MAT2A-IN-26 is an orally active MAT2A inhibitor with a human IC50 of 17.53 nM. MAT2A-IN-26 inhibits the enzymatic activity of MAT2A, thereby reducing the levels of S-adenosylmethionine (SAM) and symmetric dimethylarginine (sDMA). MAT2A-IN-26 inhibits the proliferation of MTAP-deficient cancer cells and induces anti-tumor efficacy in xenograft models. MAT2A-IN-26 can be used in non-small cell lung cancer research[1].
Molekulargewicht:
437.44
Formel:
C23H21F2N5O2
Target-Kategorie:
Methionine Adenosyltransferase (MAT)
Anwendungsbeschreibung:
MCE Product type: Reference compound
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