| Literature DB >> 17541186 |
Harunobu Mukaiyama1, Toshihiro Nishimura, Hiroaki Shiohara, Satoko Kobayashi, Yoshimitsu Komatsu, Shinji Kikuchi, Eiichi Tsuji, Noboru Kamada, Hideki Ohnota, Hiroshi Kusama.
Abstract
We synthesized a series of novel 2-anilinopyrazolo[1,5-a]pyrimidine derivatives and evaluated their ability to inhibit c-Src kinase; 7-(2-amino-2-methylpropylamino)-5-cyclopropyl-2-(3,5-dimethoxyphenylamino)pyrazolo[1,5-a]pyrimidine-3-carboxamide 7o and 7-(2-amino-2-methylpropylamino)-2-(3,5-dimethoxyphenylamino)-5-methylpyrazolo[1,5-a]pyrimidine-3-carboxamide 7f showed potent inhibitory activity. Compound 7f inhibited c-Src selectively and exhibited satisfactory central nervous system (CNS) penetration. Furthermore, 7f.HCl reduced the infarct volume in vivo in a rat middle cerebral artery (MCA) occlusion model when administrated intraperitoneally.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17541186 DOI: 10.1248/cpb.55.881
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645