Identification of new anti-mycobacterial agents based on quinoline-isatin hybrids targeting enoyl acyl carrier protein reductase (InhA)
- 20 January 2024
- journal article
- research article
- Published by Elsevier in Bioorganic Chemistry
- Vol. 144, 107138
Abstract
No abstract availableKeywords
Funding Information
- Deanship of Scientific Research, King Khalid University (RGP1/296/44)
This publication has 71 references indexed in Scilit:
- Open Babel: An open chemical toolboxJournal of Cheminformatics, 2011
- Molecular basis and mechanisms of drug resistance in Mycobacterium tuberculosis: classical and new drugsJournal of Antimicrobial Chemotherapy, 2011
- SwissParam: A fast force field generation tool for small organic moleculesJournal of Computational Chemistry, 2011
- Structure−Activity Relationships for a Series of Quinoline-Based Compounds Active against Replicating and NonreplicatingMycobacterium tuberculosisJournal of Medicinal Chemistry, 2009
- Radius of gyration as an indicator of protein structure compactnessMolecular Biology, 2008
- Multidrug-resistant tuberculosisBMC Infectious Diseases, 2008
- Pyrrolidine Carboxamides as a Novel Class of Inhibitors of Enoyl Acyl Carrier Protein Reductase from Mycobacterium tuberculosisJournal of Medicinal Chemistry, 2006
- GROMACS: Fast, flexible, and freeJournal of Computational Chemistry, 2005
- Synthesis and evaluation of anti-HIV activity of isatin β-thiosemicarbazone derivativesBioorganic & Medicinal Chemistry Letters, 2005
- In silico prediction of blood–brain barrier permeationDrug Discovery Today, 2003