VT103, an analog of VT101, is an orally active and selective TEAD1 protein palmitoylation inhibitor. VT103 inhibits YAP/TAZ-TEAD promoted gene transcription, blocks TEAD auto-palmitoylation, and disrupts interaction between YAP/TAZ and TEAD. VT103 can be used for the research of cancer[1].
Molekulargewicht:
410.41
Reinheit:
99.64
CAS Nummer:
[2290608-13-6]
Formel:
C18H17F3N4O2S
Target-Kategorie:
YAP
Anwendungsbeschreibung:
MCE Product type: Reference compound
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