AdooQ BioScience is a supplier of biochemicals located in Irvine, CA since 2006. In the past five years, we have been a renowned name engaged in manufacturing and supplying small molecule inhibitors including kinase inhibitors on kinds of signal pathway, such as PI3K, AKT, HDAC, MARP etc.
Company WebsiteAtropine is a competitive antagonist for the muscarinic acetylcholine receptor types M1, M2, M3, M4 and M5.
More Information Supplier PageAucubin is an iridoid glycoside. Irioids decrease the growth rates of many generalist herbivores.
More Information Supplier PageAucubin is an iridoid glycoside. Irioids decrease the growth rates of many generalist herbivores.
More Information Supplier PageAucubin is an iridoid glycoside. Irioids decrease the growth rates of many generalist herbivores.
More Information Supplier PageAurantio-obtusin, extracted from dry mature seeds of annual legume herb Cassia.
More Information Supplier PageAurantio-obtusin, extracted from dry mature seeds of annual legume herb Cassia.
More Information Supplier PageAurantio-obtusin, extracted from dry mature seeds of annual legume herb Cassia.
More Information Supplier PageAurora A Inhibitor I is a potent and selective inhibitor of Aurora A kinase (AurA), with IC50 values to be 3.4 nM (Aurora A) and unusually high selectivity 1000 fold against Aurora B; a useful tool compound for investigating the cellular role of Aurora A kinases.
More Information Supplier PageAurora A Inhibitor I is a potent and selective inhibitor of Aurora A kinase (AurA), with IC50 values to be 3.4 nM (Aurora A) and unusually high selectivity 1000 fold against Aurora B; a useful tool compound for investigating the cellular role of Aurora A kinases.
More Information Supplier PageAurora A Inhibitor I is a potent and selective inhibitor of Aurora A kinase (AurA), with IC50 values to be 3.4 nM (Aurora A) and unusually high selectivity 1000 fold against Aurora B; a useful tool compound for investigating the cellular role of Aurora A kinases.
More Information Supplier PageAurora A Inhibitor I is a potent and selective inhibitor of Aurora A kinase (AurA), with IC50 values to be 3.4 nM (Aurora A) and unusually high selectivity 1000 fold against Aurora B; a useful tool compound for investigating the cellular role of Aurora A kinases.
More Information Supplier PageAurora A Inhibitor I is a potent and selective inhibitor of Aurora A kinase (AurA), with IC50 values to be 3.4 nM (Aurora A) and unusually high selectivity 1000 fold against Aurora B; a useful tool compound for investigating the cellular role of Aurora A kinases.
More Information Supplier PageAUY922 (NVP-AUY922) is highly potent and oral inhibitor of Hsp90 with IC50=21 nM in Hsp90 FP binding assay and inhibits proliferation of various human cancer cell lines in vitro, with GI50 average 9 nM.
More Information Supplier PageAUY922 (NVP-AUY922) is highly potent and oral inhibitor of Hsp90 with IC50=21 nM in Hsp90 FP binding assay and inhibits proliferation of various human cancer cell lines in vitro, with GI50 average 9 nM.
More Information Supplier PageAUY922 (NVP-AUY922) is highly potent and oral inhibitor of Hsp90 with IC50=21 nM in Hsp90 FP binding assay and inhibits proliferation of various human cancer cell lines in vitro, with GI50 average 9 nM.
More Information Supplier PageAUY922 (NVP-AUY922) is highly potent and oral inhibitor of Hsp90 with IC50=21 nM in Hsp90 FP binding assay and inhibits proliferation of various human cancer cell lines in vitro, with GI50 average 9 nM.
More Information Supplier PageAUY922 (NVP-AUY922) is highly potent and oral inhibitor of Hsp90 with IC50=21 nM in Hsp90 FP binding assay and inhibits proliferation of various human cancer cell lines in vitro, with GI50 average 9 nM.
More Information Supplier PageAV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth factor receptor (EGFR) and the human epidermal growth factor receptor 2 (HER2), which may result in the inhibition of tumor growth and angiogenesis.
More Information Supplier PageAV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth factor receptor (EGFR) and the human epidermal growth factor receptor 2 (HER2), which may result in the inhibition of tumor growth and angiogenesis.
More Information Supplier PageAV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth factor receptor (EGFR) and the human epidermal growth factor receptor 2 (HER2), which may result in the inhibition of tumor growth and angiogenesis.
More Information Supplier PageAV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth factor receptor (EGFR) and the human epidermal growth factor receptor 2 (HER2), which may result in the inhibition of tumor growth and angiogenesis.
More Information Supplier PageAvanafil is a PDE5 Inhibitor for the Treatment of Erectile Dysfunction
More Information Supplier PageAvanafil is a PDE5 Inhibitor for the Treatment of Erectile Dysfunction
More Information Supplier PageAvanafil is a PDE5 Inhibitor for the Treatment of Erectile Dysfunction
More Information Supplier PageAvanafil is a PDE5 Inhibitor for the Treatment of Erectile Dysfunction
More Information Supplier PageAvanafil is a PDE5 Inhibitor for the Treatment of Erectile Dysfunction
More Information Supplier PageAvasimibe (CI-1011) is an orally bioavailable Acyl-CoA:Cholesterol O-Acyltransferase (ACAT) inhibitor.
More Information Supplier PageAvasimibe (CI-1011) is an orally bioavailable Acyl-CoA:Cholesterol O-Acyltransferase (ACAT) inhibitor.
More Information Supplier PageAvasimibe (CI-1011) is an orally bioavailable Acyl-CoA:Cholesterol O-Acyltransferase (ACAT) inhibitor.
More Information Supplier PageAvasimibe (CI-1011) is an orally bioavailable Acyl-CoA:Cholesterol O-Acyltransferase (ACAT) inhibitor.
More Information Supplier PageAvasimibe (CI-1011) is an orally bioavailable Acyl-CoA:Cholesterol O-Acyltransferase (ACAT) inhibitor.
More Information Supplier PageAvibactam is a covalent, reversible, non-??-lactam ??-lactamase inhibitor.
More Information Supplier PageAvibactam is a covalent, reversible, non-??-lactam ??-lactamase inhibitor.
More Information Supplier PageAvibactam is a covalent, reversible, non-??-lactam ??-lactamase inhibitor.
More Information Supplier PageAvibactam is a covalent, reversible, non-??-lactam ??-lactamase inhibitor.
More Information Supplier PageAvicularin is a bio-active flavonol isolated from a number of plants including Polygonum aviculare, Rhododendron aureum and Taxillus kaempferi.
More Information Supplier PageAvicularin is a bio-active flavonol isolated from a number of plants including Polygonum aviculare, Rhododendron aureum and Taxillus kaempferi.
More Information Supplier PageAvicularin is a bio-active flavonol isolated from a number of plants including Polygonum aviculare, Rhododendron aureum and Taxillus kaempferi.
More Information Supplier PageAVL-292 benzenesulfonate is a covalent, highly selective, orally active small molecule inhibitor of Btk with IC50 value of 0.5 nM, >1400-fold selectivity over the other kinases assayed.
More Information Supplier PageAVL-292 benzenesulfonate is a covalent, highly selective, orally active small molecule inhibitor of Btk with IC50 value of 0.5 nM, >1400-fold selectivity over the other kinases assayed.
More Information Supplier PageAVL-292 benzenesulfonate is a covalent, highly selective, orally active small molecule inhibitor of Btk with IC50 value of 0.5 nM, >1400-fold selectivity over the other kinases assayed.
More Information Supplier PageAVN-944 is an orally available, synthetic small molecule with potential antineoplastic activity.
More Information Supplier PageAVN-944 is an orally available, synthetic small molecule with potential antineoplastic activity.
More Information Supplier PageAVN-944 is an orally available, synthetic small molecule with potential antineoplastic activity.
More Information Supplier PageAvosentan (SPP301) is a potent and highly selective ETA receptor blocker.
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