Synthesis and evaluation of 3-phenylpyrazolo[3,4-d]pyrimidine-peptide conjugates as Src kinase inhibitors
Date of Original Version
3-Phenylpyrazolo[3,4-d]pyrimidine (PhPP) derivatives substituted with an alkyl or aryl carboxylic acid at the N1-endocyclic amine, such as PhPP-CH 2COOH (IC50=250 μm), and peptides Ac-CIYKYY (IC 50=400 μm) and Ac-YIYGSFK (IC50=570 μm) were weak inhibitors of polyE4Y phosphorylation by active c-Src. A series of PhPP-peptide conjugates were synthesized using PhPP as an ATP mimic and CIYKYY or YIYGSFK as a peptide substrate to improve the inhibitory potency against active c-Src kinase. PhPP derivatives were attached to the Nterminus or the side chain of amino acids in the peptide template. Two N-terminal substituted conjugates, PhPP-CH2CO-CIYKYY (IC50=0.38 μm) and PhPP-CH2CO-YIYGSFK (IC50=2.7 μm), inhibited the polyE4Y phosphorylation by active c-Src significantly higher than that of the parent compounds. The conjugation of PhPP with the peptides produced a synergistic inhibition effect possibly through creation of favorable interactions between the conjugate and the kinase domain as shown by molecular modeling studies. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
Publication Title, e.g., Journal
Kumar, Anil, Yuehao Wang, Xiaofeng Lin, Gongqin Sun, and Keykavous Parang. "Synthesis and evaluation of 3-phenylpyrazolo[3,4-d]pyrimidine-peptide conjugates as Src kinase inhibitors." ChemMedChem 2, 9 (2007): 1346-1360. doi: 10.1002/cmdc.200700074.