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 Website11-oxo-mogroside V showed a higher scavenging effect on O2- with EC50 of 4.79 mg/ml and H2O2 (EC50 of 16.52 mg/ ml) than those of mogroside V.
More Information Supplier Page11-oxo-mogroside V showed a higher scavenging effect on O2- with EC50 of 4.79 mg/ml and H2O2 (EC50 of 16.52 mg/ ml) than those of mogroside V.
More Information Supplier Page12-O-tetradecanoyl phorbol-13-acetate is a diester of phorbol and is a tumor promoting compound extracted from croton oil. It is a reversible, highly potent protein kinase C (PKC) activator in vitro and in vivo at nM concentrations.
More Information Supplier Page12-O-tetradecanoyl phorbol-13-acetate is a diester of phorbol and is a tumor promoting compound extracted from croton oil. It is a reversible, highly potent protein kinase C (PKC) activator in vitro and in vivo at nM concentrations.
More Information Supplier Page12-O-tetradecanoyl phorbol-13-acetate is a diester of phorbol and is a tumor promoting compound extracted from croton oil. It is a reversible, highly potent protein kinase C (PKC) activator in vitro and in vivo at nM concentrations.
More Information Supplier Page1400W Dihydrochloride is a slow, tight binding, potent and highly selective inhibitor of inducible nitric oxide synthase (Kd = 7 nM). Selective over nNOS and eNOS (Ki values are 2 and 50 ??M respectively). Cell-permeable and active in vivo.
More Information Supplier Page1400W Dihydrochloride is a slow, tight binding, potent and highly selective inhibitor of inducible nitric oxide synthase (Kd = 7 nM). Selective over nNOS and eNOS (Ki values are 2 and 50 ??M respectively). Cell-permeable and active in vivo.
More Information Supplier Page1400W Dihydrochloride is a slow, tight binding, potent and highly selective inhibitor of inducible nitric oxide synthase (Kd = 7 nM). Selective over nNOS and eNOS (Ki values are 2 and 50 ??M respectively). Cell-permeable and active in vivo.
More Information Supplier Page1400W Dihydrochloride is a slow, tight binding, potent and highly selective inhibitor of inducible nitric oxide synthase (Kd = 7 nM). Selective over nNOS and eNOS (Ki values are 2 and 50 ??M respectively). Cell-permeable and active in vivo.
More Information Supplier Page17 alpha-propionate is a new topical and peripherally selective androgen antagonist.
More Information Supplier Page17 alpha-propionate is a new topical and peripherally selective androgen antagonist.
More Information Supplier Page17 alpha-propionate is a new topical and peripherally selective androgen antagonist.
More Information Supplier Page17 alpha-propionate is a new topical and peripherally selective androgen antagonist.
More Information Supplier Page17-AAG is an ansamycin antibiotic which acts as an anti-tumor agent. Specifically, 17-AAG binds and inhibits Hsp90.
More Information Supplier Page17-AAG is an ansamycin antibiotic which acts as an anti-tumor agent. Specifically, 17-AAG binds and inhibits Hsp90.
More Information Supplier Page17-AAG is an ansamycin antibiotic which acts as an anti-tumor agent. Specifically, 17-AAG binds and inhibits Hsp90.
More Information Supplier Page17-AAG is an ansamycin antibiotic which acts as an anti-tumor agent. Specifically, 17-AAG binds and inhibits Hsp90.
More Information Supplier Page17-AAG is an ansamycin antibiotic which acts as an anti-tumor agent. Specifically, 17-AAG binds and inhibits Hsp90.
More Information Supplier Page17-DMAG is a water-soluble analog of 17-AAG and geldanamycin that binds the ATP binding site of Hsp90 and inhibits its chaperone activity. Displays more potent antitumor activity than 17-AAG.
More Information Supplier Page17-DMAG is a water-soluble analog of 17-AAG and geldanamycin that binds the ATP binding site of Hsp90 and inhibits its chaperone activity. Displays more potent antitumor activity than 17-AAG.
More Information Supplier Page17-DMAG is a water-soluble analog of 17-AAG and geldanamycin that binds the ATP binding site of Hsp90 and inhibits its chaperone activity. Displays more potent antitumor activity than 17-AAG.
More Information Supplier Page17-DMAG is a water-soluble analog of 17-AAG and geldanamycin that binds the ATP binding site of Hsp90 and inhibits its chaperone activity. Displays more potent antitumor activity than 17-AAG.
More Information Supplier Page17-DMAG is a water-soluble analog of 17-AAG and geldanamycin that binds the ATP binding site of Hsp90 and inhibits its chaperone activity. Displays more potent antitumor activity than 17-AAG.
More Information Supplier Page1alpha-Hydroxy VD4 , a 1alpha(OH)D derivative, can effectively induce the differentiation of monoblastic leukaemia U937, P39/TSU and P31/FUJ cells.
More Information Supplier Page1alpha-Hydroxy VD4 , a 1alpha(OH)D derivative, can effectively induce the differentiation of monoblastic leukaemia U937, P39/TSU and P31/FUJ cells.
More Information Supplier PageMps1-IN-1 is a highly potent and selectibe Mpsl inhibitor with IC50 of 367 nM; >1000-fold selectivity relative to the 352 member kinase panel with the major exceptions of Alk and Ltk.
More Information Supplier PageMps1-IN-1 is a highly potent and selectibe Mpsl inhibitor with IC50 of 367 nM; >1000-fold selectivity relative to the 352 member kinase panel with the major exceptions of Alk and Ltk.
More Information Supplier PageMps1-IN-1 is a highly potent and selectibe Mpsl inhibitor with IC50 of 367 nM; >1000-fold selectivity relative to the 352 member kinase panel with the major exceptions of Alk and Ltk.
More Information Supplier Page2-Atractylenolide, extracted from Atractylodes macrocephala Koidz. Rhizome.
More Information Supplier Page2-Atractylenolide, extracted from Atractylodes macrocephala Koidz. Rhizome.
More Information Supplier Page2-Atractylenolide, extracted from Atractylodes macrocephala Koidz. Rhizome.
More Information Supplier Pagea-Hydroxyglutaric acid (2-HG) is an a-hydroxy acid. It is normally metabolized to 2-oxoglutarate by D- and L-2-hydroxyglutarate dehydrogenases, and mutations in these enzymes cause 2-hydroxyglutaric aciduria, a neurometabolic disorder.
More Information Supplier Pagea-Hydroxyglutaric acid (2-HG) is an a-hydroxy acid. It is normally metabolized to 2-oxoglutarate by D- and L-2-hydroxyglutarate dehydrogenases, and mutations in these enzymes cause 2-hydroxyglutaric aciduria, a neurometabolic disorder.
More Information Supplier Page2-Hydroxysaclofen is a potent and selective antagonist at GABAB receptors.
More Information Supplier Page2-Hydroxysaclofen is a potent and selective antagonist at GABAB receptors.
More Information Supplier Page2-Hydroxysaclofen is a potent and selective antagonist at GABAB receptors.
More Information Supplier Page2-Methoxyestradiol is an apoptotic, antiproliferative and antiangiogenic agent. Induces p53-induced apoptosis via two pathways: activation of p38 and NF-??B; and activation of JNK and AP-1 leading to Bcl-2 phosphorylation.
More Information Supplier Page2-Methoxyestradiol is an apoptotic, antiproliferative and antiangiogenic agent. Induces p53-induced apoptosis via two pathways: activation of p38 and NF-??B; and activation of JNK and AP-1 leading to Bcl-2 phosphorylation.
More Information Supplier Page2-Methoxyestradiol is an apoptotic, antiproliferative and antiangiogenic agent. Induces p53-induced apoptosis via two pathways: activation of p38 and NF-??B; and activation of JNK and AP-1 leading to Bcl-2 phosphorylation.
More Information Supplier Page2-Methoxyestradiol is an apoptotic, antiproliferative and antiangiogenic agent. Induces p53-induced apoptosis via two pathways: activation of p38 and NF-??B; and activation of JNK and AP-1 leading to Bcl-2 phosphorylation.
More Information Supplier Page2-Methoxyestradiol is an apoptotic, antiproliferative and antiangiogenic agent. Induces p53-induced apoptosis via two pathways: activation of p38 and NF-??B; and activation of JNK and AP-1 leading to Bcl-2 phosphorylation.
More Information Supplier Page2,3 DCPE displays anticancer agent properties and induces ERK activation.
More Information Supplier Page2,3 DCPE displays anticancer agent properties and induces ERK activation.
More Information Supplier Page2,3 DCPE displays anticancer agent properties and induces ERK activation.
More Information Supplier Page2′-O-beta-L-galactopyranosylorientin, extracted from Flos Trollii Chinensis.
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