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 WebsiteZ-360 is a selective, orally available, 1,5-benzodiazepine-derivative gastrin/cholecystokinin 2 (CCK-2) receptor antagonist with potential antineoplastic activity.
More Information Supplier PageZ-LEHD-FMK is a synthetic peptide that irreversibly inhibits caspase-9 and related caspase activity.
More Information Supplier PageZ-LEHD-FMK is a synthetic peptide that irreversibly inhibits caspase-9 and related caspase activity.
More Information Supplier PageZ-LEHD-FMK is a synthetic peptide that irreversibly inhibits caspase-9 and related caspase activity.
More Information Supplier PageZ-VAD-FMK is a cell-permeable, irreversible pan-caspase inhibitor. Inhibits caspase processing and apoptosis induction in tumor cells in vitro (IC50 = 0.0015 – 5.8 mM). Active in vivo.
More Information Supplier PageZ-VAD-FMK is a cell-permeable, irreversible pan-caspase inhibitor. Inhibits caspase processing and apoptosis induction in tumor cells in vitro (IC50 = 0.0015 – 5.8 mM). Active in vivo.
More Information Supplier PageZ-VAD-FMK is a cell-permeable, irreversible pan-caspase inhibitor. Inhibits caspase processing and apoptosis induction in tumor cells in vitro (IC50 = 0.0015 – 5.8 mM). Active in vivo.
More Information Supplier PageZ-VAD-FMK is a cell-permeable, irreversible pan-caspase inhibitor. Inhibits caspase processing and apoptosis induction in tumor cells in vitro (IC50 = 0.0015 – 5.8 mM). Active in vivo.
More Information Supplier PageZ-VAD-FMK is a cell-permeable, irreversible pan-caspase inhibitor. Inhibits caspase processing and apoptosis induction in tumor cells in vitro (IC50 = 0.0015 – 5.8 mM). Active in vivo.
More Information Supplier PageZ-WEHD-FMK is a synthetic peptide that irreversibly inhibits caspase-5 and related caspase activity.
More Information Supplier PageZ-WEHD-FMK is a synthetic peptide that irreversibly inhibits caspase-5 and related caspase activity.
More Information Supplier PageZ-WEHD-FMK is a synthetic peptide that irreversibly inhibits caspase-5 and related caspase activity.
More Information Supplier PageZaleplon is a non-benzodiazepine agent that acts as an agonist at the benzodiazepine site.
More Information Supplier PageZaleplon is a non-benzodiazepine agent that acts as an agonist at the benzodiazepine site.
More Information Supplier PageZaleplon is a non-benzodiazepine agent that acts as an agonist at the benzodiazepine site.
More Information Supplier PageZaleplon is a non-benzodiazepine agent that acts as an agonist at the benzodiazepine site.
More Information Supplier PageZaltidine is a H2-receptor antagonist, which has the antisecretory action.
More Information Supplier PageZaltidine is a H2-receptor antagonist, which has the antisecretory action.
More Information Supplier PageZaltidine is a H2-receptor antagonist, which has the antisecretory action.
More Information Supplier PageZanamivir is a neuraminidase inhibitor used in the treatment and prophylaxis of influenza caused by influenza A virus and influenza B virus.
More Information Supplier PageZanamivir is a neuraminidase inhibitor used in the treatment and prophylaxis of influenza caused by influenza A virus and influenza B virus.
More Information Supplier PageZanamivir is a neuraminidase inhibitor used in the treatment and prophylaxis of influenza caused by influenza A virus and influenza B virus.
More Information Supplier PageZanamivir is a neuraminidase inhibitor used in the treatment and prophylaxis of influenza caused by influenza A virus and influenza B virus.
More Information Supplier PageZardaverine is a phosphodiesterase inhibitor, selective for PDE3 and 4 (IC50 values are 0.5 and 0.8 ??M respectively).
More Information Supplier PageZardaverine is a phosphodiesterase inhibitor, selective for PDE3 and 4 (IC50 values are 0.5 and 0.8 ??M respectively).
More Information Supplier PageZardaverine is a phosphodiesterase inhibitor, selective for PDE3 and 4 (IC50 values are 0.5 and 0.8 ??M respectively).
More Information Supplier PageZardaverine is a phosphodiesterase inhibitor, selective for PDE3 and 4 (IC50 values are 0.5 and 0.8 ??M respectively).
More Information Supplier PageCDP323 is a small-molecule prodrug antagonist of the vascular cell adhesion molecule 1 binding to ??4-integrins
More Information Supplier PageCDP323 is a small-molecule prodrug antagonist of the vascular cell adhesion molecule 1 binding to ??4-integrins
More Information Supplier PageCDP323 is a small-molecule prodrug antagonist of the vascular cell adhesion molecule 1 binding to ??4-integrins
More Information Supplier PageCDP323 is a small-molecule prodrug antagonist of the vascular cell adhesion molecule 1 binding to ??4-integrins
More Information Supplier PageZCL-278 is a selective inhibitor of Cdc42. Targets the binding site of the Cdc42 guanine nucleotide exchange factor, intersectin (ITSN). Inhibits Cdc42-mediated cellular effects, including microspike formation in 3T3 fibroblasts and neuronal branching in primary neonatal cortical neurons. Also suppresses cell motility and migration in PC3 cells, without cytotoxic effects.
More Information Supplier PageZCL-278 is a selective inhibitor of Cdc42. Targets the binding site of the Cdc42 guanine nucleotide exchange factor, intersectin (ITSN). Inhibits Cdc42-mediated cellular effects, including microspike formation in 3T3 fibroblasts and neuronal branching in primary neonatal cortical neurons. Also suppresses cell motility and migration in PC3 cells, without cytotoxic effects.
More Information Supplier PageZCL-278 is a selective inhibitor of Cdc42. Targets the binding site of the Cdc42 guanine nucleotide exchange factor, intersectin (ITSN). Inhibits Cdc42-mediated cellular effects, including microspike formation in 3T3 fibroblasts and neuronal branching in primary neonatal cortical neurons. Also suppresses cell motility and migration in PC3 cells, without cytotoxic effects.
More Information Supplier PageZCL-278 is a selective inhibitor of Cdc42. Targets the binding site of the Cdc42 guanine nucleotide exchange factor, intersectin (ITSN). Inhibits Cdc42-mediated cellular effects, including microspike formation in 3T3 fibroblasts and neuronal branching in primary neonatal cortical neurons. Also suppresses cell motility and migration in PC3 cells, without cytotoxic effects.
More Information Supplier PageZCL-278 is a selective inhibitor of Cdc42. Targets the binding site of the Cdc42 guanine nucleotide exchange factor, intersectin (ITSN). Inhibits Cdc42-mediated cellular effects, including microspike formation in 3T3 fibroblasts and neuronal branching in primary neonatal cortical neurons. Also suppresses cell motility and migration in PC3 cells, without cytotoxic effects.
More Information Supplier PageZearalenone is a phytoestrogenic mycotoxin usually produced by Fusarium species, is shown to be a cytotoxic compound, but alos binds to the estrogen receptor (ER) (IC50 values are 166 and 240 nM for ER?? and ER?? respectively) and was found to stimulate the transcriptional activity of both subtypes at concentrations between 1 – 10 nM.
More Information Supplier PageZearalenone is a phytoestrogenic mycotoxin usually produced by Fusarium species, is shown to be a cytotoxic compound, but alos binds to the estrogen receptor (ER) (IC50 values are 166 and 240 nM for ER?? and ER?? respectively) and was found to stimulate the transcriptional activity of both subtypes at concentrations between 1 – 10 nM.
More Information Supplier PageZearalenone is a phytoestrogenic mycotoxin usually produced by Fusarium species, is shown to be a cytotoxic compound, but alos binds to the estrogen receptor (ER) (IC50 values are 166 and 240 nM for ER?? and ER?? respectively) and was found to stimulate the transcriptional activity of both subtypes at concentrations between 1 – 10 nM.
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