Exploration of the P2–P3 SAR of aldehyde cathepsin K inhibitors
- 18 May 2004
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 14 (13) , 3425-3429
- https://doi.org/10.1016/j.bmcl.2004.04.084
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Exploration of the P1 SAR of aldehyde cathepsin K inhibitorsBioorganic & Medicinal Chemistry Letters, 2003
- Potent and Selective Inhibition of Human Cathepsin K Leads to Inhibition of Bone Resorption In Vivo in a Nonhuman PrimateJournal of Bone and Mineral Research, 2001
- A Tyrosine-Derived Benzofuranone Related to Diazonamide AOrganic Letters, 2000
- Cathepsin K and the Design of Inhibitors of Cathepsin KCurrent Pharmaceutical Design, 2000
- Asymmetric Synthesis with Chiral Hydrogenolysable Amines: A New Route to Enantiopure EthanolaminesHETEROCYCLES, 1994
- Preparation and reactions of functionalized benzylic organometallics of zinc and copperOrganometallics, 1990
- An Efficient Synthesis of (4S)-(-)-4-Isopropyl-2-oxazolidinoneSynthesis, 1989
- A convenient stereoselective synthesis of 1,2,3-aminodiols from .alpha.-amino acidsThe Journal of Organic Chemistry, 1988
- New approach to the mechanism of the reaction between benzyl Grignard reagents and carbonyl compoundsThe Journal of Organic Chemistry, 1982
- The preparation and dehydration of 1-benzylcycloalkanolsJournal of Chemical Education, 1973