Piperolein B, isopiperolein B and piperamide C9:1(8E): total synthesis and cytotoxicities

Please use this identifier to cite or link to this item: http://dspace.lamu.edu.zm:8080/handle/123456789/188

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DC Field	Value	Language
dc.contributor.author	Kayamba, Francis	-
dc.contributor.author	Dunnill, Christopher	-
dc.contributor.author	Hamnett, David J.	-
dc.contributor.author	Rodriguez, Arantxa	-
dc.contributor.author	Georgopoulos, Nikolaos T.	-
dc.contributor.author	Moran, Wesley J.	-
dc.date.accessioned	2022-06-15T09:50:23Z	-
dc.date.available	2022-06-15T09:50:23Z	-
dc.date.issued	2013	-
dc.identifier.uri	DOI: 10.1039/c3ra42060d	-
dc.identifier.uri	http://155.0.177.102:8080/jspui//xmlui/handle/123456789/188	-
dc.description	This research article can also be accessed through DOI:10.1039/c3ra42060d	en_US
dc.description.abstract	Total syntheses of the reported structures of piperolein B, isopiperolein B and piperamide C9:1(8E) have been achieved. The analytical data reported for piperolein B and piperamide C9:1(8E) match the synthetic values, however those for isopiperolein B do not. The cytotoxicities of these three structurally similar compounds against cancer cell lines of different tissue origins were evaluated and the results indicated that these compounds show differential effects on cancer cell viability.	en_US
dc.language.iso	en	en_US
dc.publisher	The Royal Society of Chemistry	en_US
dc.subject	Piper compounds	en_US
dc.subject	cytotoxic	en_US
dc.title	Piperolein B, isopiperolein B and piperamide C9:1(8E): total synthesis and cytotoxicities	en_US
dc.type	Article	en_US
Appears in Collections:	Pharmaceutical Chemistry and Pharmacognosy

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