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产品目录

编号化学名称Cas号纯度化学结构
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
121804APD597897732-93-398% 
APD597 is a potent and selective GPR119 agonist, which is potential useful for the tr
121434AT-10190141-22-398% 
AT-101 is the orally bioavailable the R-(-) enantiomer of gossypol with potential ant
1207014-Aminobenzeneboronic Acid Hydrochloride80460-73-798% 
Coming soon!
120409Alendronate sodium trihydrate121268-17-598%
Coming soon!
120408Ambroxol hydrochloride23828-92-498%
Coming soon!
120110Actinomycin D50-76-098% 
Actinomycin D is the most significant member of actinomycines, which are a class of p
120104Altiratinib1345847-93-998% 
Altiratinib is a novel c-MET/TIE-2/VEGFR inhibitor; effectively reduce tumor burden i
120103AGI-51981355326-35-098% 
AGI-5198 is a novel R132H-IDH1 inhibitor, identified through a high-throughput screen
120102Acotiamide HCl773092-05-098% 
Acotiamide is a drug approved in Japan for the treatment of postprandial fullness, up
120101A661166227-08-298% 
A66 is a potent and specific p110 inhibitor with IC50 of 32 nM, >100 fold selectiv
112101AV-412451492-95-899.38%
AV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth fact