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 WebsiteDaptomycin is a lipopeptide antibiotic used in the treatment of certain infections caused by Gram-positive organisms.
More Information Supplier PageDaptomycin is a lipopeptide antibiotic used in the treatment of certain infections caused by Gram-positive organisms.
More Information Supplier PageDaptomycin is a lipopeptide antibiotic used in the treatment of certain infections caused by Gram-positive organisms.
More Information Supplier PageDaptomycin is a lipopeptide antibiotic used in the treatment of certain infections caused by Gram-positive organisms.
More Information Supplier PageDarapladib is a reversible lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor .
More Information Supplier PageDarapladib is a reversible lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor .
More Information Supplier PageDarapladib is a reversible lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor .
More Information Supplier PageDarapladib is a reversible lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor .
More Information Supplier PageDarifenacin works by blocking the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions.
More Information Supplier PageDarifenacin works by blocking the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions.
More Information Supplier PageDarifenacin works by blocking the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions.
More Information Supplier PageDarifenacin works by blocking the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions.
More Information Supplier PageDasatinib (BMS-354825) is an oral multi- BCR/ABL and Src family tyrosine kinase inhibitor. The main targets of dasatinib, are BCR/ABL, Src, c-Kit, ephrin receptors, and several other tyrosine kinases, but not erbB kinases such as EGFR or Her2.
More Information Supplier PageDasatinib (BMS-354825) is an oral multi- BCR/ABL and Src family tyrosine kinase inhibitor. The main targets of dasatinib, are BCR/ABL, Src, c-Kit, ephrin receptors, and several other tyrosine kinases, but not erbB kinases such as EGFR or Her2.
More Information Supplier PageDasatinib (BMS-354825) is an oral multi- BCR/ABL and Src family tyrosine kinase inhibitor. The main targets of dasatinib, are BCR/ABL, Src, c-Kit, ephrin receptors, and several other tyrosine kinases, but not erbB kinases such as EGFR or Her2.
More Information Supplier PageDasatinib (BMS-354825) is an oral multi- BCR/ABL and Src family tyrosine kinase inhibitor. The main targets of dasatinib, are BCR/ABL, Src, c-Kit, ephrin receptors, and several other tyrosine kinases, but not erbB kinases such as EGFR or Her2.
More Information Supplier PageDasatinib (BMS-354825) is an oral multi- BCR/ABL and Src family tyrosine kinase inhibitor. The main targets of dasatinib, are BCR/ABL, Src, c-Kit, ephrin receptors, and several other tyrosine kinases, but not erbB kinases such as EGFR or Her2.
More Information Supplier PageDasatinib hydrochloride is a potent and dual Abl/ Src inhibitor IC50 of ??1 nM/0.8 nM respectively; also inhibit c-Kit (WT)/c-Kit (D816V) with IC50 of 79 nM/37 nM.
More Information Supplier PageDasatinib hydrochloride is a potent and dual Abl/ Src inhibitor IC50 of ??1 nM/0.8 nM respectively; also inhibit c-Kit (WT)/c-Kit (D816V) with IC50 of 79 nM/37 nM.
More Information Supplier PageDasatinib hydrochloride is a potent and dual Abl/ Src inhibitor IC50 of ??1 nM/0.8 nM respectively; also inhibit c-Kit (WT)/c-Kit (D816V) with IC50 of 79 nM/37 nM.
More Information Supplier PageDauricine is a calcium channel blocker. It is the main toxin that makes the North American vine Menispermum canadense poisonous.
More Information Supplier PageDauricine is a calcium channel blocker. It is the main toxin that makes the North American vine Menispermum canadense poisonous.
More Information Supplier PageDauricine is a calcium channel blocker. It is the main toxin that makes the North American vine Menispermum canadense poisonous.
More Information Supplier PageDaurinoline is an alkaloid from the rhizomes of Menispermum canadense and Menispermum dauricum and from Phaeanthus vietnamensis.
More Information Supplier PageDaurinoline is an alkaloid from the rhizomes of Menispermum canadense and Menispermum dauricum and from Phaeanthus vietnamensis.
More Information Supplier PageDaurinoline is an alkaloid from the rhizomes of Menispermum canadense and Menispermum dauricum and from Phaeanthus vietnamensis.
More Information Supplier PageDaurisoline alkaloid isolated from the rhizomes of Menispermum dauricum that exhibit varies pharmacological activities including antiplatelet aggregation, anti-inflammatory, neuron-protective properties, and antiarrhythmic effect.
More Information Supplier PageDaurisoline alkaloid isolated from the rhizomes of Menispermum dauricum that exhibit varies pharmacological activities including antiplatelet aggregation, anti-inflammatory, neuron-protective properties, and antiarrhythmic effect.
More Information Supplier PageDaurisoline alkaloid isolated from the rhizomes of Menispermum dauricum that exhibit varies pharmacological activities including antiplatelet aggregation, anti-inflammatory, neuron-protective properties, and antiarrhythmic effect.
More Information Supplier PageDB07268 is a potent and selective JNK1 inhibitor with an IC50 value of 9 nM.
More Information Supplier PageDB07268 is a potent and selective JNK1 inhibitor with an IC50 value of 9 nM.
More Information Supplier PageDB07268 is a potent and selective JNK1 inhibitor with an IC50 value of 9 nM.
More Information Supplier PageDbeq is a selective and reversible inhibitor of p97 ATPase (IC50 = 1.5 uM).
More Information Supplier PageDbeq is a selective and reversible inhibitor of p97 ATPase (IC50 = 1.5 uM).
More Information Supplier PageDbeq is a selective and reversible inhibitor of p97 ATPase (IC50 = 1.5 uM).
More Information Supplier PageDbeq is a selective and reversible inhibitor of p97 ATPase (IC50 = 1.5 uM).
More Information Supplier PageDbeq is a selective and reversible inhibitor of p97 ATPase (IC50 = 1.5 uM).
More Information Supplier PageDBU is a chemical compound and belongs to the class of amidine compounds.
More Information Supplier PageDBU is a chemical compound and belongs to the class of amidine compounds.
More Information Supplier PageDBU is a chemical compound and belongs to the class of amidine compounds.
More Information Supplier PageDCC-2036 is an orally bioavailable small-molecule inhibitor of multiple tyrosine kinases with potential antineoplastic activity.
More Information Supplier PageDCC-2036 is an orally bioavailable small-molecule inhibitor of multiple tyrosine kinases with potential antineoplastic activity.
More Information Supplier PageDCC-2036 is an orally bioavailable small-molecule inhibitor of multiple tyrosine kinases with potential antineoplastic activity.
More Information Supplier PageDCC-2036 is an orally bioavailable small-molecule inhibitor of multiple tyrosine kinases with potential antineoplastic activity.
More Information Supplier PageDCC-2036 is an orally bioavailable small-molecule inhibitor of multiple tyrosine kinases with potential antineoplastic activity.
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