Synthesis of Carbamate Derivatives of Biological Interest

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DC Field	Value	Language
dc.contributor.author	SHAHNAZ PERVEEN	-
dc.contributor.author	NASREEN FATIMA	-
dc.contributor.author	KHALID MOHAMMED KHAN	-
dc.contributor.author	AJMAL KHAN	-
dc.contributor.author	MUHAMMAD ALI	-
dc.contributor.author	MUHAMMAD IQBAL CHOUDHARY	-
dc.date.accessioned	2023-12-01T04:19:21Z	-
dc.date.available	2023-12-01T04:19:21Z	-
dc.date.issued	2010-06-12	-
dc.identifier.citation	Perveen, S., Fatima, N., Khan, K. M., Khan, A., Ali, M., & Choudhary, M. I. (2010). Synthesis of carbamate derivatives of biological interest. J. Chem. Soc. Pak, 32, 338-343.	en_US
dc.identifier.issn	0253-5106	-
dc.identifier.uri	http://142.54.178.187:9060/xmlui/handle/123456789/19985	-
dc.description.abstract	A number of carbamates derivatives 1-12 were synthesized and evaluated for their antioxidant, urease inhibition, anticancer, antibacterial and antifungal activities. N-Ethylamine-N¢, N¢-diethyl carbamate (4), showed remarkable metal chelating capability (RSA 98.8%) higher than the standard. Another compound, N-3-benzoic-N¢,N¢-diethyl carbamate (8) also exhibited a moderate antioxidant activity in DPPH radical scavenging assay (RSA 78.7%).	en_US
dc.description.sponsorship	The chemical society of Pakistan is an approved society from the PSF.	en_US
dc.language.iso	en	en_US
dc.publisher	HEJ Research Institute of Chemistry, University of Karachi, Karachi.	en_US
dc.title	Synthesis of Carbamate Derivatives of Biological Interest	en_US
dc.type	Article	en_US
Appears in Collections:	Issue 03

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