LT-626 is a potent PARP inhibitor with an IC50 of 1.60 nM. LT-626 inhibits cellular PAR synthesis with an EC50 of 17.9 nM and shows enhanced cytotoxicity in colorectal cancer cells harboring MRE11 mutations. LT-626 exhibits synergistic effects with Cisplatin (HY-17394), Oxaliplatin (HY-17371), and SN-38 (HY-13704) in colorectal cancer cells. LT-626 can be used for colorectal research[1].
Molekulargewicht:
379.37
CAS Nummer:
[1207456-03-8]
Formel:
C20H15F2N5O
Target-Kategorie:
PARP
Anwendungsbeschreibung:
MCE Product type: Reference compound
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