurations were investigated by experimental and TDDFT-simulated ECD spectra. Sarcoehrenbergilid D 307 was found to differ from compound 301 only in stereochemistry [96]. Furthermore, five cembranes diterpenes, Sarcoehrenolides A–E 310–314 were isolated from S. ehrenbergi. Their chemical structures were determined through extensive spectral data. All isolates were related to ehrenbergol D 251 in structure, having an α,β-unsaturated-γlactone group at carbon-6 to carbon-19, however, they differ in migration of double bonds and/or oxidative configurations. Additionally, the absolute configuration of sarcoehrenolide A 310 was investigated by a single-crystal X-ray diffraction assay by Cu Kα radiation, and the absolute configurations of sarcoehrenolides B 311 and D 313 by TDDFT/ECD calculations [97].

From S. infundibuliforme two nitrogenous diterpenoids with unusual tricycle [6.3.1.01,5] dodecane skeleton named, sarinfacetamides A and B 315 and 316 and a known compound; nanolobatin B 317 were reported. Their structures were clarified by a thorough spectral data, TDDFT-ECD calculation and the absolute configuration of sarinfacetamide A 315 was investigated. The authors proposed a probable biosynthetic pathway for sarinfacetamides A and B 315 and 316, in which, the development of the carbon-12−carbon-4 bond together with epoxide ring opening of nanolobatin B 317 created an intermediary carbon cation molecule which reacted with the nitrogen lone pair electrons attacking carbon-9 followed by the opening of carbon-1/carbon-9 bond and generation of carbon-1/carbon-8 bond offering sarinfacetamides skeleton, of which acetylation of carbon -4/carbon -8 or carbon -4/carbon -8/carbon -16 yielded sarinfacetamides B 316 and A 315, respectively [98]. From genus sarcophyton, (1S,2E,4R,6E,8S,11S,12S)-11,12-epoxy-8-hydroperoxy-4-hydroxy-2,6-cembradiene 318 was reported. Its structure was fully determined through a complete spectroscopic analysis [99].

Sarcomililatols A, B and sarcomililate A 319–321, which possessed tricyclo [11.3.0.02,16] hexadecane skeleton, along with diterpenoids sarcophytol M 322, were isolated from S. mililatensis. Absolute configuration for sarcomililatol A 319 and sarcomililate A 321 were elucidated by combination of residual dipolar coupling-based NMR analysis, Snatzke’s assay and TDDFT-ECD calculation and anomalous X-ray diffraction with sarcomililatol A 319. The authors also proposed a biogenetic pathway relationship for sarcomililatols A, B and sarcomililate A 319–321. Based on structural resemblance between the three compounds, acetylation of sarcomililatol B 320 gave sarcomililatol A 319, and with dehydration under acid, isomerization and intramolecular [4 + 2] cycloaddition, sarcomililate A 321 was formed [100]. A pyrane-cembranoid diterpenes, 9-hydroxy-7,8dehydro-sarcotrocheliol and 8,9-expoy-sarcotrocheliol acetate 323 and 324 were isolated from S. trocheliophorum [101]. Figure 4 summarizes diterpenes isolated from Sacrophyton sp.

Figure 4. Diterpenes reported from Sarcophyton sp.

2.2. Biscembranes

Four biscembranes, bisglaucumlides A–D 325–328 were isolated from S. glaucum. Spectral data showed that bisglaucumlide A 325 possessed a biscembranoid skeleton. Bisglaucumlide B 326 was confirmed to be 32-acetylbisglaucumlide A by the positive Cotton effect in the CD spectrum. As for bisglaucumlide C 327 it was found to be the geometrical isomer of bisglaucumlide B 326 while considering the geometry of the C-4 olefin. Bisglaucumlide D 328 was an isomer to bisglaucumlide C 327, its absolute configuration indicated an anticlockwise relation among the enone chromopores revealing a negative Cotton effect CD spectrum [102]. Moreover, chemical investigation of S. glaucum extract yielded two biscembranes with an uncommon α, β-unsaturated ε-lactone, Glaucumolides A and B 329–330 [103].

Ximaolides A–G 331–337, seven biscembranoid, together with methyl tortuosoate A 338 where isolated from S. tortuosum. Their structures were elucidated through spectral analysis and Ximaolide A 331 and E 335 relative stereochemistry were investigated using X-ray diffraction method. The authors demonstrated that methyl tortuosoate A 338 could be the biogenetic precursor for all isolated metabolites since their upper parts were closely related to compound 338 [104].

A cembranolide diterpene identified as isosarcophytonolide D 339, an isomer to the previously isolated compound 41 from S. tortuosum, along with two biscembranes, bislatumlides A and B 340–341, were isolated from S. latum. A detailed spectral analysis revealed that the structure of bislatumlide B 341 matched that of bislatumlide A 340. However, ¹³C NMR data revealed a significant difference from compound 340 in the chemical shifts of carbon-19 and carbon-10 demonstrating the Z nature of Δ¹¹ olefin in compound 340. Thus, compound 340 was found to be the 11Z isomer of bislatumlide B 341. Interestingly the authors have proposed a biosynthetic pathway for bislatumlides A and B 340–341 in which isosarcophytonolide D 339 was found to be one of the precursors for bislatumlide A 340. Moreover, the authors investigated the effect of long-term storage in CDCl₃, where it showed isomerization of bislatumlide A 340 to bislatumlide B 341 at ∆¹¹ [105].

Methyl tetrahydrosarcoate and methyl tetrahydroisosarcoate 342 and 343, two cembranoids isolated from S. elegans, along with four biscembranoids, nyalolide, desacetylnyalolide, diepoxynyalolide, and dioxanyalolide 344–347. The authors proposed that diepoxynyalolide 346 could be a precursor for both compound nyalolide 344 and dioxanyalolide 347 [106].

Investigation on S. elegans extract led to the isolation of six biscembranoids identified as sarcophytolides G–L 348–353, together with biscembranoids, lobophytones H, Q, K, W, U 354–358. Isolates structure were determined by spectroscopic analysis. Absolute configuration of the compound sarcophytolide G 348 was determined using Mosher reaction [22,107]. From the methanol extract of S. pauciplicatum, sarcophytolides M and N 359 and 360, along with lobophytone O 361, were isolated [108].

Two biscembranoids, sarelengans A and B 362 and 363, were reported from S. elegans. Their chemical structures were investigated by spectral and chemical methods, and the absolute configuration of sarelengans A determined by single crystal X-ray diffraction. Sarelengans A and B 362 and 363 possessed a conjuncted trans-fused A/B-ring between two cembranoid entities. The authors mentioned that this structure feature led to an uncommon biosynthetic pathway including a cembranoid-∆⁸ instead of cembranoid-∆¹ unit in endo-Diels-Alder cycloaddition [94]. Figure 5 summarizes biscembranes isolated from Sacrophyton sp.

Figure 5. Biscembranes reported from Sarcophyton sp.

2.3. Sesquiterpenes

Investigation of the methylene chloride extract of S. acutangulum yielded tetracyclic terpenoid hydrocarbon (+)-alloaromadendrene 364 which showed similar spectral data as that of (−)-alloaromadendrene but with different optical rotation [R]D +25.8° (−)-alloaromadendrene and cyclosinularane 365 [109].

Two guaiane sesquiterpenes 4α-ethoxy-10α-hydroxyguai-6-ene and 10α-hydroxy-4α-methoxyguai-6-ene 366 and 367 were isolated from S. buitendijki and their structures were elucidated through 1 and 2D NMR [110]. One 1,2-dioxolane sesquiterpene alcohol named, dioxosarcoguaiacol 368, was isolated from S. glaucum [111].

Trocheliophorin 369 was isolated from S. trocheliophorum ethyl acetate extract. Through spectral data, its structure was elucidated, revealing that it could be the result of aromatization with dehydration of ring B of sarcophytin which co-exist in the extract, and removal of ring C and the ring junction methyl and breakage of ring A [112]. In addition, aromadendrene sesquiterpenoid, palustrol 370 from S. trocheliophorum was reported [77]. Moreover, sesquiterpene guajacophine 371 and 1,4-peroxymuurol-5-ene 372 from S. ehrenbergi were stated. [62]. Continuing the abovementioned isolation from S. glaucum sesquiterpenoid, 6-oxo-germacra-4(15),8,11-triene 373 was also reported [78]. Figure 6 summarizes sesquiterpenes isolated from Sacrophyton sp.

Figure 6. Sesquiterpenes reported from Sarcophyton sp.

2.4. Polyhydroxysterol and Steroids

One polyhydroxysetrol, 23,24-dimethylcholest-16(17)-E-en-3β,5α,6β,20(S)-tetraol 374, along with 24-methylcholestane-3β,5α,6β,25-tetraol-25-monoacetate 375 and gorosten-5(E)-3β-ol 376, were reported from S. trocheliophorum. Interpretation using 1 and 2D NMR analysis pointed out the existence of 23,24-dimethyl cholesterol derivatives which were further approved by the mass fragmentation pattern [29]. The isolation of (24S)-24methylcholestane-3β,5α,6β-triol 377 from S. crassocaule were also reported [28].

Sardisterol 378 was isolated from S. digitatun Moser. The carbon NMR matched that of (22R)-methylcholest-5-en-3β, 22,25,28-tetraol-3,22,28-triacetate 379 indicating that sardisterol 378 has the same steroidal nucleus as (22R) -methylcholest-5-en-3β, 22,25,28-tetraol-3,22,28-triacetate 378 but the OH groups in carbon 22 and 28 were replaced by acetoxy groups [113].

(24S)-24-methylcholestane-3β,5α,6β,25γ,26-pentol-25,26-diacetate 380 and (24S)-24-methylcholestane-3β,5α,6β,25γ,26-pentol-26-n-decanoate 381, was isolated from S. trocheliophorum, while, (24S)-24-methylcholestane-3β,5α,6β,25γ-tetrol 382 and (24S)-24- methylcholestane-3β,5α,6β,25γ pentol-25-monoacetate 383 were reported from S. glaucum [114].

Fourteen polyoxygenated steroids with 3β,5α,6β-hydroxy group, showing ergostane, cholestane, gorgostane and 23,24-dimethyl cholestane carbon skeletons were reported from Sarcophyton sp., 11α-acetoxy-cholesta-24-en-3β,5α,6β-triol 384, (22E,24S)-11α-acetoxy-ergostane-22,25-dien-3β,5α,6β-triol 385, (24S)-ergostane-1α,3β,5α,6β,11α-pentaol 386, (24S)-23,24-dimethylcholesta-22-en-3β,5α,6β,11α-tetraol 387, (23R,24R)-23,24-dimethylcholesta-17(20)-en-3β,5α,6β-triol 388, 11α-acetoxy-gorgostane-3β,5α,6β,12α-tetraol 389 and 12α-acetoxy-gorgostane-3β,5α,6β,11α-tetraol 390, sarcoaldosterol A 391, (24S)-ergostane-3β,5α,6β-triol 392, (24S)-ergostane-3β,5α,6β,11α-tetraol 393, (24S)-ergostane-7-en-3β,5α,6β-triol 394, 11α-acetoxy-gorgostane-3β,5α,6β-triol 395, sarcoaldosterol B 396 and gorgostane-1α,3β,5α,6β,11α-pentaol 397. Structural elucidation for all isolates were done based on spectral analysis and comparing with reported literature [115].

Six polyhydroxy steroids, (24S)-ergostan-3β,5α,6β,25-tetraol-25-monoacetate 398, (24S)-24-methylcholestan-3β,6β,25-triol-25-O-acetate 399, (24S)-methylcholestan-3β,5α,6β,25-tetraol-3,25-diacetate 400, (24S)-24-methylcholestan-1β,3β,5α,6β,25-pentaol-25-monoacetate 401 and (24S)-methylcholestan-3β,5α,6β,12β,25-pentaol-25-O-acetate 402, were reported from Sarcophyton sp., one was reported as 18-oxygenated polyhydroxy steroid, (24S)-ergostan-3β,5α,6β,18,25-pentaol 18,25-diacetate 403. The structure of this compound was determined through spectroscopic data, and its absolute configuration was elucidated by the modified Mosher’s assay [116].

Chemical investigation of the polar fraction of S. trocheliophorum, yielded two poly-hydroxy steroids, identified through extensive spectral analysis as zahramycins A and B 404 and 405. Zahramycin A 404 was characterized by the existence of oxirane ring at carbon-5 and carbon-6, while zahramycin B 405 possessed a keto-hydroxy sterol structure [117].

Ten polyhydroxylated steroids were isolated from Sarcophyton sp., (23R,24R,17Z)-11α-acetoxy-16β-methoxy-23,24-dimethylcholest-17(20)-en-3β,5α,6β-triol 406, (24R)-gorgost-25-en-3β,5α,6β,11α-tetraol 407 and 11α-acetoxycholest-24-en-1α,3β,5α,6β-tetraol 408, (24R)-methylcholest-7-en-3β,5α,6β-triol 409, 11α-acetoxy-cholest-24-en-3β,5α,6β-triol 410, (22E,24S)-11α-acetoxy-ergost-22,25-dien-3β,5α,6β-triol 411, (24S)-11α-acetoxy-ergost-3β,5α,6β-triol 412, (24R)-11α-acetoxy-gorgost-3β,5α,6β-triol 413, (24S)-ergost-3β,5α,6β,11α-tetraol 414, and (24S)-23,24-dimethylcholest-22-en-3β,5α,6β,11α-tetraol 415. Their structural elucidation was based on spectral data, and it was found that all isolated compounds have a distinguishable 3β,5α,6β-trihydroxy group; however, they differ in side chains and substitutions. These steroids could be alienated structurally into four categories including, cholesterol, ergosterol, gorgosterol and 23,24-dimethyl cholesterol. (23R,24R,17Z)-11α-acetoxy-16β-methoxy-23,24-dimethylcholest-17(20)-en-3β,5α,6β-triol 406 has a distinctive 17(20)-en-23,24-dimethyl side chain, while (24R)-gorgost-25-en-3β,5α,6β,11α-tetraol 407 was a gorgosterol having a 25-ene side chain [118].

Ethanol-soluble fraction of the acetone extract of S. trocheliophorum yielded 9,11-secosteroid named, 25(26)-dehydrosarcomilasterol 416 and three polyhydroxylated steroids, 7α- hydrocrassorosterol A 417, 11α-acetoxy-7α-Hydrocrassorosterol A 418, sarcomilasterol 419, 3β,6α,11-trihydroxy-9,11-seco-5α-cholest-7-ene-9-one 420 and 3β,6α,11-trihydroxy-24-methylene-9,11-seco-5α-cholest-7-ene-9-one 421. The 9,11-secostroids nucleus can be described as the chemotaxonomic indicators for genus Sarcophyton [119].

Beside the abovementioned isoprenoids obtained from S. glaucum, 16-deacetylhalicrasterol B 422, together with sarcoaldesterol B 396, sarglaucsterol 423 were isolated too and their structures were elucidated by spectral data [70]. Furthermore, from S. ehrenbergi the isolation of two formerly isolated hippurine 424 and 425 [120] alongside pregnenolone 426 were reported [121]. Figure 7 summarizes polyhydroxylated sterols isolated from Sacrophyton sp.

Figure 7. Polyhydroxylated sterols reported from Sarcophyton sp.

2.5. Miscellaneous

From S. trocheliophorum, tetradecyl octadecenoate 427, 2,3-dihydroxypropyloctadecyl ether 428 and tetradecyl-9-Z-octadecenoate 429 were identified [29]. In addition, purification of the total lipid extract of S. trocheliophorum provided four butenolides 430–433 with different chain substitutions and saturation together with three fatty acids, arachidonic acid, eicosapentaenoic and docosahexaenoic methyl esters 434–436 and prostaglandin PGB2 437 [122].

An infrequent prostaglandin was isolated from S. crassocaule, (5Z)-9,15-dioxoprosta-5,8(12)-dien-1-oate 438 based on spectral analysis. This was the first time to report a prostaglandin with a C-15 keto group from natural origin [123]. Furthermore, from the ethyl acetate and n-butanol fractions of S. crassocaule, two isolated metabolites identified as sarcophytonone 439 a tetra-substituted quinone, and sarcophytonamine 440 a quaternary amine were reported. It might be valuable to know that these quinone derivatives are scarce in marine organisms and only sarcophytonone 439 was identified in S. mayi [124].

Five compounds were isolated from S. infundibuliforme, three were reported O-glycosylglycerol known as sarcoglycosides A–C 441–443 and chimyl alcohol and hexadecanol 444 and 445. Sarcoglycoside A 441 was the first glycoglycerolipid to be isolated from soft coral, while sarcoglycosides B and C 442 and 443 were rare marine isolates, composed of a lyxose residue and chimyl alcohol moiety [125]. Moreover, one α-tocopheryl quinone derivative, 3,5,6-trimethyl-2-14S-3,11,14-trihydroxy-3,7,11,15-tetramethylhexadecylcyclohexa-2,5-diene-1,4-dione 446, was isolated [64].

Purification of ethyl acetate extract of S. ehrenbergi yielded ten prostaglandins, sarcoehrendin A−J 447–456 together with five correlated compounds 457–461. Sarcoehrendin A 447 was found to be the acetylated derivative of arachidonic acid ethyl; previously isolated from Lobophyton depressum [126,127]. Another six prostaglandins 462–467, were reported from S. ehrenbergi, three were reported to be of marine origin [121]. From S. ehrenbergi extract, 2-methyl-1-octanol ester of (E)-3-(4methoxyphenyl) propenoic acid 468 was reported. The authors mentioned that stereochemical structure of 2-methyl-1-octanol ester of (E)-3-(4methoxyphenyl) propenoic acid 468 was ensured via synthesis of two possible isomers (S)-1 and (R)-1 which was recognized by an asymmetric synthesis using 4-benzyl-2-oxazolidinone chiral auxiliaries from octanoic acid [128]. From S. ehrenbergi ceramide 469 was reported alongside two cerebrosides, sarcoehrenosides A and B 470 and 471. A detailed spectral analysis revealed the occurrence of an amide linkage, a long chain, and a sugar, dependable with the C-9 methyl cerebroside nature of sarcoehrenoside A 470 [129].

Three carotenoids, peridinin, peridininol and peridininol-5,8-furanoxide 472–474 were reported for the first time from S. elegans. Chemical structures were interpreted by using spectral data and reported data [130]. Additionally, from Sarcophyton sp. another carotenoid, all-trans-(9′Z,11′Z)-(3R,3′S,5′R,6′R)-pyrrhoxanthin 475 was isolated [76].

Methyl tortuoate A and methyl tortuoate B 476 and 477, two tetracyclic tetraterpenoids, together with methyl sartortuoate 478 and methyl isosartortuoate 479, were reported from S. tortuosum. Methyl tortuoate A 476 was similar to methyl sartortuoate 478 in structure, except for the presence of secondary hydroxyl group in methyl tortuoate A 476 and absence of one tertiary hydroxyl functional group and conjugated diene. As for, methyl tortuoate B 477, it was found to be similar to methyl isosartortuoate 479 in structure, but with no hydroxyl group at C-27 [131]. Tetraterpenoid, methyl tortuoate C 480 after further investigation of the same ethanolic extract of S. tortuosum was isolated and a full spectral data was done to investigate its structure [132]. Another tetracyclic tetraterpenoid; methyl tortuoate D 481, was also reported from S. tortuosum and was identified using direct infusion electrospray ionization mass spectrometry [133]. Figure 8 summarizes miscellaneous isolated from Sacrophyton sp.

Figure 8. Miscellaneous isolated from Sacrophyton sp.

3. Biological Activities

3.1. Cytotoxic Activity

The capability of 13- Acetoxysarcocrassolide 9 was investigated, as a cytotoxic agent against gastric carcinoma using MTT method, colony formation method, cell morphology assessments, and wound-healing method. It suppressed the development and migration of gastric cancer cells in a dose-dependent manner and initiated both early and late cell death examined by flow cytometer assay [134]. The authors mentioned that there was a relationship between the structure of sarcrassin A, B, D, and E 76, 77, 79, and 80, and emblide 81, and its activity, showing that loss of acetoxy group as in crassocolide C 84 led to loss of activity against all tested cell lines. While, acetylation at 4-OH position in crassocolide B 83 resulted in a decrease in activity cytotoxicity. However, the existence of two hydroxy moiety present at carbon-3 and carbon-4 and no oxidation at carbon-13 as in crassocolide D 85 showed potent activity against MCF-7 and A549 cell lines. While, crassocolide A 82 and F 87 exhibited potent activity toward Hep G2, MCF-7, MDA-MB-231 and A549, because of the 5-O-acetyl group [46]. Furthermore, crassocolide H and L 90 and 94, from S. crassocaule, showed strong activity toward KB, Hela, and Daoy cell lines owing to the presence of Cl atom at C-11 instead of OH group in crassocolide H 90 [47].

Sarcocrassocolides A–D 137–140, showed potent activity toward MCF-7, WiDr, HEp-2 and Daoy cell lines [58]. The authors maintained that the existence of acetoxy group at C-13 was important for activity. Sarcocrassocolides F–I 143–146, showed cytotoxicity toward all or part cell lines. However, sarcocrassocolide I 146 was most potent toward Daoy, HEp-2, MCF-7 and WiDr cell lines while sarcocrassocolide J and L 147 and 149 13-deacetoxy derivatives, were least potent against all tested cell lines with ED₅₀ = >20 μM. Furthermore, hydroxy moiety at carbon-8 improve the cytotoxic activity in contrast with carbon-8 hydroperoxy-bearing correspondents sarcocrassocolide F and H 143 and 145 were most potent toward MCF-7 [59].

Owing to the α,β-unsaturated ε-lactone ring in glaucumolides A and B 329 and 330 both exhibited strong cytotoxicity toward HL-60 and CCRF-CEM cell [103]. The authors specified that the less degrees of oxidation the more immunosuppressive activity, yalongene A 71 was the most potent even better than the positive control Cyclosporin A [100]. (24S)-24-methylcholestane-3β,5α,6β,25-tetrol-25-monoacetate 375 exhibited potent activity toward P-388, A549, and HT-29 cell lines [114]. The authors reported that there was a structure activity relationship in which the existence of an extra free hydroxyl group at C-20 position in 23,24-dimethylcholest-16(17)-E-ene-3β,5α,6β,20(S)-tetraol 374, and acetyl group at C-25 position in 24-methylcholestane-3β,5α,6β,25-tetraol 25-monoacetate 375 led to strong cytotoxicity toward human M14, HL60, and MCF7 cells with a dose-dependent manner [29]. The occurrence of OAc moiety at carbon-11 was important for cytotoxic activity, as in (23R,24R,17Z)-11α-acetoxy-16β-methoxy-23,24-dimethylcholest-17(20)-en-3β,5α,6β-triol 406, (22E,24S)-11α-acetoxy-ergost-22, 25-dien-3β,5α,6β-triol 411 and (24R)-11α-acetoxy-gorgost-3β,5α,6β-triol 413 showed a strong cytotoxicity toward K562, HL-60, HeLa cell lines, while, 11α-acetoxycholest-24-en-1α,3β,5α,6β-tetraol 408, 11α-acetoxy-cholest-24-en-3β,5α,6β-triol 410 and (24S)-11α-acetoxy-ergost-3β,5α,6β-triol 412 exhibited a potent activity toward K562 and HL-60 [118].

3.2. Anti-Inflammatory Activity

Sarcocrassocolide M 150 could be a leading anti-inflammatory. Sarcocrassocolides M–O 150–152 might be beneficial anti-inflammatory agents because of the structure relationship and the existence of β-hydroperoxy moiety at carbon-7 [60]. Sarcocrassocolides F–L 137–143 activity was attributed to the ring-opening of the α,β-unsaturated-β-ether ketone group leading to an increase in the enzyme inhibitory activity [58]. Sarcoehrenolide A, B, and D 310, 311, and 313 and ehrenbergol D 251 showed significant TNF-α inhibition in which sarcoehrenolide B 311 was most active due to the existence of acetoxy at carbon-18. A structure activity relationship was demonstrated in which the keto moiety at carbon-13 and hydroxyl group at carbon-18 could be responsible for the slight increase in activity. However, the presence of carbomethoxy moiety at carbon-18 led to a reduction in activity [97].

3.3. Antidiabetic Activity

Methyl sarcotroate B 173 has strong inhibitory activity toward PTP1B because of the hydroperoxide group which binds to the active site of the Cys residue [67]. Potency of sarcophytonolide N 50 and sarcrassin E 80 may be because of the existence of methyl ester moiety at carbon-18, which significantly increases the enzyme inhibitory activity toward human PTP1B enzyme [39].

3.4. Antimicrobial Activity

Sarcophytolide 32 showed a strong antibacterial activity toward methicillin-sensitive S. aureus Newman strain because of the diene at C-1/C-3 [41]. The crude extract exhibited antimicrobial activity toward most of the examined bacteria, yeasts, and fungi. [77]. Trocheliophols H, I, L, N, O, and R 231, 232, 235, 237, 238, and 241, 4-epi-sarcophytol L 243 showed antibacterial activity toward Xanthomonas vesicatoria, Agrobacterium tumefaciens, Pseudomonas lachrymans, Bacillus subtilis, and Staphylococcus aureus. The authors mentioned that the structure activity relationship and the existence of exomethylene group at C-8 add to the antibacterial activity, while H-3β orientation, which was present only in compound trocheliophol S 242, gave the most potent activity against the selected bacteria [81]. The toxicity of the novel γ-lactones compounds butenolides 430–433 were evaluated by using shrimp bioassay, and bioactivity was shown. Additionally, they showed activity against Gram-positive bacteria only [122].

Because of the structure activity relationship, 11α-acetoxy-cholesta-24-en-3β,5α,6β-triol 384, (22E,24S)-11α-acetoxy-ergostane-22,25-dien-3β,5α,6β-triol 385, 11α-acetoxy-gorgostane-3β,5α,6β,12α-tetraol 389, 12α-acetoxy-gorgostane-3β,5α,6β,11α-tetraol 390, and sarcoaldosterol A 391 were more potent toward antibacterial activity toward Escherichia coli and Bacillus megaterium, and antifungal activity toward Microbotryum violaceum and Septoria tritici fungi, because of the 11α-acetoxy group, cyclopropane side chain and terminal-double bond [115].

3.5. Miscellaneous

Anticonvulsant activity of ceramide 469, measured in vivo by the pentylenetetrazole (PTZ)-induced seizure assay, has successfully opposed the lethality of pentylenetetrazole in mice. It showed also a significant anxiolytic activity when used in the light–dark transition box. This could be caused possibly by GABA and serotonin receptors modulation [135]. Table 1 summarizes the main biological activities of secondary metabolites from genus Sacrophyton.

Table 1. The main biological activities of secondary metabolites isolated from genus Sacrophyton.

Compound Name (Number)	Soft Coral	Chemical Class	Biological Activities	Geographical Area of Collection
Crassolide 7	S. crassocaule	Diterpene	Potent cytotoxic activity against A549, HT-29, KB with IC50 range of 7.55 to 9.15 and most active against P-388 cell line with ED50 = 0.16 µg/mL [28].	Green Island, Taiwan
Sarcocrassolide A 8			Potent cytotoxic activity against A549, HT-29, KB with IC50 range of 4.29 to 8.35 and most active against P-388 cell line with ED50 = 0.14 µg/mL. Significantly decreased iNOS protein levels and COX-2 expression to 1.1 ± 0.9% and 3.9 ± 2.3%, respectively, could be a promising anti-inflammatory agent [32,58].	Green Island, Taiwan. Xisha Islands, South Sea, China. Dongsha coast, Taiwan
13-Acetoxysarcocrassolide 9			Potent cytotoxic activity against A549, HT-29, KB with IC50 range of 4.66 to 7.39 and most active against P-388 cell line with ED50 = 0.38 µg/mL and gastric carcinoma [32,58].	Green Island, Taiwan
Denticulatolide 10	S. crassocaule Sarcophyton sp.		Potent cytotoxic activity against A549, HT-29, KB with IC50 range of 5.78 to 6.46 and most active against P-388 cell line with ED50 = 0.15 µg/mL. Inhibited the colony formation of Chinese hamster V79 at ED50 = 3.6 µM, respectively and decreased the TNFα-production at 3.0–10.0 µM [28,54].	Green Island, Taiwan. Manado, North Sulawesi
Sarcophin 13	S. glaucum S. elegans S. mililatensis		Significantly decrease the viability of melanoma cells and does not show toxic effect on CV-1 cells and decrease de novo DNA synthesis and PARP activity. Exhibited cytotoxic activity toward A2780 cell line with IC50 > 10 μg/mL. Significant increase in ALP activity and collagen synthesis [75,136].	Xidao Island, Hainan, China Baycanh Island, Condao District, Baria-Vungtau province, Vietnam
Sarcophytol A 15	S. infundibuliforme		Strong antifouling activity toward the larval settlement of barnacle Balanus Amphitrite (EC50 = 2.25 µg/mL) [64].	Wenchang coral reef in the South China Sea
Sarcophytol A acetate 16			Strong antifouling activity toward the larval settlement of barnacle Balanus Amphitrite (EC50 = 1.75 µg/mL) [64].
13-Dehydroxysarcoglaucol 23	S. cherbonnieri	Diterpene	Potent cytotoxic activity against hepatocellular carcinoma, gastric adenocarcinoma, and breast adenocarcinoma cell lines against cell lines with IC50 = 6.6, 5.4, 1.7 μg/mL, respectively [33].	Ra-Ra Reef, Fiji Islands, and Stanley Reef, Australia
Sarcoglaucol-16-one 25	S. cherbonnieri S. ehrenbergi		Potent cytotoxic activity against hepatocellular carcinoma, gastric adenocarcinoma, and breast adenocarcinoma cell lines against cell lines with IC50 = 8.6, 7.1, 6.1 μg/mL, respectively [33].
Decaryiol 29	S. cherbonnieri		Potent cytotoxic activity against hepatocellular carcinoma, gastric adenocarcinoma, and breast adenocarcinoma cell lines against cell lines with IC50 = 2.0, 7.1, 0.19 μg/mL, respectively [33].
Sarcophytolide 32	S. glaucum S. trocheliophorum		Cytotoxic activity at 500 µM concentration toward mouse melanoma B16F10 cells. Good antidiabetic activity with IC50 = 15.4 µM. Strong antibacterial activity toward methicillin-sensitive S. aureus Newman strain with MIC = 125 µg/mL [40,41,68].	Red Sea. Yalong Bay, Hainan Province, China
(4Z,8S,9R,12E,14E)-9-Hydroxy-1-isopropyl-8,12-dimethyloxabicyclo [9.3.2]-hexadeca-4,12,14-trien-18-one 33	Sarcophyton new sp.		Potent cytotoxicity toward breast adenocarcinoma cell line IC50 = 6.5 μg/mL [35].	Stanley Reef and Great Barrier Reef, Australia
Sarcophytolol 35	S. glaucum		Potent activity against HepG2 with IC50 = 20 ± 0.032 µM [34].	North of Jeddah, Saudi Arabia, Red Sea
Sarcophytolide B 36			Potent toward MCF-7 with IC50 = 25.0 ± 0.160 µM [34].
Sarcophytolide C 37			Potent activity against HepG2 with IC50 = 20 ± 0.153 µM [34].
Sarcophytonolide J 47	S. infundibuliforme		Strong antifouling activity toward the larval settlement of barnacle Balanus Amphitrite (EC50 = 7.50 µg/mL) [64].	Wenchang Coral Reef in the South China Sea
Sarcophytonolide N 50	S. trocheliophorum		Strong antidiabetic activity with IC50 = 5.95 µM [39].	Yalong Bay, Hainan Province, China
Ketoemblide 55	S. elegans	Diterpene	Significant cytotoxicity toward breast cancer MDA-MB-231 migration in a time dependent manner. Mild antidiabetic activity with IC50 = 27.2 µM [18,39].	Xisha Islands, South China Sea. Yalong Bay, Hainan Province, China
Yalongene A 71	S. mililatensis		Most potent immunosuppressant with IC50 = 4.8 μM and selective index = 7.2. Strong cytoprotective activity on SH-SY5Y cell injury caused by hydrogen peroxide in vitro [42,100].	Xigu Island, Hainan Province, China
Sarcrassin A 76	S. crassocaule		Potent cytotoxic activity toward KB cell lines with IC50 = 19.0 µg/mL [44].	Bay of Sanya, Hainan Island, China. Yalong Bay, Hainan Province, China
Sarcrassin B 77			Potent cytotoxic activity toward KB cell lines with IC50 = 5.0 µg/mL [44].
Sarcrassin D 79			Potent cytotoxicity toward KB cell lines with IC50 = 4.0 µg/mL [44].
Sarcrassin E 80	S. crassocaule S. trocheliophorum		Potent cytotoxic activity toward KB cell lines with IC50 = 13.0 µg/mL. Strong antidiabetic activity with IC50 = 6.33 µM [39].
Emblide 81	S. crassocaule S. tortuosum		Potent cytotoxic activity toward KB cell lines with IC50 = 5.0 µg/mL. Mild inhibition of the elastase release 29.2 ± 6.1% [44,74].	Sanya Bay, Hainan Island, China. Lanyu Island Coast, Taiwan
Crassocolide A 82	S. crassocaule		Potent cytotoxic activity toward Hep G2, MCF-7, MDA-MB-231, A549 DLD-1, and CCRF-CEM cell lines (IC50 = 3.1, 8.9, 8.6, and 11.9 µg/mL, 5.7 and 6.3 µM, respectively). Strongly decreased iNOS protein levels and COX-2 expression to 3.5% ± 0.9% and 59.4% ± 21.4%, respectively [46,61].	Kenting Coast, Taiwan. Dongsha Coast, Taiwan
Crassocolide B 83			Decrease cytotoxic activity against Liver, breast, lung, DLD-1, CCRF-CEM, and HL-60 cancer cells (IC50 = 13.1, 10.3, 12.1 11.9 µg/mL, 28.1, 8.7 and 11.1 µM, respectively). Strongly decreased iNOS protein levels to 3.2% ± 0.7% [46,61].
Crassocolide D 85	S. crassocaule	Diterpene	Potent cytotoxic activity toward MCF-7, A549, and DLD-1 cell lines with IC50 = 15.3, 12.5 µg/mL and 27.7 µM, respectively. Strongly decreased iNOS protein levels to 3.2% ± 0.6% [46,61].	Kenting Coast, Taiwan. Dongsha Coast, Taiwan
Crassocolide E 86			Potent cytotoxicity toward DLD-1, CCRF-CEM, and HL-60 cancer cells with IC50 = 8.7, 7.3, and 8.4 µM, respectively. Strongly decreased iNOS protein and COX-2 expression levels to 1.4% ± 0.4% and 32.0% ± 15.3%, respectively [46,61].	Dongsha Coast, Taiwan
Crassocolide F 87			Potent cytotoxic activity toward Hep G2, MCF-7, MDA-MB-231, and A549 with IC50 = 2.1, 7.4, 8.8, and 3.2 µg/mL, respectively [46].	Kenting Coast, Taiwan
Crassocolide H 90			Strong cytotoxic activity toward KB, Hela, and Daoy cell lines with IC50 = 5.3, 14.9, and 3.8 20 µg/mL, respectively [47].
Crassocolide I 91			Potent cytotoxic activity toward Daoy cell line with IC50 = 0.8 µg/mL [47].
Crassocolide J 92			Potent cytotoxic activity toward Daoy cell line with IC50 = 2.8 µg/mL [47].
Crassocolide K 93			Potent cytotoxic activity toward Daoy cell line with IC50 = 2.5 µg/mL [47].
Crassocolide L 94			Strong cytotoxic activity toward KB, Hela, and Daoy cell lines with IC50 = 12.2, 8.0, and 4.1 µg/mL [47].
Crassocolide M 95			Potent cytotoxic activity toward Daoy cell line with IC50 = 1.1 µg/mL [47].
Crassocolide N 96			Potent cytotoxic activity against KB, HeLa, and Daoy cells (IC50 = 4.7, 4.7, and 2.8 µg/mL, respectively) [47].	Dongsha Atoll, Taiwan
Crassocolide O 97			Potent cytotoxicity against Daoy cells IC50 = 4.5 µg/mL [47].
Crassocolide P 98	S. crassocaule	Diterpene	Potent and selective cytotoxicity against Daoy cells growth IC50 = 1.9 µg/mL [47].	Dongsha Atoll, Taiwan
Sarcostolide A 102	S. stolidotum		Potent cytotoxic activity toward HeLa and WiDr cell lines with IC50 = 22.26 and 19.97 μg/mL, respectively [50].	Kenting, off the southern coast, Taiwan
Sarcostolide B 103			Potent cytotoxic activity toward WiDr with IC50 = 8.31 μg/mL and HeLa and cell lines with IC50 = 5.88 μg/mL [50].
Sarcostolide C 104			Most potent cytotoxic activity toward HeLa cell lines with IC50 = 1.65 μg/mL and WiDr with IC50 = 19.35 μg/mL [50].
Sarcostolide D 105			Potent cytotoxic activity toward HeLa and WiDr cell lines with IC50 = 11.05 and 29.09 μg/mL, respectively [50].
Sarcostolide E 106			Potent cytotoxic activity toward HeLa and WiDr cell lines with IC50 = 16.75 and 27.48μg/mL, respectively, and Daoy with IC50 = 5.5 μg/mL [50].
Sarcostolide F 107			Potent cytotoxic activity toward HeLa and WiDr cell lines with IC50 = 7.32 and 28.84 μg/mL, respectively [50].
Sarcostolide G 108			Potent cytotoxic activity toward HeLa and WiDr cell lines with IC50 = 18.45 and 20.06 μg/mL, respectively [50].
(-)-7β-Hydroxy-8α-methoxy-deepoxy-sarcophytoxide 110	S. mililatensis		Significant increase in the ALP activity collagen synthesis [51].	Baycanh Island, Condao District, Baria-Vungtau Province, Vietnam
(+)-7β,8β-Dihydroxy-deepoxy-sarcophytoxide 111
(-)-17-Hydroxysarcophytonin A 112
Sarcophytol V 113
Sarcophytoxide 114	S. mililatensis S. glaucum Sarcophyton sp. S. trocheliophorum	Diterpene	Significant increase in the ALP activity collagen synthesis. Strong activity toward MCF-7 and HCT116 cells with IC50 = 9.9 ± 0.03 and 25.8 ± 0.03 µM, respectively. Activity toward Hep G2, Hep 3B, MDA-MB-231, A549, and Ca9-22 cell lines with IC50 = 16.2, 12.4, 13.2, 15.3, and 18.9 µg/mL, respectively [51,55,78].	Baycanh Island, Condao District, Baria-Vungtau Province, Vietnam. Red Sea, Jeddah, Saudi Arabia
7β-Acetoxy-8α-hydroxydeepoxy-sarcophine 116	S. glaucum		Potent cytotoxicity toward HepG2, HCT-116, and HeLa cells with IC50 = 3.6, 2.3, and 6.7 μg/mL, respectively [65].	Hurghada, Red Sea, Egypt
7α,8β-Dihydroxydeepoxysarcophine 117	S. elegans S. auritum S. glaucum		Cytotoxic activity toward A2780 cell line with IC50 > 10 μg/mL and against both breast and liver cancer cell lines with IC50 = 18.4 ± 0.16, 11 ± 0.22 µg/mL, respectively. Significantly decrease the viability of melanoma cells at 500 (72 hr) treatment., does not show toxic effect CV-1 cells and decrease de novo DNA synthesis and PARP activity [75,136].	Xidao Island, Hainan, China. Xidao Island, Hainan, China. Safaga Red Sea, Egypt
Ent-sarcophine 122	S. glaucum		Potent suppression of the phase I enzyme cytochrome P450 1A activity with IC50 = 3.4 µM [66].	Yalong Bay, Hainan Province, China
Lobohedleolide 125	Sarcophyton sp.		Most potent, inhibited the colony formation of Chinese hamster V79 at ED50 = 4.6 µM and decreased the TNFα-production at 3.0–10.0 µM [54].	Manado, North Sulawesi
(7Z)- Lobohedleolide 126			Most potent, inhibited the colony formation of Chinese hamster V79 at ED50 = 4.6 µM and decreased the TNFα-production at 3.0–10.0 µM [54].
7-Acetyl-8-epi- sinumaximol G 131	S. ehrenbergi		Cytotoxic activity against MCF-7 with IC50 range 22.39 to 27.12 µg/mL [56].	Hurghada, Red Sea, Egypt
8-Epi- sinumaximol G 132
12-Acetyl-7, 12-epi- sinumaximol G 133
12-Hydroxysarcoph-10-ene 134
8-Hydroxy-epi-sarcophinone 135
Sinumaximol G 136
Sarcocrassocolide A 137	S. crassocaule	Diterpene	Potent cytotoxic activity toward MCF-7, WiDr, HEp-2, and Daoy cancer with IC50 = 4.2, 3.2, 2.0, and 4.1 µg/mL, respectively. Decreased the levels of iNOS protein to 13.7 ± 5.2% at a concentration of 10 µM [58].	Dongsha Coast, Taiwan
Sarcocrassocolide B 138			Potent cytotoxic activity toward MCF-7, WiDr, HEp-2, and Daoy cancer with IC50 = 4.2, 3.2, 1.2, and 1.8 µg/mL, respectively. Significantly decreased the levels of iNOS protein to 3.3 ± 5.0% at a concentration of 10 µM [58].
Sarcocrassocolide C 139			Potent cytotoxic activity toward MCF-7, WiDr, HEp-2, and Daoy cancer with IC50 = 6.2, 4.5, 2.6, and 4.0 µg/mL, respectively. Decrease significantly iNOS protein levels to 4.6 ± 1.3% at a concentration of 10 µM [58].
Sarcocrassocolide D 140			Potent cytotoxic activity toward MCF-7, WiDr, HEp-2, and Daoy cancer with IC50 = 8.8, 5.6, 3.2, and 5.4 µg/mL, respectively. Decrease significantly iNOS protein levels to 7.0 ± 3.1% at a concentration of 10 µM [58].
Sarcocrassocolide F 143			Potent toward MCF-7 cells with ED50 = 19.4 ± 2.4 μM. Decreased iNOS protein levels [59].
Sarcocrassocolide G 144			Potent toward Daoy, HEp-2 and WiDr cells with ED50 = 8.3 ± 1.4, 16.5 ± 1.7 and 18.9 ± 1.9 μM, respectively. Decreased iNOS protein levels [59].
Sarcocrassocolide H 145			Most potent toward MCF-7 ED50 = 9.4 ± 2.5 μM. Significantly suppressed both iNOS and COX-2 proteins expression [59].
Sarcocrassocolide I 146			Most potent toward Daoy, HEp-2, MCF-7, and WiDr cell lines with ED50 = 5.1 ± 1.2, 5.8 ± 0.5, 8.4 ± 1.5, and 6.4 ± 2.0 μM. Decreased iNOS protein levels [59].
Sarcocrassocolide J 147			Least potent toward Daoy, HEp-2, MCF-7, and WiDr cell lines with ED50 = >20 μM. Decreased iNOS protein levels [59].
Sarcocrassocolide L 149	S. crassocaule	Diterpene	Least potent toward Daoy, HEp-2, MCF-7, and WiDr cell lines with ED50 = >20 μM. Reduced iNOS protein levels [59].	Dongsha Coast, Taiwan
Sarcocrassocolide M 150			Potent cytotoxicity toward Daoy, HEp-2, MCF-7, and WiDr with IC50 = 6.6 ± 0.8, 5.2 ± 0.6, and 5.0 ± 0.7 μM, respectively. Significantly decreased iNOS protein levels and COX-2 expression to 4.2 ± 1.6% and 62.8 ± 22.4%, respectively [60].
Sarcocrassocolide N 151			Potent cytotoxicity toward Daoy, HEp-2, MCF-7, and WiDr with IC50 = 10.4 ±1.1, 12.3 ± 1.6, and 12.4 ± 2.1 μM, respectively. Significantly decreased iNOS protein levels to 52.9 ± 12.8% [60].
Sarcocrassocolide O 152			Potent cytotoxicity toward Daoy, HEp-2, MCF-7, and WiDr with IC50 = 10.6 ± 0.5, 10.1 ± 2.3, and 6.4 ± 0.5 μM, respectively. Significantly decreased the levels of iNOS protein to 22.7 ± 2.8% [60].
Sarcocrassocolide P 153			Potent cytotoxic against DLD-1 and HL-6 (IC50 = 21.8 and 24.9 µM, respectively. Strongly reduced iNOS protein levels with 1.3% ± 0.3% [61].
Sarcocrassocolide Q 154			Potent cytotoxic toward only HL-6 (IC50 = 18.6 µM). Decreased iNOS protein levels and COX-2 expression with 2.4% ± 0.4% and 58.3% ± 20.5, respectively [61].
Sarcocrassocolide R 155			Potent cytotoxicity toward DLD-1, CCRF-CEM, and HL-60 cancer cells (IC50 = 10.0, 3.8, and 7.9 µM, respectively). Strongly reduced iNOS protein levels to 1.2% ± 0.3% [61].
(+)-12-Carboxy-11Z-sarcophytoxide 157	S. ehrenbergi		Antiviral activity toward HCMV with IC50 = 180.7 µM [63].
(+)-12-Methoxycarbonyl-11Z-sarcophine 158	S. ehrenbergi	Diterpene	Antiviral activity toward HCMV with IC50 = 5.8, 24.2, 24.8, 4.7, and 16.1 µM, respectively [63].	Dongsha Atoll off Taiwan
Ehrenberoxide A 159
Ehrenberoxide B 160
Ehrenberoxide C 161
Lobophynin C 162
Cembrene C 163	S. trocheliophorum		Mild antidiabetic activity with IC50 = 26.6 µM. Antifungal activity toward Aspergillus flavus and Candida albicans (MIC = 0.68 µM) [39,77].	Yalong Bay, Hainan Province, China. Red Sea, Jeddah, Saudi Arabia
Sarcophytol B 164	Sarcophyton sp.		Potent antibacterial activity toward Bacillus cereus, Staphylococcus albus, and Vibrio parahaemolyticus (MIC = 3.13, 1.56, and 0.50 μM, respectively) [73].	Xuwen Coral Reef Area, Guangdong Province, China
Sarcophytol H 166	S. infundibuliforme		Strong antifouling activity toward the larval settlement of barnacle Balanus Amphitrite (EC50 = 8.13 µg/mL) [64].	Wenchang Coral Reef in the South China Sea
(–)-Marasol 167	S. infundibuliforme S. glaucum		Antifouling activity on larval adherence of the barnacle Balanus Amphitrite at concentration of 10.0 µg/mL [73].	Xuwen Coral Reef, Guangdong Province, China
12(S)-Hydroperoxylsarcoph-10-ene 170	S. glaucum		Potent suppression of the phase I enzyme cytochrome P450 1A activity with IC50 = 2.7 µM [66].	Yalong Bay, Hainan Province, China
8-Epi-sarcophinone 171			Potent suppression of the phase I enzyme cytochrome P450 1A activity with IC50 = 3.7 µM [66].
Methyl sarcotroate B 173	S. trocheliophorum		Strong inhibitory activity toward PTP1B with IC50 = 6.97 μM [67].
(1S,2E,4R,6E,8S,11R,12S)-8,11-Epoxy-4,12-epoxy-2,6-cembradiene 175	S. glaucum		Cytotoxic activity at 500 µM concentration toward mouse melanoma B16F10 cells [68].	Red Sea
(1S,4R,13S)-Cembra-2E,7E,11E-trien-4,13-diol 177
Ehrenbergol B 179	S. ehrenbergi		Strong antiviral activity with IC50 = 5 µg/mL [69].	San-Hsian-Tai, Taitong County, Taiwan
Sarcophyolide B 181	S. elegans	Diterpene	Most potent cytotoxic activity toward A2780 with IC50 = 2.92 μM [22].	Xidao Island, Hainan, China
Sarcophyolide C 182			Cytotoxic activity toward A2780 cell line with IC50 > 10 μg/mL [22].
Sarcophyolide D 183
Sarcophyolide E 184
Sarcophytol L 185
13α-Hydroxysarcophytol L 186
Sarcophyolide A 187
Sarcophinone 188
7α-Hydroxy-Δ8(19)-deepoxysarcophine 189
4β-Hydroxy-Δ2(3)-sarcophine 190
1,15β-Epoxy-2-epi-16-deoxysarcophine 191
Sarcophytol Q 192
Lobocrasol 193			Most potent cytotoxic activity toward A2780 cell line with IC50 = 3.37 μM [22].
Acetyl ehrenberoxide B 194	S. ehrenbergi		Antiviral activity toward HCMV with IC50 = 8 µg/mL [72].	San-Hsian-Tai, Taitong County, Taiwan
Ehrenbergol C 195			Antiviral activity toward HCMV with IC50 = 20 µg/mL [72].
Tortuosene A 201	S. tortuosum		Potent inhibition 56.0 ± 3.1% against FMLP/CB-induced superoxide anion generation [74].	Lanyu Coast Island of Taiwan
Tortuosene B 202			Mild inhibition of the elastase release 13.7 ± 3.5 [74].
Sarcotrocheliol acetate 213	S. glaucum S. trocheliophorum		Strong activity against HepG2 and MCF-7 cells with IC50 = 19.9 ± 0.02 and 2.4 ± 0.04 µM, respectively. Strong antibacterial activity with inhibition zones range (12 to 18 mm) and MICs between 1.53 to 4.34 µM, toward Staphylococcus aureus, Acinetobacter sp., and MRSA [77,78].	Red Sea, Jeddah, Saudi Arabia
Sarcotrocheliol 214	S. glaucum	Diterpene	Strong antibacterial activity with inhibition zones range from 12 to 18 mm and MICs between 1.53 and 4.34 µM, toward Staphylococcus aureus, Acinetobacter sp., and MRSA. Strong activity toward MCF-7 cells with IC50 = 3.2 ± 0.02 µM, respectively [77,78].	Red Sea, Jeddah, Saudi Arabia
Sarcophinediol 215			Strong activity against HepG2 and HCT116 with IC50 = 18.8 ± 0.07 and 19.4 ± 0.02 µM, respectively [78].
2-[(E,E,E)-7′,8′-Epoxy-4′,8′,12′- trimethylcyclotetradeca-1′,3′,11′-trienyl]propan-2-ol 209	Sarcophyton sp.		Mild inhibition more than 10% at a concentration of 20 μM toward the MCF-7 cell line [76].	Dongshan island, China
Crassumol C 211
Laevigatol A 212
Sarsolilide B 220	S. trocheliophorum		Inhibited protein tyrosine phosphatase 1B IC50 = 6.8 ± 0.9 μM [80].	Yalong Bay, Hainan Province, China
Sarsolilide C 221			Inhibited protein tyrosine phosphatase 1B IC50 = 27.1 ± 2.6 μM [81].
Trocheliophol E 228			Mild inhibition toward inflammation-related NF-kB by 11% [81].	Weizhou Island, Southwestern China
Trocheliophol F 229			Mild inhibition toward inflammation-related NF-kB by 29% [81].
Trocheliophol H 231			Antibacterial activity toward Xanthomonas vesicatoria, Agrobacterium tumefaciens, Pseudomonas lachrymans, Bacillus subtilis, and Staphylococcus aureus, with MIC = 8 to 32 µg/mL [81].
Trocheliophol I 232
Trocheliophol L 235			Antibacterial activity toward Xanthomonas vesicatoria, Agrobacterium tumefaciens, Pseudomonas lachrymans, Bacillus subtilis, and Staphylococcus aureus, with MIC = 8 to 32 µg/mL [81].
Trocheliophol M 236			Mild inhibition toward inflammation-related NF-kB by 14% [81].
Trocheliophol N 237			Antibacterial activity toward Xanthomonas vesicatoria, Agrobacterium tumefaciens, Pseudomonas lachrymans, Bacillus subtilis, and Staphylococcus aureus, with MIC = 8 to 32 µg/mL [81].
Trocheliophol O 238	S. trocheliophorum	Diterpene	Antibacterial activity toward Xanthomonas vesicatoria, Agrobacterium tumefaciens, Pseudomonas lachrymans, Bacillus subtilis, and Staphylococcus aureus, with MIC = 8 to 32 µg/mL [81].	Weizhou Island, Southwestern China
Trocheliophol R 241
Trocheliophol S 242			Most potent antibacterial activity against Xanthomonas vesicatoria, Agrobacterium tumefaciens, Pseudomonas lachrymans, Bacillus subtilis, and Staphylococcus aureus [81].
4-Epi-sarcophytol L 243			Antibacterial activity toward Xanthomonas vesicatoria, Agrobacterium tumefaciens, Pseudomonas lachrymans, Bacillus subtilis, and Staphylococcus aureus, with MIC = 8 to 32 µg/mL [81].
Sarcophelegan B 245	S. elegans		Significant cytotoxicity toward breast cancer MDA-MB-231 migration in a time dependent manner [18].	Xisha Islands, South China Sea
Ehrenbergol D 251	S. ehrenbergi		Potent cytotoxic activity P-388 cell line with EC50 = 2.0 μM. Significant TNF-α inhibition IC50 = 24.2 μM [82,97].	San-Hsian-Tai Island (Taitong)
Ehrenbergol E 252			Potent cytotoxic activity P-388 cell line with EC50 = 3.0 μM [82].
Secodihydrosarsolenone 287	S. trocheliophorum		Restrained activity toward PTP1B with IC50 = 13.7 µmol/L [92].	The South China Sea Coral Reef
Sarelengan C 297	S. elegans		Significant inhibitory action on nitric oxide synthesis in RAW264.7 macrophages, with IC50 = 32.5 µM [94].	Yalong Bay, Hainan Province, China
Sarcoehrenbergilid D 307	S. ehrenbergi		Strong cytotoxicity against A549 cells with IC25 = 23.3 μM [96].	Hurghada, Red Sea, Egypt
Sarcoehrenbergilid E 308			Strong cytotoxicity activity against A549 and HepG2 cells with IC25 = 27.3 and 22.6 μM, respectively [96].
Sarcoehrenbergilid F 309			Strong cytotoxic activity against A549 cells with IC25 = 25.4 μM [96].
Sarcoehrenolide A 310			Significant TNF-α inhibition IC50 = 28.5 μM [97].	Weizhou Island, Guangxi Province, China
Sarcoehrenolide B 311			Significant TNF-α inhibition IC50 = 8.5 μM [97].
Sarcoehrenolide D 313			Significant TNF-α inhibition IC50 = 27.3 μM [97].
Sarinfacetamide A 315	S. infundibuliforme	Diterpene	Increase effects of the ConA-induced T lymphocytes with 6.18% and 36.32% proliferation rates, respectively [98].	Ximao Island, Hainan Province, China
Nanolobatin B 317
(1S,2E,4R,6E,8S,11S,12S)-11,12-Epoxy-8-hydroperoxy-4-hydroxy-2,6-cembradiene 318	Sarcophyton sp.		Potent antibacterial activity toward pathogens as Alteromonas sp., Cytophaga-Flavobacterium, and Vibrio sp. from seaweed, with antibiosis index = 0.5, 1.25, and 1.75, respectively [99].	Bohey Dulang, Semporna, Sabah
Glaucumolides A and B 329–330	S. glaucum	Biscembrane	Potent cytotoxicity toward HL-60 and CCRF-CEM cancer cell lines with IC50 = 6.6 ± 1.2, 3.8 ± 0.9, 5.3 ± 1.4, and 7.4 ± 1.5μg/mL, respectively. Strong inhibition against superoxide anion generation with IC50 = 2.79 ± 0.66 μM and 2.79 ± 0.32 μM, respectively, and elastase release with IC50 = 3.97 ± 0.10 μM for both compounds and in vitro anti-inflammatory activity both significantly prevent the accumulation nitric oxide synthase protein [103].	From the wild and cultured in cultivation tank in the National Museum of Marine Biology and Aquarium, Taiwan
Bislatumlide A and B 340–341	S. latum		Potent activity against A549 and WiDr tumor cell with IC50 = 7 µg/mL and murine lymphocytic leukemia with IC50 = of 5.8 µg/mL [105].	Ximao Island, Hainan Province, China
Methyl tetrahydrosarcoate 342	S. elegans		Lethality bioassay exhibited IC50 = 1.5 μM [106].	Kitangambwe, Kenya
Dioxanyalolide 347			Antimicrobial activity toward Escherichia coli. Lethality bioassay exhibited IC50 = 1.5 μM [106].
Sarelengan B 363			Significant inhibitory action on nitric oxide synthesis in RAW264.7 macrophages, with IC50 = 18.2 µM [94].	Yalong Bay, Hainan Province, China
(+)-alloaromadendrene 364	S. glaucum	Sesquiterpene	Most potent with IC50 = 20.0 ± 0.068, 20.0 ± 0.054, and 09.3 ± 0.164 µM toward HepG2, MCF-7, and PC-3, respectively. Significant inhibition to +SA mammary epithelial cell growth [34].	North of Jeddah, Saudi Arabia, Red sea
Palustrol 370	S. trocheliophorum		Potent activity toward Lymphoma and Erlish cell lines with LD50 range from 2.5 to 3.79 µM [77].	Red Sea, Jeddah, Saudi Arabia
6-Oxo-germacra-4(15),8,11-triene 373	S. glaucum		Strong activity against HCT116 with IC50 = 25.8 ± 0.03 µM [78].
23,24-Dimethylcholest-16(17)-E-ene-3β,5α,6β,20(S)-tetraol 374	S. trocheliophorum	Sterol	Strong cytotoxicity toward human M14, HL60, and MCF7 cells (EC50 = 4.3, 2.8, and 4.9 µg/mL, respectively), with a dose-dependent manner [29].	Pulau Hantu Island, South Singapore
24-Methylcholestane-3β,5α,6β,25-tetraol-25-monoacetate 375	S. crassocaule S. glaucum S. trocheliophorum		Potent activity toward the P-388, A549, and HT-29 cell lines with cell line with ED50 = 3.96, 6.6, and 0.6 µg/mL, respectively. Strong cytotoxicity against M14, HL60, and MCF7 cells with EC50 = 19.6, 13.2, and 34.5 µg/mL, respectively, with a dose-dependent manner [28].	Green Island, off Taiwan. Pulau Hantu Island, South Singapore
(24S)-24-Methylcholestane-3β,5α,6β-triol 377	S. crassocaule		Potent activity toward the P-388 cell line with ED50 = 0.14 µg/mL, respectively [28].	Green Island, off Taiwan
Sardisterol 378	S. ehrenbergi		Potent activity against A-549 cell line with IC50 = 27.3 μM [95].	Hurghada, Red Sea, Egypt
11α-Acetoxy-cholesta-24-en-3β,5α,6β-triol 384	Sarcophyton sp.		Potent toward antibacterial activity toward Escherichia coli and and Bacillus megaterium, and antifungal activity toward Microbotryum violaceum and Septoria tritici fungi [115].	The coast of Weizhou Island, Guangxi Province of China
(22E,24S)-11α-Acetoxy-ergostane-22,25-dien-3β,5α,6β-triol 385
11α-Acetoxy-gorgostane-3β,5α,6β,12α-tetraol 389
12α-Acetoxy-gorgostane-3β,5α,6β,11α-tetraol 390
Sarcoaldosterol A 391
Sarcoaldesterol B 396	S. glaucum		Cytotoxicity toward HepG2, MDA-MB-231, and A-549 cell lines with IC50 = 9.7, 14.0, and 15.8 µg/mL, respectively [70].	Jihui Fishing Port Coast, Taitung county, Taiwan
(24S)-Ergostan-3β,5α,6β,25-tetraol 25-monoacetate 398	Sarcophyton sp.		Potent cytotoxic toward K562 with IC50 = 12.30 µg/mL [116].	Xuwen Coral Reef, South China Sea
(24S)-24-methylcholestan-3β,6β,25-triol-25-O-acetate 399			Potent activity toward Staphylococcus albus with MIC = 20 µg/mL [116].
(24S)-24-Methylcholestan-1β,3β,5α,6β,25-pentaol-25-monoacetate 401			Potent cytotoxicity toward K562 with IC50 = 4.95 µg/mL. Potent activity toward Staphylococcus albus with MIC = 20 µg/mL [116].
(24S)-Methylcholestan-3β,5α,6β,12β,25-pentaol-25-O-acetate 402	Sarcophyton sp.	Sterol	Potent cytotoxic toward K562 with IC50 = 4.10 µg/mL [116].	Xuwen Coral Reef, South China Sea
(24S)-Ergostan-3β,5α,6β,18,25-pentaol 18,25-diacetate 403			Potent cytotoxic toward K562 with IC50 = 5.25 µg/mL [116].
Zahramycin B 405	S. trocheliophorum		Potent antimicrobial (15 mm) and (12 mm) activity toward Staphylococcus aureus and Bacillus subtilis, respectively, and potent activity toward Pythium ultimum pathogenic fungus (12 mm) [117].	Hurghada, Red Sea, Egypt
(23R,24R,17Z)-11α-Acetoxy-16β-methoxy-23,24-dimethylcholest-17(20)-en-3β,5α,6β-triol 406	Sarcophyton sp.		Strong cytotoxic activity against K562, HL-60, and HeLa cell lines with IC50 range of 6.4 to 24.7 μM [118].	South Sea, Weizhou Islands
11α-Acetoxycholest-24-en-1α,3β,5α,6β-tetraol 408			Potent activity toward K562 and HL-60 with IC50 range of 9.1 to 17.2 μM [118].
(24R)-Methylcholest-7-en-3β,5α,6β-triol 409			Potent anti-H1N1 virus activity with IC50 = 19.6 μg/mL [118].
11α-Acetoxy-cholest-24-en-3β,5α,6β-triol 410			Potent activity toward K562 and HL-60 with IC50 range of 9.1 to 17.2 μM [118].
(22E,24S)-11α-Acetoxy-ergost-22, 25-dien-3β,5α,6β-triol 411			Strong cytotoxicity against, K562, HL-60, HeLa cell lines with IC50 range of 6.4 to 24.7 μM [118].
(24S)-11α-Acetoxy-ergost-3β,5α,6β-triol 412			Potent activity toward K562 and HL-60 with IC50 range of 9.1 to 17.2 μM [118].
(24R)-11α-Acetoxy-gorgost-3β,5α,6β-triol 413			Strong cytotoxicity toward, K562, HL-60, HeLa cell lines with IC50 range of 6.4 to 24.7 μM [118].
(24S)-Ergost-3β,5α,6β,11α-tetraol 414			Potent anti-H1N1 virus activity with IC50 = 36.7 μg/mL [118].
Sarcomilasterol 419	S. glaucum		Cytotoxicity toward MDA-MB-231, MOLT-4, SUP-T, and U-937 cell lines with IC50 = 13.8, 6.7, 10.5, and 17.7 µg/mL, respectively [70].	Jihui Fishing Port Coast, Taitung County, Taiwan
Butenolides 430–433	S. trocheliophorum	Miscellaneous	Active against gram positive bacteria only [122].	Gulf of Aqaba, Tel Aviv
Sarcophytonamine 440	S. crassocaule		Protection against UV radiation for organism [124].	Lingshui Bay, Hainan Province, China
Ceramide 469	S. ehrenbergi S. auritum	Miscellaneous	Decreased iNOs to 46.9 ± 9.7% and COX-2 level to 77.2 ± 9.9%. Anticonvulsant activity, successfully opposed the lethality of pentylenetetrazole in mice. Significant anxiolytic activity [129,135].	Dongsha Islands, Taiwan Red Sea
Methyl tortuoate A 476	S. tortuosum		Strong cytotoxic activity toward CNE-2 and P-388 cell lines with IC50 = 22.7, 3.5, 24.7, and 5.0 µg/mL, respectively [131].	Sanya Bay, Hainan Island, China
Methyl tortuoate B 477			Strong cytotoxic activity toward CNE-2 and P-388 cell lines with IC50 = 24.7 and 5.0 µg/mL, respectively [131].
Methyl sartortuoate 478	S. pauciplicatum		Good cytotoxic activity toward HepG2, HL-60, KB, LNCaP, LU-1, MCF7, SK-Mel2, and SW480 cancer cells with IC50 ranged from 7.93 ± 2.08 to 19.34 ± 0.72 µM [108].	Hai Phong, Vietnam

4. Conclusions

Based on reviewing the available current literature, a huge library of metabolites was isolated, and it possessed unique structures. Up to 481 compounds with different structures belonging to different chemical classes were reported from the Sarcophyton species. The chemical structures were classified as terpenoids (majority), biscembranes, polyhydroxylated sterols, sesquiterpenes (minority), and miscellaneous compounds. S. trocheliophorum gave the highest number of compounds. Members of genus Sarcophyton possessed valuable and interesting biological activities, such as antibacterial, cytotoxicity, antifungal, and antidiabetic.