Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/8069
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dc.contributor.authorAgrawal, Y. K.-
dc.contributor.authorBhatt, H. G.-
dc.contributor.authorRaval, H. G.-
dc.contributor.authorOza, P. M.-
dc.contributor.authorGogoi, P. J.-
dc.date.accessioned2019-01-09T09:41:16Z-
dc.date.available2019-01-09T09:41:16Z-
dc.date.issued2007-
dc.identifier.urihttp://10.1.7.192:80/jspui/handle/123456789/8069-
dc.descriptionMini-Reviews in Medicinal Chemistry, 2007, 7, 451-460en_US
dc.description.abstractTo develop the newer pharmaceuticals and to spur the strong growth, being a general property of ‘handedness’, chirality plays a major role. The Easson-Stedman principle shows the differences in the biological activity between enantiomers resulted from selective reactivity of one enantiomer with its receptor. It helps to improve the pharmacokinetic properties and to remove undesirable side effects by virtue of the unique activity of enantiomers. Racemic switching and marketing drug combinations are used as tools for drug life-cycle management and to redevelop racemic mixtures as single enantiomers.en_US
dc.publisherBentham Science Publishers Ltd.en_US
dc.relation.ispartofseriesIPFP0271;-
dc.subjectChiralityen_US
dc.subjectenantiomersen_US
dc.subjectstereoselectivityen_US
dc.subjectracemic switchingen_US
dc.subjectdrug combinationen_US
dc.subjectpharmacokineticsen_US
dc.titleChirality: A New Era of Therapeuticsen_US
dc.typeFaculty Papersen_US
Appears in Collections:Faculty Papers

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