Others modulator
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 41788 | CB-6644 | 2316817-88-4 | 96.33% |  |
| CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL | ||||
| 24107 | LXH-3-71 | 2251753-65-6 | ≧97.0% |  |
| LXH-3-71是一种新型“分子胶”，可诱导PHGDH和DDB1-CUL4泛素连接酶之 | ||||
| 20645 | CP-506 ( Synonyms: SN-36506 ) | 2227304-19-8 | 98% Min. | _2227304-19-8.png) |
| CP-506 (SN-36506) 是一种缺氧激活的 DNA 烷基化氮芥化合物前药，能够 | ||||
| 822223 | Venglustat ( ibiglustat ) | 1401090-53-6 | ≧98.0% | _1401090-53-6.png) |
| Ibiglustat (Venglustat) 是一种具有口服活性的，可透过血脑屏障的葡萄 | ||||
| 822224 | 布瑞拉沙秦（Brilaroxazine） | 1239729-06-6 | ≧98.0% |  |
| RP-5063（Brilaroxazine） 是一种多模式的血清素和多巴胺受体调节剂， | ||||
| 822225 | Cadisegliatin (TTP-399) | 859525-02-3 | ≧98.0% |  |
| Cadisegliatin(TTP-399) 是一种潜在的肝脏选择性葡萄糖激酶 (GK) 激活剂 | ||||
| 231106 | PDS-0330 | 2904682-19-3 | ≧98.0% |  |
| PDS-0330 是一种特异性、有效的Claudin-1抑制剂。PDS-0330 干扰 claudin-1 | ||||
| 20258 | CRT0273750 | 1979939-16-6 | ≧98.0% |  |
| CRT0273750 modulates LPA levels in plasma and is suitable for in vivo studies. | ||||
| 20259 | Elinzanetant ( NT-814 ) | 929046-33-3 | ≧98.0% |  |
| Elinzanetant，以前称为 NT-814 (45)，是一种双重 NK1,3R 拮抗剂，因此有 | ||||
| 52002 | K-7174 dihydrochloride | 191089-60-8 | 98% |  |
| K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of | ||||
| 18381 | JPH203 HCl ( Nanvuranlat ) | 1597402-27-1 | ≧95.0% | _1597402-27-1.png) |
| JPH203,也称为KYT- 0353,是一个强有力的和选择性(l型氨基酸转运蛋白 | ||||
| 615201 | CLEFMA | 1246964-32-8 | 98% Min. |  |
| CLEFMA has anti-proliferative activity in H441 cells. CLEFMA may induce autophagic ce | ||||