Challenging the Biginelli scaffold to surpass the first line antitubercular drugs:
Mycobacterium tuberculosis
/ drug effects
Antitubercular Agents
/ pharmacology
Nucleoside-Phosphate Kinase
/ antagonists & inhibitors
Structure-Activity Relationship
Microbial Sensitivity Tests
Molecular Structure
Dose-Response Relationship, Drug
Mice
Models, Molecular
Animals
RAW 264.7 Cells
Enzyme Inhibitors
/ pharmacology
Biginelli
Mycobacterium tuberculosis thymidine monophosphate kinase
Tetrahydropyrimidine
antitubercular activity
molecular dynamics simulation
Journal
Journal of enzyme inhibition and medicinal chemistry
ISSN: 1475-6374
Titre abrégé: J Enzyme Inhib Med Chem
Pays: England
ID NLM: 101150203
Informations de publication
Date de publication:
Dec 2024
Dec 2024
Historique:
medline:
11
9
2024
pubmed:
11
9
2024
entrez:
11
9
2024
Statut:
ppublish
Résumé
New Biginelli adducts were rationalised,
Identifiants
pubmed: 39258667
doi: 10.1080/14756366.2024.2386668
doi:
Substances chimiques
Antitubercular Agents
0
Nucleoside-Phosphate Kinase
EC 2.7.4.4
dTMP kinase
EC 2.7.4.9
Enzyme Inhibitors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM