A New Renieramycin T Right-Half Analog as a Small Molecule Degrader of STAT3.
EMT
NSCLC
STAT3
degradation
molecular docking
renieramycin derivatives
structure–activity relationship
synthesis
Journal
Marine drugs
ISSN: 1660-3397
Titre abrégé: Mar Drugs
Pays: Switzerland
ID NLM: 101213729
Informations de publication
Date de publication:
14 Aug 2024
14 Aug 2024
Historique:
received:
23
07
2024
revised:
09
08
2024
accepted:
12
08
2024
medline:
28
8
2024
pubmed:
28
8
2024
entrez:
28
8
2024
Statut:
epublish
Résumé
Constitutive activation of STAT3 contributes to tumor development and metastasis, making it a promising target for cancer therapy. (1R,4R,5S)-10-hydroxy-9-methoxy-8,11-dimethyl-3-(naphthalen-2-ylmethyl)-1,2,3,4,5,6-hexahydro-1,5-epiminobenzo[d]azocine-4-carbonitrile, DH_31, a new derivative of the marine natural product Renieramycin T, showed potent activity against H292 and H460 cells, with IC
Identifiants
pubmed: 39195486
pii: md22080370
doi: 10.3390/md22080370
pii:
doi:
Substances chimiques
STAT3 Transcription Factor
0
STAT3 protein, human
0
Antineoplastic Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : National Research Council of Thailand
ID : N42A670567