UNC569 |
Catalog No.GC18308 |
UNC569는 IC50이 2.9nM이고 Ki가 4.3nM인 강력하고 가역적이며 ATP 경쟁적이며 경구 활성인 Mer 키나제 억제제입니다. UNC569는 또한 각각 37nM 및 48nM의 IC50으로 Axl 및 Tyro3를 억제합니다. UNC569는 급성 림프구성 백혈병(ALL) 및 비정형 기형/횡문근 종양 연구에 사용할 수 있습니다.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1350547-65-7
Sample solution is provided at 25 µL, 10mM.
UNC569 is a potent inhibitor of the TAM family receptor tyrosine kinases Mer, Axl, and Tyro3 (IC50s = 2.9, 37, and 48 nM, respectively). It has antiproliferative activity in vitro against acute lymphoblastic leukemia (ALL) cells (IC50s = 0.5 and 1.2 μM for 697 and Jurkat cell lines, respectively) and inhibits Mer phosphorylation (IC50s = 141 and 193 nM in 697 and Jurkat cell lines, respectively). UNC569 activates Akt and ERK1/2 phosphorylation, induces apoptosis, and sensitizes ALL cells to etoposide and methotrexate . In vivo, UNC569 (4 μM) decreases tumor burden by 47.8% relative to vehicle controls in human MYC transgenic zebrafish. UNC569 (10 mg/kg) delays leukemia onset, reduces CNS infiltration, and prolongs survival of mice implanted with patient-derived Mer-expressing ALL primary cells.
Review for UNC569
Average Rating: 5
(Based on Reviews and 27 reference(s) in Google Scholar.)Review for UNC569
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