Design, synthesis, and biological evaluation of novel analogues of archazolid: A highly potent simplified V-ATPase inhibitor
- 24 December 2006
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 17 (6) , 1732-1735
- https://doi.org/10.1016/j.bmcl.2006.12.073
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Stereochemical Determination of Archazolid A and B, Highly Potent Vacuolar-Type ATPase Inhibitors from the Myxobacterium Archangium gephyraOrganic Letters, 2006
- Archazolid and apicularen: Novel specific V-ATPase inhibitorsBMC Biochemistry, 2005
- Plasmalemmal Vacuolar-Type H+-ATPase in Cancer BiologyCell Biochemistry and Biophysics, 2004
- Archazolids, New Cytotoxic Macrolactones from Archangium gephyra (Myxobacteria) Production, Isolation, Physico-chemical and Biological PropertiesThe Journal of Antibiotics, 2003
- Concanamycin A, the Specific Inhibitor of V-ATPases, Binds to the Vo Subunit cJournal of Biological Chemistry, 2002
- The vacuolar (H+)-ATPases — nature's most versatile proton pumpsNature Reviews Molecular Cell Biology, 2002
- Animal plasma membrane energization by proton-motive V-ATPasesBioEssays, 1999
- Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafnessNature Genetics, 1999
- Semianalytical treatment of solvation for molecular mechanics and dynamicsJournal of the American Chemical Society, 1990
- Macromodel—an integrated software system for modeling organic and bioorganic molecules using molecular mechanicsJournal of Computational Chemistry, 1990