CHMFL-ABL-039
產(chǎn)品名稱:CHMFL-ABL-039
產(chǎn)品描述:
產(chǎn)品描述 | CHMFL-ABL-039 is a type II native ABL kinase and drug-resistant V299L mutant BCR-ABL inhibitor (IC50s: 7.9 nM and 27.9 nM) used in the research of chronic myeloid leukemia. |
靶點活性 | ABL V299L mutant:(kd)228 nM , Bcr-Abl:27.9 nM , ABL kinase:7.9 nM |
體外活性 | CHMFL-ABL-039 (0.01-3 μM; 4 hours) can dose-dependently inhibit the ABL Y245 phosphorylation and the subsequent downstream signaling mediators. CHMFL-ABL-039 (0-10 μM; 72 hours) is 6-10 fold more sensitive than Imatinib to BCR-ABL driven cancer cell lines, and BCR-ABL independent cell lines display a great selectivity window comparing to BCR-ABL driven cancer cell lines[1]. |
體內(nèi)活性 | CHMFL-ABL-039 (0.01-3 μM; 4 hours) can dose-dependently inhibit the ABL Y245 phosphorylation and the subsequent downstream signaling mediators. CHMFL-ABL-039 (0-10 μM; 72 hours) is 6-10 fold more sensitive than Imatinib to BCR-ABL drove cancer cell lines, and BCR-ABL independent cell lines display a great selectivity window comparing to BCR-ABL drove cancer cell lines[1]. |
分子量 | 594.63 |
分子式 | C31H33F3N6O3 |
CAS No. | 2304344-56-5 |
存儲
| Powder: -20°C for 3 years | In solvent: -80°C for 2 years
溶解度
DMSO: 55 mg/mL (92.49 mM)
( < 1 mg/mL refers to the product slightly soluble or insoluble )
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