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Synthesis and Antileishmanial Activity of 3-(α-Azolylbenzyl)indoles
- Source :
- Journal of Enzyme Inhibition and Medicinal Chemistry, Journal of Enzyme Inhibition and Medicinal Chemistry, Informa Healthcare, 2002, 17 (6), pp.353-358. ⟨10.1080/1475636021000005613⟩
- Publication Year :
- 2002
- Publisher :
- HAL CCSD, 2002.
-
Abstract
- The goal of the present study was to evaluate several azolyl-substituted indoles as new antileishmanial agents. Ten 3- (α -azolylbenzyl)indoles have been synthesized using Friedel-Crafts acylation as a key-step. All the target compounds were found to display high levels of activity when tested against Leishmania mexicana promastigotes in vitro. The most active compounds, showing an IC 50
- Subjects :
- Indoles
Stereochemistry
Meglumine antimoniate
Acylation
Leishmania mexicana
Triazole
Antiprotozoal Agents
[CHIM.THER]Chemical Sciences/Medicinal Chemistry
03 medical and health sciences
chemistry.chemical_compound
Inhibitory Concentration 50
Structure-Activity Relationship
Drug Discovery
medicine
Animals
[SDV.MP.PAR]Life Sciences [q-bio]/Microbiology and Parasitology/Parasitology
Amastigote
ComputingMilieux_MISCELLANEOUS
030304 developmental biology
Pharmacology
Indole test
0303 health sciences
biology
030306 microbiology
General Medicine
[SDV.SP]Life Sciences [q-bio]/Pharmaceutical sciences
biology.organism_classification
In vitro
chemistry
Ketoconazole
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 14756366 and 14756374
- Database :
- OpenAIRE
- Journal :
- Journal of Enzyme Inhibition and Medicinal Chemistry, Journal of Enzyme Inhibition and Medicinal Chemistry, Informa Healthcare, 2002, 17 (6), pp.353-358. ⟨10.1080/1475636021000005613⟩
- Accession number :
- edsair.doi.dedup.....6f2330ca733cd963e192c83b011cd5c5
- Full Text :
- https://doi.org/10.1080/1475636021000005613⟩