| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 26A059 | SCO-240 | 1695564-98-7 | ≧98.0% | ![]() |
| SCO-240 is an investigational, orally active, and selective somatostatin receptor sub | ||||
| 26A060 | Linvemastat (Synonyms: FP-020) | 2389060-50-6 | ≧98.0% | ![]() |
| Linvemastat (FP-020) is a highly potent and selective oral MMP-12 inhibitor. | ||||
| 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 | ||||
| 26A085 | ASP5878 | 1453208-66-6 | ≧98.0% | ![]() |
| ASP-5878 is an orally available small-molecule inhibitor of FGFR-1,-2, -3 and -4 | ||||
| 26A083 | MAT2A inhibitor-[Compound 1] | 2923986-48-3 | ≧98.0% | ![]() |
| Compound 1 is a new MAT2A inhibitor. | ||||
| 26A086 | Aderamastat ( Synonyms: FP-025 ) | 877176-23-3 | 98% Min. | ![]() |
| Aderamastat (FP-025) is an oral, selective, non-hydroxamate-based, non-competitive in | ||||
| 26A084 | GDD-261 | 3137699-54-5 | ≧98.0% | ![]() |
| GDD-261 is an orally active, allosteric inhibitor of phosphoglycerate dehydrogenase ( | ||||
| 26A087 | MRX-2843 | 1429882-07-4 | ≧98.0% | ![]() |
| MRX-2843 is an orally bioavailable inhibitor of two receptor tyrosine kinases (RTKs), | ||||
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