Phase transfer catalyzed synthesis of bis-quinolines: Antileishmanial activity in experimental visceral leishmaniasis and in vitro antibacterial evaluation
- 28 February 2009
- journal article
- Published by Elsevier BV in European Journal of Medicinal Chemistry
- Vol. 44 (2), 845-853
- https://doi.org/10.1016/j.ejmech.2008.04.014
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Aziridine-2,3-Dicarboxylates, Peptidomimetic Cysteine Protease Inhibitors with Antileishmanial ActivityAntimicrobial Agents and Chemotherapy, 2006
- Synthesis and Antileishmanial Activities of Novel 3-Substituted QuinolinesAntimicrobial Agents and Chemotherapy, 2005
- Camptothecin induced mitochondrial dysfunction leading to programmed cell death in unicellular hemoflagellate Leishmania donovaniCell Death & Differentiation, 2004
- Short‐Course of Oral Miltefosine for Treatment of Visceral LeishmaniasisClinical Infectious Diseases, 2000
- Miltefosine, an Oral Agent, for the Treatment of Indian Visceral LeishmaniasisNew England Journal of Medicine, 1999
- Leishmania–HIV Interaction: Immunopathogenic MechanismsParasitology Today, 1999
- Bisquinolines. 2. Antimalarial N,N-Bis(7-chloroquinolin-4-yl)heteroalkanediaminesJournal of Medicinal Chemistry, 1998
- Practical progress and new drugs for changing patterns of leishmaniasisParasitology Today, 1993
- Fine‐structural Alterations in Leishmania tropica within Human Macrophages Exposed to Antileishmanial Drugs in Vitro1The Journal of Protozoology, 1983
- An Eight‐day Method for Screening Compounds against Leishmania donovani in the Golden Hamster*The Journal of Protozoology, 1958