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 WebsiteNXY-059 is the disulfonyl derivative of the neuroprotective spin trap pheny lbutynitrone or “PBN” with free radical-trapping properties. It substantially lessens the functional disability resulting from cerebral ischemia in a primate species.
More Information Supplier PageNXY-059 is the disulfonyl derivative of the neuroprotective spin trap pheny lbutynitrone or “PBN” with free radical-trapping properties. It substantially lessens the functional disability resulting from cerebral ischemia in a primate species.
More Information Supplier PageNXY-059 is the disulfonyl derivative of the neuroprotective spin trap pheny lbutynitrone or “PBN” with free radical-trapping properties. It substantially lessens the functional disability resulting from cerebral ischemia in a primate species.
More Information Supplier PageNXY-059 is the disulfonyl derivative of the neuroprotective spin trap pheny lbutynitrone or “PBN” with free radical-trapping properties. It substantially lessens the functional disability resulting from cerebral ischemia in a primate species.
More Information Supplier PageNXY-059 is the disulfonyl derivative of the neuroprotective spin trap pheny lbutynitrone or “PBN” with free radical-trapping properties. It substantially lessens the functional disability resulting from cerebral ischemia in a primate species.
More Information Supplier PageO4I1 increases Oct3/4 mRNA levels in HEK293 cells by 2.5- and 4-fold at 10 uM and 20 uM, respectively.
More Information Supplier PageO4I1 increases Oct3/4 mRNA levels in HEK293 cells by 2.5- and 4-fold at 10 uM and 20 uM, respectively.
More Information Supplier PageO4I1 increases Oct3/4 mRNA levels in HEK293 cells by 2.5- and 4-fold at 10 uM and 20 uM, respectively.
More Information Supplier PageO6-Benzylguanine is an effective substrate and efficient inactivator of DNA alkyltransferase. O6-Benzylguanine is an inhibitor of MGMT.
More Information Supplier PageO6-Benzylguanine is an effective substrate and efficient inactivator of DNA alkyltransferase. O6-Benzylguanine is an inhibitor of MGMT.
More Information Supplier PageO6-Benzylguanine is an effective substrate and efficient inactivator of DNA alkyltransferase. O6-Benzylguanine is an inhibitor of MGMT.
More Information Supplier PageOAC1 enhances iPSC reprogramming efficiency by enhancing Oct4 and Nanog driven gene expression.
More Information Supplier PageOAC1 enhances iPSC reprogramming efficiency by enhancing Oct4 and Nanog driven gene expression.
More Information Supplier PageOAC1 enhances iPSC reprogramming efficiency by enhancing Oct4 and Nanog driven gene expression.
More Information Supplier PageOAC1 enhances iPSC reprogramming efficiency by enhancing Oct4 and Nanog driven gene expression.
More Information Supplier PageOAC1 enhances iPSC reprogramming efficiency by enhancing Oct4 and Nanog driven gene expression.
More Information Supplier PageBcl-2 homology domain-3 (BH3) mimetic,antagonize all antiapoptotic Bcl-2 family proteins (average IC50, 3 umol/L), including Mcl-1 (IC50, 2.9 umol/L) and Bfl-1 (IC50, 5 umol/L).
More Information Supplier PageBcl-2 homology domain-3 (BH3) mimetic,antagonize all antiapoptotic Bcl-2 family proteins (average IC50, 3 umol/L), including Mcl-1 (IC50, 2.9 umol/L) and Bfl-1 (IC50, 5 umol/L).
More Information Supplier PageBcl-2 homology domain-3 (BH3) mimetic,antagonize all antiapoptotic Bcl-2 family proteins (average IC50, 3 umol/L), including Mcl-1 (IC50, 2.9 umol/L) and Bfl-1 (IC50, 5 umol/L).
More Information Supplier PageBcl-2 homology domain-3 (BH3) mimetic,antagonize all antiapoptotic Bcl-2 family proteins (average IC50, 3 umol/L), including Mcl-1 (IC50, 2.9 umol/L) and Bfl-1 (IC50, 5 umol/L).
More Information Supplier PageBcl-2 homology domain-3 (BH3) mimetic,antagonize all antiapoptotic Bcl-2 family proteins (average IC50, 3 umol/L), including Mcl-1 (IC50, 2.9 umol/L) and Bfl-1 (IC50, 5 umol/L).
More Information Supplier PageObeticholic Acid is a potent and selective farnesoid X receptor (FXR) agonist with EC50 of 99 nM
More Information Supplier PageObeticholic Acid is a potent and selective farnesoid X receptor (FXR) agonist with EC50 of 99 nM
More Information Supplier PageObeticholic Acid is a potent and selective farnesoid X receptor (FXR) agonist with EC50 of 99 nM
More Information Supplier PageObeticholic Acid is a potent and selective farnesoid X receptor (FXR) agonist with EC50 of 99 nM
More Information Supplier PageObtusifolin Suppresses Phthalate ESTERS-Induced Breast Cancer Bone Metastasis By Targeting Parathyroid HORMONE-Related Proteins.
More Information Supplier PageObtusifolin Suppresses Phthalate ESTERS-Induced Breast Cancer Bone Metastasis By Targeting Parathyroid HORMONE-Related Proteins.
More Information Supplier PageObtusifolin Suppresses Phthalate ESTERS-Induced Breast Cancer Bone Metastasis By Targeting Parathyroid HORMONE-Related Proteins.
More Information Supplier PageOC 000459 is a potent, oral and selective CRTH2 (also known as DP2) antagonist.
More Information Supplier PageOC 000459 is a potent, oral and selective CRTH2 (also known as DP2) antagonist.
More Information Supplier PageOC 000459 is a potent, oral and selective CRTH2 (also known as DP2) antagonist.
More Information Supplier PageOC 000459 is a potent, oral and selective CRTH2 (also known as DP2) antagonist.
More Information Supplier PageOctopamine hydrochloride is an invertebrate biogenic amine neurotransmitter, related to noradrenalin, that is an adrenoceptor agonist.
More Information Supplier PageOctopamine hydrochloride is an invertebrate biogenic amine neurotransmitter, related to noradrenalin, that is an adrenoceptor agonist.
More Information Supplier PageOctopamine hydrochloride is an invertebrate biogenic amine neurotransmitter, related to noradrenalin, that is an adrenoceptor agonist.
More Information Supplier PageOctopamine hydrochloride is an invertebrate biogenic amine neurotransmitter, related to noradrenalin, that is an adrenoceptor agonist.
More Information Supplier PageOctopamine hydrochloride is an invertebrate biogenic amine neurotransmitter, related to noradrenalin, that is an adrenoceptor agonist.
More Information Supplier PageOctreotide is a peptide agonist for sst2, sst3 and sst5 somatostatin receptors. IC50/Kd values (nM) at cloned human somatostatin receptors are: 290 – 1140 (sst1), 0.4 – 2.1 (sst2), 4.4 – 34.5 (sst3), > 1000 (sst4), and 5.6 – 32 (sst5).
More Information Supplier PageOctreotide is a peptide agonist for sst2, sst3 and sst5 somatostatin receptors. IC50/Kd values (nM) at cloned human somatostatin receptors are: 290 – 1140 (sst1), 0.4 – 2.1 (sst2), 4.4 – 34.5 (sst3), > 1000 (sst4), and 5.6 – 32 (sst5).
More Information Supplier PageOctreotide is a peptide agonist for sst2, sst3 and sst5 somatostatin receptors. IC50/Kd values (nM) at cloned human somatostatin receptors are: 290 – 1140 (sst1), 0.4 – 2.1 (sst2), 4.4 – 34.5 (sst3), > 1000 (sst4), and 5.6 – 32 (sst5).
More Information Supplier PageOctreotide is a peptide agonist for sst2, sst3 and sst5 somatostatin receptors. IC50/Kd values (nM) at cloned human somatostatin receptors are: 290 – 1140 (sst1), 0.4 – 2.1 (sst2), 4.4 – 34.5 (sst3), > 1000 (sst4), and 5.6 – 32 (sst5).
More Information Supplier PageOdanacatib is an inhibitor of cathepsin K,an enzyme involved in bone resorption.
More Information Supplier PageOdanacatib is an inhibitor of cathepsin K,an enzyme involved in bone resorption.
More Information Supplier PageOdanacatib is an inhibitor of cathepsin K,an enzyme involved in bone resorption.
More Information Supplier PageOdanacatib is an inhibitor of cathepsin K,an enzyme involved in bone resorption.
More Information Supplier PageOdanacatib is an inhibitor of cathepsin K,an enzyme involved in bone resorption.
More Information Supplier PageODM-201 is a potent and full antagonists for human AR (hAR) with IC50 values of 26 nM by transactivation assays in AR-HEK293 cells.
More Information Supplier PageODM-201 is a potent and full antagonists for human AR (hAR) with IC50 values of 26 nM by transactivation assays in AR-HEK293 cells.
More Information Supplier PageODM-201 is a potent and full antagonists for human AR (hAR) with IC50 values of 26 nM by transactivation assays in AR-HEK293 cells.
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