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THZ1 is a covalent CDK7 inhibitor that binds to cysteine residues located at the outer end of classical kinase structures and is highly selective to CDK7.
Brand: BCM
Solubility: ≥28.3 mg/mL in DMSO; insoluble in H2O; insoluble in EtOH
Attribute [Chem Name] N-[3-[[5-chloro-4-(1H-indol-3-yl)-2-pyrimidinyl]amino]phenyl]-4-[[(2E)-4-(dimethylamino)-1-oxo-2-buten-1-yl]amino]-benzamide [Synonym] THZ1 [CAS No.] 1604810-83-4 [Formula] C31H28ClN7O2 [Molecular] 566.05300 [Form] Powder [MDL No.] MFCD28167785
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