Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21845
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSrivastava, Arun K-
dc.contributor.authorShakeel, Mohd-
dc.contributor.authorKhan, Arbab A-
dc.date.accessioned2013-10-10T11:59:13Z-
dc.date.available2013-10-10T11:59:13Z-
dc.date.issued2002-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21845-
dc.description436-439en_US
dc.description.abstractQSAR studies, using structural parameters such as equalized electronegativity 'Xeq', molecular connectivity ‘1b' and hydrophobicity ‘logP' on a novel series of ω-amino alkanoic acid derivatives of betulinic acid, have been discussed. Anti HIV-1 activity of these compounds both in CEM-4 and MT-4 cell cultures is found to correlate well with steric 1b as well as electronic Xeq parameters. The presence of an amide function is found to be important for activity.  en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.41B(02) [February 2002]en_US
dc.titleQSAR studies on anti HIV-1 N-substituted betulinic acid amidesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.41B(02) [February 2002]

Files in This Item:
File Description SizeFormat 
IJCB 41B(2) 436-439.pdf720.25 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.