Literature DB >> 15582406

Anti-coxsackievirus B3 activity of 2-amino-3-nitropyrazolo[1,5-a]pyrimidines and their analogs.

Vadim A Makarov1, Olga B Riabova, Vladimir G Granik, Hans-Martin Dahse, Axel Stelzner, Peter Wutzler, Michaela Schmidtke.   

Abstract

A novel class of 2-amino-4-nitropyrazolo[1,5-a]pyrimidines has been identified as potent inhibitors of coxsackievirus B3 replication. The synthesis of these compounds is based on the regioselective reaction of 3,5-diamino-5-nitropyrazole with unsymmetrical beta-diketones at catalysis by hydrochloric acid leading to 2-amino-4-nitropyrazolo[1,5-a]pyrimidines as key steps.

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Year:  2005        PMID: 15582406     DOI: 10.1016/j.bmcl.2004.10.043

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Benzylidene/2-chlorobenzylidene hydrazides: synthesis, antimicrobial activity, QSAR studies and antiviral evaluation.

Authors:  Davinder Kumar; Vikramjeet Judge; Rakesh Narang; Sonia Sangwan; Erik De Clercq; Jan Balzarini; Balasubramanian Narasimhan
Journal:  Eur J Med Chem       Date:  2010-03-07       Impact factor: 6.514

2.  Crystal structure of 5,5'-[(4-fluoro-phen-yl)methyl-ene]bis-[6-amino-1,3-di-methyl-pyrimidine-2,4(1H,3H)-dione].

Authors:  Naresh Sharma; Goutam Brahmachari; Bubun Banerjee; Rajni Kant; Vivek K Gupta
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-09-10
  2 in total

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