Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/20419
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dc.contributor.authorBhattacharyya, P K-
dc.contributor.authorMedhi, C-
dc.date.accessioned2013-08-05T10:52:47Z-
dc.date.available2013-08-05T10:52:47Z-
dc.date.issued2004-10-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/20419-
dc.description2043-2048en_US
dc.description.abstractAb initio calculations of some DNA binding drugs, nitrogen mustards, have been performed for studying the effect of substituents in the alkylation reaction. The aziridinium ion of different drugs having different substituents has been studied. The substituents do not affect the formation of aziridinium ion of most drugs but for bendamustine and some model drugs of nitrogen mustards with substituents, ethyl and ethoxy groups, the energies of forming the aziridinium ion are high. The geometrical parameters of the aziridinium ions of drugs remain almost the same. However in bendamustine and some other derivatives of nitrogen mustards, distortion of aziridinium rings are observed. The results do not basically encourage the modification drugs with various substituents in the process of designing new drugs of enhanced alkylating ability. Unlike other drugs, bendamustine and some derivatives may generate carbonium ion in the intermediate state of alkylation.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-A Vol.43A(10) [October 2004]en_US
dc.titleAb initio calculation on the effect of substituents in the alkylation mechanism by nitrogen mustards at N -7 of guanineen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.43A(10) [October 2004]

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