Thiophene-2结构式
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常用名 | Thiophene-2 | 英文名 | TP2 |
|---|---|---|---|---|
| CAS号 | 420089-51-6 | 分子量 | 419.37 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C18H14F5NO3S | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | N/A |
Thiophene-2用途Thiophene-2 (TP2) 是一种特定的 Pks13 抑制剂。Thiophene-2 抑制分枝酸的生物合成,并迅速导致分枝杆菌细胞死亡。Thiophene-2 对结核分枝杆菌具有活性,MIC 值为 1 μM,并具有有效的抗结核活性。 |
| 英文名 | Thiophene-2 |
|---|---|
| 英文别名 | 更多 |
| 描述 | Thiophene-2 (TP2) 是一种特定的 Pks13 抑制剂。Thiophene-2 抑制分枝酸的生物合成,并迅速导致分枝杆菌细胞死亡。Thiophene-2 对结核分枝杆菌具有活性,MIC 值为 1 μM,并具有有效的抗结核活性。 |
|---|---|
| 相关类别 | |
| 靶点实验 |
MIC: 1 μM (Mycobacterium tuberculosis) |
| 体外研究 | 体外脂肪负荷,抑制脂肪酸激酶3。噻吩-2(TP2;0-125μM)以剂量依赖的方式抑制野生型结核分枝杆菌(Mtb)Pks13(Pks13_-WT)的负载。噻吩-2还抑制棕榈酸(FL C16)负载到抗TP的F79S突变蛋白上[1]。噻吩-2对猴肾Vero细胞和人肝癌HepG2细胞的IC50分别为17.5和7.30μM。当噻吩-2浓度为12.8μM时,在卡介苗感染的J774A.1巨噬细胞内观察到显著的细胞内杀伤活性[1]。 |
| 参考文献 |
| 分子式 | C18H14F5NO3S |
|---|---|
| 分子量 | 419.37 |
| InChIKey | AVRWEULSKHQETA-UHFFFAOYSA-N |
| SMILES | COC(=O)c1c(NC(=O)c2c(F)c(F)c(F)c(F)c2F)sc2c1CCCCC2 |
| 储存条件 | 2-8°C,避光,干燥,密封 |
| 危害码 (欧洲) | Xi |
|---|---|
| 危险品运输编码 | NONH for all modes of transport |
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| MFCD01337175 |