GK921 |
| Catalog No.GC36142 |
GK921은 인간 재조합 TGase 2에 대한 IC50이 7.71μM인 트랜스글루타미나제 2(TGase) 억제제입니다.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1025015-40-0
Sample solution is provided at 25 µL, 10mM.
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GK921 is a transglutaminase 2 (TGase) inhibitor with an IC50 of 7.71 μM for human recombinant TGase 2. IC50: 7.71 μM (TGase)[1]
GK921 inhibits the TGase 2-induced polymerization of I-κBα and p53 in a dose-dependent manner. The cytotoxicity of GK921 ranged from GI50 of 10-10 to 10-4 M. The average GI50 is 9.05×10-7 M. GK921 rescues p53 levels and consequently induces apoptosis; a concentration-dependent increase in cleaved poly(ADP-ribose) polymerase (c-PARP) and p53 levels is observed[1].
A single treatment with GK921 almost completely reduces tumor growth by stabilizing p53 in the ACHN and CAKI-1 preclinical xenograft tumor models[1].
[1]. Ku BM, et al. Transglutaminase 2 inhibitor abrogates renal cell carcinoma in xenograft models. J Cancer Res Clin Oncol. 2014 May;140(5):757-67.
Average Rating: 5 (Based on Reviews and 19 reference(s) in Google Scholar.)
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