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 WebsiteFP-Biotin is a biotinylated organophosphorus agent. It could be useful for identifying proteins that react with organophosphorus toxicants (OP).
More Information Supplier PageFP-Biotin is a biotinylated organophosphorus agent. It could be useful for identifying proteins that react with organophosphorus toxicants (OP).
More Information Supplier PageFPH1 is a small molecule, which promotes expansion of iPS-derived hepatocytes.
More Information Supplier PageFPH1 is a small molecule, which promotes expansion of iPS-derived hepatocytes.
More Information Supplier PageFPH1 is a small molecule, which promotes expansion of iPS-derived hepatocytes.
More Information Supplier PageFPH1 is a small molecule, which promotes expansion of iPS-derived hepatocytes.
More Information Supplier PageFPH2 (BRD-9424) is a small molecule, which promotes differentiation of iPS-derived hepatocytes.
More Information Supplier PageFPH2 (BRD-9424) is a small molecule, which promotes differentiation of iPS-derived hepatocytes.
More Information Supplier PageFPH2 (BRD-9424) is a small molecule, which promotes differentiation of iPS-derived hepatocytes.
More Information Supplier PageFPH2 (BRD-9424) is a small molecule, which promotes differentiation of iPS-derived hepatocytes.
More Information Supplier PageFPS-ZM1 inhibits A??40- and A??42-induced cellular stress in RAGE-expressing cells.
More Information Supplier PageFPS-ZM1 inhibits A??40- and A??42-induced cellular stress in RAGE-expressing cells.
More Information Supplier PageFPS-ZM1 inhibits A??40- and A??42-induced cellular stress in RAGE-expressing cells.
More Information Supplier PageFR 180204 is a novel and selective inhibitor of extracellular signal-regulated kinase (ERK), which may be a potential new therapy for rheumatoid arthritis.
More Information Supplier PageFR 180204 is a novel and selective inhibitor of extracellular signal-regulated kinase (ERK), which may be a potential new therapy for rheumatoid arthritis.
More Information Supplier PageFR 180204 is a novel and selective inhibitor of extracellular signal-regulated kinase (ERK), which may be a potential new therapy for rheumatoid arthritis.
More Information Supplier PageFR 180204 is a novel and selective inhibitor of extracellular signal-regulated kinase (ERK), which may be a potential new therapy for rheumatoid arthritis.
More Information Supplier PageFR901464 is a potent anticancer natural product that lowers the mRNA levels of oncogenes and tumor suppressor genes.
More Information Supplier PageFR901464 is a potent anticancer natural product that lowers the mRNA levels of oncogenes and tumor suppressor genes.
More Information Supplier PageFR901464 is a potent anticancer natural product that lowers the mRNA levels of oncogenes and tumor suppressor genes.
More Information Supplier PageFR901464 is a potent anticancer natural product that lowers the mRNA levels of oncogenes and tumor suppressor genes.
More Information Supplier PageFraxetin is an O-methylated coumarin. It can be found in Fraxinus rhynchophylla.
More Information Supplier PageFraxetin is an O-methylated coumarin. It can be found in Fraxinus rhynchophylla.
More Information Supplier PageFraxetin is an O-methylated coumarin. It can be found in Fraxinus rhynchophylla.
More Information Supplier PageFraxinellone is an insecticidal agent, inhibiting growth of larvae, used in the treatment and protection of crops and produce. Also, a naturally occurring compound used in the treatment of tumors.
More Information Supplier PageFraxinellone is an insecticidal agent, inhibiting growth of larvae, used in the treatment and protection of crops and produce. Also, a naturally occurring compound used in the treatment of tumors.
More Information Supplier PageFraxinellone is an insecticidal agent, inhibiting growth of larvae, used in the treatment and protection of crops and produce. Also, a naturally occurring compound used in the treatment of tumors.
More Information Supplier PageFructose is a simple ketonic monosaccharide found in many plants, where it is often bonded to glucose to form the disaccharide sucrose.
More Information Supplier PageFructose is a simple ketonic monosaccharide found in many plants, where it is often bonded to glucose to form the disaccharide sucrose.
More Information Supplier PageFructose is a simple ketonic monosaccharide found in many plants, where it is often bonded to glucose to form the disaccharide sucrose.
More Information Supplier PageFruquintinib is an orally available, small molecule inhibitor of vascular endothelial growth factor receptors (VEGFRs), with potential anti-angiogenic and antineoplastic activities.
More Information Supplier PageFruquintinib is an orally available, small molecule inhibitor of vascular endothelial growth factor receptors (VEGFRs), with potential anti-angiogenic and antineoplastic activities.
More Information Supplier PageFruquintinib is an orally available, small molecule inhibitor of vascular endothelial growth factor receptors (VEGFRs), with potential anti-angiogenic and antineoplastic activities.
More Information Supplier PageFTI 276 is an inhibitor that inhibits farnesyltransferase (FTase) (IC50 = 0.5 nM). Inhibits H-Ras and K-Ras processing in whole cells (IC50 values are 0.1 and 10 ??M respectively) and disrupts constitutive H-Ras-specific actvation of MAPK. Causes significant antiproliferative effects in human malignant glioma cells and many other tumor cell lines.
More Information Supplier PageFTI 276 is an inhibitor that inhibits farnesyltransferase (FTase) (IC50 = 0.5 nM). Inhibits H-Ras and K-Ras processing in whole cells (IC50 values are 0.1 and 10 ??M respectively) and disrupts constitutive H-Ras-specific actvation of MAPK. Causes significant antiproliferative effects in human malignant glioma cells and many other tumor cell lines.
More Information Supplier PageFTI 276 is an inhibitor that inhibits farnesyltransferase (FTase) (IC50 = 0.5 nM). Inhibits H-Ras and K-Ras processing in whole cells (IC50 values are 0.1 and 10 ??M respectively) and disrupts constitutive H-Ras-specific actvation of MAPK. Causes significant antiproliferative effects in human malignant glioma cells and many other tumor cell lines.
More Information Supplier PageFTI 276 is an inhibitor that inhibits farnesyltransferase (FTase) (IC50 = 0.5 nM). Inhibits H-Ras and K-Ras processing in whole cells (IC50 values are 0.1 and 10 ??M respectively) and disrupts constitutive H-Ras-specific actvation of MAPK. Causes significant antiproliferative effects in human malignant glioma cells and many other tumor cell lines.
More Information Supplier PageFTI-277 HCl is an inhibitor of farnesyl transferase (FTase); a highly potent Ras CAAX peptidomimetic which antagonizes both H- and K-Ras oncogenic signaling.
More Information Supplier PageFTI-277 HCl is an inhibitor of farnesyl transferase (FTase); a highly potent Ras CAAX peptidomimetic which antagonizes both H- and K-Ras oncogenic signaling.
More Information Supplier PageFTI-277 HCl is an inhibitor of farnesyl transferase (FTase); a highly potent Ras CAAX peptidomimetic which antagonizes both H- and K-Ras oncogenic signaling.
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