YM-90709 is an interleukin-5 receptor antagonist. YM-90709 inhibits the binding of IL-5 to its receptor on peripheral human eosinophils and butyric acid-treated eosinophilic HL-60 clone 15 cells, with IC50 values of 1.0 and 0.57 microM, respectively. In functional assays, YM-90709 inhibited IL-5-prolonged eosinophil survival with an IC50 value of 0.45 microM and did not affect the GM-CSF-prolonged eosinophil survival. Furthermore, YM-90709 inhibited the IL-5-induced but not GM-CSF-induced tyrosine phosphorylation of Janus kinase 2 (JAK2) in eosinophilic HL-60 clone 15 cells.
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化学信息
名称 | YM-90709 |
Iupac 化学名称 | YM-90709 |
同义词 | YM-90709; YM 90709; YM90709 |
英文同义词 | YM-90709; YM 90709; YM90709 |
分子式 | C22H21N3O2 |
分子量 | 359.429 |
Smile | CC1(Cc2cc(c(cc2-c3n1c4c(c3)nc5ccccc5n4)OC)OC)C |
InChiKey | HIXSPVQXXDULHS-UHFFFAOYSA-N |
InChi | InChI=1S/C22H21N3O2/c1-22(2)12-13-9-19(26-3)20(27-4)10-14(13)18-11-17-21(25(18)22)24-16-8-6-5-7-15(16)23-17/h5-11H,12H2,1-4H3 |
Cas号 | 163769-88-8 |
MDL | MFCD00354370 |
相关CAS号 | |
外观性状 | crystalline solid |
纯度 | 98% |
存储 | 3 years -20ºCpowder |
可溶性 | Soluble in DMSO |
处理方式 | |
运输条件 | Shipped under ambient temperature as non-hazardous chemical. |
海关编码 | |
Targets | |
Mechanism | |
Cell study | |
Animal study | |
Clinical study | |