Potent In vitro methicillin-resistant Staphylococcus aureus activity of 2-(1H-indol-3-yl)quinoline derivatives
Authors:
- G. KumaravelGKG. Kumaravel
- Roger L. XieRXRoger L. Xie
- Richard F. RossiRRRichard F. Rossi
- Sylvia MeyerSMSylvia Meyer
- Alban SidhuASAlban Sidhu
- Gregory D. CunyGCGregory D. Cuny
- James R. HauskeJHJames R. Hauske
- 1 December 2000
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 10 (23) , 2675-2678
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Solid-phase synthesis of substituted quinoline and isoquinoline derivatives using heterocyclic N-oxide chemistryTetrahedron Letters, 1998
- Recent Developments in Antibacterial Research1998
- Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibilityJournal of Antimicrobial Chemotherapy, 1997
- Zur Geschichte der AniluvitoninsäureEuropean Journal of Inorganic Chemistry, 1883