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 WebsiteBax channel blocker is a potent inhibitor of Bax-mediated mitochondrial cytochrome C release (IC50 = 0.52 ??M).
More Information Supplier PageBax channel blocker is a potent inhibitor of Bax-mediated mitochondrial cytochrome C release (IC50 = 0.52 ??M).
More Information Supplier PageBax inhibitor peptide P5, cell-permeable synthetic peptide inhibitor of Bax translocation to mitochondria; designed from Ku70, a protein that is suggested to suppress the mitochondrial translocation of Bax. Inhibits Bax-mediated apoptosis in vitro.
More Information Supplier PageBax inhibitor peptide P5, cell-permeable synthetic peptide inhibitor of Bax translocation to mitochondria; designed from Ku70, a protein that is suggested to suppress the mitochondrial translocation of Bax. Inhibits Bax-mediated apoptosis in vitro.
More Information Supplier PageBax inhibitor peptide P5, cell-permeable synthetic peptide inhibitor of Bax translocation to mitochondria; designed from Ku70, a protein that is suggested to suppress the mitochondrial translocation of Bax. Inhibits Bax-mediated apoptosis in vitro.
More Information Supplier PageBax inhibitor peptide V5, cell-permeable synthetic peptide inhibitor of Bax translocation to mitochondria; designed from Ku70, a protein that is suggested to suppress the mitochondrial translocation of Bax. Inhibits Bax-mediated apoptosis in vitro.
More Information Supplier PageBax inhibitor peptide V5, cell-permeable synthetic peptide inhibitor of Bax translocation to mitochondria; designed from Ku70, a protein that is suggested to suppress the mitochondrial translocation of Bax. Inhibits Bax-mediated apoptosis in vitro.
More Information Supplier PageBax inhibitor peptide V5, cell-permeable synthetic peptide inhibitor of Bax translocation to mitochondria; designed from Ku70, a protein that is suggested to suppress the mitochondrial translocation of Bax. Inhibits Bax-mediated apoptosis in vitro.
More Information Supplier PageBax inhibitor peptide, negative control, negative control peptide for the Bax inhibitor peptides V5 and P5 , which inhibit Bax translocation to mitochondria and Bax-mediated apoptosis in vitro.
More Information Supplier PageBax inhibitor peptide, negative control, negative control peptide for the Bax inhibitor peptides V5 and P5 , which inhibit Bax translocation to mitochondria and Bax-mediated apoptosis in vitro.
More Information Supplier PageBAY 1000394 is an orally bioavailable cyclin dependent kinase (CDK) inhibitor with potential antineoplastic activity.
More Information Supplier PageBAY 1000394 is an orally bioavailable cyclin dependent kinase (CDK) inhibitor with potential antineoplastic activity.
More Information Supplier PageBAY 1000394 is an orally bioavailable cyclin dependent kinase (CDK) inhibitor with potential antineoplastic activity.
More Information Supplier PageBAY 1000394 is an orally bioavailable cyclin dependent kinase (CDK) inhibitor with potential antineoplastic activity.
More Information Supplier PageBAY 11-7085 is an irreversible inhibitor of TNF??-induced I??B?? phosphorylation with IC50 of 10 ??M.
More Information Supplier PageBAY 11-7085 is an irreversible inhibitor of TNF??-induced I??B?? phosphorylation with IC50 of 10 ??M.
More Information Supplier PageBAY 11-7085 is an irreversible inhibitor of TNF??-induced I??B?? phosphorylation with IC50 of 10 ??M.
More Information Supplier PageBAY 11-7085 is an irreversible inhibitor of TNF??-induced I??B?? phosphorylation with IC50 of 10 ??M.
More Information Supplier PageBay 11-7821 is an irreversible inhibitor of TNF-??-stimulated I??B?? phosphorylation.
More Information Supplier PageBay 11-7821 is an irreversible inhibitor of TNF-??-stimulated I??B?? phosphorylation.
More Information Supplier PageBay 11-7821 is an irreversible inhibitor of TNF-??-stimulated I??B?? phosphorylation.
More Information Supplier PageBay 11-7821 is an irreversible inhibitor of TNF-??-stimulated I??B?? phosphorylation.
More Information Supplier PageBay 11-7821 is an irreversible inhibitor of TNF-??-stimulated I??B?? phosphorylation.
More Information Supplier PageBAY 60-7550 is a potent PDE2 inhibitor with IC50 values of 2.0 nM (bovine) and 4.7 nM (human).
More Information Supplier PageBAY 60-7550 is a potent PDE2 inhibitor with IC50 values of 2.0 nM (bovine) and 4.7 nM (human).
More Information Supplier PageBAY 60-7550 is a potent PDE2 inhibitor with IC50 values of 2.0 nM (bovine) and 4.7 nM (human).
More Information Supplier PageBAY 60-7550 is a potent PDE2 inhibitor with IC50 values of 2.0 nM (bovine) and 4.7 nM (human).
More Information Supplier PageBAY 61-3606 is a cell-permeable imidazopyrimidine compound that acts as a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity with no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
More Information Supplier PageBAY 61-3606 is a cell-permeable imidazopyrimidine compound that acts as a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity with no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
More Information Supplier PageBAY 61-3606 is a cell-permeable imidazopyrimidine compound that acts as a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity with no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
More Information Supplier PageBAY 61-3606 is a cell-permeable imidazopyrimidine compound that acts as a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity with no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
More Information Supplier PageBAY 61-3606 is a potent (Ki = 7.5 nM) and selective inhibitor of Syk kinase.
More Information Supplier PageBAY 61-3606 is a potent (Ki = 7.5 nM) and selective inhibitor of Syk kinase.
More Information Supplier PageBAY 61-3606 is a potent (Ki = 7.5 nM) and selective inhibitor of Syk kinase.
More Information Supplier PageBay 65-1942 is an ATP-competitive inhibitor that selectively targets IKK?? kinase activity.
More Information Supplier PageBay 65-1942 is an ATP-competitive inhibitor that selectively targets IKK?? kinase activity.
More Information Supplier PageBay 65-1942 is an ATP-competitive inhibitor that selectively targets IKK?? kinase activity.
More Information Supplier PageBay 65-1942 is an ATP-competitive inhibitor that selectively targets IKK?? kinase activity.
More Information Supplier PageBay 65-1942 is an ATP-competitive inhibitor that selectively targets IKK?? kinase activity.
More Information Supplier PageBay 65-1942 is an ATP-competitive inhibitor that selectively targets IKK?? kinase activity.
More Information Supplier PageBay 65-1942 is an ATP-competitive inhibitor that selectively targets IKK?? kinase activity.
More Information Supplier PageBay 65-1942 (R form) is an ATP-competitive inhibitor that selectively targets IKK?? kinase.
More Information Supplier PageBay 65-1942 (R form) is an ATP-competitive inhibitor that selectively targets IKK?? kinase.
More Information Supplier PageBay 65-1942 (R form) is an ATP-competitive inhibitor that selectively targets IKK?? kinase.
More Information Supplier PageBAY 80-6946 is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity.
More Information Supplier PageBAY 80-6946 is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity.
More Information Supplier PageBAY 80-6946 is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity.
More Information Supplier PageBAY 80-6946 is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity.
More Information Supplier PageBAY 87-2243, a highly potent and selective inhibitor of hypoxia-induced gene activation has antitumor activities by inhibition of mitochondrial complex I.
More Information Supplier PageBAY 87-2243, a highly potent and selective inhibitor of hypoxia-induced gene activation has antitumor activities by inhibition of mitochondrial complex I.
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