Inhibition Mechanisms of Indoleamine 2,3-Dioxygenase 1 (IDO1).
Crystallography, X-Ray
Density Functional Theory
Enzyme Inhibitors
/ chemistry
Humans
Indoleamine-Pyrrole 2,3,-Dioxygenase
/ antagonists & inhibitors
Molecular Conformation
Oximes
/ chemistry
Protein Binding
Quinones
/ chemistry
Recombinant Proteins
/ biosynthesis
Sulfonamides
/ chemistry
Temperature
Triazoles
/ chemistry
Journal
Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531
Informations de publication
Date de publication:
10 10 2019
10 10 2019
Historique:
pubmed:
19
9
2019
medline:
17
6
2020
entrez:
19
9
2019
Statut:
ppublish
Résumé
Indoleamine 2,3-dioxygenase 1 (IDO1) catalyzes the rate-limiting step in the kynurenine pathway of tryptophan metabolism, which is involved in immunity, neuronal function, and aging. Its implication in pathologies such as cancer and neurodegenerative diseases has stimulated the development of IDO1 inhibitors. However, negative phase III clinical trial results of the IDO1 inhibitor epacadostat in cancer immunotherapy call for a better understanding of the role and the mechanisms of IDO1 inhibition. In this work, we investigate the molecular inhibition mechanisms of four known IDO1 inhibitors and of two quinones in detail, using different experimental and computational approaches. We also determine for the first time the X-ray structure of the highly efficient 1,2,3-triazole inhibitor MMG-0358. Based on our results and a comprehensive literature overview, we propose a classification scheme for IDO1 inhibitors according to their inhibition mechanism, which will be useful for further developments in the field.
Identifiants
pubmed: 31525930
doi: 10.1021/acs.jmedchem.9b00942
doi:
Substances chimiques
Enzyme Inhibitors
0
Indoleamine-Pyrrole 2,3,-Dioxygenase
0
Oximes
0
Quinones
0
Recombinant Proteins
0
Sulfonamides
0
Triazoles
0
epacadostat
71596A9R13
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM