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 WebsiteMyricitrin is the 3-O-rhamnoside of myricetin. Myricitrin is used by several beetle species in their communication system.
More Information Supplier PageMyricitrin is the 3-O-rhamnoside of myricetin. Myricitrin is used by several beetle species in their communication system.
More Information Supplier PageMyricitrin is the 3-O-rhamnoside of myricetin. Myricitrin is used by several beetle species in their communication system.
More Information Supplier PageMyricitrin is the 3-O-rhamnoside of myricetin. Myricitrin is used by several beetle species in their communication system.
More Information Supplier PageMyricitrin is the 3-O-rhamnoside of myricetin. Myricitrin is used by several beetle species in their communication system.
More Information Supplier PageMyrislignan existing in nutmeg has been reported to possess inhibition of neoplasm and vascular smooth muscle contraction, and cause a prolonging of hexobarbital-induced hypnosis in mice.
More Information Supplier PageMyrislignan existing in nutmeg has been reported to possess inhibition of neoplasm and vascular smooth muscle contraction, and cause a prolonging of hexobarbital-induced hypnosis in mice.
More Information Supplier PageMyrislignan existing in nutmeg has been reported to possess inhibition of neoplasm and vascular smooth muscle contraction, and cause a prolonging of hexobarbital-induced hypnosis in mice.
More Information Supplier PageN-(p-Coumaroyl) Serotonin is an antibacterial agent which inhibits the production of proinflammatory cytokines by LPS-stimulated human blood monocytes.
More Information Supplier PageN-(p-Coumaroyl) Serotonin is an antibacterial agent which inhibits the production of proinflammatory cytokines by LPS-stimulated human blood monocytes.
More Information Supplier PageN-(p-Coumaroyl) Serotonin is an antibacterial agent which inhibits the production of proinflammatory cytokines by LPS-stimulated human blood monocytes.
More Information Supplier PageN-desethyl sunitinib is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFR?? and KIT inhibitor (Ki values are 2, 9, 17, 8 and 4 nM for VEGFR -1, -2, -3, PDGFR?? and KIT respectively).
More Information Supplier PageN-desethyl sunitinib is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFR?? and KIT inhibitor (Ki values are 2, 9, 17, 8 and 4 nM for VEGFR -1, -2, -3, PDGFR?? and KIT respectively).
More Information Supplier PageN-desethyl sunitinib is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFR?? and KIT inhibitor (Ki values are 2, 9, 17, 8 and 4 nM for VEGFR -1, -2, -3, PDGFR?? and KIT respectively).
More Information Supplier PageN-desMethyl EnzalutaMide is used in the treatment of disorders involving androgen, estrogen and progesterone receptors.
More Information Supplier PageN-desMethyl EnzalutaMide is used in the treatment of disorders involving androgen, estrogen and progesterone receptors.
More Information Supplier PageN-desMethyl EnzalutaMide is used in the treatment of disorders involving androgen, estrogen and progesterone receptors.
More Information Supplier PageN-Desmethylclozapine is a potent and selective 5-HT2C serotonin receptor antagonist
More Information Supplier PageN-Desmethylclozapine is a potent and selective 5-HT2C serotonin receptor antagonist
More Information Supplier PageN-Desmethylclozapine is a potent and selective 5-HT2C serotonin receptor antagonist
More Information Supplier PageN-Methyl Metribuzin is an aminotriazinone and the methylamine analogue of the herbicide Metribuzin.
More Information Supplier PageN-Methyl Metribuzin is an aminotriazinone and the methylamine analogue of the herbicide Metribuzin.
More Information Supplier PageN-Methyl Metribuzin is an aminotriazinone and the methylamine analogue of the herbicide Metribuzin.
More Information Supplier PageN-methylcytisine, a selective ligand of nicotinic receptors of acetylcholine in the CNS.
More Information Supplier PageN-methylcytisine, a selective ligand of nicotinic receptors of acetylcholine in the CNS.
More Information Supplier PageN3PT is a potent and selective transketolase(TK) inhibitor (IC50= 22 nM for Apo-TK) both in vitro and in vivo.
More Information Supplier PageN3PT is a potent and selective transketolase(TK) inhibitor (IC50= 22 nM for Apo-TK) both in vitro and in vivo.
More Information Supplier PageN3PT is a potent and selective transketolase(TK) inhibitor (IC50= 22 nM for Apo-TK) both in vitro and in vivo.
More Information Supplier PageN6022 is a potent, specific, and fully reversible inhibitor of S-nitrosoglutathione reductase (GSNOR) with an IC50 of 8 nM and a Ki of 2.5 nM.
More Information Supplier PageN6022 is a potent, specific, and fully reversible inhibitor of S-nitrosoglutathione reductase (GSNOR) with an IC50 of 8 nM and a Ki of 2.5 nM.
More Information Supplier PageN6022 is a potent, specific, and fully reversible inhibitor of S-nitrosoglutathione reductase (GSNOR) with an IC50 of 8 nM and a Ki of 2.5 nM.
More Information Supplier PageN6022 is a potent, specific, and fully reversible inhibitor of S-nitrosoglutathione reductase (GSNOR) with an IC50 of 8 nM and a Ki of 2.5 nM.
More Information Supplier PageNAD 299 hydrochloride (Robalzotan) is a selective, high affinity 5-HT1A receptor antagonist (Ki = 0.6 nM in vitro).
More Information Supplier PageNAD 299 hydrochloride (Robalzotan) is a selective, high affinity 5-HT1A receptor antagonist (Ki = 0.6 nM in vitro).
More Information Supplier PageNAD 299 hydrochloride (Robalzotan) is a selective, high affinity 5-HT1A receptor antagonist (Ki = 0.6 nM in vitro).
More Information Supplier PageNAD 299 hydrochloride (Robalzotan) is a selective, high affinity 5-HT1A receptor antagonist (Ki = 0.6 nM in vitro).
More Information Supplier PageNadifloxacin is a cell-permeable, synthetic, broad-spectrum fluoroquinolone antibiotic that inhibits the growth of both gram-positive and gram-negative microbes.
More Information Supplier PageNadifloxacin is a cell-permeable, synthetic, broad-spectrum fluoroquinolone antibiotic that inhibits the growth of both gram-positive and gram-negative microbes.
More Information Supplier PageNadifloxacin is a cell-permeable, synthetic, broad-spectrum fluoroquinolone antibiotic that inhibits the growth of both gram-positive and gram-negative microbes.
More Information Supplier PageNadifloxacin is a cell-permeable, synthetic, broad-spectrum fluoroquinolone antibiotic that inhibits the growth of both gram-positive and gram-negative microbes.
More Information Supplier PageNafamostat is an anticoagulant. Broad spectrum serine protease inhibitor. Reduces eosinophil infiltration, mast cell activation and airway responsiveness in a murine model of asthma.
More Information Supplier PageNafamostat is an anticoagulant. Broad spectrum serine protease inhibitor. Reduces eosinophil infiltration, mast cell activation and airway responsiveness in a murine model of asthma.
More Information Supplier PageNafamostat is an anticoagulant. Broad spectrum serine protease inhibitor. Reduces eosinophil infiltration, mast cell activation and airway responsiveness in a murine model of asthma.
More Information Supplier PageNafamostat is an anticoagulant. Broad spectrum serine protease inhibitor. Reduces eosinophil infiltration, mast cell activation and airway responsiveness in a murine model of asthma.
More Information Supplier PageNafamostat is an anticoagulant. Broad spectrum serine protease inhibitor. Reduces eosinophil infiltration, mast cell activation and airway responsiveness in a murine model of asthma.
More Information Supplier PageNaftopidil (Flivas) is a selective ??1-adrenergic receptor antagonist or alpha blocker with a Ki of 58.3 nM.
More Information Supplier PageNaftopidil (Flivas) is a selective ??1-adrenergic receptor antagonist or alpha blocker with a Ki of 58.3 nM.
More Information Supplier PageNaftopidil (Flivas) is a selective ??1-adrenergic receptor antagonist or alpha blocker with a Ki of 58.3 nM.
More Information Supplier PageNaftopidil (Flivas) is a selective ??1-adrenergic receptor antagonist or alpha blocker with a Ki of 58.3 nM.
More Information Supplier Page
