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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
011107AMG-47a882663-88-998% 
AMG-47a is a potent inhibitor of Lck and T cell proliferation.
011104ARQ-7361228237-57-798% 
ARQ 736 is a potent and selective BRAF inhibitor.
010820AZD45471035270-39-398% 
AZD4547 is a novel selective FGFR inhibitor targeting FGFR1/2/3 with IC50 of 0.2 nM/2
010816AZD-1480935666-88-998% 
AZD1480 is a novel ATP-competitive JAK2 inhibitor with IC50 of 0.26 nM, selectivity a
010809AZD8330869357-68-698% 
AZD8330 is a novel, selective, non-ATP competitive MEK 1/2 inhibitor with IC50 of 7 n
010808AS7030261236699-92-598% 
AS703026 is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2)
010803AZ5051035227-43-098% 
AZ505 is a potent and highly selective inhibitor of the oncogenic protein SMYD2(IC50=
010428AG-L-59687793035-88-898% 
Coming soon!
010422AG102465678-07-198% 
AG-1024 inhibits IGF-1R autophosphorylation with IC50 of 7 M, less potent to IR with
010418Almotriptan154323-57-698% 
Almotriptan is a 5-HT1B/1D-receptor agonist used to treat migraine.
010410AM630164178-33-098% 
AM630 is a selectivity CB2 antagonist with Ki of 31.2 nM; > 150 fold selectivity o
123019AZD-80551009298-09-298% 
AZD-8055 is an inhibitor of the mammalian target of rapamycin (mTOR) with potential a
123016Amuvatinib850879-09-398% 
Amuvatinib is a potent and multi-targeted inhibitor of c-Kit, PDGFR and Flt3 with IC5
123009AR-42935881-37-198% 
AR-42 is a novel, oral cancer therapy currently in early clinical development.
123006A-966492934162-61-598% 
A-966492 is a novel and potent inhibitor of PARP1 and PARP2 with Ki of 1 nM and 1.5 n
122942AMG 487473719-41-498% 
AMG 487 is a small molecule antagonist of the chemokine receptor CXCR3.
122931Atosiban acetate90779-69-498% 
Atosiban is a nonapeptide, desamino-oxytocin analogue, and a competitive vasopressin/
122926AST-1306897383-62-998% 
AST-1306 is a novel irreversible inhibitor of EGFR and ErbB2 with IC50 of 0.5 nM and
122925AZD81861627494-13-698% 
AZD8186 is an isoform-specific small-molecule PI3K inhibitor, potently inhibits PI3K
122906AG-1201448346-63-198% 
AG-120 is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1), wi
122902AZD-54231034148-04-398% 
Coming soon!
122843A 83-01909910-43-698% 
A 83-01 is a selective inhibitor of TGF- type I receptor ALK5 kinase, type I activin/
122842AM251183232-66-898% 
AM251 is a potent CB1 receptor antagonist (IC50 = 8 nM, Ki = 7.49 nM) that displays 3
122838AZD2858486424-20-898% 
AZD2858 is a selective GSK-3 inhibitor with an IC50 of 68 nM, inhibits tau phosphoryl
122824Adjudin252025-52-898% 
Adjudin is a drug which is under development as a potential non-hormonal male contrac
122822AdipoRon924416-43-398% 
AdipoRon is a novel small-molecule AdipoR agonist; binds to both AdipoR1(Kd= 1.8 uM)
122407Anamorelin249921-19-598% 
Anamorelin is a synthetic orally active ghrelin receptor agonist which is under devel
122303Atorvastatin sodium134523-01-698% 
Atorvastatin has the potential to ameliorate arsenic-induced vascular dysfunction and
122211Amrubicin110267-81-798% 
Amrubicin is a novel anthracycline derivative for treatment of bladder carcinoma.
122210AG 490134036-52-598% 
AG-490 is a tyrosine kinase inhibitor of JAK2, EGFR, and Neu that belongs to the fami