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抑制剂/激活剂

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凋亡与自噬

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G-749

G-749 是一种高效的, ATP 竞争性的 FLT3 抑制剂，对野生型 FLT3 和突变型 FLT3-D835Y 作用的 IC50 值分别为 0.4 nM 和 0.6 nM。G-749 可用于急性髓系白血病 (AML) 的耐药研究。

货号：
TK0562
规格：

1mg

5mg

10mg
价格：
￥0.00

产品参数

CAS No.	1457983-28-6
生物活性	G-749 is a potent, oral active and ATP competitive FLT3 inhibitor, with IC50s of 0.4 nM and 0.6 nM for FLT3 wild type and FLT3-D835Y, respectively. G-749 can be used for the research of drug resistance for acute myeloid leukemia (AML).
分子式	C25H25N6O2Br
分子量	521.41
运输条件	Room temperature in continental US; may vary elsewhere.
储存条件	Powder -20°C 3 years
溶解性数据	DMSO : 25 mg/mL (47.95 mM; Need ultrasonic)
体内研究	G-749 (3-30 mg/kg; p.o.; daily; for 28 days) shows effective antitumor activity in mouse models.
体外研究	G-749 shows potent and sustained inhibition of the FLT3 wild type and mutants including FLT3-ITD, FLT3-D835Y, FLT3-ITD/N676D, and FLT3-ITD/F691L in cellular assays. G-749 inhibits autophosphorylation of FLT3 with an IC50 value of ≤8 nM in FLT3-WT bearing RS4-11 and in FLT3-ITD harboring MV4-11 and Molm-14 cells. G-749 (0.0001-10 nM; 72 hours) shows strong antiproliferation of leukemia cells addicted to FLT3-ITD (MV4-11 and Molm-14) in a dose-dependent manner. G-749 (25-100 nM; 36 hours) causes antiproliferative activity through apoptosis. G-749 (1.6-1000 nM; 2 hours) shows more potent inhibition of p-FLT3, p-ERK1/2, and p-AKT than AC220 and PKC412.
纯度及产品资料	98%

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