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首页-小分子抑制剂&激动剂-Tyrosine Kinase-BTK-LFM-A13
LFM-A13

Chemical Structure : LFM-A13

CAS No.: 244240-24-2

LFM-A13 ((Z)-LFM-A13 )

货号: PC-45399Not For Human Use, Lab Use Only.

LFM-A13 is a highly specific inhibitor of BTK with Ki of 1.4 uM, IC50 of 17.2 uM, shows no activity against EGFR, IRK, JAK1, JAK3, or HCK.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

LFM-A13 is a highly specific inhibitor of BTK with Ki of 1.4 uM, IC50 of 17.2 uM, shows no activity against EGFR, IRK, JAK1, JAK3, or HCK.
LFM-A13 enhances the sensitivity to ceramide- or vincristine-induced apoptosis in BTK+ B-lineage leukemic cells; prolongs the median survival time of VPL-treated mice.
LFM-A13 also inhibits Plk3 with IC50 of 61 uM, prevented bipolar mitotic spindle assembly in human breast cancer cells and glioblastoma cells, delays tumor progression in MMTV/neu transgenic mouse model of HER2 positive breast cancer.

物理化学性质&存储条件

分子量 360.0014
分子式 C11H8Br2N2O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

DMSO: ≥ 42 mg/mL

Chemical Name/SMILES

2-Butenamide, 2-cyano-N-(2,5-dibromophenyl)-3-hydroxy-,(2Z)-

参考文献

1. Mahajan S, et al. J Biol Chem. 1999 Apr 2;274(14):9587-99.

2. Uckun FM, et al. Bioorg Med Chem. 2007 Jan 15;15(2):800-14.

3. Uckun FM, et al. Clin Cancer Res. 2002 May;8(5):1224-33.

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