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 WebsiteSRT3109 is a CXCR2 ligand for use in the treatment of chemokine mediated diseases and conditions.
More Information Supplier PageSRT3109 is a CXCR2 ligand for use in the treatment of chemokine mediated diseases and conditions.
More Information Supplier PageSRT3109 is a CXCR2 ligand for use in the treatment of chemokine mediated diseases and conditions.
More Information Supplier PageSSR 69071 is a high affinity, potent inhibitor of Neutrophil Elastase (human leukocyte elastase, HLE) (IC50 = 3.9 nM).
More Information Supplier PageSSR 69071 is a high affinity, potent inhibitor of Neutrophil Elastase (human leukocyte elastase, HLE) (IC50 = 3.9 nM).
More Information Supplier PageSSR128129E is an orally-active and allosteric FGFR1 inhibitor with IC50 of 1.9 ??M
More Information Supplier PageSSR128129E is an orally-active and allosteric FGFR1 inhibitor with IC50 of 1.9 ??M
More Information Supplier PageSSR128129E is an orally-active and allosteric FGFR1 inhibitor with IC50 of 1.9 ??M
More Information Supplier PageSSR128129E is an orally-active and allosteric FGFR1 inhibitor with IC50 of 1.9 ??M
More Information Supplier PageST 101 (ZSET1446) is a novel cognitive enhancer that promotes hippocampal neurogenesis and ameliorates depressive behavior in olfactory bulbectomized mice.
More Information Supplier PageST 101 (ZSET1446) is a novel cognitive enhancer that promotes hippocampal neurogenesis and ameliorates depressive behavior in olfactory bulbectomized mice.
More Information Supplier PageST 101 (ZSET1446) is a novel cognitive enhancer that promotes hippocampal neurogenesis and ameliorates depressive behavior in olfactory bulbectomized mice.
More Information Supplier PageST7612AA1 is a new and potent HDCA inhibitor with potential anticancer activity.
More Information Supplier PageST7612AA1 is a new and potent HDCA inhibitor with potential anticancer activity.
More Information Supplier PageST7612AA1 is a new and potent HDCA inhibitor with potential anticancer activity.
More Information Supplier PageSTAT5 Inhibitor is a cell-permeable, nonpetidic nicotinoyl hydrazone that suppresses STAT5 by targeting its SH2 domain (IC50 = 47 ?M against STAT5?? SH2 domain EPO peptide binding activity).
More Information Supplier PageSTAT5 Inhibitor is a cell-permeable, nonpetidic nicotinoyl hydrazone that suppresses STAT5 by targeting its SH2 domain (IC50 = 47 ?M against STAT5?? SH2 domain EPO peptide binding activity).
More Information Supplier PageSTAT5 Inhibitor is a cell-permeable, nonpetidic nicotinoyl hydrazone that suppresses STAT5 by targeting its SH2 domain (IC50 = 47 ?M against STAT5?? SH2 domain EPO peptide binding activity).
More Information Supplier PageStattic is a small molecule shown to selectively inhibit the activation of the Stat3 transcription factor by blocking phosphorylation and dimerization events.
More Information Supplier PageStattic is a small molecule shown to selectively inhibit the activation of the Stat3 transcription factor by blocking phosphorylation and dimerization events.
More Information Supplier PageStaurosporine is a natural product originally isolated in 1977 from the bacterium Streptomyces staurosporeus. The main biological activity of staurosporine is the inhibition of protein kinases through the prevention of ATP binding to the kinase. This is achieved through the stronger affinity of staurosporine to the ATP-binding site on the kinase.
More Information Supplier PageStaurosporine is a natural product originally isolated in 1977 from the bacterium Streptomyces staurosporeus. The main biological activity of staurosporine is the inhibition of protein kinases through the prevention of ATP binding to the kinase. This is achieved through the stronger affinity of staurosporine to the ATP-binding site on the kinase.
More Information Supplier PageStaurosporine is a natural product originally isolated in 1977 from the bacterium Streptomyces staurosporeus. The main biological activity of staurosporine is the inhibition of protein kinases through the prevention of ATP binding to the kinase. This is achieved through the stronger affinity of staurosporine to the ATP-binding site on the kinase.
More Information Supplier PageStaurosporine is a natural product originally isolated in 1977 from the bacterium Streptomyces staurosporeus. The main biological activity of staurosporine is the inhibition of protein kinases through the prevention of ATP binding to the kinase. This is achieved through the stronger affinity of staurosporine to the ATP-binding site on the kinase.
More Information Supplier PageStemRegenin 1 (SR1) is a cell-permeable purine derivative that acts as an antagonist of aryl hydrocarbon receptor and promotes the self-renewal of hematopoietic stem cells (HSCs).
More Information Supplier PageStemRegenin 1 (SR1) is a cell-permeable purine derivative that acts as an antagonist of aryl hydrocarbon receptor and promotes the self-renewal of hematopoietic stem cells (HSCs).
More Information Supplier PageStemRegenin 1 (SR1) is a cell-permeable purine derivative that acts as an antagonist of aryl hydrocarbon receptor and promotes the self-renewal of hematopoietic stem cells (HSCs).
More Information Supplier PageStemRegenin 1 (SR1) is a cell-permeable purine derivative that acts as an antagonist of aryl hydrocarbon receptor and promotes the self-renewal of hematopoietic stem cells (HSCs).
More Information Supplier PageStemRegenin 1 (SR1) is a cell-permeable purine derivative that acts as an antagonist of aryl hydrocarbon receptor and promotes the self-renewal of hematopoietic stem cells (HSCs).
More Information Supplier PageStevioside is a reagent that exhibits transepithelial p-aminohippurate transport.
More Information Supplier PageStevioside is a reagent that exhibits transepithelial p-aminohippurate transport.
More Information Supplier PageStevioside is a reagent that exhibits transepithelial p-aminohippurate transport.
More Information Supplier PageSTF 118804 is a highly specific NAMPT inhibitor that reduces the viability of most B-ALL cell lines with high potency IC50 values in the low nanomolar range and improves survival in an orthotopic xenotransplant model of high-risk acute lymphoblastic leukemia.
More Information Supplier PageSTF 118804 is a highly specific NAMPT inhibitor that reduces the viability of most B-ALL cell lines with high potency IC50 values in the low nanomolar range and improves survival in an orthotopic xenotransplant model of high-risk acute lymphoblastic leukemia.
More Information Supplier PageSTF 118804 is a highly specific NAMPT inhibitor that reduces the viability of most B-ALL cell lines with high potency IC50 values in the low nanomolar range and improves survival in an orthotopic xenotransplant model of high-risk acute lymphoblastic leukemia.
More Information Supplier PageSTF 118804 is a highly specific NAMPT inhibitor that reduces the viability of most B-ALL cell lines with high potency IC50 values in the low nanomolar range and improves survival in an orthotopic xenotransplant model of high-risk acute lymphoblastic leukemia.
More Information Supplier PageSTF-31 is an inhibitor of glucose transporter 1 (GLUT1, IC50 = 1 muM),
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