Reactant for synthesis of: A coumarin-based HIV-1 Vpr inhibitor Antitumor agents as potent chemosensitizers Oxime carbamates as reversible inhibitors of fatty acid amide hydrolase Dipeptidyl peptidase 4 inhibitors for the treatment of type 2 diabetes Bisarylmaleimide glycogen synthase kinase-3 inhibitors Lysosomal acid lipase inhibitors and potential Niemann-Pick type C disease therapeutics
Journal of medicinal chemistry, 58(17), 6928-6937 (2015-08-19)
Cathepsin K is a major drug target for osteoporosis and related-bone disorders. Using a combination of virtual combinatorial chemistry, QSAR modeling, and molecular docking studies, a series of cathepsin K inhibitors based on N-(functionalized benzoyl)-homocycloleucyl-glycinonitrile scaffold was developed. In order
Correlation of the rates of solvolysis of 1-piperidincarbonyl chloride using the extended Grunwald-Winstein equation.
Choi H, et al.
Bull. Korean Chem. Soc., 32(11), 3941-3941 (2011)
New nordihydroguaiaretic acid derivatives as anti-HIV agents.
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