2014
DOI: 10.1016/j.tet.2014.07.042
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Novel cytotoxic nine-membered macrocyclic polysulfur cembranoid lactones from the soft coral Sinularia sp.

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Cited by 18 publications
(17 citation statements)
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“…Of the thirty-six cembrane related metabolites 1113-1149 reported from cnidarians in 2014, [709][710][711][712][713][714][715][716][717][718][719][720][721][722] secocrassumol 1113 (Lobophytun crassum) 709 is notable as it is derived from the cembrane skeleton via an unusual C-11-C-12 bond cleavage, sinugyrosanolide A 1114 (Sinularia gyrosa) is an unprecedented C-4 norcembranoid, 710 tortuosenes A 1146 and B 1147 (Sarcophyton tortuosum) 721 represent the rst examples of cembranoids containing a C-2-C-20 ring closure, and sinularbols A 1148 and B 1149 (Sinularia arborea) contain a rare C-3-C-9 ring closure. 722 Cnidarian chemistry is dominated by metabolites derived from terpene biosynthesis, with particularly large numbers falling into the diterpenoid classication.…”
Section: Cnidariansmentioning
confidence: 99%
“…Of the thirty-six cembrane related metabolites 1113-1149 reported from cnidarians in 2014, [709][710][711][712][713][714][715][716][717][718][719][720][721][722] secocrassumol 1113 (Lobophytun crassum) 709 is notable as it is derived from the cembrane skeleton via an unusual C-11-C-12 bond cleavage, sinugyrosanolide A 1114 (Sinularia gyrosa) is an unprecedented C-4 norcembranoid, 710 tortuosenes A 1146 and B 1147 (Sarcophyton tortuosum) 721 represent the rst examples of cembranoids containing a C-2-C-20 ring closure, and sinularbols A 1148 and B 1149 (Sinularia arborea) contain a rare C-3-C-9 ring closure. 722 Cnidarian chemistry is dominated by metabolites derived from terpene biosynthesis, with particularly large numbers falling into the diterpenoid classication.…”
Section: Cnidariansmentioning
confidence: 99%
“…Interestingly, the cytotoxic activity of 8 and 152 against the multidrug-resistant cell lines HepG2/ADM and MCF-7/ADM was comparable to that of the positive control doxorubicin. Furthermore, it was found that compound 152 induced apoptosis, and its selective toxicity toward HepG2/ADM cells was not related to P-glycoproteins [122]. In another chemical investigation, Roy et al [123] reported the isolation of two new alcyonolide congeners, trisnorditerpenoid 1 and diterpenoid 2, from the coral Cespitularia sp.…”
Section: Bioactive Compounds From Coralmentioning
confidence: 99%
“…In previous studies, a series of secondary metabolites, including steroids and cembrane-and capnosane-type diterpenoids, [12][13][14] were isolated from the octocoral Sinularia humilis, and sulfurcontaining natural products were obtained from various octocorals belonging to the genus Sinularia. [9][10][11] Metabolism of the sulfur element was proven to be processed by the associated bacteria. 15,16 To the best of our knowledge, this is the first occasion on which cyclooctasulfur was obtained from a marine invertebrate.…”
Section: Resultsmentioning
confidence: 99%