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 WebsiteRo 61-8048 is a potent and competitive kynurenine 3-hydroxylase inhibitor (Ki = 4.8 nM, IC50 = 37 nM).
More Information Supplier PageRo 61-8048 is a potent and competitive kynurenine 3-hydroxylase inhibitor (Ki = 4.8 nM, IC50 = 37 nM).
More Information Supplier PageRo 61-8048 is a potent and competitive kynurenine 3-hydroxylase inhibitor (Ki = 4.8 nM, IC50 = 37 nM).
More Information Supplier PageRo 61-8048 is a potent and competitive kynurenine 3-hydroxylase inhibitor (Ki = 4.8 nM, IC50 = 37 nM).
More Information Supplier PageRo 90-7501 is an inhibitor of amyloid ??42 (A??42) fibril assembly; reduces A??42-induced toxicity (EC50 = 2 ??M).
More Information Supplier PageRo 90-7501 is an inhibitor of amyloid ??42 (A??42) fibril assembly; reduces A??42-induced toxicity (EC50 = 2 ??M).
More Information Supplier PageRo 90-7501 is an inhibitor of amyloid ??42 (A??42) fibril assembly; reduces A??42-induced toxicity (EC50 = 2 ??M).
More Information Supplier PageRo 90-7501 is an inhibitor of amyloid ??42 (A??42) fibril assembly; reduces A??42-induced toxicity (EC50 = 2 ??M).
More Information Supplier PageRO-9187 is a potent inhibitor of HCV virus replication in the replicon system (IC(50) = 171 +/- 12 nM; CC(50) >1 mM).
More Information Supplier PageRO-9187 is a potent inhibitor of HCV virus replication in the replicon system (IC(50) = 171 +/- 12 nM; CC(50) >1 mM).
More Information Supplier PageRO-9187 is a potent inhibitor of HCV virus replication in the replicon system (IC(50) = 171 +/- 12 nM; CC(50) >1 mM).
More Information Supplier PageRO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with IC50 of 3 nM.
More Information Supplier PageRO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with IC50 of 3 nM.
More Information Supplier PageRO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with IC50 of 3 nM.
More Information Supplier PageRO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with IC50 of 3 nM.
More Information Supplier PageRO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with IC50 of 3 nM.
More Information Supplier PageRO4927350 a potent and highly selective non-ATP-competitive MEK1/2 inhibitor.
More Information Supplier PageRO4927350 a potent and highly selective non-ATP-competitive MEK1/2 inhibitor.
More Information Supplier PageRO4927350 a potent and highly selective non-ATP-competitive MEK1/2 inhibitor.
More Information Supplier PageRO4927350 a potent and highly selective non-ATP-competitive MEK1/2 inhibitor.
More Information Supplier PageRO4929097 is an orally bioavailable, small-molecule gamma secretase (GS) inhibitor with an IC50 of 4 nM.
More Information Supplier PageRO4929097 is an orally bioavailable, small-molecule gamma secretase (GS) inhibitor with an IC50 of 4 nM.
More Information Supplier PageRO4929097 is an orally bioavailable, small-molecule gamma secretase (GS) inhibitor with an IC50 of 4 nM.
More Information Supplier PageRO4929097 is an orally bioavailable, small-molecule gamma secretase (GS) inhibitor with an IC50 of 4 nM.
More Information Supplier PageRO4929097 is an orally bioavailable, small-molecule gamma secretase (GS) inhibitor with an IC50 of 4 nM.
More Information Supplier PageRO4987655 is an orally active small molecule, targeting mitogen-activated protein kinase kinase 1 (MAP2K1 or MEK1), with potential antineoplastic activity.
More Information Supplier PageRO4987655 is an orally active small molecule, targeting mitogen-activated protein kinase kinase 1 (MAP2K1 or MEK1), with potential antineoplastic activity.
More Information Supplier PageRO4987655 is an orally active small molecule, targeting mitogen-activated protein kinase kinase 1 (MAP2K1 or MEK1), with potential antineoplastic activity.
More Information Supplier PageRO5126766, also known as CH5126766, is a protein kinase inhibitor specific for the Raf and MEK mitogen-activated protein kinases (MAPKs) with potential anti-neoplastic activity.
More Information Supplier PageRO5126766, also known as CH5126766, is a protein kinase inhibitor specific for the Raf and MEK mitogen-activated protein kinases (MAPKs) with potential anti-neoplastic activity.
More Information Supplier PageRO5126766, also known as CH5126766, is a protein kinase inhibitor specific for the Raf and MEK mitogen-activated protein kinases (MAPKs) with potential anti-neoplastic activity.
More Information Supplier PageROCK inhibitor is a highly potent inhibitor of human ROCK-1 and ROCK-2 isoenzymes with IC50 values of 0.6 and 1.1 nM, respectively.
More Information Supplier PageROCK inhibitor is a highly potent inhibitor of human ROCK-1 and ROCK-2 isoenzymes with IC50 values of 0.6 and 1.1 nM, respectively.
More Information Supplier PageROCK inhibitor is a highly potent inhibitor of human ROCK-1 and ROCK-2 isoenzymes with IC50 values of 0.6 and 1.1 nM, respectively.
More Information Supplier PageRocuronium bromide is an aminosteroid non-depolarizing neuromuscular blocker and also is used as a muscle relaxant used in modern anesthesia to facilitate endotracheal intubation.
More Information Supplier PageRocuronium bromide is an aminosteroid non-depolarizing neuromuscular blocker and also is used as a muscle relaxant used in modern anesthesia to facilitate endotracheal intubation.
More Information Supplier PageRocuronium bromide is an aminosteroid non-depolarizing neuromuscular blocker and also is used as a muscle relaxant used in modern anesthesia to facilitate endotracheal intubation.
More Information Supplier PageRocuronium bromide is an aminosteroid non-depolarizing neuromuscular blocker and also is used as a muscle relaxant used in modern anesthesia to facilitate endotracheal intubation.
More Information Supplier PageRocuronium bromide is an aminosteroid non-depolarizing neuromuscular blocker and also is used as a muscle relaxant used in modern anesthesia to facilitate endotracheal intubation.
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