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 WebsiteAZD8055 is a potent, selective, and orally bioavailable ATP-competitive mTOR kinase inhibitor with an IC50 of 0.8 nM.
More Information Supplier PageAZD8186 is an isoform-specific small-molecule PI3K inhibitor, potently inhibits PI3K?? (IC50=4 nM) and PI3K?? (IC50=12 nM) with selectivity over PI3K?? (IC50=35 nM) and PI3K?? (IC50=675 nM).
More Information Supplier PageAZD8186 is and inhibitor of the beta isoform of phosphoinositide-3 kinase (PI3K), with potential antineoplastic activity.
More Information Supplier PageAZD8186 is an isoform-specific small-molecule PI3K inhibitor, potently inhibits PI3K?? (IC50=4 nM) and PI3K?? (IC50=12 nM) with selectivity over PI3K?? (IC50=35 nM) and PI3K?? (IC50=675 nM).
More Information Supplier PageAZD8186 is and inhibitor of the beta isoform of phosphoinositide-3 kinase (PI3K), with potential antineoplastic activity.
More Information Supplier PageAZD8186 is an isoform-specific small-molecule PI3K inhibitor, potently inhibits PI3K?? (IC50=4 nM) and PI3K?? (IC50=12 nM) with selectivity over PI3K?? (IC50=35 nM) and PI3K?? (IC50=675 nM).
More Information Supplier PageAZD8186 is and inhibitor of the beta isoform of phosphoinositide-3 kinase (PI3K), with potential antineoplastic activity.
More Information Supplier PageAZD8330 is a MEK inhibitor that specifically inhibits mitogen-activated protein kinase kinase 1 (MEK or MAP/ERK kinase1), resulting in inhibition of growth factor-mediated cell signaling and tumor cell proliferation.
More Information Supplier PageAZD8330 is a MEK inhibitor that specifically inhibits mitogen-activated protein kinase kinase 1 (MEK or MAP/ERK kinase1), resulting in inhibition of growth factor-mediated cell signaling and tumor cell proliferation.
More Information Supplier PageAZD8330 is a MEK inhibitor that specifically inhibits mitogen-activated protein kinase kinase 1 (MEK or MAP/ERK kinase1), resulting in inhibition of growth factor-mediated cell signaling and tumor cell proliferation.
More Information Supplier PageAZD8330 is a MEK inhibitor that specifically inhibits mitogen-activated protein kinase kinase 1 (MEK or MAP/ERK kinase1), resulting in inhibition of growth factor-mediated cell signaling and tumor cell proliferation.
More Information Supplier PageAZD8330 is a MEK inhibitor that specifically inhibits mitogen-activated protein kinase kinase 1 (MEK or MAP/ERK kinase1), resulting in inhibition of growth factor-mediated cell signaling and tumor cell proliferation.
More Information Supplier PageAZD8931 is an oral, equipotent inhibitor of ErbB1, ErbB2 and ErbB3 receptor signaling.
More Information Supplier PageAZD8931 is an oral, equipotent inhibitor of ErbB1, ErbB2 and ErbB3 receptor signaling.
More Information Supplier PageAZD8931 is an oral, equipotent inhibitor of ErbB1, ErbB2 and ErbB3 receptor signaling.
More Information Supplier PageAZD8931 is an oral, equipotent inhibitor of ErbB1, ErbB2 and ErbB3 receptor signaling.
More Information Supplier PageAZD8931 is an oral, equipotent inhibitor of ErbB1, ErbB2 and ErbB3 receptor signaling.
More Information Supplier PageAZD9496 is a potent and orally bioavailable selective estrogen receptor downregulator and antagonist.
More Information Supplier PageAZD9496 is a potent and orally bioavailable selective estrogen receptor downregulator and antagonist.
More Information Supplier PageAZD9496 is a potent and orally bioavailable selective estrogen receptor downregulator and antagonist.
More Information Supplier PageAzelastine is a potent, second-generation, selective, histamine antagonist (histamine-H1-receptor antagonist).
More Information Supplier PageAzelastine is a potent, second-generation, selective, histamine antagonist (histamine-H1-receptor antagonist).
More Information Supplier PageAzelastine is a potent, second-generation, selective, histamine antagonist (histamine-H1-receptor antagonist).
More Information Supplier PageAzelnidipine is a calcium blocker that attenuates liver fibrosis and may increase antioxidant defence. that attenuates liver fibrosis and may increase antioxidant defence.
More Information Supplier PageAzelnidipine is a calcium blocker that attenuates liver fibrosis and may increase antioxidant defence. that attenuates liver fibrosis and may increase antioxidant defence.
More Information Supplier PageAzelnidipine is a calcium blocker that attenuates liver fibrosis and may increase antioxidant defence. that attenuates liver fibrosis and may increase antioxidant defence.
More Information Supplier PageAzelnidipine is a calcium blocker that attenuates liver fibrosis and may increase antioxidant defence. that attenuates liver fibrosis and may increase antioxidant defence.
More Information Supplier PageAzilsartan (TAK-536) is an angiotensin II receptor antagonist used in the treatment of hypertension.
More Information Supplier PageAzilsartan (TAK-536) is an angiotensin II receptor antagonist used in the treatment of hypertension.
More Information Supplier PageAzilsartan (TAK-536) is an angiotensin II receptor antagonist used in the treatment of hypertension.
More Information Supplier PageAzilsartan (TAK-536) is an angiotensin II receptor antagonist used in the treatment of hypertension.
More Information Supplier PageAzilsartan (TAK-536) is an angiotensin II receptor antagonist used in the treatment of hypertension.
More Information Supplier PageAzithromycin is an azalide antibiotic, which inhibits the growth of gram negative bacteria, such as Haemophilus influenza.
More Information Supplier PageAzithromycin is an azalide antibiotic, which inhibits the growth of gram negative bacteria, such as Haemophilus influenza.
More Information Supplier PageAzithromycin is an azalide antibiotic, which inhibits the growth of gram negative bacteria, such as Haemophilus influenza.
More Information Supplier PageAzithromycin is an azalide antibiotic, which inhibits the growth of gram negative bacteria, such as Haemophilus influenza.
More Information Supplier PageAzithromycin is an azalide antibiotic, which inhibits the growth of gram negative bacteria, such as Haemophilus influenza.
More Information Supplier PageAzomycin(2-Nitroimidazole) is an antimicrobial antibiotic produced by a strain of Nocardia mesenterica, which is active against aerobic Gram-positive and Gram-negative bacteria.
More Information Supplier PageAzomycin(2-Nitroimidazole) is an antimicrobial antibiotic produced by a strain of Nocardia mesenterica, which is active against aerobic Gram-positive and Gram-negative bacteria.
More Information Supplier PageAzomycin(2-Nitroimidazole) is an antimicrobial antibiotic produced by a strain of Nocardia mesenterica, which is active against aerobic Gram-positive and Gram-negative bacteria.
More Information Supplier PageAzomycin(2-Nitroimidazole) is an antimicrobial antibiotic produced by a strain of Nocardia mesenterica, which is active against aerobic Gram-positive and Gram-negative bacteria.
More Information Supplier PageAztreonam is a synthetic monocyclic beta-lactam antibiotic (a monobactam), with the nucleus based on a simpler monobactam isolated from Chromobacterium violaceum.
More Information Supplier PageAztreonam is a synthetic monocyclic beta-lactam antibiotic (a monobactam), with the nucleus based on a simpler monobactam isolated from Chromobacterium violaceum.
More Information Supplier PageAztreonam is a synthetic monocyclic beta-lactam antibiotic (a monobactam), with the nucleus based on a simpler monobactam isolated from Chromobacterium violaceum.
More Information Supplier PageAztreonam is a synthetic monocyclic beta-lactam antibiotic (a monobactam), with the nucleus based on a simpler monobactam isolated from Chromobacterium violaceum.
More Information Supplier PageAztreonam is a synthetic monocyclic beta-lactam antibiotic (a monobactam), with the nucleus based on a simpler monobactam isolated from Chromobacterium violaceum.
More Information Supplier PageB-HT 920 is a dopamine agonist that has been proposed as an antiparkinsonian agent. It also has ??1-adrenergic and ??2-adrenergic agonist activity.
More Information Supplier PageB-HT 920 is a dopamine agonist that has been proposed as an antiparkinsonian agent. It also has ??1-adrenergic and ??2-adrenergic agonist activity.
More Information Supplier PageB-HT 920 is a dopamine agonist that has been proposed as an antiparkinsonian agent. It also has ??1-adrenergic and ??2-adrenergic agonist activity.
More Information Supplier PageB-HT 920 is a dopamine agonist that has been proposed as an antiparkinsonian agent. It also has ??1-adrenergic and ??2-adrenergic agonist activity.
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