Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/19832
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMohan, C Gopi-
dc.contributor.authorMishra, PC-
dc.date.accessioned2013-07-16T08:52:09Z-
dc.date.available2013-07-16T08:52:09Z-
dc.date.issued2000-08-
dc.identifier.issn0975-0959 (Online); 0301-1208 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/19832-
dc.description268-272en_US
dc.description.abstractA series of 6, 11 -dihydro-11-oxodibenz[b,e]oxepin-2-acetic acids (DOAA) which are known to be anti-inflammatory agents were studied. The geometries of some of the molecules obtained from X-ray crystallography were used in the calculations as such while the geometries of their derivatives were obtained by local, partial geometry optimization around the sites of substitution employing the AM1 method, keeping the remaining parts of the geometries the same as those in the parent molecules. Molecular electrostatic potential (MEP) mapping was performed for the molecules using optimized hybridization displacement charges (HDC) combined with Lowdin charges, as this charge distribution has been shown earlier to yield near ab initio quality results. A good correlation has been found between the MEP values near the oxygen atoms of the hydroxyl groups of the carboxy groups of the molecules and their anti-inflammatory activities. The result is broadly in agreement with the model proposed earlier by other authors regarding the structure-activity relationship for other similar molecules.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rightsCC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJBB Vol.37(4) [August 2000]en_US
dc.titleMolecular structure-activity relationship study of some non-steroidal antiinflammatory agents using electrostatic potential mappingen_US
dc.typeArticleen_US
Appears in Collections: IJBB Vol.37(4) [August 2000]

Files in This Item:
File Description SizeFormat 
IJBB 37(4) 268-272.pdf1.12 MBAdobe PDFView/Open


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