1993
DOI: 10.1021/np50099a035
|View full text |Cite
|
Sign up to set email alerts
|

A Novel Norditerpenoid from the Okinawan Soft Coral Sinularia Sp.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

4
42
0

Year Published

2003
2003
2020
2020

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 44 publications
(46 citation statements)
references
References 2 publications
4
42
0
Order By: Relevance
“…[1][2][3][4][5][6][7][8][9][10][11][12][13][14][15] A number of these macrocyclic norcembraniods were recently shown to exhibit an array of bioactivities such as antifungal 6 and cytotoxic properties. 6,[10][11][12][13] The continuing search for bioactive constituents urged us to investigate the secondary metabolites of the soft coral Sinularia gyrosa (Tixier-Durivault, 1970), which was collected by hand using SCUBA along the coast of the Dongsha Atoll off Taiwan.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5][6][7][8][9][10][11][12][13][14][15] A number of these macrocyclic norcembraniods were recently shown to exhibit an array of bioactivities such as antifungal 6 and cytotoxic properties. 6,[10][11][12][13] The continuing search for bioactive constituents urged us to investigate the secondary metabolites of the soft coral Sinularia gyrosa (Tixier-Durivault, 1970), which was collected by hand using SCUBA along the coast of the Dongsha Atoll off Taiwan.…”
Section: Introductionmentioning
confidence: 99%
“…10) Misinterpretation of the X-ray data and of the configuration at C-11 has led to confusion in the literature, and this error has been propagated in many of the later papers 11,12) and reviews. 13) Sato et al reported the C-11 epimer 14) and Shoji et al reported its C-5 epimer and named it sinuleptolide, 15) hence the name 5-episinuleptolide for compound 1. Recently, Tseng et al isolated and determined unambiguously the absolute configuration of 5-episinuleptolide (1) by a modified Mosher's method as 1R, 5S, 8R, 10S, 11R.…”
mentioning
confidence: 99%
“…Gorgonians and soft corals, two groups of coelenterates that belong to the orders Gorgonacea and Alcyonacea respectively, are [45,46,50] Sarcophyton flexuosum 15-17, [11] Sarcophyton stolidotum 372-378 [114] Sarcophyton elegans 18, 19 [12] Sarcophyton cherbonnieri 277, 279, 541 [89] Sarcophyton ehrenbergi 20-23, 204, 205, 263, 542, 543 [13,14] Sarcophyton tortrrosurn 154, 592-594 [58] Sarcophyton tortuosum 585-591 [169,170] Sinularia dissecta 482, 618 [146,176] Sinularia maxima Sinularia polydactyla 516-518, 635-637 [156,180,181] Sinularia maxima 478, 479 [144] Sinularia scabra 507-512 [153][154][155] Sarcophyton crassocaule 440, 441 [17,127,128] Sinularia manaarensis 383-391 [117] Sinularia erecta 498, 500, 609, 610 [151,152] Sinularia leptoclados 491-493 [150] Sinularia lochmodes 496-498, 461 [174,189] Sinularia querciformis 432-435 [126] Sinularia polydactyla 290, 291 [88] Sinularia grandilobata 112-116 [41] [125,150] Sinularia mayi 292-294, 615 [92] Sinularia gyrosaisolated 500-505 [53] Sinularia ovispiculata 56 [26] unidentified soft coral 134-141 [51] Euniceu sp. 52, 58-63, 627-631, 640-644 [24...…”
Section: Resultsmentioning
confidence: 99%
“…Investigation of the chemical constituents of a Taiwanese soft coral Sinularia scabra has afforded five new norditerpenoids, scabrolides C-G (507-510), which were found to be analogs with those of sinuleptolide (511) and 5-epi-sinuleptolide (512) also isolated previously from the same species and other Sinularia. Metabolite 508 was found to exhibit significant cytotoxicity against the growth of Hepa59T/VGH and KB cell lines (ED 50 's 0.5 and 0.7 μg/mL, respectively) [153][154][155]. Four new norcembrene diterpenolds (513-515) have been isolated from several species of the soft coral Sinularia collected in Palau, Western Caroline Islands [52].…”
Section: Furanocembranoidsmentioning
confidence: 99%