CYP1B1-IN-14 TFA is a metabolically stable hCYP1B1 competitive inhibitor with an IC50 of 1.32 nM and a Ki of 0.72 µM. CYP1B1-IN-14 TFA reverses the resistance of cancer cells to Paclitaxel (HY-B0015). CYP1B1-IN-14 TFA acts synergistically with Paclitaxel (HY-B0015) to inhibit tumor growth in xenograft models without obvious toxicity. CYP1B1-IN-14 TFA can be used for the research of cancers such as paclitaxel-resistant lung cancer[1].
Molekulargewicht:
641.27
Formel:
C23H26Br2F3N3O5
Target-Kategorie:
Cytochrome P450,P-glycoprotein
Anwendungsbeschreibung:
MCE Product type: Reference compound
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