Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
011107 | AMG-47a | 882663-88-9 | 98% | |
AMG-47a is a potent inhibitor of Lck and T cell proliferation. | ||||
011104 | ARQ-736 | 1228237-57-7 | 98% | |
ARQ 736 is a potent and selective BRAF inhibitor. | ||||
010820 | AZD4547 | 1035270-39-3 | 98% | |
AZD4547 is a novel selective FGFR inhibitor targeting FGFR1/2/3 with IC50 of 0.2 nM/2 | ||||
010816 | AZD-1480 | 935666-88-9 | 98% | |
AZD1480 is a novel ATP-competitive JAK2 inhibitor with IC50 of 0.26 nM, selectivity a | ||||
010809 | AZD8330 | 869357-68-6 | 98% | |
AZD8330 is a novel, selective, non-ATP competitive MEK 1/2 inhibitor with IC50 of 7 n | ||||
010808 | AS703026 | 1236699-92-5 | 98% | |
AS703026 is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) | ||||
010803 | AZ505 | 1035227-43-0 | 98% | |
AZ505 is a potent and highly selective inhibitor of the oncogenic protein SMYD2(IC50= | ||||
010428 | AG-L-59687 | 793035-88-8 | 98% | |
Coming soon! | ||||
010422 | AG1024 | 65678-07-1 | 98% | |
AG-1024 inhibits IGF-1R autophosphorylation with IC50 of 7 M, less potent to IR with | ||||
010418 | Almotriptan | 154323-57-6 | 98% | |
Almotriptan is a 5-HT1B/1D-receptor agonist used to treat migraine. | ||||
010410 | AM630 | 164178-33-0 | 98% | |
AM630 is a selectivity CB2 antagonist with Ki of 31.2 nM; > 150 fold selectivity o | ||||
123019 | AZD-8055 | 1009298-09-2 | 98% | |
AZD-8055 is an inhibitor of the mammalian target of rapamycin (mTOR) with potential a | ||||
123016 | Amuvatinib | 850879-09-3 | 98% | |
Amuvatinib is a potent and multi-targeted inhibitor of c-Kit, PDGFR and Flt3 with IC5 | ||||
123009 | AR-42 | 935881-37-1 | 98% | |
AR-42 is a novel, oral cancer therapy currently in early clinical development. | ||||
123006 | A-966492 | 934162-61-5 | 98% | |
A-966492 is a novel and potent inhibitor of PARP1 and PARP2 with Ki of 1 nM and 1.5 n | ||||
122942 | AMG 487 | 473719-41-4 | 98% | |
AMG 487 is a small molecule antagonist of the chemokine receptor CXCR3. | ||||
122931 | Atosiban acetate | 90779-69-4 | 98% | |
Atosiban is a nonapeptide, desamino-oxytocin analogue, and a competitive vasopressin/ | ||||
122926 | AST-1306 | 897383-62-9 | 98% | |
AST-1306 is a novel irreversible inhibitor of EGFR and ErbB2 with IC50 of 0.5 nM and | ||||
122925 | AZD8186 | 1627494-13-6 | 98% | |
AZD8186 is an isoform-specific small-molecule PI3K inhibitor, potently inhibits PI3K | ||||
122906 | AG-120 | 1448346-63-1 | 98% | |
AG-120 is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1), wi | ||||
122902 | AZD-5423 | 1034148-04-3 | 98% | |
Coming soon! | ||||
122843 | A 83-01 | 909910-43-6 | 98% | |
A 83-01 is a selective inhibitor of TGF- type I receptor ALK5 kinase, type I activin/ | ||||
122842 | AM251 | 183232-66-8 | 98% | |
AM251 is a potent CB1 receptor antagonist (IC50 = 8 nM, Ki = 7.49 nM) that displays 3 | ||||
122838 | AZD2858 | 486424-20-8 | 98% | |
AZD2858 is a selective GSK-3 inhibitor with an IC50 of 68 nM, inhibits tau phosphoryl | ||||
122824 | Adjudin | 252025-52-8 | 98% | |
Adjudin is a drug which is under development as a potential non-hormonal male contrac | ||||
122822 | AdipoRon | 924416-43-3 | 98% | |
AdipoRon is a novel small-molecule AdipoR agonist; binds to both AdipoR1(Kd= 1.8 uM) | ||||
122407 | Anamorelin | 249921-19-5 | 98% | |
Anamorelin is a synthetic orally active ghrelin receptor agonist which is under devel | ||||
122303 | Atorvastatin sodium | 134523-01-6 | 98% | |
Atorvastatin has the potential to ameliorate arsenic-induced vascular dysfunction and | ||||
122211 | Amrubicin | 110267-81-7 | 98% | |
Amrubicin is a novel anthracycline derivative for treatment of bladder carcinoma. | ||||
122210 | AG 490 | 134036-52-5 | 98% | |
AG-490 is a tyrosine kinase inhibitor of JAK2, EGFR, and Neu that belongs to the fami |
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