Facile isolation of (<i style="mso-bidi-font-style: normal">E</i>)-labda-8(17),12-diene-15,16-dial from <i style="mso-bidi-font-style: normal">Curcuma amada </i>and its conversion to other biologically active compounds

Sheeja, Alan D B; Nair, Mangalam S

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Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/27400

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DC Field	Value	Language
dc.contributor.author	Sheeja, Alan D B	-
dc.contributor.author	Nair, Mangalam S	-
dc.date.accessioned	2014-03-13T04:59:30Z	-
dc.date.available	2014-03-13T04:59:30Z	-
dc.date.issued	2014-03	-
dc.identifier.issn	0975-0983(Online); 0376-4699(Print)	-
dc.identifier.uri	http://hdl.handle.net/123456789/27400	-
dc.description	319-324	en_US
dc.description.abstract	Curcuma amada Roxb. (Zingiberaceae) rhizomes have been found to be a good source of (E)-labda-8(17),12-diene-15,16-dial. This has been chemically transformed to other biologically active compounds like aframodial, zerumin A as well as other natural products like (E)-labda-8(17),12-diene-15,16-olide, 15,16-epoxy-8(17),13(16),14-labdatriene and (-)-marginatone. The antimicrobial activity of zerumin A sodium salt as well as other derivatives of the dialdehyde has been established.	en_US
dc.language.iso	en_US	en_US
dc.publisher	NISCAIR-CSIR, India	en_US
dc.rights	CC Attribution-Noncommercial-No Derivative Works 2.5 India	en_US
dc.source	IJC-B Vol.53B(03) [March 2014]	en_US
dc.subject	Curcuma amada	en_US
dc.subject	Zerumin A	en_US
dc.subject	(E)-labda-8(17),12-diene-15,16-dial	en_US
dc.subject	Aframodial	en_US
dc.subject	Antimicrobial	en_US
dc.subject	Chemical transformation	en_US
dc.title	Facile isolation of (E)-labda-8(17),12-diene-15,16-dial from Curcuma amada and its conversion to other biologically active compounds	en_US
dc.type	Article	en_US
Appears in Collections:	IJC-B Vol.53B(03) [March 2014]

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