1078736-39-6Relevant articles and documents
Synthesis and biological evaluation of pyrazoline analogues with β-amino acyl group as dipeptidyl peptidase IV inhibitors
Jun, Mi Ae,Park, Woul Seong,Kang, Seung Kyu,Kim, Ki Young,Kim, Kwang Rok,Rhee, Sang Dal,Bae, Myung Ae,Kang, Nam Sook,Sohn, Sang-Kwon,Kim, Sung Gyu,Lee, Jie Oh,Lee, Duck Hyung,Cheon, Hyae Gyeong,Kim, Sung Soo,Ahn, Jin Hee
, p. 1889 - 1902 (2008/12/22)
A series of pyrazoline derivatives with β-amino acyl group were synthesized and evaluated for their ability to inhibit dipeptidyl peptidase IV. Several pyrazoline derivatives exhibited submicromolar inhibitory activities against DPP-IV. X-ray co-crystal structure of initial hit compound 1h was determined. Among this series, carboxylic acid substituted pyrazoline derivative 2u was the most active and greatly decreased the inhibitory activity toward CYP3A4 enzyme.