| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 24041 | ASN-90 ( ASN-120290, FNP-223 ) | 2129093-74-7 | ≧98.0% | ![]() |
| ASN-90 (ASN-120290, FNP-223) is an oral, brain-penetrant, small-molecule inhibitor of | ||||
| 24048 | Sebetralstat free base | 1933514-13-6 | 98% Min. | ![]() |
| Sebetralstat (KVD-900), an oral plasma kallikrein inhibitor. | ||||
| 24073 | Dabogratinib ( TYRA-300 ) | 2800223-30-5 | ≧98.0% | ![]() |
| Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the | ||||
| 24108 | JHU-083 | 1998725-11-3 | ≧98.0% | ![]() |
| JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de | ||||
| 24110 | VVD-130037 ( BAY-3605349 ) | 3034880-93-5 | ≧98.0% | ![]() |
| VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2). | ||||
| 24112 | HC-5404-FU | 3034479-99-4 | ≧98.0% | ![]() |
| HC-5404-FU is a novel, highly selective and potent PERK inhibitor. | ||||
| 25001 | HC-5404 | 2247396-91-2 | ≧98.0% | ![]() |
| HC-5404 is a novel, highly selective and potent PERK inhibitor. | ||||
| 25032 | BMS-466442 | 1598424-76-0 | ≧98.0% | ![]() |
| BMS-466442 is a small molecule inhibitor of asc-1. | ||||
| 25033 | Azeliragon | 603148-36-3 | ≧98.0% | ![]() |
| Azeliragon (TTP488) is an orally bioavailable small molecule inhibitor of the recepto | ||||
| 25052 | Lazertinib mesylate | 2247995-37-3 | ≧98.0% | ![]() |
| Lazertinib is a an orally available third-generation, selective inhibitor of certain | ||||
| 25062 | GP130 modulator-1 | 2375779-31-8 | ≧98.0% | ![]() |
| GP130 modulator-1 (compound A33) is agp130signaling pathway modulator. GP130 modulato | ||||
| 25063 | Seladelpar sodium salt | 3026272-26-1 | ≧98.0% | ![]() |
| Seladelpar is a PPAR-delta agonist. | ||||
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