THZ1 is a selective and potent covalent CDK7 inhibitor with an IC50 of 3.2 nM. THZ1 also inhibits the closely related kinases CDK12 and CDK13 and downregulates MYC expression[1][2].
Molecular Weight:
566.05
Purity:
99.84
CAS Number:
[1604810-83-4]
Formula:
C31H28ClN7O2
Target:
CDK
Application Notes:
MCE Product type: Reference compound1
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