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 Website5-o-methylvisammioside has analgesic, antipyretic, anti-inflammatory and anti-platelet aggregation effect.
More Information Supplier Page5-R-Rivaroxaban is (R) enantiomer of Rivaroxaban. Rivaroxaban is a novel, oral, direct Factor Xa (FXa) inhibitor in late-stage development for the prevention and treatment of thromboembolic disorders.
More Information Supplier Page5-R-Rivaroxaban is (R) enantiomer of Rivaroxaban. Rivaroxaban is a novel, oral, direct Factor Xa (FXa) inhibitor in late-stage development for the prevention and treatment of thromboembolic disorders.
More Information Supplier Page5-R-Rivaroxaban is (R) enantiomer of Rivaroxaban. Rivaroxaban is a novel, oral, direct Factor Xa (FXa) inhibitor in late-stage development for the prevention and treatment of thromboembolic disorders.
More Information Supplier Page5,15-Diacetyl-3-benzoyllathyrol, extracted from Euphorbiaceae Euphorbia lathyris dry mature seeds.
More Information Supplier Page6-Maleimido-1-hexanol is a maleimide compound with a pendant hexanol moiety.
More Information Supplier Page6-Maleimido-1-hexanol is a maleimide compound with a pendant hexanol moiety.
More Information Supplier Page6-Maleimidocaproic acid is a sulfhydryl reactive heterobifunctional crosslinking reagent.
More Information Supplier Page6-OAU is a surrogate agonist of GPR84; activates human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.
More Information Supplier Page6-OAU is a surrogate agonist of GPR84; activates human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.
More Information Supplier Page6-OAU is a surrogate agonist of GPR84; activates human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.
More Information Supplier Page6-shogaol is a pungent constituent of ginger similar in chemical structure to gingerol.
More Information Supplier Page6-shogaol is a pungent constituent of ginger similar in chemical structure to gingerol.
More Information Supplier Page6-shogaol is a pungent constituent of ginger similar in chemical structure to gingerol.
More Information Supplier PageEsculetin, a phenolic compound, acts as a 5-LO (5-lipoxygenase, 5-LOX) inhibitor.
More Information Supplier Page6H05 is a selective, and allosteric inhibitor of oncogenic K-Ras(G12C).
More Information Supplier Page6H05 is a selective, and allosteric inhibitor of oncogenic K-Ras(G12C).
More Information Supplier Page6H05 is a selective, and allosteric inhibitor of oncogenic K-Ras(G12C).
More Information Supplier Page7-Aminocephalosporanic acid is the core chemical structure for the synthesis of cephalosporin antibiotics and intermediates.
More Information Supplier Page7-Aminocephalosporanic acid is the core chemical structure for the synthesis of cephalosporin antibiotics and intermediates.
More Information Supplier Page7-Epi 10-Desacetyl Paclitaxel is a derivative of Paclitaxel, which is a microtubule polymer stabilizer with IC50 of 0.1 pM in human endothelial cells.
More Information Supplier Page7-Epi 10-Desacetyl Paclitaxel is a derivative of Paclitaxel, which is a microtubule polymer stabilizer with IC50 of 0.1 pM in human endothelial cells.
More Information Supplier Page7-Epi 10-Desacetyl Paclitaxel is a derivative of Paclitaxel, which is a microtubule polymer stabilizer with IC50 of 0.1 pM in human endothelial cells.
More Information Supplier Page7-xylosyltaxol is a taxol derivative, Paclitaxel binds to tubulin and inhibits the disassembly of microtubules.
More Information Supplier Page7-xylosyltaxol is a taxol derivative, Paclitaxel binds to tubulin and inhibits the disassembly of microtubules.
More Information Supplier Page7-xylosyltaxol is a taxol derivative, Paclitaxel binds to tubulin and inhibits the disassembly of microtubules.
More Information Supplier Page7ACC2 is a new potent MCT inhibitor with IC50 of 11 nM for inhibition of [14C]-lactate influx; new antitumor treatment targeting lactate transport in cancer cells.
More Information Supplier Page7ACC2 is a new potent MCT inhibitor with IC50 of 11 nM for inhibition of [14C]-lactate influx; new antitumor treatment targeting lactate transport in cancer cells.
More Information Supplier Page7ACC2 is a new potent MCT inhibitor with IC50 of 11 nM for inhibition of [14C]-lactate influx; new antitumor treatment targeting lactate transport in cancer cells.
More Information Supplier Page8-Gingerol is a bioactive ingredient of ginger (Zingiber officinale) having anti-nausea, anti-inflammatory, and anti-carcinogenic properties.
More Information Supplier Page8-Gingerol is a bioactive ingredient of ginger (Zingiber officinale) having anti-nausea, anti-inflammatory, and anti-carcinogenic properties.
More Information Supplier Page8-Gingerol is a bioactive ingredient of ginger (Zingiber officinale) having anti-nausea, anti-inflammatory, and anti-carcinogenic properties.
More Information Supplier Page8-O-acetyl shanzhiside methyl ester was isolated from the leaves of Lamiophlomis rotata (Benth.) Kudo.
More Information Supplier Page8-O-acetyl shanzhiside methyl ester was isolated from the leaves of Lamiophlomis rotata (Benth.) Kudo.
More Information Supplier Page8-O-acetyl shanzhiside methyl ester was isolated from the leaves of Lamiophlomis rotata (Benth.) Kudo.
More Information Supplier Page9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
More Information Supplier Page9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
More Information Supplier Page9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
More Information Supplier PageA 438079 Hcl is a competitive P2X7 receptor antagonist (pIC50 = 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line).
More Information Supplier PageA 438079 Hcl is a competitive P2X7 receptor antagonist (pIC50 = 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line).
More Information Supplier PageA 438079 Hcl is a competitive P2X7 receptor antagonist (pIC50 = 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line).
More Information Supplier PageA 740003 is a novel competitive antagonist of P2X7 receptors (IC50 values = 40 nM for human and 18 nM for rat).
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