Title of article :
N-4-Pyrimidinyl-1H-indazol-4-amine inhibitors of Lck: Indazoles as phenol isosteres with improved pharmacokinetics
Author/Authors :
Paul Bamborough، نويسنده , , Richard M. Angell، نويسنده , , Inder Bhamra، نويسنده , , David Brown، نويسنده , , James Bull، نويسنده , , John A. Christopher، نويسنده , , Anthony W.J. Cooper، نويسنده , , Lynsey H. Fazal، نويسنده , , Ilaria Giordano، نويسنده , , S. Lucy Hind، نويسنده , , Vipulkumar K. Patel، نويسنده , , Lisa E. Ranshaw، نويسنده , , Martin J. Sims، نويسنده , , Philip A. Skone، نويسنده , , Kathryn J. Smith، نويسنده , , Emma Vickerstaff، نويسنده , , Melanie Washington، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
6
From page :
4363
To page :
4368
Abstract :
2,4-Dianilino pyrimidines are well-known inhibitors of tyrosine kinases including lymphocyte specific kinase (Lck). Structure–activity relationships at the 4-position are discussed and rationalised. Examples bearing a 2-methyl-5-hydroxyaniline substituent at the 4-position were especially potent but showed poor oral pharmacokinetics. Replacement of this substituent by 4-amino(5-methyl-1H-indazole) yielded compounds with comparable enzyme potency and improved pharmacokinetic properties.
Keywords :
2 , 4-Dianilino pyrimidines , p56Lck inhibitors , Lck inhibitors , Protein kinase inhibitors
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
2007
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
798426
Link To Document :
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