| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 25197 | Bexobrutideg ( NX-5948 ) | 2649400-34-8 | ≧98.0% | ![]() |
| Bexobrutideg (NX-5948) is a BTK degrader. | ||||
| 25198 | Bezuclastinib | 1616385-51-3 | ≧98.0% | ![]() |
| Bezuclastinib is an oral, small-molecule inhibitor of the kinase activity of the KIT | ||||
| 25199 | JX06 | 729-46-4 | ≧98.0% | ![]() |
| JX06 is an effective, selective, covalent PDK inhibitor. | ||||
| 25194 | Oveporexton ( TAK-861 ) | 2460722-04-5 | ≧98.0% | ![]() |
| Oveporexton isan oral small molecule selective orexin type-2 receptor (OX2R) agonist. | ||||
| 25201 | KL1333 | 1800405-30-4 | ≧98.0% | ![]() |
| KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon | ||||
| 25202 | Flurpiridaz-Precursor | 863888-32-8 | ≧98.0% | ![]() |
| Flurpiridaz-Precursor in stock. | ||||
| 25204 | MAT2A inhibitor 5 | 2957874-18-7 | ≧98.0% | ![]() |
| MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit | ||||
| 25205 | AF710B | N/A | ≧98.0% ; EE≧98.0% | ![]() |
| AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1 | ||||
| 25206 | MA242 TFA | 1049704-18-8 | ≧98.0% | ![]() |
| MA242 isMDM2 and NFAT1 dual inhibitorthat induces MDM2 auto-ubiquitination and degrad | ||||
| 25207 | NSD1 inhibitor BT5 | 2351225-46-0 | ≧98.0% | ![]() |
| BT5 potently inhibits NSD1, engages the SET domain in cells, and reduces H3K36me2 lev | ||||
| 25208 | MK256 | 2271348-04-8 | ≧98.0% | ![]() |
| MK256 is a novel CDK8 inhibitor with potent antitumor activity in AML through downreg | ||||
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