Literature DB >> 11201210

Structure-activity relationships for a collection of structurally diverse inhibitors of purine nucleoside phosphorylase.

A D Andricopulo1, R A Yunes.   

Abstract

Values of inhibition constants, Ki, and concentrations required for 50% inhibition, IC50, for a collection of structurally diverse competitive inhibitors of calf spleen purine nucleoside phosphorylase have been determined employing inosine as substrate. These values have been employed to create predictive quantitative structure-activity relationships (QSAR) which link structure to values of Ki and IC50. These QSAR models have substantial power to predict values and the associated uncertainties for Ki and IC50 for unknown, structurally diverse inhibitors of purine nucleoside phosphorylase.

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Year:  2001        PMID: 11201210     DOI: 10.1248/cpb.49.10

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents.

Authors:  Carolina H Andrade; Livia de B Salum; Marcelo S Castilho; Kerly F M Pasqualoto; Elizabeth I Ferreira; Adriano D Andricopulo
Journal:  Mol Divers       Date:  2008-03-29       Impact factor: 2.943

  1 in total

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