Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 26A047 | BH-30643 | 3062177-59-4 | ≧98.0% |  |
| BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM | ||||
| 26A048 | Apecotrep (BI 764198) | 2311863-36-0 | ≧98.0% | _2311863-36-0.png) |
| Apecotrep (BI 764198) is a potential first-in-class, oral, selective TRPC6 inhibitor. | ||||
| 72602 | Imisopasem manganese ( M40403; GC4403 ) | 218791-21-0 | ≧97.0% | .png) |
| Imisopasem manganese ( M40403; GC4403 ) is a stable non-peptidyl mimetic of MnSOD tha | ||||
| 26A049 | SCY-770 ( Synonyms: PXL-770 ) | 1523493-78-8 | ≧98.0% | _1523493-78-8.png) |
| SCY-770 (PXL-770) is a direct adenosine monophosphate-activated protein kinase (AMPK) | ||||
| 26A050 | Eratrectinib ( Synonyms: VC-004 ) | 2396516-98-4 | ≧98.0% | _2396516-98-4.png) |
| Eratrectinib (VC-004) is a small molecule inhibitor of the nerve growth factor recept | ||||
| 26A051 | Mocaciclib ( Synonyms: Q-901 ) | 2766124-39-2 | ≧98.0% | _2766124-39-2.png) |
| Mocaciclib (Q-901) is a cyclin-dependent kinase-7 (CDK-7) inhibitor. | ||||
| 26A052 | IPG-7236 | 2756350-91-9 | ≧98.0% |  |
| IPG-7236 is a C-C chemokine receptor type 8 (CCR8) antagonist. | ||||
| 26A053 | Palacaparib ( Synonyms: AZD-9574 ) | 2756333-39-6 | ≧98.0% |  |
| Palacaparib (AZD-9574) is an orally available, CNS penetrant, PARP-1 inhibitor. | ||||
| 26A054 | ART-6043 | 2923356-52-7 | ≧98.0% |  |
| ART-6043 is an oral, small-molecule inhibitor of the DNA polymerase theta (POLQ). | ||||
| 26A055 | Privosegtor ( Synonyms: OCS-05, ACT-01 ) | 1361200-34-1 | ≧98.0% |  |
| Privosegtor (OCS-05, ACT-01) is a small molecule peptidomimetic, BDNF/NT-3 growth fac | ||||
| 26A056 | Repinatrabit ( Synonyms: JNT-517 ) | 2837993-05-0 | ≧98.0% |  |
| Repinatrabit (JNT-517) is an investigational, selective, small-molecule inhibitor of | ||||
| 26A058 | N-Methylamisulpride ( Synonyms: LB-102 ) | 2227154-23-4 | ≧98.0% | _2227154-23-4.png) |
| N-Methylamisulpride (Synonyms: LB-102) is a dopamine D2 and D3 receptor antagonist an | ||||