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 WebsiteGSK343 is a potent histone H3-lysine 27 (H3K27) methyltransferase EZH2 inhibitor (IC= 4 nM). Diplays 1000-fold selectivity for other HMTs except EZH1 (60-fold selectivity). GSK343 inhibits H3K27 methylation in HCC1806 cells with an IC of
More Information Supplier PageGSK343 is a potent histone H3-lysine 27 (H3K27) methyltransferase EZH2 inhibitor (IC= 4 nM). Diplays 1000-fold selectivity for other HMTs except EZH1 (60-fold selectivity). GSK343 inhibits H3K27 methylation in HCC1806 cells with an IC of
More Information Supplier PageShows antimalerial activity with IC50 values of 11.2 nM for 3D7 strain, 12.6 nM for HB3 strain, 17.6 nM for K1 strain
More Information Supplier PageShows antimalerial activity with IC50 values of 11.2 nM for 3D7 strain, 12.6 nM for HB3 strain, 17.6 nM for K1 strain
More Information Supplier PageShows antimalerial activity with IC50 values of 11.2 nM for 3D7 strain, 12.6 nM for HB3 strain, 17.6 nM for K1 strain
More Information Supplier PageShows antimalerial activity with IC50 values of 11.2 nM for 3D7 strain, 12.6 nM for HB3 strain, 17.6 nM for K1 strain
More Information Supplier PageGSK429286A is a cell-permeable, selective small molecule inhibitor of Rho-associated, coiled-coil containing protein kinase (ROCK).
More Information Supplier PageGSK429286A is a cell-permeable, selective small molecule inhibitor of Rho-associated, coiled-coil containing protein kinase (ROCK).
More Information Supplier PageGSK429286A is a cell-permeable, selective small molecule inhibitor of Rho-associated, coiled-coil containing protein kinase (ROCK).
More Information Supplier PageGSK429286A is a cell-permeable, selective small molecule inhibitor of Rho-associated, coiled-coil containing protein kinase (ROCK).
More Information Supplier PageGSK429286A is a cell-permeable, selective small molecule inhibitor of Rho-associated, coiled-coil containing protein kinase (ROCK).
More Information Supplier PageGSK461364 is an ATP-competitive inhibitor of polo-like kinase 1 (Plk1).
More Information Supplier PageGSK461364 is an ATP-competitive inhibitor of polo-like kinase 1 (Plk1).
More Information Supplier PageGSK461364 is an ATP-competitive inhibitor of polo-like kinase 1 (Plk1).
More Information Supplier PageGSK461364 is an ATP-competitive inhibitor of polo-like kinase 1 (Plk1).
More Information Supplier PageGSK-503 is a potent EZH2 inhibitor with potential anticancer activity.
More Information Supplier PageGSK-503 is a potent EZH2 inhibitor with potential anticancer activity.
More Information Supplier PageGSK-503 is a potent EZH2 inhibitor with potential anticancer activity.
More Information Supplier PageGSK690693 is a novel ATP-competitive, low-nanomolar pan-Akt kinase inhibitor.
More Information Supplier PageGSK690693 is a novel ATP-competitive, low-nanomolar pan-Akt kinase inhibitor.
More Information Supplier PageGSK690693 is a novel ATP-competitive, low-nanomolar pan-Akt kinase inhibitor.
More Information Supplier PageGSK690693 is a novel ATP-competitive, low-nanomolar pan-Akt kinase inhibitor.
More Information Supplier PageGSK690693 is a novel ATP-competitive, low-nanomolar pan-Akt kinase inhibitor.
More Information Supplier PageGuanabenz acetate is an a2A-AR adrenergic agonist and IGRS (imidazoline I2 binding site) selective ligand.
More Information Supplier PageGuanabenz acetate is an a2A-AR adrenergic agonist and IGRS (imidazoline I2 binding site) selective ligand.
More Information Supplier PageGuanabenz acetate is an a2A-AR adrenergic agonist and IGRS (imidazoline I2 binding site) selective ligand.
More Information Supplier PageGuanfacine hydrochloride, an anti-hypertensive agent, is a selective ??2A-adrenoceptor agonist with Kd of 31 nM and displays 60-fold selectivity over ??2B-adrenoceptors.
More Information Supplier PageGuanfacine hydrochloride, an anti-hypertensive agent, is a selective ??2A-adrenoceptor agonist with Kd of 31 nM and displays 60-fold selectivity over ??2B-adrenoceptors.
More Information Supplier PageGuanfacine hydrochloride, an anti-hypertensive agent, is a selective ??2A-adrenoceptor agonist with Kd of 31 nM and displays 60-fold selectivity over ??2B-adrenoceptors.
More Information Supplier PageGuanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a ??-N9-glycosidic bond.
More Information Supplier PageGuanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a ??-N9-glycosidic bond.
More Information Supplier PageGuanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a ??-N9-glycosidic bond.
More Information Supplier PageGuanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a ??-N9-glycosidic bond.
More Information Supplier PageGuanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a ??-N9-glycosidic bond.
More Information Supplier PageGuvacine hydrochloride inhibits GABA uptake (IC50 values are 14, 58, 119 and 1870 uM for hGABA T-1, rGABA T-2, hGABA T-3 and hBGT-1 respectively).
More Information Supplier PageGuvacine hydrochloride inhibits GABA uptake (IC50 values are 14, 58, 119 and 1870 uM for hGABA T-1, rGABA T-2, hGABA T-3 and hBGT-1 respectively).
More Information Supplier PageW4869 is a cell permeable, selective inhibitor of N-SMase (neutral sphingomyelinase).
More Information Supplier PageW4869 is a cell permeable, selective inhibitor of N-SMase (neutral sphingomyelinase).
More Information Supplier PageW4869 is a cell permeable, selective inhibitor of N-SMase (neutral sphingomyelinase).
More Information Supplier PageGW501516 (GW1516 or GSK-516) is a drug that acts as a PPAR?? modulator.
More Information Supplier PageGW501516 (GW1516 or GSK-516) is a drug that acts as a PPAR?? modulator.
More Information Supplier PageGW501516 (GW1516 or GSK-516) is a drug that acts as a PPAR?? modulator.
More Information Supplier PageGW501516 (GW1516 or GSK-516) is a drug that acts as a PPAR?? modulator.
More Information Supplier PageGW 5074 is a potent, selective and cell-permeable c-Raf1 kinase inhibitor
More Information Supplier PageGW 5074 is a potent, selective and cell-permeable c-Raf1 kinase inhibitor
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