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A Novel Series of [1,2,4]Triazolo[4,3-a]Pyridine Sulfonamides as Potential Antimalarial Agents: In Silico Studies, Synthesis and In Vitro Evaluation.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2020 Sep 30; Vol. 25 (19). Date of Electronic Publication: 2020 Sep 30. - Publication Year :
- 2020
-
Abstract
- For the development of new and potent antimalarial drugs, we designed the virtual library with three points of randomization of novel [1,2,4]triazolo[4,3- a ]pyridines bearing a sulfonamide fragment. The library of 1561 compounds has been investigated by both virtual screening and molecular docking methods using falcipain-2 as a target enzyme. 25 chosen hits were synthesized and evaluated for their antimalarial activity in vitro against Plasmodium falciparum . 3-Ethyl- N -(3-fluorobenzyl)- N -(4-methoxyphenyl)-[1,2,4]triazolo[4,3- a ]pyridine-6-sulfonamide and 2-(3-chlorobenzyl)-8-(piperidin-1-ylsulfonyl)-[1,2,4]triazolo[4,3- a ]pyridin-3(2 H )-one showed in vitro good antimalarial activity with inhibitory concentration IC <subscript>50</subscript> = 2.24 and 4.98 μM, respectively. This new series of compounds may serve as a starting point for future antimalarial drug discovery programs.
- Subjects :
- Antimalarials chemistry
Antimalarials pharmacokinetics
Binding Sites
Cell Line
Drug Evaluation, Preclinical
Humans
Ligands
Molecular Docking Simulation
Plasmodium falciparum drug effects
Pyridines chemistry
Pyridines pharmacokinetics
Sulfonamides chemistry
Sulfonamides pharmacokinetics
Triazoles chemistry
Triazoles pharmacokinetics
Antimalarials chemical synthesis
Antimalarials pharmacology
Computer Simulation
Pyridines chemical synthesis
Pyridines pharmacology
Sulfonamides chemical synthesis
Sulfonamides pharmacology
Triazoles chemical synthesis
Triazoles pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 25
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 33007887
- Full Text :
- https://doi.org/10.3390/molecules25194485