Genus Smenospongia: Untapped Treasure of Biometabolites—Biosynthesis, Synthesis, and Bioactivities

Marine sponges continue to attract remarkable attention as one of the richest pools of bioactive metabolites in the marine environment. The genus Smenospongia (order Dictyoceratida, family Thorectidae) sponges can produce diverse classes of metabolites with unique and unusual chemical skeletons, including terpenoids (sesqui-, di-, and sesterterpenoids), indole alkaloids, aplysinopsins, bisspiroimidazolidinones, chromenes, γ-pyrones, phenyl alkenes, naphthoquinones, and polyketides that possessed diversified bioactivities. This review provided an overview of the reported metabolites from Smenospongia sponges, including their biosynthesis, synthesis, and bioactivities in the period from 1980 to June 2022. The structural characteristics and diverse bioactivities of these metabolites could attract a great deal of attention from natural-product chemists and pharmaceuticals seeking to develop these metabolites into medicine for the treatment and prevention of certain health concerns.


Introduction
Marine organisms are renowned as a prosperous pool of diverse metabolites with unparalleled structural features and prominent bioactivities that display potential advantages as lead candidates for developing new pharmaceuticals [1,2]. The rate of discovery of marine metabolites has dramatically increased in the last decades [3]. It has been estimated that, since 2010, more than 15,000 marine natural metabolites have been reported [3,4].
Marine sponges (phylum Porifera) are a substantial part of the benthic biomass and have many essential ecosystem functions such as food, shelter, or regulation of substrate settlement [5]. They are sessile invertebrates that developed an efficacious chemical system based on secondary biometabolite production for communication and defense purposes [6]. In addition, the metabolites produced by sponges and their associated microorganisms are particularly beneficial to repel their surface colonization by harmful biofouling and to fight diseases [6,7]. These metabolites displayed not only unique chemical structures but also interesting bioactivities and made sponges a potential pool of lead compounds for drug discovery [8][9][10][11][12].
The genus Smenospongia (order Dictyoceratida, family Thorectidae) comprises 19 species [13]. The sponges of this genus have the capacity to produce diverse classes of secondary metabolites including phenyl alkenes, indole alkaloids, terpenoids (sesqui-, di-, and sesterterpenoids), aplysinopsins, bisspiroimidazolidinones, chromenes, γ-pyrones, naphthoquinones, and polyketides. Many reported metabolites from this genus possess unique and Several studies reported the isolation of a variety of indole alkaloids as well as closely related brominated derivatives from this genus, which are summarized in the current work along with their characterization, isolation, and bioactivities.

Aplysinopsin Derivatives
Aplysinopsins are tryptophan-derived metabolites that vary in the indole moiety bromination pattern and variation in the C ring structure, including the position and number of N-methyl, oxidation state, absence and presence of the C-1 -C-8 double bond, and stereochemistry [23].
Two new aplysinopsin derivatives, 6-bromo-aplysinopsin (27) and 6-bromo-4 -Ndemethylaplysinopsin (28), were purified from the Caribbean S. aurea extract (toluene: MeOH 1:3) using SiO 2 CC and crystallization from MeOH: H 2 O and elucidated using NMR, MS, and chemical synthesis (Supplementary Materials Table S3) [16]. In addition, aplysinopsins 27-35 separated from S. aurea were assessed for their in vitro antimycobacterial and antimalarial activity, as well as human 5-HT2 receptor binding antagonists in FP and FRET assays [18] (Figure 3).  5-HT2C organizes food intake in mammals, whereas the 5-HT2A receptor displays a role in depression's pathophysiology. Hence, these receptors' modulators could be potential antiobesity and antidepressant agents, respectively. Only 27 exhibited antimalarial activity at endpoint 0.34 μg/mL with a selectivity index of 14, whereas 31 and  5-HT 2C organizes food intake in mammals, whereas the 5-HT 2 A receptor displays a role in depression's pathophysiology. Hence, these receptors' modulators could be potential antiobesity and antidepressant agents, respectively. Only 27 exhibited antimalarial activity at endpoint 0.34 µg/mL with a selectivity index of 14, whereas 31 and 33 were moderately active (conc. 0.97 and 1.1 µg/mL, respectively, with selectivity indexes of >4.9 and >4.3, respectively). Compounds 27, 33, and 35 displaced high-affinity [ 3 H] antagonist binding from cloned 5-HT 2C receptors, whereas 27 and 35 also displaced high-affinity [ 3 H] antagonist binding from the 5-HT 2A receptor subtype, and 33 had only partial displacement at the highest concentration at the 5-HT 2A subtype. None of the others (31, 33, and 34) had displacement effectiveness at the highest concentration tested. Among the tested metabolites, 27 had the highest overall affinity, which was like that of endogenous serotonin at the 5-HT 2C receptor subtype, while 33 and 35 had a 5-to 27-fold lower affinity than serotonin. The structure-activity study revealed the role of functional groups at C-6, C-2 , and C-3 , in the binding to 5-HT 2 human serotonin receptors. The C-3 alkyl chain length displayed a substantial role in binding to the 5-HT receptors, and the presence of the ethyl group (as in 35) enhanced the binding potential compared with the methyl group (as in 34). Additionally, the Br atom at C-6 in the absence of C-3 -ethyl increased the binding affinity (as in 27 and 33 versus 32) and selectivity to the 5-HT 2C receptor subtype over the 5-HT 2A receptor subtype. Additionally, C-2 -methylation facilitated the binding to the 5-HT 2A receptor subtype (as in 27 versus 33) [20]. Chemical investigation of Smenospongia sp. CH 2 Cl 2 fraction by SiO 2 CC and HPLC yielded brominated alkaloids derivatives 26 and 30 that revealed antibacterial capacity (MICs 25 and 12.5 µg/mL) versus S. epidermidis ATCC12228 compared with vancomycin (MIC 0.625 µg/mL) in the microbroth dilution assay [22].

Bisspiroimidazolidinone Alkaloids
Imidazolidinones are a class of heterocyclic metabolites characterized by a nitrogencontaining five-membered ring that have received remarkable attention from medicinal chemists, as many derivatives of this scaffold class possessed variable bioactivities and are used as chiral catalysts by organic chemists [24].
Two new bisspiroimidazolidinone alkaloids, dictazolines A (38) and B (39), along with related metabolites tubastrindoles A (40) and B (41) were obtained from S. cerebriformis using Sephadex LH20/SiO 2 flash column and HPLC and elucidated by NMR analyses (Supplementary Materials Table S4). Only 40 and 41 were evaluated for the inhibition of the serine and threonine kinase PKC. Initially, 41 displayed weak inhibition of PKCδ, whereas 40 and 41 were inactive at reducing the β-secretase-proteolytic cleavage of the amyloid precursor protein, an assay of Alzheimer's disease treatment [25] (Figure 4).

Polyketides
Smenamides A (42) and B (43) are hybrid polyketide-peptide metabolites having dolapyrrolidinone, N-methylacetamide, and chlorovinyl moieties that were separated from Caribbean S. aurea and assigned using HRESIMS/MS and NMR experiments. They demonstrated no notable cytotoxic potential (conc. 30 nM) on Calu-1 in the MTT assay after 27 h of treatment; however, they (conc. 50 nM) had remarkable effectiveness (IC 50 48 nM for 42 and 49 nM for 43) ( Figure 5). Compound 42 exerted its powerful cytotoxic potential via a proapoptotic mechanism with increasing apoptotic cells and no or little necrotic cells, whereas in 43, the apoptotic cells' percentage was much less, and the necrotic cells' percentage was high (47%, conc. 100 nM) in the Annexin-V PI/FITC kit assays. These different mechanisms could be attributed to the difference in the C13-C15 doublebond configuration.
are used as chiral catalysts by organic chemists [24].
Two new bisspiroimidazolidinone alkaloids, dictazolines A (38) and B (39), along with related metabolites tubastrindoles A (40) and B (41) were obtained from S. cerebriformis using Sephadex LH20/SiO2 flash column and HPLC and elucidated by NMR analyses (Supplementary Materials Table S4). Only 40 and 41 were evaluated for the inhibition of the serine and threonine kinase PKC. Initially, 41 displayed weak inhibition of PKCδ, whereas 40 and 41 were inactive at reducing the β-secretase-proteolytic cleavage of the amyloid precursor protein, an assay of Alzheimer's disease treatment [25] ( Figure  4).   potential via a proapoptotic mechanism with increasing apoptotic cells and no or little necrotic cells, whereas in 43, the apoptotic cells' percentage was much less, and the necrotic cells' percentage was high (47%, conc. 100 nM) in the Annexin-V PI/FITC kit assays. These different mechanisms could be attributed to the difference in the C13-C15 double-bond configuration.  These metabolites could be promising leads for designing antitumor agents [26]. Caso et al. reported the synthesis of ent-smenamide (I) and 16-epi-smenamide A (II) and established smenamide A's 16-R configuration. The carboxylic acid moiety was created starting from S-citronellene via a Grignard process and two Wittig reactions. Furthermore, the Andrus protocol was used for carboxylic acid moiety coupling with either (R)-or (S)-dolapyrrolidinone [27]. In 2018, Caso et al. attempted to study if the C-16 configuration influenced the bioactivities. They synthesized 16-epi-smenamide A and eight analogs of the 16-epi-series that were tested for antiproliferative capacity versus MM (multiple myeloma) cell lines. It was found that the C-16 configuration had a slight influence on the activity since the 16-epi-analogs were active at nanomolar concentrations [28]. Interestingly, 44 and 46 revealed moderate neurotoxicity versus neuro-2A cells, whereas 45, the geometric isomer of 44, had no potential [29]. Using a molecular-networking dereplication strategy, two new members of smenamides, 47 and 48, were separated through Rp-HPLC separations and elucidated by NMR, ECD, and Marfey's analyses (Supplementary Materials Table S5). Compound 47 was a hydrated analog of 42 with 8S/13S/15S/16R/20Z-configuration [30], whereas 48 is a C-8-epimer of 47 having 8S/13S/15S/16R/20Z-configuration. Their cytotoxic potential versus MCF-7, MDA-MB-231, and MG-63 was estimated in the xCELLIgence assays. It is noteworthy that they exerted (conc. 5 µM) a moderate selective antiproliferative capacity on MDA-MB-231 and MCF-7; however, they had no effectiveness versus MG-63. It was found that the dolapyrrolinone C-8 absolute configuration did not affect the activity [30]. From the same Caribbean S. aurea using RP-18 CC and HPLC, smenothiazoles A (49) and B (50), which are hybrid peptide-polyketide compounds, were separated; these are biogenetically related and structurally vary from smenamides ( Figure 6). myeloma) cell lines. It was found that the C-16 configuration had a slight influence on the activity since the 16-epi-analogs were active at nanomolar concentrations [28]. Interestingly, 44 and 46 revealed moderate neurotoxicity versus neuro-2A cells, whereas 45, the geometric isomer of 44, had no potential [29]. Using a molecular-networking dereplication strategy, two new members of smenamides, 47 and 48, were separated through Rp-HPLC separations and elucidated by NMR, ECD, and Marfey's analyses (Supplementary Materials Table S5). Compound 47 was a hydrated analog of 42 with 8S/13S/15S/16R/20Z-configuration [30], whereas 48 is a C-8-epimer of 47 having 8S/13S/15S/16R/20Z-configuration. Their cytotoxic potential versus MCF-7, MDA-MB-231, and MG-63 was estimated in the xCELLIgence assays. It is noteworthy that they exerted (conc. 5 μM) a moderate selective antiproliferative capacity on MDA-MB-231 and MCF-7; however, they had no effectiveness versus MG-63. It was found that the dolapyrrolinone C-8 absolute configuration did not affect the activity [30]. From the same Caribbean S. aurea using RP-18 CC and HPLC, smenothiazoles A (49) and B (50), which are hybrid peptide-polyketide compounds, were separated; these are biogenetically related and structurally vary from smenamides ( Figure 6). They were tested versus Calu-1, LC31, A2780, and MCF7 in the MTT assay. These metabolites displayed a potent cytotoxic potential at low nanomolar concentrations with selectivity versus ovarian cancer cells. They showed a comparable effect on LC31, Calu-1, and A2780 cell lines and a lower effect on MCF7 in the MTT assay, whereas in Annexin-V FITC/PI assays, smenothiazoles showed a strong apoptotic effect on A2780 (ovarian They were tested versus Calu-1, LC31, A2780, and MCF7 in the MTT assay. These metabolites displayed a potent cytotoxic potential at low nanomolar concentrations with selectivity versus ovarian cancer cells. They showed a comparable effect on LC31, Calu-1, and A2780 cell lines and a lower effect on MCF7 in the MTT assay, whereas in Annexin-V FITC/PI assays, smenothiazoles showed a strong apoptotic effect on A2780 (ovarian cancer cells) that is accompanied with an S phase decrease resulting in blocking the cellular cell-cycle G0G1 phase [31].

Polyketides
Four chlorinated polyketides, smenolactones A-D (51-54), and trichophycin B (55) were separated from S. aurea and characterized by NMR, ECD, and Mosher analyses. The cytotoxic capacity of 51 and 53-55 was evaluated versus MCF-7, PANC-1, and BxPC-3 tumor cell lines using the MTS assay and an xCELLigence System Real-Time Cell Analyzer (RTCA). They displayed cytotoxic activity at low-or submicromolar concentrations [32]. Smenolactones were found (conc. 250 and 500 nM and 1 and 2 µM for 48 h) to reduce the cell viability and increase the tumor cell doubling time, revealing their antiproliferative potential on MCF-7 cells. Notably, 53 (conc. 1 and 2 µM) was the most potent one (IC 50 918 and 652 nM, respectively); however, 51 and 54 (conc. 2 µM) caused less notable MCF-7 growth inhibition. For in vitro antiproliferative selectivity assessment, PANC-1 experienced induced or unaffected proliferation with 51 and 54 (conc. 500 nM and 1 µM, 48 h), while BXPC-3 displayed a delayed growth at 1 µM. The results demonstrated that the polyketide chain length and flexibility influence the activity as in 53, which had no double bonds, and a longer chain was the most bioactive. Furthermore, lactone moiety C-5R configuration led to strong activity as in 51 versus 54 with C-5-S stereochemistry that had a weaker inhibition, whereas chlorovinylidene configuration had no dramatic influence on the activity [32].
Phytochemical investigation of the Caribbean S. conulosa led to the separation of two new chlorinated thiazole-involving metabolites, conulothiazoles A (56) and B (57), along with 42, 43, 49, and 50 that were elucidated by NMR and MS analyses, and their absolute configuration was assigned by chemical degradation and Marfy's and HRLCM analyses [33]. These metabolites possessed molecular features of several cyanobacterial metabolites, including a terminal thiazole ring as in barbamide and middle vinyl chloride as in jamaicamides [33].

Terpenoids
Terpenoids of variable carbon skeletons have been reported from this genus, including sesqui-, sester-, and diterpenoids (Supplementary Materials Table S6). These metabolites along with their reported bioactivities and synthesis were summarized here.

Hydroquinone and Quinone Sesquiterpenoids
Compounds 58 and 63 were purified from the less-polar fraction of S. aurea and characterized by NMR and chemical interconversion. The 5S/8S/9R/10S configuration of 58 was established based on X-ray analysis [15]. In addition, the EtOH extract of the Jamaican S. aurea afforded sesquiterpenes 58, 59, and 61 using SiO 2 and Sephadex LH-20 ( Figure 7).
From Snenospongia sp., smenoqualone (78) was purified, which is structurally related to strongylin A separated from Strongylophora hartmani [40]. It had no antimicrobial and cytotoxic potential, suggesting that the free OH group on the quinone ring is substantial for the activity [41].
Do et al. reported that the 75 pretreatment remarkably boosted TRAIL-produced apoptosis in HCT-116 cells and stimulated TRAIL-caused apoptosis on colon cancer cells via increased caspase-8 and -3 activation, DNA damage, and PARP cleavage. It also lessened Bcl-xL and Bcl2 cell survival proteins, while it strongly upregulated death receptors' DR4 and DR5 expression through the upregulation of CCAAT/CHOP (enhancer-binding protein homologous protein). The DR4, CHOP, and DR5 expression upregulation had occurred through the activation of ERK (extracellular-signal-regulated kinase) and p38 MAPK (mitogen-activated protein kinase) signaling pathways, as well as ROS generation. Therefore, 75 boosted the human colon cancer cells' sensitivity to TRAIL-caused apoptosis via the ERK-ROS/CHOP-p38 MAPK-mediated upregulation of DR4 and DR5 expression, indicating that 75 could be developed into a chemotherapeutic agent [42].
Aerobic glycolysis is preferred more in cancer cells than the oxidative phosphorylation for ATP production. In different cancers, the upregulation of PDK1 (pyruvate dehydrogenase kinase 1) minimizes the PDH (pyruvate dehydrogenase) activity via the induction of its E1α subunit (PDHA1) phosphorylation and, subsequently, turns the energy metabolism from oxidative phosphorylation to aerobic glycolysis [43]. Therefore, PDK1 is regarded as a target for anticancer therapy. Compound 75 decreased the viability of A549, DLD-1, RKO, HEK293T, Detroit-551, and LLC cells (GI 50 10.5, 8.61, 50.16, 37.30, and >100 µM respectively) in the MTT sassy. It reduced the PDHA1 phosphorylation in the A549 cells by suppressing the PDK activity. It also increased oxygen consumption and decreased secretory lactate levels. Thus, it increased the oxidative phosphorylation and PDH activity while subsequently reducing cell viability via the suppression of the PDK activity. It could be a candidate for anticancer agents that acted via the PDK1 activity inhibition [44].
nAMD (neovascular age-related macular degeneration) is a common reason for irreversible vision loss in the elderly. Son

et al. stated that 75 topical and oral administrations in mice and rabbits caused the inhibition and regression of laser-induced CNV (choroidal neovascularization) by β-catenin downregulation in RPE (retinal pigment epithelial) cells ((hTERT-RPE1 and ARPE-19), and it prohibited p53-mediated apoptosis induction in HU-VECs (human umbilical vein endothelial cells). It repressed the expression of inflammatory and angiogenic factors and restored the E-cadherin expression in RPE cells by prohibiting
the Wnt-β-catenin pathway. Therefore, it functioned through the p53-Wnt-β-catenin pathway regulation with advantages over the available cytokine-targeted anti-angiogenic therapies. It has a unique mechanism by suppressing the expression of proinflammatory and angiogenic factors and prohibiting the growth of vascular endothelial cells; it could be administered more safely, cost-effectively, and conveniently in the form of eye drops or oral drugs to patients than the currently used intravitreal drugs [45].
From S. aurea and S. cerebriformis, 77, 87-90, and 97-99 were purified and assigned based on various NMR data ( Figure 10). Compounds 89 and 90 have an unprecedented 2,2dimethylbenzo[d]oxazol-6(2H)-one moiety. GIAO (gauge-invariant atomic orbital) NMR chemical shift calculations along with the application of CP3 and DP4 advanced statistics were utilized for stereochemistry determination. The downregulation of β-catenin expression has been considered a promising approach for cytotoxic drug formulation. Compounds 77 and 88 and the mixture of 89 and 90 suppressed CRT (β-catenin response transcription) via degrading β-catenin and exhibited cytotoxic potential versus colon cancer cells through their anti-CRT potential using a CellTiter-Glo assay kit [46]. Compounds 88 and 89/90 mixture started to produce antiproliferative potential (conc. > 20 μM), whereas 77 began to inhibit tumor growth (conc. 1.5 and 0.75 μM) versus HCT-116 cells (IC50 2.95 μM) and SW4 (IC50 3.24 μM), revealing that 77 had more potent cytotoxic potential than the other compounds [46]. It was reported that a competitive intramolecular Michael addition might be involved in these metabolites' formation. The intramolecular addition of enolate II onto the C-20 carbonyl would result in the generation of 97 and 99 or 98, relying on si-or re-face addition (path I). Alternatively, the addition of enolate onto the C-21 carbonyl group and tautomerization followed by trans-etherification would result in 77 formation (path II). Additionally, reductive amination of IV followed by Schiff's base formation with acetone or acetaldehyde and consecutive isomerization generates VI and VII, respectively (Scheme 1). Lastly, the oxidation of these two intermediates leads to the formation of benzoxazole moieties in 87-90 [46]. The downregulation of β-catenin expression has been considered a promising approach for cytotoxic drug formulation. Compounds 77 and 88 and the mixture of 89 and 90 suppressed CRT (β-catenin response transcription) via degrading β-catenin and exhibited cytotoxic potential versus colon cancer cells through their anti-CRT potential using a CellTiter-Glo assay kit [46]. Compounds 88 and 89/90 mixture started to produce antiproliferative potential (conc. > 20 µM), whereas 77 began to inhibit tumor growth (conc. 1.5 and 0.75 µM) versus HCT-116 cells (IC 50 2.95 µM) and SW4 (IC 50 3.24 µM), revealing that 77 had more potent cytotoxic potential than the other compounds [46]. It was reported that a competitive intramolecular Michael addition might be involved in these metabolites' formation. The intramolecular addition of enolate II onto the C-20 carbonyl would result in the generation of 97 and 99 or 98, relying on si-or re-face addition (path I). Alternatively, the addition of enolate onto the C-21 carbonyl group and tautomerization followed by transetherification would result in 77 formation (path II). Additionally, reductive amination of IV followed by Schiff's base formation with acetone or acetaldehyde and consecutive isomerization generates VI and VII, respectively (Scheme 1). Lastly, the oxidation of these two intermediates leads to the formation of benzoxazole moieties in 87-90 [46]. New sesquiterpenes, 66, 67, 91, 100, and 101, along with 68-70, 71, and 75 were separated from S. cerebriformis and assigned using NMR, MS, and ECD spectra. Compounds 100 and 101 featured cyclopentenone and 4,9-friedodrim-4(11)-ene sesquiterpene skeleton with 16R/20R and 16S/20R, respectively. Compound 91 had C-15 benzoxazole moiety instead of cyclopentenone in 100 and 101; however, 67 was structurally similar to 70 and 69 with a different C-8-configuration. Their inhibitory potential versus NO production in BV2 microglia cells stimulated with LPS in the immune-fluorescence assay using the Griess reaction was estimated [47]. Compounds 67, 69, 70, 75, 100, and 101 (conc. 10, 20, and 40 μM) noticeably prohibited (IC50 ranged from 10.40 to 30.43 μM) LPS-induced NO production in BV2 cells, whereas 75 had a significant activity (IC50 10.40 μM) compared with L-NMMA (IC50 22.1 μM). The structure-activity study suggested that the C-14-OH group had an important role in the NO production inhibition. Thus, 75 could be a marked anti-inflammation constituent of S. cerebriformis [47].
Their activation of AMPK (5 adenosine monophosphate-activated protein kinase) in L6 myoblast cells was tested utilizing an AMPK phosphorylation assay. Only 128 displayed a dark band that indicated the creation of phosphorylated AMPK at a concentration of 10 mM [53].

Chromene Derivatives
Unusual macrocyclic chromenes, smenochromenes A-D (130-133), were purified from the Smenospongia sp. EtOAc fraction by Sephadex LH-20 and HPLC and characterized by NMR and X-ray tools [55] (Supplementary Materials Table S7). Compound 130 was a racemate, whereas 131-133 were optically active. These metabolites possessed a chromene core fused to a 14-membered ring system that could be derived from farnesyl hydroquinone I (Scheme 2) that undergoes dehydrogenation to produce II. Subsequently, the oxa-6π electrocyclization of II affords chromene III featuring the hydroxy-chromene core. Furthermore, an allylic cation IV is formed by the terminal allylic position oxidation that undergoes various cyclizations between C1 and C14 giving the 14-membered carbocyclic 130 after that ∆ 6,7 -double-bond isomerization produces 131. On the other side, the formation of a bond between C1 and the phenolic oxygen yields 132's and 133 s 16-membered heterocyclic system (Scheme 2).

γ-Pyrone Derivatives
The Caribbean S. aurea MeOH/CHCl 3 extract afforded 134 by RP-18 CC and HPLC that featured a γ-pyrone polypropionate framework. It was assigned by NMR, MS, and ECD [57]. It is noteworthy that pyrone polypropionates are uncommon in sponges; however, they are commonly encountered in marine mollusks and bacteria [58,59].

Phenyl Alkenes
From Florida sponges S. aurea and S. cerebriformi, a novel phenyl alkene, 135, with unprecedented linear phenyl alkene skeleton was separated (Supplementary Materials  Table S8). Its 4R absolute configuration was established by a modified Mosher's method. It showed in vitro cytotoxic activity versus HL-60 (IC 50 8.1 µM). The molecular docking study suggested that 135 produced its cytotoxic potential through the inhibition of microtubule activity [60].

γ-Pyrone Derivatives
The Caribbean S. aurea MeOH/CHCl3 extract afforded 134 by RP-18 CC and HPLC that featured a γ-pyrone polypropionate framework. It was assigned by NMR, MS, and

Antimicrobial Activity
Smenospongia sp. extracts were found to exhibit noticeable antimicrobial capacity. The CH2Cl2 extract appeared the most active versus Staph. aureus and E. coli (inhibition zone diameters (IZDs) 23 and 11 mm, respectively at conc. 500 μg/disk), whereas the MeOH extract had weaker activity (IZD 20 mm/disk versus Staph. aureus), and the aqueous extract displayed no activity [39].

Antimicrobial Activity
Smenospongia sp. extracts were found to exhibit noticeable antimicrobial capacity. The CH 2 Cl 2 extract appeared the most active versus Staph. aureus and E. coli (inhibition zone diameters (IZDs) 23 and 11 mm, respectively at conc. 500 µg/disk), whereas the MeOH extract had weaker activity (IZD 20 mm/disk versus Staph. aureus), and the aqueous extract displayed no activity [39].

Conclusions
Marine sponges are a wealth of biometabolites with chemical diversity that have been proven to be beneficial sources for novel drug target discovery. Among the marine sponges, Smenospongia sponges have been reported as a reservoir of diverse biometabolites. In the current work, Smenospongia, one of the most interesting sponge genera, was highlighted. The species of this genus have been collected from various regions ( Figure 16). The bigger number of metabolites has been reported from the Smenospongia species obtained from Thailand (21 compounds), whereas the least number (4 compounds) was isolated from sponge samples that were collected from both the Milne Bay region, Papua New Guinea, and the Ninamijima and Nichinan-oshima Islands.

Conclusions
Marine sponges are a wealth of biometabolites with chemical diversity that have been proven to be beneficial sources for novel drug target discovery. Among the marine sponges, Smenospongia sponges have been reported as a reservoir of diverse biometabolites. In the current work, Smenospongia, one of the most interesting sponge genera, was highlighted. The species of this genus have been collected from various regions ( Figure 16). The bigger number of metabolites has been reported from the Smenospongia species obtained from Thailand (21 compounds), whereas the least number (4 compounds) was isolated from sponge samples that were collected from both the Milne Bay region, Papua New Guinea, and the Ninamijima and Nichinan-oshima Islands.  The results revealed that sesqui-and sesterterpenoids and indole derivatives are the major metabolites of this genus. Additionally, few studies reported the isolation of aplysinopsins, bisspiroimidazolidinones, chromenes, γ-pyrones, phenyl alkenes, naphthoquinones, polyketides, fatty acids, sterols, and phthalates ( Figure 18).  The results revealed that sesqui-and sesterterpenoids and indole derivatives are the major metabolites of this genus. Additionally, few studies reported the isolation of aplysinopsins, bisspiroimidazolidinones, chromenes, γ-pyrones, phenyl alkenes, naphthoquinones, polyketides, fatty acids, sterols, and phthalates ( Figure 18). The results revealed that sesqui-and sesterterpenoids and indole derivatives are the major metabolites of this genus. Additionally, few studies reported the isolation of aplysinopsins, bisspiroimidazolidinones, chromenes, γ-pyrones, phenyl alkenes, naphthoquinones, polyketides, fatty acids, sterols, and phthalates ( Figure 18). These metabolites have been assessed for diverse bioactivities, including antimalarial, antimicrobial, cytotoxic, 5-HT2 receptor antagonistic, antifouling, and anti-inflammation. Some metabolites displayed moderated to potent cytotoxic, anti-inflammation, and antimicrobial capacities ( Figure 19). Among these metabolites, 80, 117, 119, 120, 126, and 128 exhibited more potent cytotoxic capacity than standard anticancer drugs, whereas 114, 115, 117, 118, 122, 126, and 129 demonstrated marked antimicrobial activity versus some microbial strains. These metabolites have been assessed for diverse bioactivities, including antimalarial, antimicrobial, cytotoxic, 5-HT2 receptor antagonistic, antifouling, and anti-inflammation. Some metabolites displayed moderated to potent cytotoxic, anti-inflammation, and antimicrobial capacities ( Figure 19). Among these metabolites, 80, 117, 119, 120, 126, and 128 exhibited more potent cytotoxic capacity than standard anticancer drugs, whereas 114, 115, 117, 118, 122, 126, and 129 demonstrated marked antimicrobial activity versus some microbial strains. Interestingly, Smenospongia genus sponges have been reported to biosynthesize chlorinated mixed polyketide-peptide compounds, including smenamides, smenothiazoles, and conulothiazoles, that shared chlorovinylidene, dolapyrrolidone ring, and terminal alkyne that are characteristics of cyanobacterial metabolites. Some of these compounds possessed potential antitumor capacity that could be promising leads for antitumor drug design. Structure-activity assessments of some reported metabolites from Interestingly, Smenospongia genus sponges have been reported to biosynthesize chlorinated mixed polyketide-peptide compounds, including smenamides, smenothiazoles, and conulothiazoles, that shared chlorovinylidene, dolapyrrolidone ring, and terminal alkyne that are characteristics of cyanobacterial metabolites. Some of these compounds possessed potential antitumor capacity that could be promising leads for antitumor drug design. Structure-activity assessments of some reported metabolites from this genus revealed that the chemical skeletons' nature of these metabolites and substituent patterns greatly affected the bioactivities. In addition, reported synthetic work established that the modifications of structures and replacement by some functional groups resulted in more potential and useful tags for further functionalization through click chemistry, which is a new area for drug-like molecule synthesis that can boost the drug discovery process. Unfortunately, the bioassays of some reported metabolites demonstrated no notable effectiveness, suggesting a more potential for searching and running other bioevaluations. For enriching the metabolite discovery from this genus, advanced techniques, including LC-MS-NMR, metabolomics, and UPLC-MS, could be utilized. This work aimed to be beneficial for the Smenospongia genus's bioprospecting process and to bring attention to the chemical diversity of their metabolites. Finally, we think that the genus and its metabolites still warrant considerable research attention. SW480 Human colorectal cancer cell line TLC Thin layer chromatography TRAIL Tumor necrosis factor-related apoptosis-inducing ligand UPLC-MS Ultra performance liquid chromatography-tandem mass spectrometer