Rational Design of Original Fused-Cycle ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Rational Design of Original Fused-Cycle Selective Inhibitors of Tryptophan 2,3-Dioxygenase.
Auteur(s) :
Kozlova, A. [Auteur]
Thabault, L. [Auteur]
Liberelle, Maxime [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Klaessens, S. [Auteur]
Prévost, J. R. C. [Auteur]
Mathieu, C. [Auteur]
Pilotte, L. [Auteur]
Stroobant, V. [Auteur]
Van Den Eynde, B. [Auteur]
Frédérick, R. [Auteur]
Thabault, L. [Auteur]
Liberelle, Maxime [Auteur]

Lille Neurosciences & Cognition (LilNCog) - U 1172
Klaessens, S. [Auteur]
Prévost, J. R. C. [Auteur]
Mathieu, C. [Auteur]
Pilotte, L. [Auteur]
Stroobant, V. [Auteur]
Van Den Eynde, B. [Auteur]
Frédérick, R. [Auteur]
Titre de la revue :
Journal of Medicinal Chemistry
Numéro :
64
Pagination :
10967–10980
Date de publication :
2021-08-08
ISSN :
1520-4804
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Tryptophan 2,3-dioxygenase (TDO2) is a heme-containing enzyme constitutively expressed at high concentrations in the liver and responsible for l-tryptophan (l-Trp) homeostasis. Expression of TDO2 in cancer cells results ...
Lire la suite >Tryptophan 2,3-dioxygenase (TDO2) is a heme-containing enzyme constitutively expressed at high concentrations in the liver and responsible for l-tryptophan (l-Trp) homeostasis. Expression of TDO2 in cancer cells results in the inhibition of immune-mediated tumor rejection due to an enhancement of l-Trp catabolism via the kynurenine pathway. In the study herein, we disclose a new 6-(1H-indol-3-yl)-benzotriazole scaffold of TDO2 inhibitors developed through rational design, starting from existing inhibitors. Rigidification of the initial scaffold led to the synthesis of stable compounds displaying a nanomolar cellular potency and a better understanding of the structural modulations that can be accommodated inside the active site of hTDO2.Lire moins >
Lire la suite >Tryptophan 2,3-dioxygenase (TDO2) is a heme-containing enzyme constitutively expressed at high concentrations in the liver and responsible for l-tryptophan (l-Trp) homeostasis. Expression of TDO2 in cancer cells results in the inhibition of immune-mediated tumor rejection due to an enhancement of l-Trp catabolism via the kynurenine pathway. In the study herein, we disclose a new 6-(1H-indol-3-yl)-benzotriazole scaffold of TDO2 inhibitors developed through rational design, starting from existing inhibitors. Rigidification of the initial scaffold led to the synthesis of stable compounds displaying a nanomolar cellular potency and a better understanding of the structural modulations that can be accommodated inside the active site of hTDO2.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
Inserm
CHU Lille
Inserm
CHU Lille
Collections :
Date de dépôt :
2024-01-16T01:56:56Z
2024-06-10T07:18:13Z
2024-06-10T07:18:13Z