Symbiotic Microbiomes of Coral Reefs Sponges and Corals 2019
DOI: 10.1007/978-94-024-1612-1_16
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Natural Products from Corals

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Cited by 9 publications
(12 citation statements)
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“…Seven new diterpenoids, flexibilisolides C-G, flexibilisin C, and 11,12-secoflexibillin along with seven known compounds, were derived from the soft coral Sinularia flexibilis [103]. Flexibilisolide C (201), 11-dehydrosinulariolide (197), 14-deoxycrassin (44), 11-episinulariolide acetate (202), and 3,4:8,11-bisepoxy-7-acetoxycembra-15(17)-en-1,12olide (203) showed cytotoxicity toward human cervical epithelioid carcinoma (HeLa) with ED 50 values ranging from 11.6 to 15.6 µg/mL. Moreover, flexibilisolide C (201), 11dehydrosinulariolide (197), 14-deoxycrassin (44), and 11-episinulariolide acetate (202) were found to exhibit cytotoxicity against B-16 (human melanin carcinoma) cell line with ED 50 values comparable to that of the positive control 5-fluorouracil (9.9 ± 0.8 µg/mL).…”
Section: Cytotoxic Compounds From the Genus Sinulariamentioning
confidence: 99%
“…Seven new diterpenoids, flexibilisolides C-G, flexibilisin C, and 11,12-secoflexibillin along with seven known compounds, were derived from the soft coral Sinularia flexibilis [103]. Flexibilisolide C (201), 11-dehydrosinulariolide (197), 14-deoxycrassin (44), 11-episinulariolide acetate (202), and 3,4:8,11-bisepoxy-7-acetoxycembra-15(17)-en-1,12olide (203) showed cytotoxicity toward human cervical epithelioid carcinoma (HeLa) with ED 50 values ranging from 11.6 to 15.6 µg/mL. Moreover, flexibilisolide C (201), 11dehydrosinulariolide (197), 14-deoxycrassin (44), and 11-episinulariolide acetate (202) were found to exhibit cytotoxicity against B-16 (human melanin carcinoma) cell line with ED 50 values comparable to that of the positive control 5-fluorouracil (9.9 ± 0.8 µg/mL).…”
Section: Cytotoxic Compounds From the Genus Sinulariamentioning
confidence: 99%
“…Compound (2) exhibited moderate cytotoxicity against acute leukemia (HL-60) cell line with IC50 value of 33.5 µM and a weak effect on the hepatoma cancer (HepG2) and colon adenocarcinoma (SW480) cell lines with IC50 values of 64.3 and 71.0 µM, respectively [50]. The structures of the steroids (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18) are shown in Figure 1 and the potential biological activities are shown in Table 1. Steroids, 8αH-3β,11-dihydroxy-5α,6α-expoxy-24-methylene-9,11-secocholestan-9-one (4) and crassarosteroside A (5) were obtained from Sinularia granosa and S. crassa soft coral extracts [51,52], respectively.…”
Section: Steroids Derived From the Genus Sinulariamentioning
confidence: 99%
“…In addition, photosynthetic corals are successfully cultivated in artificial conditions and are the subject of chemical and biomedical investigation [3,4]. Soft corals produce more than 5800 secondary metabolites [5], including rare and unusual fatty acids [6][7][8][9][10][11][12][13], terpenoids [14][15][16], quinones [17], alkaloids [18][19][20][21][22][23], glycosides [24][25][26][27][28][29][30][31] and steroids [18,[32][33][34][35][36][37]. It is known that many secondary metabolites isolated from marine invertebrates including soft corals, exhibit anticancer and other pharmacological activities [38][39][40][41][42][43][44][45].…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, MNPs play an important ecological role amongst marine organisms, especially invertebrates, which compete intensely for nutrients, light, and space [ 13 ]. In this context, invertebrates, such as the soft coral Xenia sp., are recognized as a source of secondary marine natural products such as terpenoids, including diterpenes and sesquiterpenes, capnellenes, and steroids [ 14 ]. The diversity of marine-derived sterols was predicted by Bergmann in 1962, who extensively reviewed sterols’ structures and distribution [ 15 ].…”
Section: Introductionmentioning
confidence: 99%