Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 26A003 | Pimicotinib hydrochloride | 2759304-23-7 | ≧98.0% |  |
| Pimicotinib (ABSK021) hydrochloride is a selective and orally active CSF1R inhibitor. | ||||
| 26A002 | Quecitinib | 2416858-84-7 | ≧98.0% |  |
| Quecitinib is a dual inhibitor of JAK1 and TYK2. | ||||
| 26A001 | Enterololin | 1445830-39-6 | ≧98.0% |  |
| Enterololin is an antibacterial compound with targeted activity against Enterobacteri | ||||
| 26B001 | 5-azaspiro[4.5]decan-5-ium bromide | 16431-36-0 | ≧98.0% |  |
| 25210 | MAT2A-IN-23 | 2925324-58-7 | ≧98.0% |  |
| MAT2A-IN-23 39 is a potent MTA2A inhibitor. | ||||
| 25211 | AXKO-0046 | 3103525-82-9 | ≧98.0% |  |
| AXKO-0046 is a small-molecule LDHB selective inhibitor. | ||||
| 25209 | Temozolomide | 85622-93-1 | ≧98.0% |  |
| Temozolomide is an alkylating agent. | ||||
| 25208 | MK256 | 2271348-04-8 | ≧98.0% |  |
| MK256 is a novel CDK8 inhibitor with potent antitumor activity in AML through downreg | ||||
| 25207 | NSD1 inhibitor BT5 | 2351225-46-0 | ≧98.0% |  |
| BT5 potently inhibits NSD1, engages the SET domain in cells, and reduces H3K36me2 lev | ||||
| 25206 | MA242 TFA | 1049704-18-8 | ≧98.0% |  |
| MA242 isMDM2 and NFAT1 dual inhibitorthat induces MDM2 auto-ubiquitination and degrad | ||||
| 25205 | AF710B | N/A | ≧98.0% ; EE≧98.0% |  |
| AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1 | ||||
| 25204 | MAT2A inhibitor 5 | 2957874-18-7 | ≧98.0% |  |
| MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit | ||||