PYZD-4409 |
Catalog No.GC17801 |
PYZD-4409는 IC50이 20μM(무세포 효소 분석)인 유비퀴틴 활성화 효소 UBA1의 특이적 억제제입니다. PYZD-4409는 악성 세포에서 세포 사멸을 유도하고 원발성 급성 골수성 백혈병 세포의 클론 생성 성장을 우선적으로 억제합니다.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 423148-78-1
Sample solution is provided at 25 µL, 10mM.
PYZD-4409 is a novel small molecule inhibitor of the ubiquitin-activating enzyme E1 with IC50 value of 20μM [1].
The ubiquitin-activating enzyme E1 is involved in the fist step of protein degradation. It uses ATP to adenylate and transfers the ubiquitin molecule to the next enzyme E2. It is demonstrated that the ubiquitination pathway is increased in the primary leukemia cells. Thus, inhibition of E1 can be a target of hematologic malignancies treatment. PYZD-4409 is screened out from a chemical library based on the pyrazolidine pharmacophore. The IC50 value(20μM) of it has been evaluated in a cell-free enzymatic assay. PYZD-4409 can also inhibit E1 in cultured K562 leukemia cells. PYZD-4409 causes cell death in leukemia, myeloma and solid tumor cell lines. In clonogenic growth assays, PYZD-4409 is found to reduce the growth of AML cells over normal hematopoietic cells. As an essential role of protein degradation, the inhibition of E1 resluts in the increased amounts of cyclin D3 and p53 [1].
References:
[1] G. Wei Xu, Mohsin Ali, Tabitha E. Wood et al. The ubiquitin-activating enzyme E1 as a therapeutic target for the treatment of leukemia and multiple myeloma. Blood. 2010, 115(11): 2251-2259.
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