SAR125884
CAS No. 1116743-46-4
SAR125884 ( —— )
产品货号. M20207 CAS No. 1116743-46-4
SAR125844 是一种有效且高度选择性的 MET 受体酪氨酸激酶 (RTK) 抑制剂,用于静脉内给药。 (IC50 值为 4.2 nmol/L)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥356 | 有现货 |
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| 5MG | ¥583 | 有现货 |
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| 10MG | ¥956 | 有现货 |
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| 25MG | ¥1936 | 有现货 |
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| 50MG | ¥3102 | 有现货 |
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| 100MG | ¥5038 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称SAR125884
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述SAR125844 是一种有效且高度选择性的 MET 受体酪氨酸激酶 (RTK) 抑制剂,用于静脉内给药。 (IC50 值为 4.2 nmol/L)。
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产品描述SAR125844 a potent and highly selective inhibitor of the MET receptor tyrosine kinase (RTK) for intravenous administration.?(IC50 value of 4.2 nmol/L).
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体外实验Cell Proliferation Assay Cell Line:H-460 cells, HCT116 cells, H1993 cells, EBC-1 cells, SNU-5 cells, OE33 cells, Hs 746T cells and MKN-45 cellsConcentration:1 nM, 3 nM, 10 nM, 30 nM, 100 nM, 300 nM, 1000 nM, 3000 nM, 10000 nMIncubation Time:96 hResult:Inhibited cell proliferation in all cell lines with MET gene amplification, with IC50 values in the nanomolar range (1-7 nM), with the exception of the lung cancer cell line NCI-H1573.Apoptosis Analysis Cell Line:SNU-5 cells Concentration:1 nM, 3 nM, 10 nM, 30 nM, 100 nM, 300 nM Incubation Time:24 h, 48 h, 72 h Result:Induced massive apoptosis in SNU-5 cells at 48 and 72 hours, with a relative EC50 value of 6 nM and a plateau of 60% at 72 hours.Cell Migration Assay Cell Line:H-460 cells, HCT116 cells, H1993 cells, EBC-1 cells, SNU-5 cells, OE33 cells, Hs 746T cells and MKN-45 cells Concentration:3 nM, 10 nM, 30 nM, 100 nM, 300 nM, 1000 nMIncubation Time:20 h Result:Inhibited cell migration with an IC50 value of 26 nM。
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体内实验Animal Model:SNU-5 and Hs 746T tumor-bearing miceDosage:45 mg/kg Administration:Intravenous injection (i.v.)Result:Resulted in complete and almost complete tumor regression in 3 of 8 mice and 5 of 8 mice, respectively. Animal Model:MET-amplified gastric tumor model mice Dosage:5 mg/kg, 11 mg/kg, 21 mg/kg, 53 mg/kg, 106 mg/kg, 213 mg/kg Administration:Intravenous injection (i.v.)Result:Resulted complete tumor regression in 7 of 8 of mice at 53, 106, and 213 mg/kg and partial regression at 11 and 21 mg/kg.Showed more than 80% MET inhibition at all doses and maintained for 96 hours at 213 mg/kg, 72 hours at.106 mg/kg, and 48 hours at 53 mg/kg.Showed complete or near-complete regression (92%–99%) and maintained for 7 days at 106 mg/kg, and 48 hours at 53 mg/kg.
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同义词——
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通路Angiogenesis
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靶点c-Met/HGFR
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受体MET RTK
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研究领域——
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适应症——
化学信息
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CAS Number1116743-46-4
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分子量550.63
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分子式C25H23FN8O2S2
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纯度>98% (HPLC)
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溶解度DMSO:45 mg/mL (81.72 mM)
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SMILESFc1ccc(cc1)-c1ccc2nnc(Sc3ccc4nc(NC(=O)NCCN5CCOCC5)sc4c3)n2n1
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化学全称1-(6-((6-(4-fluorophenyl)-[124]triazolo[43-b]pyridazin-3-yl)thio)benzo[d]thiazol-2-yl)-3-(2-morpholinoethyl)urea
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Egile C et al. The selective intravenous inhibitor of the MET tyrosine kinase SAR125844 inhibits tumor growth in MET-amplified cancer. Mol Cancer Ther. 2015 Feb;14(2):384-94.
产品手册
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