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 WebsiteCimaterol is a potent agonist of β-adrenergic receptors (pEC50 = 8.13, 8.78, and 6.62 for human β1, β2, and β3, respectively).
More Information Supplier PageCimetidine is a histamine H2-receptor antagonist that inhibits stomach acid production.
More Information Supplier PageCimetidine is a histamine H2-receptor antagonist that inhibits stomach acid production.
More Information Supplier PageCimetidine is a histamine H2-receptor antagonist that inhibits stomach acid production.
More Information Supplier PageCiMigenol 3-beta-D-xylopyranoside, extracted from Beesia calthifolia( Maxim. ) Ulhr. Rhizome.
More Information Supplier PageCiMigenol 3-beta-D-xylopyranoside, extracted from Beesia calthifolia( Maxim. ) Ulhr. Rhizome.
More Information Supplier PageCiMigenol 3-beta-D-xylopyranoside, extracted from Beesia calthifolia( Maxim. ) Ulhr. Rhizome.
More Information Supplier PageCimigenol-3-O-alpha-L-arabinoside is extracted from Cimicifuga foetida L. dried rhizome.
More Information Supplier PageCimigenol-3-O-alpha-L-arabinoside is extracted from Cimicifuga foetida L. dried rhizome.
More Information Supplier PageCimigenol-3-O-alpha-L-arabinoside is extracted from Cimicifuga foetida L. dried rhizome.
More Information Supplier PageCinchonidine is an alkaloid used in asymmetric synthesis in organic chemistry. It is a stereoisomer and pseudo-enantiomer of cinchonine.
More Information Supplier PageCinchonidine is an alkaloid used in asymmetric synthesis in organic chemistry. It is a stereoisomer and pseudo-enantiomer of cinchonine.
More Information Supplier PageCinchonidine is an alkaloid used in asymmetric synthesis in organic chemistry. It is a stereoisomer and pseudo-enantiomer of cinchonine.
More Information Supplier PageCinnamaldehyde is the organic compound that gives cinnamon its flavor and odor.
More Information Supplier PageCinnamaldehyde is the organic compound that gives cinnamon its flavor and odor.
More Information Supplier PageCinnamaldehyde is the organic compound that gives cinnamon its flavor and odor.
More Information Supplier PageCinnamic acid is a white crystalline organic acid, which is slightly soluble in water. It is obtained from oil of cinnamon, or from balsams such as storax.
More Information Supplier PageCinnamyl alcohol is an organic compound that is found in esterified form in storax, Balsam of Peru, and cinnamon leaves.
More Information Supplier PageCinnamyl alcohol is an organic compound that is found in esterified form in storax, Balsam of Peru, and cinnamon leaves.
More Information Supplier PageCinnamyl alcohol is an organic compound that is found in esterified form in storax, Balsam of Peru, and cinnamon leaves.
More Information Supplier PageCinobufagin is a specific Na+/K+-ATPase inhibitor. About as active as ouabain
More Information Supplier PageCinobufagin is a specific Na+/K+-ATPase inhibitor. About as active as ouabain
More Information Supplier PageCinobufagin is a specific Na+/K+-ATPase inhibitor. About as active as ouabain
More Information Supplier PageCinobufagin is a specific Na+/K+-ATPase inhibitor. About as active as ouabain
More Information Supplier PageCiproxifan is an extremely potent histamine H3 inverse agonist/antagonist.
More Information Supplier PageCiproxifan is an extremely potent histamine H3 inverse agonist/antagonist.
More Information Supplier PageCiproxifan is an extremely potent histamine H3 inverse agonist/antagonist.
More Information Supplier PageCiproxifan is an extremely potent histamine H3 inverse agonist/antagonist.
More Information Supplier PageCiproxifan is an extremely potent histamine H3 inverse agonist/antagonist.
More Information Supplier PageCiproxifan maleate is a potent, selective H3 histamine receptor antagonist.
More Information Supplier PageCiproxifan maleate is a potent, selective H3 histamine receptor antagonist.
More Information Supplier PageCiproxifan maleate is a potent, selective H3 histamine receptor antagonist.
More Information Supplier PageCiproxifan maleate is a potent, selective H3 histamine receptor antagonist.
More Information Supplier PageCIQ is a subunit-selective potentiator of NMDA receptors containing the NR2C or NR2D subunit.
More Information Supplier PageCIQ is a subunit-selective potentiator of NMDA receptors containing the NR2C or NR2D subunit.
More Information Supplier PageCIQ is a subunit-selective potentiator of NMDA receptors containing the NR2C or NR2D subunit.
More Information Supplier Pagecis-(Z)-Flupentixol dihydrochloride is a dopamine receptor antagonist, antipsychotic, neuroleptic agent.
More Information Supplier Pagecis-(Z)-Flupentixol dihydrochloride is a dopamine receptor antagonist, antipsychotic, neuroleptic agent.
More Information Supplier Pagecis-(Z)-Flupentixol dihydrochloride is a dopamine receptor antagonist, antipsychotic, neuroleptic agent.
More Information Supplier Pagecis-Urocanic acid is a major ultraviolet-absorbing component of the stratum corneum.
More Information Supplier Pagecis-Urocanic acid is a major ultraviolet-absorbing component of the stratum corneum.
More Information Supplier Pagecis-Urocanic acid is a major ultraviolet-absorbing component of the stratum corneum.
More Information Supplier PageCisplatin was the first member of a class of platinum-containing anti-cancer drugs, which now also includes carboplatin and oxaliplatin. These platinum complexes react in vivo, binding to and causing crosslinking of DNA, which ultimately triggers apoptosis (programmed cell death).
More Information Supplier PageCisplatin was the first member of a class of platinum-containing anti-cancer drugs, which now also includes carboplatin and oxaliplatin. These platinum complexes react in vivo, binding to and causing crosslinking of DNA, which ultimately triggers apoptosis (programmed cell death).
More Information Supplier PageCisplatin was the first member of a class of platinum-containing anti-cancer drugs, which now also includes carboplatin and oxaliplatin. These platinum complexes react in vivo, binding to and causing crosslinking of DNA, which ultimately triggers apoptosis (programmed cell death).
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