Literature DB >> 20832916

Structure activity relationship studies of imidazo[1,2-a]pyrazine derivatives against cancer cell lines.

Shailaja Myadaraboina1, Manjula Alla, Venkateshwarlu Saddanapu, Vittal Rao Bommena, Anthony Addlagatta.   

Abstract

Designed novel imidazo[1,2-a]pyrazine based inhibitors, synthesized by condensing α-aminopyrazines with α-halocarbonyl compounds followed by electrophilic substitutions. Cytotoxic effects on four cancer cell lines evaluated. Based on preliminary data, imidazo[1,2-a]pyrazine template redesigned to improve activity.
Copyright © 2010 Elsevier Masson SAS. All rights reserved.

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Year:  2010        PMID: 20832916     DOI: 10.1016/j.ejmech.2010.08.035

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  2 in total

1.  Crystal structure of 2-[12-methyl-14-phenyl-10,13,14,16-tetra-aza-tetra-cyclo[7.7.0.0(2,7).0(11,15)]hexa-deca-1(16),2,4,6,9,11(15),12-heptaen-8-yl-idene]propandi-nitrile.

Authors:  Joel T Mague; Shaaban K Mohamed; Mehmet Akkurt; Hussein M S El-Kashef; Mustafa R Albayati
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-11-08

2.  Synthesis and Antibacterial Activity of Benzo[4,5]isothiazolo[2,3-a]pyrazine-6,6-dioxide Derivatives.

Authors:  Jatinder P Bassin; Michelle J Botha; Rajesh Garikipati; Madhu Goyal; Lee Martin; Amit Shah
Journal:  Molecules       Date:  2017-11-04       Impact factor: 4.411

  2 in total

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