Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 122524 | GW2580 | 870483-87-7 | 98% |  |
| GW2580 is an orally bioavailable inhibitor of c-FMS kinase; completely inhibited huma | ||||
| 122805 | Balipodect ( TAK-063 ) | 1238697-26-1 | 98% | _1238697-26-1.png) |
| Balipodect (TAK 063 ) is a novel PDE10A inhibitor. It has shown high inhibitory activ | ||||
| 122919 | Tenapanor | 1234423-95-0 | 98% |  |
| Tenapanoris an inhibitor of the sodium-proton exchanger NHE3. Thisantiporter protein | ||||
| 122941 | Pacritinib ( SB1518 ) | 937272-79-2 | ≧98.0% | _937272-79-2.png) |
| Pacritinib(SB1518) is a highly selective kinaseinhibitorwith specificity for JAK2, FL | ||||
| 51627 | MK7622 | 1227923-29-6 | 98% by HPLC |  |
| MK-7622isused as adjunctive therapy to acetylcholinesterase inhibitors (AChEIs) for t | ||||
| 20267 | Almonertinib | 1899921-05-1 | 98% Min. |  |
| Almonertinib is an orally available inhibitor of the epidermal growth factor receptor | ||||
| 10403 | CAY 10566 | 944808-88-2 | ≧98.0% |  |
| CAY 10566 is a potent selective SCD-1 inhibitor. | ||||
| 25152 | Avutometinib ( Synonyms: Ro 5126766; CH5126766 ) | 946128-88-7 | ≧98.0% | _946128-88-7.png) |
| Avutometinib ( Synonyms: Ro 5126766; CH5126766 )is a potent and selective dual RAF/ME | ||||
| 011813 | Avoralstat | 918407-35-9 | 95.0% |  |
| Avoralstat (formerly BCX4161) is a potent small-molecule oral plasma kallikrein inhib | ||||
| 1662118 | MK-8931 ( Verubecestat ) | 1286770-55-5 | 98% by HPLC/HNMR | -cas-1286770-55-5.png) |
| Verubecestat(MK-8931) is a small-molecule inhibitor of beta-secretase cleaving enzyme | ||||
| 611902 | PF-04979064 | 1220699-06-8 | ≧98.0% |  |
| PF-04979064 is a potent and selective PI3K/mTOR dual kinase inhibitor with an IC(50) | ||||
| 6111110 | Nastorazepide | 209219-38-5 | 98% |  |
| Nastorazepide (Z-360) is a selective, orally available, 1,5-benzodiazepine-derivative | ||||