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 WebsiteSorafenib (Nexavar) is a novel, small molecular inhibitor of several tyrosine protein kinases (VEGFR and PDGFR) and RAF/MEK/ERK cascade inhibitor with an IC50 of 6, 22, 38 nM for Raf-1, wt BRAF and V599E mutant BRAF.
More Information Supplier PageSorafenib (Nexavar) is a novel, small molecular inhibitor of several tyrosine protein kinases (VEGFR and PDGFR) and RAF/MEK/ERK cascade inhibitor with an IC50 of 6, 22, 38 nM for Raf-1, wt BRAF and V599E mutant BRAF.
More Information Supplier PageSorafenib (Nexavar) is a novel, small molecular inhibitor of several tyrosine protein kinases (VEGFR and PDGFR) and RAF/MEK/ERK cascade inhibitor with an IC50 of 6, 22, 38 nM for Raf-1, wt BRAF and V599E mutant BRAF.
More Information Supplier PageSorafenib (Nexavar) is a novel, small molecular inhibitor of several tyrosine protein kinases (VEGFR and PDGFR) and RAF/MEK/ERK cascade inhibitor with an IC50 of 6, 22, 38 nM for Raf-1, wt BRAF and V599E mutant BRAF.
More Information Supplier PageSorafenib (Nexavar) is a novel, small molecular inhibitor of several tyrosine protein kinases (VEGFR and PDGFR) and RAF/MEK/ERK cascade inhibitor with an IC50 of 6, 22, 38 nM for Raf-1, wt BRAF and V599E mutant BRAF.
More Information Supplier PageSotrastaurin is a protein kinase C inhibitor for the prevention of transplant rejection and treatment of psoriasis.
More Information Supplier PageSotrastaurin is a protein kinase C inhibitor for the prevention of transplant rejection and treatment of psoriasis.
More Information Supplier PageSotrastaurin is a protein kinase C inhibitor for the prevention of transplant rejection and treatment of psoriasis.
More Information Supplier PageSotrastaurin is a protein kinase C inhibitor for the prevention of transplant rejection and treatment of psoriasis.
More Information Supplier PageSotrastaurin is a protein kinase C inhibitor for the prevention of transplant rejection and treatment of psoriasis.
More Information Supplier PageSoyasaponin Bb can impede kidney enlargement and cyst growth in the pcy mouse model of PKD.
More Information Supplier PageSoyasaponin Bb can impede kidney enlargement and cyst growth in the pcy mouse model of PKD.
More Information Supplier PageSoyasaponin Bb can impede kidney enlargement and cyst growth in the pcy mouse model of PKD.
More Information Supplier PageSP-420 is an orally active small molecule that selectively binds iron and removes it from the body. In animal studies, SP-420 has shown excellent tissue penetration, highly efficient iron binding and a promising safety profile.
More Information Supplier PageSP-420 is an orally active small molecule that selectively binds iron and removes it from the body. In animal studies, SP-420 has shown excellent tissue penetration, highly efficient iron binding and a promising safety profile.
More Information Supplier PageSP-420 is an orally active small molecule that selectively binds iron and removes it from the body. In animal studies, SP-420 has shown excellent tissue penetration, highly efficient iron binding and a promising safety profile.
More Information Supplier PageSP2509 is a novel histone demethylase LSD1 (KDM1A) antagonist with IC50 of 13 nM; no inhibition on MAO-A and MAO-B.
More Information Supplier PageSP2509 is a novel histone demethylase LSD1 (KDM1A) antagonist with IC50 of 13 nM; no inhibition on MAO-A and MAO-B.
More Information Supplier PageSP2509 is a novel histone demethylase LSD1 (KDM1A) antagonist with IC50 of 13 nM; no inhibition on MAO-A and MAO-B.
More Information Supplier PageSP600125 is a JNK inhibitor with IC50=40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3.
More Information Supplier PageSP600125 is a JNK inhibitor with IC50=40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3.
More Information Supplier PageSP600125 is a JNK inhibitor with IC50=40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3.
More Information Supplier PageSP600125 is a JNK inhibitor with IC50=40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3.
More Information Supplier PageSP600125 is a JNK inhibitor with IC50=40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3.
More Information Supplier PageSpautin-1 is a novel autophagy inhibitor, IM inhibited the growth of K562 cells with IC50 of 1.03??M. In contrast, co-treatment with Spautin-1 increased IM-induced inhibition of cell viability with IC50 of 0.45 uM.
More Information Supplier PageSpautin-1 is a novel autophagy inhibitor, IM inhibited the growth of K562 cells with IC50 of 1.03??M. In contrast, co-treatment with Spautin-1 increased IM-induced inhibition of cell viability with IC50 of 0.45 uM.
More Information Supplier PageSpautin-1 is a novel autophagy inhibitor, IM inhibited the growth of K562 cells with IC50 of 1.03??M. In contrast, co-treatment with Spautin-1 increased IM-induced inhibition of cell viability with IC50 of 0.45 uM.
More Information Supplier PageSpecnuezhenide, extracted from dried ripe fruit of Ligustum lucidum Ait privet .
More Information Supplier PageSpecnuezhenide, extracted from dried ripe fruit of Ligustum lucidum Ait privet .
More Information Supplier PageSpecnuezhenide, extracted from dried ripe fruit of Ligustum lucidum Ait privet .
More Information Supplier PageSpectinomycin is an antibiotic useful for the treatment of the bacterial infection, gonorrhea.
More Information Supplier PageSpectinomycin is an antibiotic useful for the treatment of the bacterial infection, gonorrhea.
More Information Supplier PageSpectinomycin is an antibiotic useful for the treatment of the bacterial infection, gonorrhea.
More Information Supplier PageSpectinomycin is an antibiotic useful for the treatment of the bacterial infection, gonorrhea.
More Information Supplier PageSpinorphin is an endogenous factor that exhibits inhibitory effects on enkephalin-degrading enzymes.
More Information Supplier PageSpinorphin is an endogenous factor that exhibits inhibitory effects on enkephalin-degrading enzymes.
More Information Supplier PageSpinorphin is an endogenous factor that exhibits inhibitory effects on enkephalin-degrading enzymes.
More Information Supplier PageSpinosin, a C-glycoside flavonoid from semen Zizhiphi Spinozae, potentiated pentobarbital-induced sleep via the serotonergic system.
More Information Supplier PageSpinosin, a C-glycoside flavonoid from semen Zizhiphi Spinozae, potentiated pentobarbital-induced sleep via the serotonergic system.
More Information Supplier PageSpinosin, a C-glycoside flavonoid from semen Zizhiphi Spinozae, potentiated pentobarbital-induced sleep via the serotonergic system.
More Information Supplier PageSpliceostatin A targets SF3b and inhibits both splicing and nuclear retention of pre-mRNA.
More Information Supplier PageSpliceostatin A targets SF3b and inhibits both splicing and nuclear retention of pre-mRNA.
More Information Supplier PageSpliceostatin A targets SF3b and inhibits both splicing and nuclear retention of pre-mRNA.
More Information Supplier PageSpliceostatin A targets SF3b and inhibits both splicing and nuclear retention of pre-mRNA.
More Information Supplier PageSplitomicin is a selective NAD(+)-dependent histone deacetylase Sir2p inhibitor with IC50 of 60 ??M, showing a higher activity in a cell-based assay.
More Information Supplier PageSplitomicin is a selective NAD(+)-dependent histone deacetylase Sir2p inhibitor with IC50 of 60 ??M, showing a higher activity in a cell-based assay.
More Information Supplier PageSplitomicin is a selective NAD(+)-dependent histone deacetylase Sir2p inhibitor with IC50 of 60 ??M, showing a higher activity in a cell-based assay.
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