Literature DB >> 1120982

Synthesis and biological evaluation of xanthine oxidase inhibitors. Pyrazolo(3,4-d)pyrimidines and pyrazolo(3,4-b)pyridines.

I Chu, B M Lynch.   

Abstract

1-, 3-, and 5-substituted pyrazolo[3,4-d]pyrimidines and pyrazolo[3,4-b]pyridines related to allopurinol were synthesized and evaluated as xanthine oxidase inhibitors. Among these compounds, 4-hydroxypyrazolo[3,4-b]pyridine-5-carboxylic acids 12 were found to possess potency in the same order of allopurinol. The influence of the substitutions on the enzyme inhibitory effect and the bulk tolerance of the enzyme-inhibitor complex are discussed.

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Year:  1975        PMID: 1120982     DOI: 10.1021/jm00236a010

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

1.  Regioselective multi-component synthesis of 1H-pyrazolo[3,4-d]pyrimidine-6(7H)-thiones.

Authors:  Shirin Safaei; Iraj Mohammadpoor-Baltork; Ahmad Reza Khosropour; Majid Moghadam; Shahram Tangestaninejad; Valiollah Mirkhani
Journal:  Mol Divers       Date:  2012-08-29       Impact factor: 2.943

2.  3,4,6-Trimethyl-1-phenyl-1H-pyrazolo-[3,4-b]pyridine.

Authors:  Salha Hamri; Abderrafia Hafid; Hafid Zouihri; Saïd Lazar; Mostafa Khouili
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-07-10

3.  Crystal structure of [4-(2-meth-oxy-phen-yl)-3-methyl-1-phenyl-6-tri-fluoro-methyl-1H-pyrazolo-[3,4-b]pyridin-5-yl](thio-phen-2-yl)methanone.

Authors:  V Rajni Swamy; P Gunasekaran; R V Krishnakumar; N Srinivasan; P Müller
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-08-06
  3 in total

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