Literature DB >> 6718460

New guanine deaminase inhibitors.

A K Saxena, S Ahmad, K Shanker, K Kishor.   

Abstract

2-Aryl/alkyl-3-(5'-carboxamido-imidazol-4'-yl)-quinazolin-4-(3H)-o nes have been reported as Guanine deaminase inhibitors. These compounds were prepared from 4-amino-5-imidazol-carboxamide and suitable 2-aryl/alkyl-benzoxazin-4-ones. Compounds were characterized by their m.ps., elemental analyses and I. R. spectra. These compounds have shown significant inhibition, aryl substituent was more effective than alkyl group. This is the first report when quinazolones have been reported as Guanine deaminase inhibitors. Inhibitors of this enzyme can enhance the bioavailability of purine antagonists and in turn are helpful for the chemotherapy of cancer.

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Year:  1984        PMID: 6718460     DOI: 10.1016/s0031-6989(84)80107-1

Source DB:  PubMed          Journal:  Pharmacol Res Commun        ISSN: 0031-6989


  3 in total

1.  A novel transition state analog inhibitor of guanase based on azepinomycin ring structure: Synthesis and biochemical assessment of enzyme inhibition.

Authors:  Saibal Chakraborty; Niti H Shah; James C Fishbein; Ramachandra S Hosmane
Journal:  Bioorg Med Chem Lett       Date:  2010-11-27       Impact factor: 2.823

Review 2.  Nucleobase deaminases: a potential enzyme system for new therapies.

Authors:  Vandana Gaded; Ruchi Anand
Journal:  RSC Adv       Date:  2018-06-28       Impact factor: 4.036

3.  Analogs of iso-azepinomycin as potential transition-state analog inhibitors of guanase: synthesis, biochemical screening, and structure-activity correlations of various selectively substituted imidazo[4,5-e][1,4]diazepines.

Authors:  Saritha Tantravedi; Saibal Chakraborty; Niti H Shah; James C Fishbein; Ramachandra S Hosmane
Journal:  Bioorg Med Chem       Date:  2013-07-11       Impact factor: 3.641

  3 in total

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