(5Z,2E)-CU-3结构式
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常用名 | (5Z,2E)-CU-3 | 英文名 | CU-3 |
|---|---|---|---|---|
| CAS号 | 1815598-71-0 | 分子量 | 392.47 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C16H12N2O4S3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
(5Z,2E)-CU-3用途(5Z,2E)-CU-3 是一种有效的选择性抗 DGKα 同工酶抑制剂,IC50 值为 0.6 μM,竞争性抑制 DGKα 对 ATP 的亲和力,Km 值为 0.48 mM。(5Z,2E)-CU-3 靶向 DGKα 催化区域,但不靶向调节区域。(5Z,2E)-CU-3 具有抗肿瘤和免疫原性作用,增强癌细胞的凋亡和 T 细胞的活化。 |
| 中文名 | N-{5-[(E)-3-Furan-2-yl-prop-2-en-(Z)-ylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}-benzenesulfonamide |
|---|---|
| 英文名 | (5Z,2E)-CU-3 |
| 描述 | (5Z,2E)-CU-3 是一种有效的选择性抗 DGKα 同工酶抑制剂,IC50 值为 0.6 μM,竞争性抑制 DGKα 对 ATP 的亲和力,Km 值为 0.48 mM。(5Z,2E)-CU-3 靶向 DGKα 催化区域,但不靶向调节区域。(5Z,2E)-CU-3 具有抗肿瘤和免疫原性作用,增强癌细胞的凋亡和 T 细胞的活化。 |
|---|---|
| 相关类别 | |
| 靶点实验 |
IC50: 0.6 μM (DGKα)[1] |
| 参考文献 |
| 分子式 | C16H12N2O4S3 |
|---|---|
| 分子量 | 392.47 |
| InChIKey | YIUMXULORVBWLL-SPGDJUBISA-N |
| SMILES | O=C1C(=CC=Cc2ccco2)SC(=S)N1NS(=O)(=O)c1ccccc1 |
| 外观性状 | 固体 |
| 储存条件 | 2-8°C,密封,干燥 |
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