SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 M. It can inhibit PGE1-stimulated increases in cAMP levels in intact human platelets.SQ22536(250 mol/L) attenuates the inhibitory effect of adenosine against ADP-induced platelet aggregation from 85 to 575%, respectively (p<0.001). SQ22536 also attenuates an increase of intraplatelet levels of cAMP by adenosine from 292 to 91 pmol/108 platelets (p<0.05). It has no effect on the platelet antiaggregant activity of inosine (1 to 4 mmol/L) and ADP-induced platelet aggregation
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化学信息
| 名称 | SQ22536 |
| Iupac 化学名称 | SQ22536 |
| 同义词 | 9-(tetrahydrofuran-2-yl)-9h-purin-6-amine |
| 英文同义词 | 9-(tetrahydrofuran-2-yl)-9h-purin-6-amine |
| 分子式 | C9H11N5O |
| 分子量 | 205.22 |
| Smile | c1nc(c2c(n1)n(cn2)C3CCCO3)N |
| InChiKey | UKHMZCMKHPHFOT-UHFFFAOYSA-N |
| InChi | InChI=1S/C9H11N5O/c10-8-7-9(12-4-11-8)14(5-13-7)6-2-1-3-15-6/h4-6H,1-3H2,(H2,10,11,12) |
| Cas号 | 17318-31-9 |
| MDL | MFCD00210216 |
| 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 | |