Amanote Research
Register
Sign In
Design, Synthesis, and Evaluation of Aza-Peptide Michael Acceptors as Selective and Potent Inhibitors of Caspases-2, -3, -6, -7, -8, -9, and -10
doi 10.1021/jm0601405.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Design, Synthesis, and Pharmacological Evaluation of Novel NAcylhydrazone Derivatives as Potent Histone Deacetylase 6/8 Dual Inhibitors
Synthesis and Evaluation of Macrocyclic Peptide Aldehydes as Potent and Selective Inhibitors of the 20S Proteasome
Design and Synthesis of Novel Potent Non-Peptide and Orally Active Renin Inhibitors
Acta Crystallographica Section A Foundations of Crystallography
Design, Synthesis and Pharmacological Evaluation of Indolylsulfonamide Amines as Potent and Selective 5-HT6receptor Antagonists
Journal of Enzyme Inhibition and Medicinal Chemistry
Medicine
Drug Discovery
Pharmacology
Synthesis of 7, 5', 6'- And 7, 6', 7'-Trimethoxybenzofurano (3', 2'; 3, 4) Coumarin
Nippon kagaku zassi
Potent Antimicrobial Agents of 8-Aza-Bicyclo[3.2.1]octyl Hydrazide Derivatives: Synthesis and Biological Evaluation
Asian Journal of Chemistry
Chemistry
A Synthesis of 2, 3-Methylenedioxy-7, 8, 10, 11-Tetrahydro-9h-Cyclohepta [A] Naphthalen-9-One
Yakugaku Zasshi
Pharmacology
Pharmaceutical Science
Furan-2-Ylmethylene Thiazolidinediones as Novel, Potent, and Selective Inhibitors of Phosphoinositide 3-Kinase G
Structure-Based Design of Potent and Selective CK1γ Inhibitors
ACS Medicinal Chemistry Letters
Organic Chemistry
Biochemistry
Drug Discovery
