作者
Philip A. Carpino,Bruce A. Lefker,Steven M. Toler,Lydia C. Pan,John R. Hadcock,Ewell R. Cook,Joseph DiBrino,Anthony M. Campeta,Shari L. DeNinno,Kristin L. Chidsey‐Frink,William A. Hada,John Inthavongsay,F.Michael Mangano,Michelle Mullins,David F. Nickerson,Oicheng Ng,C.M. Pirie,John A. Ragan,Colin R. Rose,David A. Tess,Ann S. Wright,Lap-Fai Yu,Michael P. Zawistoski,Paul DaSilva‐Jardine,Theresa C. Wilson,David D. Thompson
摘要
Novel pyrazolinone-piperidine dipeptide derivatives were synthesized and evaluated as growth hormone secretagogues (GHSs). Two analogues, capromorelin (5, CP-424391-18, hGHS-R1a K(i)=7 nM, rat pituicyte EC(50)=3 nM) and the des-methyl analogue 5c (hGHS-R1a K(i)=17 nM, rat pituicyte EC(50)=3 nM), increased plasma GH levels in an anesthesized rat model, with ED(50) values less than 0.05 mg/kg iv. Capromorelin showed enhanced intestinal absorption in rodent models and exhibited superior pharmacokinetic properties, including high bioavailabilities in two animal species [F(rat)=65%, F(dog)=44%]. This short-duration GHS was orally active in canine models and was selected as a development candidate for the treatment of musculoskeletal frailty in elderly adults.