TYRA-200 is a potent and orally active FGFR2 inhibitor. TYRA-200 inhibits the kinase activity of wild-type FGFR2 and its mutants. TYRA-200 induces significant tumor regression in FGFR2-driven cancer models. TYRA-200 can be used for the research of FGFR2-altered advanced solid tumors, intrahepatic cholangiocarcinoma, and endometrial cancer[1][2].
Molekulargewicht:
449.48
Reinheit:
98.06
CAS Nummer:
[2823289-77-4]
Formel:
C23H24FN7O2
Target-Kategorie:
FGFR
Anwendungsbeschreibung:
MCE Product type: Reference compound
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