109511-58-2
基本信息
1,4-二氨基-2,3-二氰基-1,4-双(邻氨基苯硫基)丁二烯
1,4-二氨基-2,3-二氰基-1,4-双(邻氨基苯巯基)丁二烯
UO 126
CS-1122
U0126 >99%
U0126, >=98%
U0126
U 0126
U0126 (Uo126)
U 0126 - U 126
1,4-DIAMINO-2,3-DICYANO-1
Bis[amino(o-aminophenylthio)methylene]succinonitrile
物理化学性质
| 熔点 | approximate 154℃(dec.) |
| 沸点 | 565.1±50.0 °C(Predicted) |
| 密度 | 1.44 |
| RTECS号 | EJ9710000 |
| 储存条件 | Desiccate at +4°C |
| 溶解度 | 溶于DMSO（高达200mg/ml）。 |
| 酸度系数(pKa) | 2.11±0.10(Predicted) |
| 形态 | 白色固体 |
| 颜色 | 白色 |
| 水溶解性 | Soluble in DMSO. Poorly soluble in ethanol and water |
| 稳定性 | 自购买之日起 1 年内保持稳定。 DMSO 中的溶液可在 -20° 下保存长达 3 个月。 |
安全数据
| 危险性符号(GHS) |  GHS07 |
| 警示词 | 警告 |
| 危险性描述 | H302-H315-H319-H335 |
| 防范说明 | P261-P280a-P304+P340-P305+P351+P338-P405-P501a |
| 海关编码 | 2930909899 |
常见问题列表
|
MEK2 60 nM (IC 50 ) |
MEK1 70 nM (IC 50 ) |
Treatment with U0126 efficiently reduces progeny virus titers of all tested strains in A549 cells. While nM concentrations of U0126 are efficient to reduce H1N1v and H5N1 (MB1), μM concentrations of U0126 are required to reduce the virus titer of H5N1 (GSB) and H7N7. The EC
50
values for U0126-EtOH against H1N1v are 1.2±0.4 μM in A549 cells and 74.7±1.0 μM in MDCKII cells.
Rat hepatocarcinoma cells (FAO) stimulated by fetal calf serum (FCS) exhibits a significant proportion in S phase (32.62%) whereas U0126 strongly decreases the proportion of cells in S phase (9.92%) and increases the proportion of cells in G
0
-G
1
phase and to a lesser extent in G
2
/M.
Cell Viability Assay
| Cell Line: | A549 and MDCK II cells. |
| Concentration: | 0.001-1000 μM. |
| Incubation Time: | 48 h. |
| Result: | The EC 50 values for U0126 against H1N1v were 1.2 ± 0.4 μM in A549 cells and 74.7 ± 1.0 μM in MDCKII cells |
Mice are treated daily with U0126-EtOH (U0126; i.p., 10.5 mg/kg). In control experiment, tumor sizes are constant or slightly increase all over the kinetic. At the opposite, in all U0126-EtOH experiments, engraftment and early tumor growth are significantly decreased. Furthermore, a 60-70% reduction in the volume of tumors treated with U0126-EtOH is obtained 9 days after injection and thereafter.
Rats are subjected to 120 minutes transient middle cerebral artery occlusion (tMCAO) and thereafter treated with the U0126-EtOH (U0126; i.p., 30 mg/kg) at 0 and 24 hours of reperfusion. After treatment with U0126-EtOH, the vasoconstriction to S6c is markedly reduced.
| Animal Model: | Athymic female nude mice (SWISS, nu/nu). |
| Dosage: | 10.5 mg/kg. |
| Administration: | Intraperitoneal injection daily. |
| Result: | Inhibited tumor growth. |
| Animal Model: | Twelve-week-old female Wistar rats (250 to 265 g) . |
| Dosage: | 30 mg/kg. |
| Administration: | Intraperitoneally. |
| Result: | The vasoconstriction to S6c is markedly reduced. |