Synthesis and structure-activity optimization of azepane-containing derivatives as PTPN2/PTPN1 inhibitors.
Journal
European journal of medicinal chemistry
ISSN: 1768-3254
Titre abrégé: Eur J Med Chem
Pays: France
ID NLM: 0420510
Informations de publication
Date de publication:
15 Apr 2024
15 Apr 2024
Historique:
received:
05
03
2024
revised:
03
04
2024
accepted:
03
04
2024
pubmed:
12
4
2024
medline:
12
4
2024
entrez:
11
4
2024
Statut:
ppublish
Résumé
Protein tyrosine phosphatases PTPN2 and PTPN1 (also known as PTP1B) have been implicated in a number of intracellular signaling pathways of immune cells. The inhibition of PTPN2 and PTPN1 has emerged as an attractive approach to sensitize T cell anti-tumor immunity. Two small molecule inhibitors have been entered the clinic. Here we report the design and development of compound 4, a novel small molecule PTPN2/N1 inhibitor demonstrating nanomolar inhibitory potency, good in vivo oral bioavailability, and robust in vivo antitumor efficacy.
Identifiants
pubmed: 38604096
pii: S0223-5234(24)00270-8
doi: 10.1016/j.ejmech.2024.116390
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
116390Informations de copyright
Copyright © 2024 Elsevier Masson SAS. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors are all employees of Insilico Medicine. The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.