RECOMMENDED PRODUCTS
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 25076 | HC-7366 | 2803470-63-3 | ≧98.0% |  |
| HC-7366 is a potent and selective activator of the general control nonderepressible 2 | ||||
| 41788 | CB-6644 | 2316817-88-4 | 96.33% |  |
| CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL | ||||
| 25148 | Atebimetinib | 2669009-92-9 | ≧98.0% |  |
| Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1 | ||||
| 25075 | LLL12 | 1260247-42-4 | ≧97.0% |  |
| LLL12 is a potent STAT3 inhibitor. | ||||
| 181121 | AZD-5904 | 618913-30-7 | ≧98.0% |  |
| AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590 | ||||
| 237071 | Flavopiridol ( Alvocidib ) | 146426-40-6 | ≧98.0% | .png) |
| Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst | ||||
| 24107 | LXH-3-71 | 2251753-65-6 | ≧97.0% |  |
| LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH | ||||
| 20509 | GLPG3667 | 2308520-97-8 | ≧98.0% |  |
| GLPG3667 is an oral potent and selective small-molecule TYK2 inhibitor in development | ||||
| 121431 | KW-2478 | 819812-04-9 | 98% |  |
| KW-2478 is an agent that targets the human heat-shock protein 90 (Hsp90) with potenti | ||||
| 18576 | VU0467154 | 1451993-15-9 | ≧98.0% |  |
| VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept | ||||
| 171452 | BGB-15025 | 2766481-17-6 | ≧98.0% |  |
| BGB-15025 is a potent and selective HPK1 inhibitor that is efficacious as a single ag | ||||
| 17021601 | LY3039478 ( Crenigacestat ) | 1421438-81-4 | ≧98.0% | _1421438-81-4.png) |
| LY3039478 ( Crenigacestat ), a selective NOTCH1 inhibitor, reduces intrahepatic chola | ||||