DSpace at EWHA: Synthesis and biological properties of benzo-annulated rutaecarpines

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DC Field	Value	Language
dc.contributor.author	권영주	*
dc.date.accessioned	2016-08-28T12:08:44Z	-
dc.date.available	2016-08-28T12:08:44Z	-
dc.date.issued	2010	*
dc.identifier.issn	0918-6158	*
dc.identifier.other	OAK-6942	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/221076	-
dc.description.abstract	A series of benzo-annulated rutaecarpines were prepared from anthranilic acid and 3-aminonaphthalene-2- carboxylic acid by Fischer indole synthesis as key reaction. Cytotoxicity was somewhat increased by the introduction of benzo-annulation, which was not directly related to the inhibitory activity against topoisomerases (topo) I and II. Benzo-annulation on ring A led to significant increase of inhibitory activity against topo II while annulations on ring E increased inhibitory activity against topo I. © 2010 Pharmaceutical Society of Japan.	*
dc.language	English	*
dc.title	Synthesis and biological properties of benzo-annulated rutaecarpines	*
dc.type	Article	*
dc.relation.issue	10	*
dc.relation.volume	33	*
dc.relation.index	SCI	*
dc.relation.index	SCIE	*
dc.relation.index	SCOPUS	*
dc.relation.startpage	1704	*
dc.relation.lastpage	1709	*
dc.relation.journaltitle	Biological and Pharmaceutical Bulletin	*
dc.identifier.wosid	WOS:000282420300011	*
dc.identifier.scopusid	2-s2.0-77958008285	*
dc.author.google	Hong Y.H.	*
dc.author.google	Lee W.J.	*
dc.author.google	Lee S.H.	*
dc.author.google	Son J.K.	*
dc.author.google	Kim H.L.	*
dc.author.google	Nam J.M.	*
dc.author.google	Kwon Y.	*
dc.author.google	Jahng Y.	*
dc.contributor.scopusid	권영주(12446435600)	*
dc.date.modifydate	20240422124907	*