tcsc3245 THZ2

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Product Description

THZ2 is a potent and selective CDK7 inhibitor with IC50 of 13.9 nM.

IC50 & Target: IC50: 13.9 nM (CDK7)[1]

In Vitro: THZ2 selectively targets CDK7 and potently inhibits the growth of triple-negative but not ER/PR+ breast cancer cells. THZ2 at low nanomolar doses also efficiently suppresses the clonogenic growth of TNBC cells with IC50 of appr 10 nM. THZ2 induces apoptotic cell death in triple-negative but not ER/PR+ breast cancer cells or normal human cells[1].

In Vivo: THZ2 (10 mg/Kg) markedly reduces the growth rate of tumors in mice and demonstrates an anti-tumor activity. Compared to vehicle-treated tumors, tumor tissues isolated from mice treated with THZ2 has reduced proliferation and increased apoptosis, as indicated by immunostaining against Ki67 and cleaved Caspase 3 respectively. THZ2 in NOD-SCID mice leads to reduced body weight, suggesting that THZ2 mayt be less well-tolerated in this particular mouse strain[1].

Information

CAS No1604810-84-5
FormulaC31H28ClN7O2
Clinical Informationclinicalinformation
PathwayCell Cycle/DNA Damage
TargetCDK

Specifications

Purity / Grade>98%
SolubilityDMSO : ≥ 39 mg/mL (68.90 mM)
Smilessmiles

Misc Information

Observed Molecular Weight566.05
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