DSpace at EWHA: Solandelactones A-I, lactonized cyclopropyl oxylipins isolated from the hydroid Solanderia secunda

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DC Field	Value	Language
dc.contributor.author	송준임	*
dc.date.accessioned	2016-08-28T11:08:33Z	-
dc.date.available	2016-08-28T11:08:33Z	-
dc.date.issued	1996	*
dc.identifier.issn	0040-4020	*
dc.identifier.other	OAK-12490	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/228629	-
dc.description.abstract	Solandelactones A-I(1-9), cyclopropyl and lactone containing novel docosanoids have been isolated from the hydroid Solanderia secunda. The structure of these compounds have been elucidated by combined spectral and chemical studies. Configuration of the cyclopropyl ring has been essigned as the opposite of related oxylipins by NOESY experiments. Absolute stereochemistry has been determined on the basis of chemical transformations and CD measurements of synthetic derivatives. In addition, the biogenetic origin of solandelactones has been discussed. Solandelactones C, D and G exhibited moderate inhibitory activity against Farnesyl Protein Transferase.	*
dc.language	English	*
dc.title	Solandelactones A-I, lactonized cyclopropyl oxylipins isolated from the hydroid Solanderia secunda	*
dc.type	Article	*
dc.relation.issue	32	*
dc.relation.volume	52	*
dc.relation.index	SCI	*
dc.relation.index	SCIE	*
dc.relation.index	SCOPUS	*
dc.relation.startpage	10583	*
dc.relation.lastpage	10596	*
dc.relation.journaltitle	Tetrahedron	*
dc.identifier.doi	10.1016/0040-4020(96)00606-0	*
dc.identifier.scopusid	2-s2.0-0030570847	*
dc.author.google	Seo Y.	*
dc.author.google	Cho K.W.	*
dc.author.google	Rho J.-R.	*
dc.author.google	Shin J.	*
dc.author.google	Kwon B.-M.	*
dc.author.google	Bok S.-H.	*
dc.author.google	Song J.-I.	*
dc.contributor.scopusid	송준임(55500861300)	*
dc.date.modifydate	20231116111945	*