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Review

Marine Nucleosides: Structure, Bioactivity, Synthesis and Biosynthesis

by
Ri-Ming Huang
1,2,
Yin-Ning Chen
3,
Ziyu Zeng
4,
Cheng-Hai Gao
5,
Xiangdong Su
2 and
Yan Peng
6,*
1
Key Laboratory of Plant Resources Conservation and Sustainable Utilization, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China
2
Department of Pharmacy and Pharmacology, University of Bath, Bath BA2 7AY, UK
3
College of Light Industry and Food Engineering, Guangxi University, Nanning 530004, China
4
School of Pharmaceutical Sciences, Shandong University, Jinan 250012, China
5
Key Laboratory of Marine Environmental Science, Guangxi Academy of Sciences, Nanning 530007, China
6
Life Science & Technology School, Lingnan Normal University, Zhanjiang 52048, China
*
Author to whom correspondence should be addressed.
Mar. Drugs 2014, 12(12), 5817-5838; https://doi.org/10.3390/md12125817
Submission received: 4 August 2014 / Revised: 20 November 2014 / Accepted: 21 November 2014 / Published: 2 December 2014
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Abstract

:
Nucleosides are glycosylamines that structurally form part of nucleotide molecules, the building block of DNA and RNA. Both nucleosides and nucleotides are vital components of all living cells and involved in several key biological processes. Some of these nucleosides have been obtained from a variety of marine resources. Because of the biological importance of these compounds, this review covers 68 marine originated nucleosides and their synthetic analogs published up to June 2014. The review will focus on the structures, bioactivities, synthesis and biosynthetic processes of these compounds.

1. Introduction

Nucleosides belong to a class of organic compounds with their structures being composed of a nitrogen-containing heterocyclic nucleobase and a 5-carbon sugar (Figure 1). The nucleobase is bound to the 5-carbon sugar, either a ribose or a deoxyribose, through a β-glycosidic linkage. Phosphorylation of nucleosides on the primary hydroxyl group of the sugar moiety forms nucleotides, the building blocks of DNA and RNA. Both nucleosides and nucleotides are vital components of all living cells and involved in several fundamental biological processes. Discoveries made in the area of purine and pyrimidine nucleosides and nucleotide chemistry [1,2,3] have contributed substantially to the better understanding of the biological processes at the molecular levels. Therefore scientists show great interest in not only the naturally occurring nucleosides and their biochemical properties but also the effects of synthetic nucleosides on living organisms [4,5,6].
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Figure 1. The structural compositions of nucleosides and nucleotides.
Figure 1. The structural compositions of nucleosides and nucleotides.
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Microorganisms and marine organisms are capable of producing different nucleosides with unusual structures and biological properties [7,8,9]. Some of these molecules with significant bioactivities have been isolated previously from a variety of marine resources [8,9]. The discoveries of these remarkable biological activities in the marine nucleosides have promoted a great amount of research work on the synthesis of various analogs of these nucleosides and the further evaluation of their biological activities [10,11,12]. The searching for novel analogs of natural nucleosides with potential antibiotic, antiviral, antiparasitic and antitumor properties has driven the rapid progress in the area of nucleoside chemistry research [13].
Bioactive marine nucleosides have been reviewed [14,15]. However, there is no comprehensive review of marine nucleosides since the first unusual marine nucleoside was isolated by Bergmann in 1950 [14]. Thus, this review aims to summarize 68 marine-derived nucleosides and their synthetic analogues reported up to the first half year of 2014. The structures, bioactivities, synthesis and biosynthetic processes of these marine derived nucleosides are included.

2. Purine Nucleosides

Purine nucleoside is composed of a purine base and a five-carbon sugar (either a ribose or a deoxyribose). The common purine bases include purine, adenine, guanine, hypoxanthine, xanthine, theobromine, caffeine, uric acid and isoguanine (Figure 2).
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Figure 2. The structures of the common purine derivatives.
Figure 2. The structures of the common purine derivatives.
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2.1. Purine-d-Arabinosides

Spongoadenosine (Ara-A, 1) and its 3′-O-acetyl derivative (2) were isolated from gorgonian Eunicella cavolini [16]. It is interesting to note that 1 was synthesized [17] prior to its isolation from a natural source. Ara-A exhibited significant antiviral activity against DNA viruses, which was the first antiviral drug for the treatment of fatal Herpes encephalitis [18]. The significance of its biological properties [11] has ensured continued interest since the compound was first synthesized in 1960 [19,20]. It was found that 9-β-d-darabinofuranosyl-adenine-5′-phosphate, which penetrated the cell without degradation had more sustained toxicity against mouse fibroblasts (L-cells) than that of its nucleoside. Ara-A had a firmly established role in the management of certain human herpes virus infections and was also effective in the therapy of H. keratitis, H. encephalitis and Varicella zoster infections in immunosuppressed patients [21]. In addition, the biosynthesis of Ara-A has been studied [22]. It was suggested that Ara-A is produced by direct epimerization of C-2′ hydroxy group of adenosine or a derivative thereof. It is also likely that a 2′-keto compound is involved as an intermediate [23]. However, there is no detailed report on biological activity of compound 2. Since compound 2 has a very similar structure to compound 1, it will be worthy to further investigate whether 2 has similar biological properties as 1, or whether 2′-OH in 1 and 2′-AcO in 2 have their own contribution to the biological activity. In addition, as both compounds 1 and 2 were produced by the same gorgonian E. cavolini, they may have the same biosynthesis pathway in the gorgonian. The corresponding chemical structures are shown in Figure 3.
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Figure 3. The structures of purine-d-arabinosides (1 and 2).
Figure 3. The structures of purine-d-arabinosides (1 and 2).
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2.2. Purine-2′-Deoxyribosides

2′-Deoxyadenosine (3), possessing significant biological properties [24], is a normal component of nucleic acids. However, it was isolated in free state from the marine sponge Dasychalina cyathina [25], and also isolated later from the marine sponge Callyspongia species [26]. 2′-Deoxy-spongosine (4), known as a synthetic product, was first isolated from the Caribbean sponge Cryptotethia crypta [27], and also isolated from the same sponge collected from Western Australia [28]. Aplysidine (5) was isolated from the Okinawan marine sponge Aplysina sp. Its structure was elucidated by spectroscopic methods and confirmed by the synthesis of aplysidine (5) [29]. This compound is the first nucleoside with theophylline ring as a base isolated from a marine source. Aplysidine (5) was found to have the antagonistic activity for adenosine A1 receptor comparable with xanthine-N-7-ribosides [30]. Xanthosine (6) was isolated from a starfish Asterias rollestoni (Yellow Sea, China) [31]. 2′-Deoxy-guanosine (7) was isolated from the marine sponge Haliclona sp. [32]. Avinosol (8) was isolated from the marine sponge Dysidea sp. collected in Papua New Guinea. Avinosol (8) was apparently the first example of a naturally occurring meroterpenoid-nucleoside conjugate, showing anti-invasion activity in a cell-based assay [33]. Among these purine-2′-deoxyribosides, seven of total eight compounds were isolated from marine sponges. Therefore, it is possible that this type compounds are mainly produced by marine sponge origin as they there share the similar biosynthesis pathways for purine-2′-deoxyribosides in marine sponges. The corresponding chemical structures are shown in Figure 4.
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Figure 4. The structures of purine-2′-deoxyribosides (3–8).
Figure 4. The structures of purine-2′-deoxyribosides (3–8).
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2.3. Purine-1-β-d-Ribosides

Spongosine (9) was first isolated from the marine sponge Cryptotethia crypta in 1950 [14,34]. It was also obtained from the marine sponge Haliclona sp. [32] and the marine bryozoan Bugula neritina [35]. The structure of spongosine (9) as 3-methoxy adenosine, was confirmed by its chemical synthesis from 2-chloroadenine [36]. Three syntheses of spongosine (9) were reported [37,38]. Spongosine (9) was also synthesized from isoguanosine (10) through a new method [39]. Isoguanosine (10) was isolated from the marine nudibranch mollusk Diaulula sandiegensis (Monterey, California) [40]. Isoguanosine (10) exhibited hypotension, bradycardia and relaxation of smooth muscle activities [41]. The compound was more potent and much longer acting than adenosine. Like adenosine and its analogs, isoguanosine (10) stimulated accumulation of adenosine 3′,5′-monophosphate (cAMP) in brain tissue [41]. Effect of the size of alkoxy groups at position 2 in spongosine has been extensively studied with respect to its coronary vasodilating activity [42]. The result revealed that using an n-propoxy group at position 2 to replace a methoxy group resulted in eight-fold increase in its activity. Adenosine (11) was reported to be the cardioactive constituents of D. cyathina [25]. Its transportation, formation and inactivation in different tissues and involvement in the pathophysiology of renal changes observed in various types of renal insufficiency have been discussed [43]. The bronchodilation efficiency of methylxanthine is believed to be due to the adenosine antagonism action. The role of its uptake inhibitors as probe has been established [44]. Doridosine (12) [45,46,47] was isolated from marine sponge Tedania digitata and nudibranch Anisodoris nobilis at approximately the same time by two groups working independently in different continents (Australia and USA) [48,49]. The function and origin of this compound in these marine organisms is not known. Doridosine (12) exhibited muscle relaxant, hypothermic and cardiovascular effects following oral administration in mice and rats [46,47]. It interacted directly with adenosine receptors in guinea-pig brain to stimulate adenylate cyclase [50]. Its muscle relaxant activity and other properties have been compared with its various analogs. It has been found that the potency is retained in compounds in which the 1-methylisoguanine moiety is unaltered. 1-Methylisoguanosine (13) is a close derivative of doridosine (12) that occurs in the marine animals, which was isolated from the sponge T. digitata [45,51]. It has also been reported to occur in the nudibranch A. nobilis [48] and coral Madracis mirabilis [52]. This nucleoside showed potent muscle relaxant, blood pressure lowering, cardiovascular and anti-inflammatory activity [53,54]. Two known cytotoxic nucleosides, toyomycin (14) [55] and 5-(methoxycarbonyl)-tubercidin (15) [56], were isolated from Jaspis johnstoni from Fiji [57]. Tubercidin (16), a known nucleoside antibiotic, was isolated as the major metabolite from a marine sponge Caulospongia biflabellata. Tubercidin (16) exhibited potent cytotoxic activity against P388 and A549 tumor cells. The isolation, structure elucidation and biological activities of tubercidin (16) were described in the literature, which was the first report of the isolation of tubercidin from a marine organism [58]. A bromophenol coupled with deoxyguanosine (17) was isolated from Rhodomela confervoides (Qingdao, China) [59]. 3-Deazainosine (18), previously known as a synthetic compound [60], was isolated from the Egyptian ascidian Eudistoma laysani [61]. Shimofuridin A (19), a cytotoxic nucleoside derivative embracing an acylfucopyranoside unit, was isolated from the Okinawan marine tunicate Aplidium multiplicatum [62]. The compound has also been synthesized [63]. Shimofuridins B–G (20–25) with acylfucopyranoside moiety were minor metabolites from the same organism [64]. Inosine (26) was isolated from the extract of the didemnid ascidian Lissoclinum sp. [65]. The crustacean Ligia exotica from Korea contained 3′-O-(α-d-glucosyl)inosine (27), for which the structure was confirmed by a total synthesis [66]. Among these purine-1-β-d-ribosides, compounds 14–16 are cytotoxic metabolites. Further investigation on their pharmacological action mechanism and structure-activity-relationships (SAR) are needed to explore potential use for these compounds. In addition, shimofuridins B–G (20–25) represent compounds with interesting structural backbone. However, there is no reported biological data for this type of molecules. Their synthetic analogues are needed to further evaluate their biological properties. The corresponding chemical structures are shown in Figure 5.
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Figure 5. The structures of purine-1-β-d-ribosides (9–27).
Figure 5. The structures of purine-1-β-d-ribosides (9–27).
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2.4. Purine Nucleoside Analogues

An unusual nucleoside isolated from marine nudibranch mollusk Doris verrucosa [67] was characterized as 9-[5′-deoxy-5′-(methylthio)-β-d-xylofuranosyl]adenine (28). It was the first naturally occurring analog of methylthio-adenosine (MTA). In the biological system MTA is formed from S-sadenosyl-l-methionine (AdoMet), a ubiquitous enzyme that occurs both in normal and malignant tissues. AdoMet acts as methyl group donor in transmethylation reaction. The nucleoside (28) was the first naturally occurring purine nucleoside carrying a substituted xylose sugar moiety. It has been synthesized [68] prior to its isolation from a marine nudibranch. An arsenic containing the nucleoside characterized as 5′-deoxy-5′-dimethylarsinyladenosine (29) was isolated from the kidney of the giant clam Tridacna maxima [69]. Marine alga Hypnea valendia [70] has furnished 5-iodo-5-deoxytubercidine (30), whose sugar moiety is 5-deoxyribose. The nucleoside (30) displayed prominent muscle relaxant property. It also produced hypothermia in mice [70]. A species of Mycale collected in Japan contained two novel nucleosides, mycalsines A (31) and B (32), both inhibited cell division in the fertilized-starfish-egg assay [71]. Kumusine (33) isolated from an Indonesian sponge Theonella sp. was characterized as 2-chloro-9-(5′-deoxy-2′-methyl-β-d-ribofuranosyl)-adenine [72]. 2′-C-methyl-5′-deoxyribofuranosyl nucleosides, trachycladine A (34) and trachycladine B (35), were isolated from the marine sponge Trachycladus laevispirulifer (Western Australia) [73]. The nucleosides 5′-deoxytubercidin (36) and 5′-deoxy-3-bromotubercidin (37) were isolated from Didemnum voeltzkowi from Philippines [74]. Australian Atriolum robustum was the source of amino acid-derived metabolites 38 and 39 [75]. Compound 38 was a relatively potent partial agonist of human A3 adenosine receptors. As an unusual nucleoside, 4-amino-7-(5′-deoxy-β-d-xylofuranosyl)-5-iodopyrrolo[2,3-d]pyrimidine (40), was isolated from an ascidian, Diplosoma sp. Compound 40 was found to inhibit the division of fertilized sea urchin eggs [76]. Ostrerine A (41) was isolated from extracts of the mollusk Ostrea rivularis, which is a food source and traditional Chinese medicine [77]. The iodinated nucleoside (42), isolated from Diplosoma sp. (Hateruma Is., Okinawa), inhibited the division of fertilized sea urchin eggs [76]. The first naturally occurring nucleoside disulfide (43) has been reported to be isolated from a dredges South Australian T. laevispirulifer [78]. A species of Erylus (Australia) was the source of N3,5-cycloxanthosine (44), the first naturally occurring cyclonucleoside. The compound is a known synthetic product prior to the isolation [79]. A new cyclonucleoside (45) was isolated from Axinella polypoides (Calvi, Corsica, France) [80]. Investigation of the secondary metabolites of the ascidian Herdmania momus led to the isolation and characterization of four new nucleoside derivatives (46–49) [81]. Structural studies showed that these derivatives could represent a series of rare methylsulfinyladenosine derivatives of interconvertible transesterification isomers and/or sulfinyl epimers. The antiviral activities of 46–49 were evaluated against a series of human pathogenic viruses [81]. The corresponding chemical structures are shown in Figure 6.
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Figure 6. The structures of purine nucleoside analogues (28–49).
Figure 6. The structures of purine nucleoside analogues (28–49).
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3. Pyrimidine Nucleosides

A pyrimidine nucleoside simply consists of a pyrimidine base and a five-carbon sugar (either a ribose or a deoxyribose). The pyrimidine base belongs to the diazines family with two nitrogen atoms position at 1 and 3 of the six-membered aromatic heterocyclic ring. In nucleic acids, pyrimidine nucleosides and pyrimidine nucleotides are composed of three types of nucleobases, they are cytosine (C), uracil (U) and thymine (T) (Figure 1).

3.1. Pyrimidine-d-Arabinosides

In 1950, Bergmann for the first time isolated an unusual nucleoside, spongothymidine (Ara-T, 50) from the sponge C. crypta [14]. This pioneering work of late Prof. Bergmann stimulated a wide interest in the sponges as a source of novel compounds. Spongothymidine (50) was obtained from the sponge C. crypta by acetone extraction [34], and also isolated from the marine sponge Callyspongia sp. [26]. Spongothymidine (50) was found to be effective against HSV-l, HSV-2 and V. zoster virus (VSV) (ID50 0.25–0.5 μg/mL) [82,83]. Its inhibition against HSV-l and HSV-2 was selective and was effective orally [82]. Ara-T was also effective against EMV, but inactive against CMV [83]. Extensive purification of the mixture of nucleosides obtained by Soxhlet extraction of the sponge C. crypta with acetone yielded spongouridine (51) [84]. Spongouridine (51) isolated first from a marine sponge, was subsequently obtained from the gorgonian E. cavolini [85]. Spongouridine has been used as a starting material for the synthesis of marine nucleoside, spongoadenosine (Ara-A), by a combination of chemical and microbial process [85]. Spongouridine was cleaved reversibly [86] to d-arabinose-l-phosphate and uracil by the enzyme nucleoside phosphorylase. Its phosphate has been prepared for antiviral evaluation. It showed weak antiviral properties [87] and very weak activity against HSV-l as compared to spongothymidine. The corresponding chemical structures are shown in Figure 7.
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Figure 7. The structures of pyrimidine-d-arabinosides (50 and 51).
Figure 7. The structures of pyrimidine-d-arabinosides (50 and 51).
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3.2. Pyrimidine-2′-Deoxyribosides

1-(2′-Deoxy-β-d-ribofuranosyl) uracil (2′-deoxyuridine, 52) and 1-(2′-deoxy-β-d-ribofuranosyl) thymine (thymidine, 53) were isolated from starfish Acanthaster planci [88] and also isolated from the marine sponges Haliclona sp. [32] and Callyspongia sp. [26]. The usual pyrimidine nucleosides, 3-methyl-2′-deoxyuridine (54) and 3-methyl-2′-deoxycytidine (55) were identified as the metabolites of Geodia baretti that caused strong contractile activity in the guinea-pig ileum assay [89]. One new nucleoside derivative, named 3-acetyl-5-methyl-2′-deoxyuridine (56), was isolated from the cultures of Streptomyces microflavus. This strain was an associated actinomycete isolated from the marine sponge Hymeniacidon perlevis collected from the coast of Dalian (China) [90]. Based on the analysis of the origin of these pyrimidine-2′-deoxyribosides, they were produced by different species, such as starfish, marine sponges and symbiotic microorganisms. We therefore think whether these different species have some common gene clusters for producing this type of nucleosides are still needed more investigations. The corresponding chemical structures are shown in Figure 8.
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Figure 8. The structures of pyrimidine-2′-deoxyribosides (52–56).
Figure 8. The structures of pyrimidine-2′-deoxyribosides (52–56).
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3.3. Pyrimidine-1-β-d-Ribosides

3-Methylcytidine (57) is the only pyrimidine riboside isolated from marine sponge G. baretti [89], and 57 displayed contractile activity in the ileum assay. Thymidine analogues (58) and (59), previously known as synthetic compounds, were isolated from extracts of Cladiella australis (Taiwan) [91]. Mild cytotoxicity was exhibited by 58 and 59. Famesides A and B (60 and 61), linear sesquiterpenoids connected by ether links to a ribose dihydrouracil nucleoside, were isolated from a marine-derived Streptomyces sp., strain CNT-372, grown in saline liquid culture. The farnesides are only the second example of this exceedingly rare class of microbial terpenoid nucleoside metabolites. Farneside A (60) was found to have modest antimalarial activity against the parasite Plasmodium falciparum [92]. Kipukasins H and I (62 and 63) were isolated from the fungus Aspergillus versicolor derived from the gorgonian Dichotella gemmacea collected in the South China Sea. Compounds 62 and 63 exhibited selective antibacterial activity against Staphylococcus epidermidis with a MIC value of 12.5 μM. This is the first report about their isolation, structure elucidation and biological activities of compounds 62 and 63 [93]. Apart from compound 60, all these pyrimidine-1-β-d-ribosides in this article were found to possess interesting biological properties, further investigations on their pharmacological action mechanism should be carried out, and more analogs should be synthesized to understand their SAR. The corresponding chemical structures are shown in Figure 9.
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Figure 9. The structures of pyrimidine-1-β-d-ribosides (57–63).
Figure 9. The structures of pyrimidine-1-β-d-ribosides (57–63).
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3.4. Analogues of Pyrimidine Nucleosides

Two unusual 2′-deoxy-nucleoside uronic acids, thymidine-5′-carboxylic acid (64) and 2′-deoxyuridine-5′-carboxylic acid (65), were isolated from the Mediterranean tunicate Aplidium fuscum [94]. The synthetically known antiviral agent 2′,3′-didehydro-2′,3′-dideoxyuridine (66) has been obtained from Okinawan marine sponge Aplysina sp. which was collected off the Kerama Islands, Okinawa [29]. The corresponding chemical structures are shown in Figure 10.
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Figure 10. The structures of analogues of pyrimidine nucleosides (64–66).
Figure 10. The structures of analogues of pyrimidine nucleosides (64–66).
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4. Indole Nucleosides

The kahakamides A (67) and B (68) are two new indole nucleosides, which were isolated from the actinomycete Nocardiopsis dassonvillei obtained from a shallow water sediment sample from Kauai, Hawaii. Kahakamide A (67) exhibited slight inhibition of the Gram-positive bacterium Bacillus subtilis in a disc-diffusion assay [95]. These indole nucleosides are seldom found in marine organisms, it is necessary to clarify their biosynthesis pathways in natural resources, and to discover their biological functions. The corresponding chemical structures are shown in Figure 11.
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Figure 11. The structures of indole nucleosides (67 and 68).
Figure 11. The structures of indole nucleosides (67 and 68).
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5. Synthesis

Although studies for the synthesis of the nucleosides began in 1948 [96], the preparations of the nucleosides and their analogues are still a particularly challenging and attractive target for the synthetic community because of their promising pharmacological profiles.
To confirm the proposed structure of avinosol (8) [33], the natural product was synthesized from avarone and 2′-deoxyinosine as shown in Scheme 1. Avarone was prepared in quantitative yield by oxidation of naturally occurring avarol [97], obtained from the Dysidea sp. extract, with MnO2 in Et2O at room temperature for 10 min. Reaction of avarone with 2′-deoxyinosine in DMF and K2CO3 at room temperature for 30 min gave avinosol (8) in 22% yield (Scheme 1) [98].
To further confirm the correct structure of the new inosine disaccharide, the four stereoisomers 2′-O-(α-d-glucosyl)- and 2′-O-(β-d-glucosyl)inosine and 3′-O-(α-d-glucosyl)- and 3′-O-(β-d-glucosyl) inosine were synthesized. The synthetic approach to these compounds must include an O-glycosylation step to form the disaccharide. Although there are plenty of examples of efficient nucleoside formation from simple, elaborated, or disaccharidal glycosyl donors, there are few cases of successful O-glycosylation of a nucleoside [63,99]. Attachment of a glucopyranosyl subunit at O-3′ of inosine would represent a rare example of O-glycosylation of a purine nucleoside because it requires overcoming the double obstacle of steric hindrance and competing depurination. Glycosyl acceptor 26B-a was prepared through two steps (Scheme 2). The protection of inosine (26) with tert-butyldimethylsilyl chloride in pyridine gave a mixture of 2′,5′-di-O- and 3′,5′-di-O-(tert-butyldimethylsilyl) inosines (26A-a, 26A-b). N-1-Benzylation of the 26A-a and 26A-b mixture with benzyl bromide yielded the glycosylation acceptor mixture of 26B-a and 26B-b, which was separated by Silica gel column chromatography. The TBDMS moiety is known to migrate to adjacent hydroxyl groups (from 26B-a to 26B-b and vice versa) under basic conditions [100]. Thus, the second step was performed without separation of 26A-a and 26A-b. Benzyl-protected glucopyranosyl donor was prepared according to a literature procedure [101]. The nonparticipating benzyloxy group at C-2″ was expected to direct α-glycosylation. Scheme 3 showed the synthetic procedure used for the synthesis of 3′-O-(α-d-glucosyl)inosine (27) [66].
A reappraisal of the data for xanthosine suggested an alternative cyclonucleoside structure, namely, N3,5′-cycloxanthosine (44). First it was synthesized in 1963 [102], and further characterized by ORD studies [103], N3,5′-cycloxanthosine remained dormant in the scientific literature until 2004, at which time it came to Robert’s attention through the publication of a convenient one-step synthesis from xanthosine (Scheme 4) [79].
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Scheme 1. Synthesis of avinosol (8) from avarol.
Scheme 1. Synthesis of avinosol (8) from avarol.
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Scheme 2. Synthesis from inosine (26).
Scheme 2. Synthesis from inosine (26).
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Scheme 3. Synthesis of avinosol (27).
Scheme 3. Synthesis of avinosol (27).
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Marinedrugs 12 05817 g015 1024
Scheme 4. Synthesis of N3,5′-cycloxanthosine (44).
Scheme 4. Synthesis of N3,5′-cycloxanthosine (44).
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6. Biosynthetic Pathways

Nucleosides are vital components of all living cells and involved in several biological processes, the biological properties and the chemistry of some nucleosides have been well studied. Some of these molecules are even developed to be approved as drugs. However, the biosynthetic pathways of some promising molecules remain largely unexplored.
Arsenic is naturally present in seawater at concentrations of 2–3 μg dm−3, mainly as arsenate. The major forms of arsenic in marine algae are dimethylarsinylribosides [104]. 5a-e, which are probably metabolized to arsenobetaine (Me3As+CH2CO2−), the usual form of arsenic in marine animals [105] within food chains. It has been proposed that algae biosynthesized dimethylarsinylribosides from absorbed oceanic arsenate by mechanisms first described by Challenger [106] for the biosynthesis of trimethylarsine by microorganisms, and involving S-adenosylmethionine (AdoMet) [107] as the methyl donor and 5′-deoxy-5′-dimethylarsinyladenosine (29) as a key intermediate (Scheme 5) [69].
2′/3′-Transesterification has been known to occur in some ribose derivatives [108,109,110]. The interconversion between 62 and 63, which were isolated from the fungus A. versicolor, was observed during the extraction and purification processes [93]. The 2′-O-acyl ribofuranoside or 3′-O-acyl ribofuranoside was labile and reactive in MeOH-H2O solution and underwent the intramolecular acyl migration to produce isomers. The aroyl in 62 was transferred from the 2′-OH position to the neighboring 3′-OH on the ribose moiety via an ortho-acid ester intermediate [111], yielding the regioisomer 63 (Scheme 6). This aroyl migration was reversible, which finally achieved a dynamic equilibrium (n1:n2 = 7:10, approximately).
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Scheme 5. Proposed biosynthetic pathway for dimethylarsinylribosides.
Scheme 5. Proposed biosynthetic pathway for dimethylarsinylribosides.
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Marinedrugs 12 05817 g017 1024
Scheme 6. Mechanism of the interconversion for 62 and 63 in MeOH-H2O.
Scheme 6. Mechanism of the interconversion for 62 and 63 in MeOH-H2O.
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7. Conclusions

Up to June 2014, studies on marine nucleosides have been focused on the structure, bioactivity, synthesis and proposed biosynthetic pathway. Several bioactive marine nucleosides have been isolated from marine organisms. According to the reported data, marine sponges are the best source of these marine nucleosides. The heterocyclic moiety in marine nucleoside is either a substituted pyrimidine, purine or pyrrolo[2,3-d]pyrimidine moiety. The sugar moiety is either d-arabinose, d-ribose, 2′-deoxyribose, 2′,3′-didehydro, 2′,3′-dideoxyribose or a substituted xylose sugar. The discoveries of these remarkable biological activities found in the marine nucleosides have promoted the great amount of research work on the chemical synthesis of various analogs of these nucleosides. In some cases the compounds have been synthesized prior to the isolation from marine source. These molecules exhibited antiviral, anticancer, vasodilator, muscle relaxant, and hypertensive activities. Among them, the biological activity of the arabinosides is most prominent. Ara-A (1) is one of the best antiviral drugs. The searching for novel analogs of natural nucleosides with potential biological properties has driven the rapid progress in the area of nucleoside chemistry research. Marine nucleosides have provided new “Lead compounds” for drug design, particularly in the area of viral and parasitic infections. Several analogs of bioactive marine nucleosides have been synthesized and evaluated for biological activities. Consequently marine organisms can be a promising source for this class of bioactive compounds. Thus, much more investigations on the chemistry and the biological properties of marine nucleosides should be carried out in order to disclose the potency, selectivity, toxicity and availability of the bioactive marine nucleosides.

Acknowledgments

We thank the authors of all the references cited herein for their valuable contributions. This study was supported by grants from National Natural Science Foundation of China (No. 31100260), Natural Science Foundation of Lingnan Normal University (No. 2L1312), Zhanjiang City-Science and Technology Program (No. 2013A01024), Foundation of Key Laboratory of Plant Resources Conservation and Sustainable Utilization, South China Botanical Garden, Chinese Academy of Sciences (No. 201210ZS). Ri-Ming Huang acknowledges the support of a CAS Academic Visitor Fellowship as academic visitor at University of Bath (with Ian S Blagbrough).

Author Contributions

Ri-Ming Huang contributed in writing the manuscript. Yan Peng conceived and designed the format of the manuscript. All the authors contributed in critical reading and discussion on the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kukhanova, M.K. Anti-HIV nucleoside drugs: A retrospective view into the future. Mol. Biol. 2012, 46, 768–779. [Google Scholar] [CrossRef]
  2. Damaraju, V.L.; Damaraju, S.; Young, J.D.; Baldwin, S.A.; Mackey, J.; Sawyer, M.B.; Cass, C.E. Nucleoside anticancer drugs: The role of nucleoside transporters in resistance to cancer chemotherapy. Oncogene 2003, 22, 7524–7536. [Google Scholar] [CrossRef] [PubMed]
  3. Cooperwood, J.S.; Gumina, G.; Boudinot, F.D.; Chu, C.K. Nucleoside and Nucleotide Prodrugs. In Recent Advances in Nucleosides: Chemistry and Chemotherapy; Elsevier: Amsterdam, The Netherlands, 2002; pp. 91–147. [Google Scholar]
  4. Huryn, D.M.; Okabe, M. Aids-driven nucleoside chemistry. Chem. Rev. 1992, 92, 1745–1768. [Google Scholar] [CrossRef]
  5. Agrofoglio, L.A.; Gillaizeau, I.; Saito, Y. Palladium-assisted routes to nucleosides. Chem. Rev. 2003, 103, 1875–1916. [Google Scholar] [CrossRef] [PubMed]
  6. Mikhailopulo, I.A.; Miroshnikov, A.I. New trends in nucleoside biotechnology. Acta Nat. 2010, 2, 36–58. [Google Scholar]
  7. Faulkner, D.J. Marine natural products. Nat. Prod. Rep. 1993, 10, 497–539. [Google Scholar] [CrossRef] [PubMed]
  8. Isono, K. Nucleoside antibiotics—Structure, biologicalactivity, and biosynthesis. J. Antibiot. 1988, 41, 1711–1739. [Google Scholar] [CrossRef] [PubMed]
  9. Isono, K. Current progress on nucleoside antibiotics. Pharmacol. Ther. 1991, 52, 269–286. [Google Scholar] [CrossRef] [PubMed]
  10. Newman, D.J.; Cragg, G.M. Advanced preclinical and clinical trials of natural products and related compounds from marine sources. Curr. Med. Chem. 2004, 11, 1693–1713. [Google Scholar] [CrossRef] [PubMed]
  11. Newman, D.J.; Cragg, G.M. Marine natural products and related compounds in clinical and advanced preclinical trials. J. Nat. Prod. 2004, 67, 1216–1238. [Google Scholar] [CrossRef] [PubMed]
  12. Proksch, P.; Edrada-Ebel, R.A.; Ebel, R. Drugs from the sea—Opportunities and obstacles. Mar. Drugs 2003, 1, 5–17. [Google Scholar] [CrossRef]
  13. Kijjoa, A.; Sawangwong, P. Drugs and cosmetics from the sea. Mar. Drugs 2004, 2, 73–82. [Google Scholar] [CrossRef]
  14. Bergmann, W.; Feeney, R.J. The isolation of a new thymine pentoside from sponges. J. Am. Chem. Soc. 1950, 72, 2809–2810. [Google Scholar] [CrossRef]
  15. Bhakuni, D.S.; Rawat, D.S. Bioactive Marine Natural Products; Springer: New Delhi, India, 2005; pp. 208–234. [Google Scholar]
  16. Cimino, G.; de Rosa, S.; de Stefano, S. Antiviral agents from a gorgonian, Eunicella cavolini. Experientia 1984, 40, 339–340. [Google Scholar] [CrossRef]
  17. Lee, W.W.; Benitez, A.; Goodman, L.; Baker, B.R. Potential anticancer agents .40. Synthesis of the β-anomer of 9-(d-arabinofuranosyl)-adenine. J. Am. Chem. Soc. 1960, 82, 2648–2699. [Google Scholar] [CrossRef]
  18. Ch’ien, L.T.; Cannon, N.J.; Charamella, L.J.; Dismukes, W.E.; Whitley, R.J.; Buchanan, R.A.; Alford, C.A. Effect of adenine arabinoside on severe Herpesvirus hominis infections in man. J. Infect. Dis. 2004, 190, 1362–1367. [Google Scholar] [CrossRef] [PubMed]
  19. Tsimberidou, A.M.; Keating, M.J.; Giles, F.J.; Wierda, W.G.; Ferrajoli, A.; Lerner, S.; Beran, M.; Andreeff, M.; Kantarjian, H.M.; O’Brien, S. Fludarabine and mitoxantrone for patients with chronic lymphocytic leukemia. Cancer Am. Cancer Soc. 2004, 100, 2583–2591. [Google Scholar]
  20. Plosker, G.L.; Figgitt, D.P. Oral fludarabine. Drugs 2003, 63, 2317–2323. [Google Scholar] [CrossRef] [PubMed]
  21. Whitley, R.; Aford, C.; Hess, F.; Buchanan, R. Vidarbine: A preliminary review of its pharmacological properties and therapeutic use. Drugs 1980, 20, 267–282. [Google Scholar] [CrossRef] [PubMed]
  22. Farmer, P.B.; Suhadoln, R.J. Nucleoside antibiotics—Biosynthesis of arabinofuranosyladenine by Streptomyces antibioticus. Biochemistry 1972, 11, 911–916. [Google Scholar] [CrossRef] [PubMed]
  23. Farmer, P.B.; Uematsu, T.; Hogenkam, H.P.; Suhadoln, R.J. Nucleoside antibiotics—Epimerization of carbon 2′ of adenosine during biosynthesis of 9-β-d-arabinofuranosyladenine by Streptomyces antibioticus. J. Biol. Chem. 1973, 248, 1844–1847. [Google Scholar] [PubMed]
  24. Zemlicka, J. Unusual analogues of nucleosides: Chemistry and biological activity. In Recent Advances in Nucleosides: Chemistry and Chemotherapy; Chu, C.K., Ed.; Elsevier Science B.V.: Amsterdam, The Netherlands, 2002; pp. 327–357. [Google Scholar]
  25. Weinheimer, A.J.; Chang, C.W.; Matson, J.A.; Kaul, P.N. Marine cardioactive agents—Adenosine and 2′-deoxyadenosine from Dasychalina cyathina. Lloydia 1978, 41, 488–490. [Google Scholar] [PubMed]
  26. Huang, R.M.; Zhou, X.F.; Peng, Y.; Yang, X.W.; Xu, T.H.; Liu, Y.H. Nucleosides from the marine sponge Callyspongia sp. Chem. Nat. Compd. 2011, 46, 1010–1011. [Google Scholar] [CrossRef]
  27. Bergmann, W.; Burke, D.C. Contributions to the study of marine products. The nucleosides of sponges .4. Spongosine. J. Org. Chem. 1956, 21, 226–228. [Google Scholar] [CrossRef]
  28. Searle, P.A.; Molinski, T.F. Isolation of spongosine and 2′-deoxyspongosine from a Western Australian sponge of the order Hadromerida (Tethyidae). J. Nat. Prod. 1994, 57, 1452–1454. [Google Scholar]
  29. Kondo, K.; Shigemori, H.; Ishibashi, M.; Kobayashi, J. Aplysidine, a new nucleoside from the Okinawan marine sponge Aplysina sp. Tetrahedron 1992, 48, 7145–7148. [Google Scholar] [CrossRef]
  30. de Koning, H.P.; Bridges, D.J.; Burchmore, R.J. Purine and pyrimidine transport in pathogenic protozoa: From biology to therapy. FEMS Microbiol. Rev. 2005, 29, 987–1020. [Google Scholar] [CrossRef] [PubMed]
  31. Li, G.Q.; Deng, Z.W.; Ii, J.; Fu, H.Z.; Lin, H.W. Chemical constituents from starfish Asterias rollestoni. J. Chin. Pharm. Sci. 2004, 13, 81–86. [Google Scholar]
  32. Wang, B.; Dong, J.; Zhou, X.F.; Lee, K.J.; Huang, R.M.; Zhang, S.; Liu, Y.H. Nucleosides from the marine sponge Haliclona sp. Z. Naturforsch C 2009, 64, 143–148. [Google Scholar] [PubMed]
  33. Diaz-Marrero, A.R.; Austin, P.; van Soest, R.; Matainaho, T.; Roskelley, C.D.; Roberge, M.; Andersen, R.J. Avinosol, a meroterpenoid-nucleoside conjugate with antiinvasion activity isolated from the marine sponge Dysidea sp. Org. Lett. 2006, 8, 3749–3752. [Google Scholar] [CrossRef] [PubMed]
  34. Bergmann, W.; Feeney, R.J. Contributions to the study of marine products: The nucleosides of sponges. J. Org. Chem. 1951, 16, 981–987. [Google Scholar] [CrossRef]
  35. Tian, X.R.; Tang, H.F.; Feng, J.T.; Li, Y.S.; Lin, H.W.; Fan, X.P.; Zhang, X. Neritinaceramides A-E, new ceramides from the marine bryozoan Bugula neritina inhabiting South China Sea and their cytotoxicity. Mar. Drugs 2014, 12, 1987–2003. [Google Scholar] [CrossRef] [PubMed]
  36. Bergmann, W.; Stempien, M.F. Contributions to the study of marine products: The nucleosides of sponges. 5. The synthesis of spongosine. J. Org. Chem. 1957, 22, 1575–1577. [Google Scholar] [CrossRef]
  37. Schaeffer, H.J.; Thomas, H.J. Synthesis of potential anticancer agents. 15. Ribonucleosides of 2-substituted purines. J. Am. Chem. Soc. 1958, 80, 4896–4899. [Google Scholar] [CrossRef]
  38. Matsuda, A.; Nomoto, Y.; Ueda, T. Nucleosides and nucleotides: Synthesis of 2-cyanoadenosines and 8-cyanoadenosines and their derivatives. Chem. Pharm. Bull. 1979, 27, 183–192. [Google Scholar] [CrossRef]
  39. Stimac, A.; Leban, I.; Kobe, J. An efficient stereospecific method for the synthesis of 8-aza-3-deazaguanine nucleosides from glycosyl azides. Synlett 1999, 7, 1069–1073. [Google Scholar] [CrossRef]
  40. Fuhrman, F.A.; Fuhrman, G.J.; Nachman, R.J.; Mosher, H.S. Isoguanosine—Isolation from an animal. Science 1981, 212, 557–558. [Google Scholar] [CrossRef] [PubMed]
  41. Ewing, P.L.; Schlenk, F.; Emerson, G.A. Comparison of smooth muscle effects of crotonoside (isoguanosine) and adenosine. J. Pharm. Exp. Ther. 1949, 97, 379–383. [Google Scholar]
  42. Kaul, P.N. Biomedical potential of the sea. Pure Appl. Chem. 1982, 54, 1963–1972. [Google Scholar] [CrossRef]
  43. Ohisalo, J.J. Regulatory functions of adenosine. Med. Biol. 1987, 65, 181–191. [Google Scholar] [PubMed]
  44. Deckert, J.; Morgan, P.F.; Marangos, P.J. Adenosine uptake site heterogeneity in the mammalian CNS—Uptake Inhibitors as probes and potential neuropharmaceuticals. Life Sci. 1988, 42, 1331–1345. [Google Scholar] [CrossRef] [PubMed]
  45. Quinn, R.J.; Gregson, R.P.; Cook, A.F.; Bartlett, R.T. Isolation and synthesis of 1-methylisoguanosine, a potent pharmacologically active constituent from the marine sponge Tedania digitata. Tetrahedron Lett. 1980, 21, 567–568. [Google Scholar] [CrossRef]
  46. Bairdlambert, J.; Marwood, J.F.; Davies, L.P.; Taylor, K.M. 1-Methylisoguanosine—Orally active marine natural product with skeletal-muscle and cardiovascular effects. Life Sci. 1980, 26, 1069–1077. [Google Scholar] [CrossRef] [PubMed]
  47. Tao, P.L.; Yen, M.H.; Shyu, W.S.; Chern, J.W. Doridosine derivatives—Binding at adenosine receptors and in vivo effects. Eur. J. Pharmacol. 1993, 243, 135–139. [Google Scholar] [CrossRef] [PubMed]
  48. Fuhrman, F.A.; Fuhrman, G.J.; Kim, Y.H.; Pavelka, L.A.; Mosher, H.S. Doridosine—New hypotensive N-methylpurine riboside from the nudibranch Anisodoris nobilis. Science 1980, 207, 193–195. [Google Scholar] [CrossRef] [PubMed]
  49. Kim, Y.H.; Nachman, R.J.; Pavelka, L.; Mosher, H.S.; Fuhrman, F.A.; Fuhrman, G.J. Doridosine, 1-methylisoguanosine, from Anisodoris nobilis—Structure, pharmacological properties and synthesis. J. Nat. Prod. 1981, 44, 206–214. [Google Scholar] [CrossRef] [PubMed]
  50. Davies, L.P.; Taylor, K.M.; Gregson, R.P.; Quinn, R.J. Stimulation of guinea pig brain adenylate cyclase by adenosine analogs with potent pharmacological activity in vivo. Life Sci. 1980, 26, 1079–1088. [Google Scholar] [CrossRef] [PubMed]
  51. Cook, A.F.; Bartlett, R.T.; Gregson, R.P.; Quinn, R.J. 1-Methylisoguanosine, a pharmacologically active agent from a marine sponge. J. Org. Chem. 1980, 45, 4020–4025. [Google Scholar] [CrossRef]
  52. Grozinger, K.; Freter, K.R.; Farina, P.; Gladczuk, A. Synthesis of 7-substituted and 9-substituted 1-methylisoguanines from 4(5)-amino-5(4)-cyanoimidazole. Eur. J. Med. Chem. 1983, 18, 221–226. [Google Scholar]
  53. Jamieson, D.; Davis, P. Inhibition of nerve-mediated contractions in isolated guinea pig ileum by 1-methylisoguanosine, a novel purine from a sponge. Eur. J. Pharm. 1980, 67, 295–300. [Google Scholar] [CrossRef]
  54. Bartlett, R.T.; Cook, A.F.; Holman, M.J.; Mccomas, W.W.; Nowoswait, E.F.; Poonian, M.S.; Bairdlambert, J.A.; Baldo, B.A.; Marwood, J.F. Synthesis and pharmacological evaluation of a deries of snalogs of 1-methylisoguanosine. J. Med. Chem. 1981, 24, 947–954. [Google Scholar] [CrossRef] [PubMed]
  55. Ohkuma, K. Chemical structure of toyocamycin. J. Antibiot. 1960, 13, 361–361. [Google Scholar]
  56. Bergstrom, D.E.; Brattesani, A.J.; Ogawa, M.K.; Schweickert, M.J. Pyrrolo[2,3-d]pyrimidine nucleoside antibiotic analogs—Synthesis viaorganopalladium intermediates derived from 5-mercuritubercidin. J. Org. Chem. 1981, 46, 1423–1431. [Google Scholar] [CrossRef]
  57. Zabriskie, T.M.; Ireland, C.M. The isolation and structure of modified bioactive nucleosides from Jaspis johnstoni. J. Nat. Prod. 1989, 52, 1353–1356. [Google Scholar] [CrossRef] [PubMed]
  58. Biabani, M.F.; Gunasekera, S.P.; Longley, R.E.; Wright, A.E.; Pomponi, S.A. Tubercidin, a cytotoxic agent from the marine sponge Caulospongia biflabellata. Pharm. Biol. 2002, 40, 302–303. [Google Scholar] [CrossRef]
  59. Zhao, J.L.; Ma, M.; Wang, S.J.; Li, S.; Cao, P.; Yang, Y.C.; Lu, Y.; Shi, J.G.; Xu, N.J.; Fan, X.; et al. Bromophenols coupled with derivatives of amino acids and nucleosides from the red alga Rhodomela confervoides. J. Nat. Prod. 2005, 68, 691–694. [Google Scholar] [CrossRef] [PubMed]
  60. Minakawa, N.; Matsuda, A. Nucleosides and nucleotides: Convenient syntheses of 3-deazaadenosine, 3-deazaguanosine, and 3-deazainosine via ring-closure of 5-ethynyl-1-β-d-ribofuranosylimidazole-4-carboxamide or carbonitrile. Tetrahedron 1993, 49, 557–570. [Google Scholar] [CrossRef]
  61. AbouHussein, Dina. R.; Diaa, J.B.; Youssef, T.A. Nucleoside constituents of the Egyptian tunicate Eudistoma laysani. Nat. Prod. Sci. 2007, 13, 229–233. [Google Scholar]
  62. Kobayashi, J.; Doi, Y.; Ishibashi, M. Shimofuridin A, a nucleoside derivative embracing an acylfucopyranoside unit isolated from the Okinawan marine tunicate Aplidium multiplicatum. J. Org. Chem. 1994, 59, 255–257. [Google Scholar] [CrossRef]
  63. Knapp, S.; Gore, V.K. Synthesis of the shimofuridin nucleoside disaccharide. J. Org. Chem. 1996, 61, 6744–6747. [Google Scholar] [CrossRef] [PubMed]
  64. Doi, Y.; Ishibashi, M.; Kobayashi, J. Isolation and structure of shimofuridins B–G from the Okinawan marine tunicate Aplidium multiplicatum. Tetrahedron 1994, 50, 8651–8656. [Google Scholar] [CrossRef]
  65. Ogi, T.; Margiastuti, P.; Teruya, T.; Taira, J.; Suenaga, K.; Ueda, K. Isolation of C-11 cyclopentenones from two didemnidspecies, Lissoclinum sp. and Diplosoma sp. Mar. Drugs 2009, 7, 816–832. [Google Scholar] [CrossRef] [PubMed]
  66. Kim, S.H.; Yoo, S.M.; Park, I.S.; Kim, Y.H. A new inosine disaccharide from the crustacean Ligia exotica: Isolation and structure elucidation by total synthesis. J. Nat. Prod. 2000, 63, 1188–1191. [Google Scholar] [CrossRef] [PubMed]
  67. Cimino, G.; Crispino, A.; Destefano, S.; Gavagnin, M.; Sodano, G. A naturally-occurring analog of methylthioadenosine (MTA) from the nudibranch mollusk Doris verrucosa. Experientia 1986, 42, 1301–1302. [Google Scholar] [CrossRef]
  68. Montgome, J.A.; Shortnacy, A.T.; Thomas, H.J. Analogs of 5′-deoxy-5′-(methylthio)adenosine. J. Med. Chem. 1974, 17, 1197–1207. [Google Scholar] [CrossRef] [PubMed]
  69. Francesconi, K.A.; Stick, R.V.; Edmonds, J.S. An arsenic-containing nucleoside from the kidney of the giant clam, Tridacna maxima. J. Chem. Soc. Chem. Comm. 1991, 14, 928–929. [Google Scholar] [CrossRef]
  70. Kazlauskas, R.; Murphy, P.T.; Wells, R.J.; Baird-Lambert, J.A.; Jamieson, D.D. Halogenated pyrrolo[2,3-d]pyrimidine nucleosides from marine organisms. Aust. J. Chem. 1983, 36, 165–170. [Google Scholar] [CrossRef]
  71. Kato, Y.; Fusetani, N.; Matsunaga, S.; Hashimoto, K. Bioactive marine metabolites, Mycalisine A and mycalisine B, novel nucleosides which inhibit cell-division of fertilized starfish eggs, from the marine sponge Mycale sp. Tetrahedron Lett. 1985, 26, 3483–3486. [Google Scholar] [CrossRef]
  72. Ichiba, T.; Nakao, Y.; Scheuer, P.J.; Sata, N.U.; Kellyborges, M. Kumusine, a chloroadenine riboside from a sponge, Theonella sp. Tetrahedron Lett. 1995, 36, 3977–3980. [Google Scholar] [CrossRef]
  73. Searle, P.A.; Molinski, T.F. Trachycladine A and trachycladine B—2′-C-methyl-5′-deoxyribofuranosyl nucleosides from the marine sponge Trachycladus laevispirulifer. J. Org. Chem. 1995, 60, 4296–4298. [Google Scholar]
  74. Mitchell, S.S.; Pomerantz, S.C.; Concepcion, G.P.; Ireland, C.M. Tubercidin analogs from the ascidian Didemnum voeltzkowi. J. Nat. Prod. 1996, 59, 1000–1001. [Google Scholar] [CrossRef] [PubMed]
  75. Kehraus, S.; Gorzalka, S.; Hallmen, C.; Iqbal, J.; Muller, C.E.; Wright, A.D.; Wiese, M.; Konig, G.M. Novel amino acid derived natural products from the ascidian Atriolum robustum: Identification and pharmacological characterization of a unique adenosine derivative. J. Med. Chem. 2004, 47, 2243–2255. [Google Scholar] [CrossRef] [PubMed]
  76. Margiastuti, P.; Ogi, T.; Teruya, T.; Taira, J.; Suenaga, K.; Ueda, K. An unusual iodinated 5′-deoxyxylofuranosyl nucleoside from an Okinawan ascidian, Diplosoma sp. Chem. Lett. 2008, 37, 448–449, correction in 670. [Google Scholar] [CrossRef]
  77. Ouyang, M.A. A new adenosyl-alkaloid from Ostrea rivularis. Nat. Prod. Res. 2006, 20, 79–83. [Google Scholar] [CrossRef] [PubMed]
  78. Peng, C.S.; Gunaherath, G.M. K.B.; Piggott, A.M.; Khalil, Z.; Conte, M.; Capon, R.J. 9-(5′-Deoxy-5′-thio-β-d-xylofuranosyl)adenine disulfide from the Southern Australian marine sponge Trachycladus laevispirulifer: The first natural occurrence of a nucleoside disulfide. Aust. J. Chem. 2010, 63, 873–876. [Google Scholar] [CrossRef]
  79. Capon, R.J.; Trotter, N.S. N3,5′-cycloxanthosine, the first natural occurrence of a cyclonucleoside. J. Nat. Prod. 2005, 68, 1689–1691. [Google Scholar] [CrossRef] [PubMed]
  80. Menna, M.; Aiello, A.; D’Aniello, F.; Fattorusso, E.; Imperatore, C.; Luciano, P.; Vitalone, R. Further investigation of the mediterranean sponge Axinella polypoides: Isolation of a new cyclonucleoside and a new betaine. Mar. Drugs 2012, 10, 2509–2518. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  81. Li, J.L.; La Kim, E.; Wang, H.; Hong, J.; Shin, S.; Lee, C.K.; Jung, J.H. Epimeric methylsulfinyladenosine derivatives from the marine ascidian Herdmania momus. Bioorg. Med. Chem. Lett. 2013, 23, 4701–4704. [Google Scholar] [CrossRef] [PubMed]
  82. Aswell, J.F.; Allen, G.P.; Jamieson, A.T.; Campbell, D.E.; Gentry, G.A. Antiviral activity of arabinosylthymine in herpesviral replication: Mechanism of action in vivo and in vitro. Antimicrob. Agent Chemother. 1977, 12, 243–254. [Google Scholar] [CrossRef]
  83. Miller, R.L.; Iltis, J.P.; Rapp, F. Differential effect of arabinofuranosylthymine of the replication of human herpesviruses. J. Virol. 1977, 23, 679–684. [Google Scholar] [PubMed]
  84. Bergmann, W.; Burke, D.C. Contributions to the study of marine products: The nucleosides of sponges .3. Spongothymidine and spongouridine. J. Org. Chem. 1955, 20, 1501–1507. [Google Scholar] [CrossRef]
  85. Utagawa, T.; Morisawa, H.; Miyoshi, T.; Yoshinaga, F.; Yamazaki, A.; Mitsugi, K. Novel and simple method for the preparation of adenine arabinoside by bacterial transglycosylation reaction. FEBS Lett. 1980, 109, 261–263. [Google Scholar] [CrossRef] [PubMed]
  86. Tono, H.; Cohen, S.S. Activity of nucleoside phosphorylase on 1-β-d-arabinosyluracil within Escherichia coli. J. Biol. Chem. 1962, 237, 1271–1282. [Google Scholar]
  87. Declercq, E.; Krajewska, E.; Descamps, J.; Torrence, P.F. Anti-herpes activity of deoxythymidine analogs—Specific dependence on virus-induced deoxythymidine kinase. Mol. Pharmacol. 1977, 13, 980–984. [Google Scholar] [PubMed]
  88. Komori, T.; Sanechika, Y.J.; Ito, Y.S.; Matsuo, J.J.; Nohara, T.; Kawasaki, T.; Schulten, H.R. Biologisch aktive glykoside aus Asteroidea, I. Strukturen eines neuen cerebrosidgemischs und von nucleosiden aus dem seestern Acanthaster planci. Leibigs Ann. Chem. 1980, 1980, 653–668. [Google Scholar] [CrossRef]
  89. Lidgren, G.; Bohlin, L.; Christophersen, C. Studies of Swedish marine organisms, biologically active compounds from the marine sponge Geodia baretti. J. Nat. Prod. 1988, 51, 1277–1280. [Google Scholar] [CrossRef]
  90. Li, K.; Li, Q.L.; Ji, N.Y.; Liu, B.; Zhang, W.; Cao, X.P. Deoxyuridines from the marine sponge associated actinomycete Streptomyces microflavus. Mar. Drugs 2011, 9, 690–695. [Google Scholar] [PubMed]
  91. Ahmed, A.F.; Wu, M.H.; Wu, Y.C.; Dai, C.F.; Sheu, J.H. Metabolites with cytotoxic activity from the Formosan soft coral Cladiella australis. J. Chin. Chem. Soc. 2006, 53, 489–494. [Google Scholar]
  92. Ilan, E.Z.; Torres, M.R.; Prudhomme, J.; Le Roch, K.; Jensen, P.R.; Fenical, W. Farnesides A and B, sesquiterpenoid nucleoside ethers from a marine-rerived Streptomyces sp. strain CNT-372 from Fiji. J. Nat. Prod. 2013, 76, 1815–1818. [Google Scholar] [CrossRef] [PubMed]
  93. Chen, M.; Fu, X.M.; Kong, C.J.; Wang, C.Y. Nucleoside derivatives from the marine-derived fungus Aspergillus versicolor. Nat. Prod. Res. 2014, 28, 895–900. [Google Scholar] [CrossRef] [PubMed]
  94. Nicola, D.; Antonio, G.; Françoise, L.; Francesco, P. 2′-Deoxynucleoside uronic acids from the ascidian Aplidium (= Amaroucium) fuscum. Comp. Biochem. Physiol. B 1986, 84, 11–13. [Google Scholar]
  95. Schumacher, R.W.; Harrigan, B.L.; Davidson, B.S. Kahakamides A and B, new neosidomycin metabolites from a marine-derived actinomycete. Tetrahedron Lett. 2001, 42, 5133–5135. [Google Scholar] [CrossRef]
  96. Davoll, J.; Lythgoe, B.; Todd, A.R. Experiments on the synthesis of purine nucleosides: A synthesis of guanosine. J. Chem. Soc. 1948, 1685–1687. [Google Scholar]
  97. Ling, T.T.; Xiang, A.X.; Theodorakis, E.A. Enantioselective total synthesis of avarol and avarone. Angew. Chem. Int. Ed. 1999, 38, 3089–3091. [Google Scholar] [CrossRef]
  98. Narukulla, R.; Shuker, D.E.G.; Xu, Y.Z. Post-synthetic and site-specific modification of endocyclic nitrogen atoms of purines in DNA and its potential for biological and structural studies. Nucleic. Acids Res. 2005, 33, 1767–1778. [Google Scholar] [CrossRef] [PubMed]
  99. Knapp, S. Synthesis of complex nucleoside antibiotics. Chem. Rev. 1995, 95, 1859–1876. [Google Scholar] [CrossRef]
  100. Ogilvie, K.K.; Entwistle, D.W. Silyl protecting groups in nucleoside and nucleotide chemistry, isomerization of tert-butyldimethylsilyl protecting groups in ribonucleosides. Carbohydr. Res. 1981, 89, 203–210. [Google Scholar] [CrossRef]
  101. Abdel-Rahman, S.Z.; Nouraldeen, A.M.; Abo-Elwafa, A.A.; Ahmed, A.E. Acrylonitrile-induced reversible inhibition of uridine uptake by isolated rat intestinal epithelial-cells. Toxicol. Vitro 1994, 8, 139–143. [Google Scholar] [CrossRef]
  102. Holmes, R.E.; Robins, R.K. Purine nucleosides, preparation and reactions of some 9-β-d-ribofuranosyl-3,5′-purine cyclonucleosides. J. Org. Chem. 1963, 28, 3483–3486. [Google Scholar] [CrossRef]
  103. Hampton, A.; Nichol, A.W. Nucleotides, preparation and optical rotatory dispersion of some 9-β-d-ribofuranosyl-3,5′-purine cyclonucleosides. J. Org. Chem. 1967, 1967, 32, 1688–1691. [Google Scholar] [CrossRef]
  104. Edmonds, J.S.; Francesconi, K.A. Transformations of arsenic in the marine-environment. Experientia 1987, 43, 553–557. [Google Scholar]
  105. Cullen, W.R.; Reimer, K.J. Arsenic speciation in the environment. Chem. Rev. 1989, 89, 713–764. [Google Scholar]
  106. Challenger, F. Biological Methylation. Chem. Rev. 1945, 36, 315–361. [Google Scholar] [CrossRef]
  107. Cantoni, G.L. The nature of the active methyl donor formed enzymatically from l-methionine and adenosinetriphosphate. J. Am. Chem. Soc. 1952, 74, 2942–2943. [Google Scholar] [CrossRef]
  108. Hasegawa, H.; Akira, K.; Shinohara, Y.; Kasuya, Y.; Hashimoto, T. Kinetics of intramolecular acyl migration of 1-β-O-acyl glucuronides of (R)- and (S)-2-phenylpropionic acids. Biol. Pharm. Bull. 2001, 24, 852–855. [Google Scholar] [CrossRef] [PubMed]
  109. Jackson, A.D.; Denu, J.M. Structural identification of 2′- and 3′-O-acetyl-ADP-ribose as novel metabolites derived from the Sir2 family of β-NAD(+)-dependent histone/protein deacetylases. J. Biol. Chem. 2002, 277, 18535–18544. [Google Scholar]
  110. Sauve, A.A.; Celic, I.; Avalos, J.; Deng, H.T.; Boeke, J.D.; Schramm, V.L. Chemistry of gene silencing: The mechanism of NAD(+)-dependent deacetylation reactions. Biochemistry 2001, 40, 15456–15463. [Google Scholar] [CrossRef] [PubMed]
  111. Spahnlangguth, H.; Benet, L.Z. Acyl glucuronides revisited—Is the glucuronidation process a toxification as well as a detoxification mechanism. Drug Metab. Rev. 1992, 24, 5–48. [Google Scholar] [CrossRef] [PubMed]

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MDPI and ACS Style

Huang, R.-M.; Chen, Y.-N.; Zeng, Z.; Gao, C.-H.; Su, X.; Peng, Y. Marine Nucleosides: Structure, Bioactivity, Synthesis and Biosynthesis. Mar. Drugs 2014, 12, 5817-5838. https://doi.org/10.3390/md12125817

AMA Style

Huang R-M, Chen Y-N, Zeng Z, Gao C-H, Su X, Peng Y. Marine Nucleosides: Structure, Bioactivity, Synthesis and Biosynthesis. Marine Drugs. 2014; 12(12):5817-5838. https://doi.org/10.3390/md12125817

Chicago/Turabian Style

Huang, Ri-Ming, Yin-Ning Chen, Ziyu Zeng, Cheng-Hai Gao, Xiangdong Su, and Yan Peng. 2014. "Marine Nucleosides: Structure, Bioactivity, Synthesis and Biosynthesis" Marine Drugs 12, no. 12: 5817-5838. https://doi.org/10.3390/md12125817

APA Style

Huang, R. -M., Chen, Y. -N., Zeng, Z., Gao, C. -H., Su, X., & Peng, Y. (2014). Marine Nucleosides: Structure, Bioactivity, Synthesis and Biosynthesis. Marine Drugs, 12(12), 5817-5838. https://doi.org/10.3390/md12125817

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