<span style="font-size:10.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-US;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-US">Carbohydrate hydrolyzing enzymes inhibitory and free radical scavenging activities of substituted 2H-chromene-3-carboxylates, 2H-chromenyl Knoevenagel derivatives and 6H-chromenoquinolinones

Vishnu, S; Srikanth, P; Tiwari, Ashok K; Kumar, D Anand; Raju, B China

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Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/33034

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DC Field	Value	Language
dc.contributor.author	Vishnu, S	-
dc.contributor.author	Srikanth, P	-
dc.contributor.author	Tiwari, Ashok K	-
dc.contributor.author	Kumar, D Anand	-
dc.contributor.author	Raju, B China	-
dc.date.accessioned	2015-10-28T09:38:19Z	-
dc.date.available	2015-10-28T09:38:19Z	-
dc.date.issued	2015-11	-
dc.identifier.issn	0975-0983(Online); 0376-4699(Print)	-
dc.identifier.uri	http://hdl.handle.net/123456789/33034	-
dc.description	1332-1341	en_US
dc.description.abstract	Three series of compounds namely ethyl 2-hydroxy-2-(trifluoromethyl)-2H-chromene-3-carboxylates 3a-q, 2H-chromenyl Knoevenagel derivatives 7a-j and 6H-chromenoquinolinones 9a-l have been prepared. The synthesized compounds 3a-q, 7a-j and 9a-g have been screened for anti-oxidant and anti-diabetic activity. Compound 3i shows the most potent ABTS inhibitory activity when compared to trolox. Compounds 3b, 3d, 3j and 3l show α-amylase inhibitory activity.	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.54B(11) [November 2015]	en_US
dc.subject	2H-Chromene-3-carboxylates	en_US
dc.subject	2H-chromenyl Knoevenagel derivatives	en_US
dc.subject	6H-chromenoquino-linones	en_US
dc.subject	Salicylaldehydes	en_US
dc.subject	4-chloro-3-formylcoumarin	en_US
dc.subject	Anti-oxidant	en_US
dc.subject	Anti-diabetic	en_US
dc.title	Carbohydrate hydrolyzing enzymes inhibitory and free radical scavenging activities of substituted 2H-chromene-3-carboxylates, 2H-chromenyl Knoevenagel derivatives and 6H-chromenoquinolinones	en_US
dc.type	Article	en_US
Appears in Collections:	IJC-B Vol.54B(11) [November 2015]

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