| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 26A084 | GDD-261 | 3137699-54-5 | ≧98.0% | ![]() |
| GDD-261 is an orally active, allosteric inhibitor of phosphoglycerate dehydrogenase ( | ||||
| 26A086 | Aderamastat ( Synonyms: FP-025 ) | 877176-23-3 | 98% Min. | ![]() |
| Aderamastat (FP-025) is an oral, selective, non-hydroxamate-based, non-competitive in | ||||
| 26A083 | MAT2A inhibitor-[Compound 1] | 2923986-48-3 | ≧98.0% | ![]() |
| Compound 1 is a new MAT2A inhibitor. | ||||
| 26A085 | ASP5878 | 1453208-66-6 | ≧98.0% | ![]() |
| ASP-5878 is an orally available small-molecule inhibitor of FGFR-1,-2, -3 and -4 | ||||
| 26A061 | Osivelotor (Synonyms: GBT-601; GBT-021601) | 2417955-18-9 | ≧98.0% | ![]() |
| Osivelotor (Synonyms: GBT-601; GBT-021601) is a next-generation sickle hemoglobin (Hb | ||||
| 26A060 | Linvemastat (Synonyms: FP-020) | 2389060-50-6 | ≧98.0% | ![]() |
| Linvemastat (FP-020) is a highly potent and selective oral MMP-12 inhibitor. | ||||
| 26A059 | SCO-240 | 1695564-98-7 | ≧98.0% | ![]() |
| SCO-240 is an investigational, orally active, and selective somatostatin receptor sub | ||||
| 26A058 | N-Methylamisulpride ( Synonyms: LB-102 ) | 2227154-23-4 | ≧98.0% | ![]() |
| N-Methylamisulpride (Synonyms: LB-102) is a dopamine D2 and D3 receptor antagonist an | ||||
| 26A056 | Repinatrabit ( Synonyms: JNT-517 ) | 2837993-05-0 | ≧98.0% | ![]() |
| Repinatrabit (JNT-517) is an investigational, selective, small-molecule inhibitor of | ||||
| 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 | ||||
| 26A054 | ART-6043 | 2923356-52-7 | ≧98.0% | ![]() |
| ART-6043 is an oral, small-molecule inhibitor of the DNA polymerase theta (POLQ). | ||||
| 26A053 | Palacaparib ( Synonyms: AZD-9574 ) | 2756333-39-6 | ≧98.0% | ![]() |
| Palacaparib (AZD-9574) is an orally available, CNS penetrant, PARP-1 inhibitor. | ||||
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