您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > AKN-028
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
AKN-028
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
AKN-028图片
CAS NO:1175017-90-9
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
AKN-028 是一种新型酪氨酸激酶 (TKI) 抑制剂,是一种有效的口服活性的 FMS 样受体酪氨酸激酶 3 (FLT3) 抑制剂,其IC50值为 6 nM。AKN-028 抑制 FLT3 自磷酸化。AKN-028 诱导剂量依赖性的细胞毒性反应 (平均IC50=1 μM)。AKN-028 通过激活 caspase 3 诱导细胞凋亡 (apoptosis)。AKN-028 可用于急性髓系白血病 (AML) 的研究。
生物活性

AKN-028, a noveltyrosine kinase (TK)inhibitor, is a potent, orally activeFMS-like receptor tyrosine kinase 3 (FLT3)inhibitor with anIC50value of 6 nM. AKN-028 inhibitsFLT3autophosphorylation. AKN-028 induces dose-dependent cytotoxic response (meanIC50=1 μM). AKN-028 inducesapoptosisby activation ofcaspase 3. AKN-028 can be used in research of acute myeloid leukemia (AML)[1].

IC50& Target

IC50: 6 nM (FLT3), 140 nM (CLK1), 220 nM (RPS6KA), 520 nM (VEGFR2), and 120 nM (FGFR2)[1]

体外研究
(In Vitro)

AKN-028 (0.1 nM-100 μM; 15 h; mouse embryonal fibroblasts and human acute megakaryoblastic leukemia M07 cells) inhibits FLT3 and KIT autophosphorylation in a dose-dependent manner[1].
AKN-028 (10 μM; 72 h; tumor cell lines) is cytotoxic to AML cell lines and induces apoptosis in the AML cell line MV4-11[1].

Western Blot Analysis[1]

Cell Line:Mouse embryonal fibroblasts either overexpressing FLT-wt, FLT3-TKD or FLT3-ITD and human acute megakaryoblastic leukemia M07 cells overexpressing KIT
Concentration:0.1 nM-100 μM
Incubation Time:15 hours
Result:Inhibited FLT3 and KIT autophosphorylation.

Cell Cytotoxicity Assay[1]

Cell Line:Tumor cell lines
Concentration:10 μM
Incubation Time:72 hours
Result:Had cytotoxic activity was highest in MV4-11 and MOLM-13 (IC50<50 nM), followed by the three other AML cell lines (IC50=0.5-6 μM).
体内研究
(In Vivo)

AKN-028 (15 mg/kg; i.h.; twice daily, for 6 days; male C57 black mice with MV4-11 xenografts) inhibits growth of primary AML and MV4-11 cells in mice[1].

Animal Model:Male C57 black mice with MV4-11 xenografts[1]
Dosage:15 mg/kg
Administration:Subcutaneous injection; twice daily, for 6 days
Result:Inhibited tumor growth and did not affect body weight.
Clinical Trial
分子量

302.33

Formula

C17H14N6

CAS 号

1175017-90-9

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

溶解性数据
In Vitro: 

DMSO : 125 mg/mL(413.46 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.3076 mL16.5382 mL33.0764 mL
5 mM0.6615 mL3.3076 mL6.6153 mL
10 mM0.3308 mL1.6538 mL3.3076 mL