Literature DB >> 10853665

Substituted 5,7-diphenyl-pyrrolo[2,3d]pyrimidines: potent inhibitors of the tyrosine kinase c-Src.

M Missbach1, E Altmann, L Widler, M Susa, E Buchdunger, H Mett, T Meyer, J Green.   

Abstract

5,7-Diphenyl-pyrrolo[2,3d]pyrimidines represent a new class of highly potent inhibitors of the tyrosine kinase c-Src (IC50 < 50 nM) with specificity against a panel of different tyrosine kinases. The substitution pattern on the two phenyl rings determines potency and specificity and provides a means to modulate cellular activity.

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Year:  2000        PMID: 10853665     DOI: 10.1016/s0960-894x(00)00131-1

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


  3 in total

1.  The alternative TrkAIII splice variant targets the centrosome and promotes genetic instability.

Authors:  Antonietta Rosella Farina; Antonella Tacconelli; Lucia Cappabianca; Gesilia Cea; Sonia Panella; Antonella Chioda; Alessandra Romanelli; Carlo Pedone; Alberto Gulino; Andrew Reay Mackay
Journal:  Mol Cell Biol       Date:  2009-06-29       Impact factor: 4.272

2.  OCLI-023, a Novel Pyrimidine Compound, Suppresses Osteoclastogenesis In Vitro and Alveolar Bone Resorption In Vivo.

Authors:  Hye Jung Ihn; Taeho Lee; Ju Ang Kim; Doohyun Lee; Nam Doo Kim; Hong-In Shin; Yong Chul Bae; Eui Kyun Park
Journal:  PLoS One       Date:  2017-01-13       Impact factor: 3.240

3.  Development and experimental test of support vector machines virtual screening method for searching Src inhibitors from large compound libraries.

Authors:  Bucong Han; Xiaohua Ma; Ruiying Zhao; Jingxian Zhang; Xiaona Wei; Xianghui Liu; Xin Liu; Cunlong Zhang; Chunyan Tan; Yuyang Jiang; Yuzong Chen
Journal:  Chem Cent J       Date:  2012-11-23       Impact factor: 4.215

  3 in total

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