| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 6111902 | Blarcamesine ( AVex-73 ; AE-37 ) | 195615-83-9 | 98.0% | ![]() |
| ANAVEX2-73 (blacamesine) 是一种 Sigma-1 受体激动剂和毒蕈碱受体调节剂 | ||||
| 1812292 | UC-1728 | 948304-40-3 | ≧98.0% | ![]() |
| UC-1728,又称t-TUCB,是一种可溶性环氧化物水解酶抑制剂。 | ||||
| 1811161 | Tulrampator ( CX-1632 ) | 1038984-31-4 | ≧98.0% | ![]() |
| Tulrampator,也被称为S-47445和CX-1632,是AMPA受体(AMPAR)的积极变构调制 | ||||
| 218701 | TOVINONTRINE ( IMR-687 ) | 2062661-53-2 | ≧98.0% | ![]() |
| TOVINONTRINE (IMR-687) 是一种高选择性和有效的磷酸二酯酶 9 (PDE9) 小分 | ||||
| 2073104 | Enarodustat ( JTZ-951 ) | 1262132-81-9 | 98% Min. | ![]() |
| Enarodustat ( JTZ-951 ) is an orally-active HIF-PH inhibitor with an EC50 of 0.22 Μm | ||||
| 24017 | AMG-193 | 2790567-82-5 | 98.62%; EE 98.28% | ![]() |
| AMG-193是一种口服小分子甲硫腺苷协同PRMT5酶抑制剂。 | ||||
| 111895 | Oteseconazole | 1340593-59-0 | ≧98.0% | ![]() |
| Oteseconazole,也称为 VT-1161,是第一个批准的口服生物利用度和选择 | ||||
| 17031303 | Tirabrutinib游离 ( ONO-4059 ) | 1351636-18-4 | ≧98.0% | ![]() |
| Tirabrutinib,也被称为ONO- 4059,是在抑制剂中,一种强大的、具有口 | ||||
| 17012103 | ONO-4059盐酸盐 | 1439901-97-9 | ≧98.0% | ![]() |
| ONO-4059是BTK的选择性和新型抑制剂,IC50为2.2 nm,ONO-4059与B细胞内的 | ||||
| 181121 | AZD-5904 | 618913-30-7 | ≧98.0% | ![]() |
| AZD5904是一个有效的口服生物利用率MPO抑制剂。在临床前研究中,AZ | ||||
| 237071 | Flavopiridol ( 夫拉平度 ) | 146426-40-6 | ≧98.0% | ![]() |
| Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst | ||||
| 25076 | HC-7366 | 2803470-63-3 | ≧98.0% | ![]() |
| HC-7366 is a potent and selective activator of the general control nonderepressible 2 | ||||
