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RECOMMENDED PRODUCTS

Catalog NoChemical NameCAS NumberPurityChemical Structure
24110VVD-130037 ( BAY-3605349 )3034880-93-5≧98.0%
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
24112HC-5404-FU3034479-99-4≧98.0%
HC-5404-FU is a novel, highly selective and potent PERK inhibitor.
25001HC-54042247396-91-2≧98.0%
HC-5404 is a novel, highly selective and potent PERK inhibitor.
25032BMS-4664421598424-76-0≧98.0%
BMS-466442 is a small molecule inhibitor of asc-1.
25033Azeliragon603148-36-3≧98.0%
Azeliragon (TTP488) is an orally bioavailable small molecule inhibitor of the recepto
25052Lazertinib mesylate2247995-37-3≧98.0%
Lazertinib is a an orally available third-generation, selective inhibitor of certain
25062GP130 modulator-12375779-31-8≧98.0%
GP130 modulator-1 (compound A33) is agp130signaling pathway modulator. GP130 modulato
25063Seladelpar sodium salt3026272-26-1≧98.0%
Seladelpar is a PPAR-delta agonist.
25078CFT19462882165-79-7≧98.0%
CFT1946 is an investigational, orally bioavailable small molecule degrader of BRAF V6
24058NST-6283002056-30-3≧98.0%
NST-628 is a potent pan-RAF-MEK molecular glue that prevents the phosphorylation and
25149Safusidenib1898206-17-1≧98.0%
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl