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Dennis S Yamashita / Robert W Marquis / Ren Xie / Sirishkumar D Nidamarthy / Hye-Ja Oh / Jae U Jeong / Karl F Erhard / ( -- ) / Daniel F Veber, J Med Chem, Mar 2006 The syntheses, in vitro characterizations, and rat and monkey in vivo pharmacokinetic profiles of a series of 5-, 6-, and 7-methyl-substituted azepanone-based cathepsin K inhibitors are described. Depending on the particular regiochemical substitution -- MEDLINE/PubMed Citation on Lysosomal cysteine proteases: Structure, function and inhibition of cathepsins. Rebecca Roberts, Drug News Perspect, Dec 2005 Lysosomal cysteine proteases, a subgroup of the cathepsin family, are critical for normal cellular functions such as general protein turnover, antigen processing and bone remodeling. In the past decade, the number of identified human cathepsins has more -- MEDLINE/PubMed Citation on Pharmacokinetics and metabolic disposition of sirolimus in healthy male volunteers after a single oral dose. Louis Y Leung / Heng-Keang Lim / Madelyn W Abell / James J Zimmerman, Ther Drug Monit, Feb 2006 The pharmacokinetics and metabolic disposition of sirolimus (rapamycin, Rapamune), a macrocyclic immunosuppressive agent for the prevention of allograft rejection in organ transplantation, were investigated in 6 healthy male volunteers after a single -- MEDLINE/PubMed Citation on |
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