Synthesis of a bromotyrosine-derived natural product inhibitor of mycothiol-S-conjugate amidase
- 16 July 2004
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 14 (14) , 3785-3788
- https://doi.org/10.1016/j.bmcl.2004.04.095
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Solution Conformations of Mycothiol Bimane, 1-d-GlcNAc-α- (1 → 1)-d-myo-Ins and 1-d-GlcNAc-α-(1 → 1)-l-myo-InsThe Journal of Organic Chemistry, 2003
- Inhibition and kinetics of mycobacterium tuberculosis and mycobacterium smegmatis mycothiol-S-conjugate amidase by natural product inhibitorsBioorganic & Medicinal Chemistry, 2003
- Mycothiol biochemistryArchiv für Mikrobiologie, 2002
- Erasing the World's Slow Stain: Strategies to Beat Multidrug-Resistant TuberculosisScience, 2002
- Multidrug-resistant tuberculosis and HIV infection.Annals of the New York Academy of Sciences, 2001
- Combinatorial Synthesis through Disulfide Exchange: Discovery of Potent Psammaplin A Type Antibacterial Agents Active against Methicillin-ResistantStaphylococcus aureus (MRSA)Chemistry – A European Journal, 2001
- Novel Bromotyrosine Alkaloids: Inhibitors of Mycothiol S-Conjugate AmidaseOrganic Letters, 2001
- Paradox of the global emergency of tuberculosisThe Lancet, 1999
- Brominated tyrosine metabolites from an unidentified spongeThe Journal of Organic Chemistry, 1987
- Phenolic constituents ofTetrahedron Letters, 1987