Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
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. | ||||
25078 | CFT1946 | 2882165-79-7 | ≧98.0% | ![]() |
CFT1946 is an investigational, orally bioavailable small molecule degrader of BRAF V6 | ||||
24058 | NST-628 | 3002056-30-3 | ≧98.0% | ![]() |
NST-628 is a potent pan-RAF-MEK molecular glue that prevents the phosphorylation and | ||||
25149 | Safusidenib | 1898206-17-1 | ≧98.0% | ![]() |
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl |
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