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Catalog NoChemical NameCAS NumberPurityChemical Structure
2073104Enarodustat ( JTZ-951 )1262132-81-998% Min.
Enarodustat ( JTZ-951 ) is an orally-active HIF-PH inhibitor with an EC50 of 0.22 Μm
Oteseconazole, also known as VT-1161,is the first Approved Orally Bioavailable and Se
17031303Tirabrutinib free base ( ONO-4059 )1351636-18-4≧98.0%
Tirabrutinib, also known as ONO-4059 is a potent and orally active Bruton agammaglobu
17012103Tirabrutinib HCl1439901-97-9≧98.0%
ONO-4059 is a selective and novel inhibitor of BTK with IC50 2.2 nm, ONO-4059 binds t
CRT0273750 modulates LPA levels in plasma and is suitable for in vivo studies.
20376TOFA ( RMI14514; MDL14514)54857-86-2≧98.0%
TOFA ( RMI14514; MDL14514) is an allosteric inhibitor of acetyl-CoA carboxylase-α (A
Razuprotafib, also known as AKB-9778, is a small molecule inhibitor of vascular endot
2105071AP1189 acetate959850-74-9≧98.0%
AP1189 is a melanocortin receptor agonist on MC1 and MC3 receptors.
ML380 is a highly potent and the first CNS penetrant M5 positive allosteric modulator
Danicopan, aslo known as ACH-4471 and ACH-0144471, is a highly potent, orally active
20259Elinzanetant ( NT-814 )929046-33-3≧98.0%
Elinzanetant, previously known as NT-814 (45), is a dual NK1,3R antagonist and theref
SRT1720 is a selectiveSIRT1activator withEC50of 0.16 M, but is >230-fold less pote