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 WebsitePranoprofen is a non-steroidal anti-inflammatory drug used in ophthalmology
More Information Supplier PagePranoprofen is a non-steroidal anti-inflammatory drug used in ophthalmology
More Information Supplier PagePranoprofen is a non-steroidal anti-inflammatory drug used in ophthalmology
More Information Supplier PagePrasugrel is a novel platelet inhibitor used for the reduction of thrombotic cardiovascular events (including stent thrombosis) in patients with acute coronary syndrome who are to be managed with PCI.
More Information Supplier PagePrasugrel is a novel platelet inhibitor used for the reduction of thrombotic cardiovascular events (including stent thrombosis) in patients with acute coronary syndrome who are to be managed with PCI.
More Information Supplier PagePrasugrel is a novel platelet inhibitor used for the reduction of thrombotic cardiovascular events (including stent thrombosis) in patients with acute coronary syndrome who are to be managed with PCI.
More Information Supplier PagePrasugrel is a novel platelet inhibitor used for the reduction of thrombotic cardiovascular events (including stent thrombosis) in patients with acute coronary syndrome who are to be managed with PCI.
More Information Supplier PagePrasugrel is a novel platelet inhibitor used for the reduction of thrombotic cardiovascular events (including stent thrombosis) in patients with acute coronary syndrome who are to be managed with PCI.
More Information Supplier PagePravadoline (WIN 48,098) is antiinflammatory and prostaglandin synthesis inhibitor, acting through inhibition of the enzyme cyclooxygenase (COX).
More Information Supplier PagePravadoline (WIN 48,098) is antiinflammatory and prostaglandin synthesis inhibitor, acting through inhibition of the enzyme cyclooxygenase (COX).
More Information Supplier PagePravadoline (WIN 48,098) is antiinflammatory and prostaglandin synthesis inhibitor, acting through inhibition of the enzyme cyclooxygenase (COX).
More Information Supplier PagePravadoline (WIN 48,098) is antiinflammatory and prostaglandin synthesis inhibitor, acting through inhibition of the enzyme cyclooxygenase (COX).
More Information Supplier PagePravastatin sodium is a water-soluble, competitive inhibitor of 3-hydroxy-3-methyl coenzyme A (HMG-CoA) reductase. Potently blocks cholesterol synthesis in vivo (Ki~ 1 nM) and displays cardioprotective properties.
More Information Supplier PagePravastatin sodium is a water-soluble, competitive inhibitor of 3-hydroxy-3-methyl coenzyme A (HMG-CoA) reductase. Potently blocks cholesterol synthesis in vivo (Ki~ 1 nM) and displays cardioprotective properties.
More Information Supplier PagePravastatin sodium is a water-soluble, competitive inhibitor of 3-hydroxy-3-methyl coenzyme A (HMG-CoA) reductase. Potently blocks cholesterol synthesis in vivo (Ki~ 1 nM) and displays cardioprotective properties.
More Information Supplier PagePravastatin sodium is a water-soluble, competitive inhibitor of 3-hydroxy-3-methyl coenzyme A (HMG-CoA) reductase. Potently blocks cholesterol synthesis in vivo (Ki~ 1 nM) and displays cardioprotective properties.
More Information Supplier PagePravastatin sodium is a water-soluble, competitive inhibitor of 3-hydroxy-3-methyl coenzyme A (HMG-CoA) reductase. Potently blocks cholesterol synthesis in vivo (Ki~ 1 nM) and displays cardioprotective properties.
More Information Supplier PagePraziquantel is a highly effective anthelmintic against all Schistosoma species.
More Information Supplier PagePraziquantel is a highly effective anthelmintic against all Schistosoma species.
More Information Supplier PagePraziquantel is a highly effective anthelmintic against all Schistosoma species.
More Information Supplier PagePraziquantel is a highly effective anthelmintic against all Schistosoma species.
More Information Supplier PagePraziquantel is a highly effective anthelmintic against all Schistosoma species.
More Information Supplier PagePrazosin HCl is an ??1 and ??2B-adrenoceptor antagonist. Also a potent antagonist at the melatonin MT3 receptor (Ki = 10.2 nM).
More Information Supplier PagePrazosin HCl is an ??1 and ??2B-adrenoceptor antagonist. Also a potent antagonist at the melatonin MT3 receptor (Ki = 10.2 nM).
More Information Supplier PagePrazosin HCl is an ??1 and ??2B-adrenoceptor antagonist. Also a potent antagonist at the melatonin MT3 receptor (Ki = 10.2 nM).
More Information Supplier PagePrazosin HCl is an ??1 and ??2B-adrenoceptor antagonist. Also a potent antagonist at the melatonin MT3 receptor (Ki = 10.2 nM).
More Information Supplier PagePrednisolone is a synthetic glucocorticoid, a derivative of cortisol, which is used to treat a variety of inflammatory and auto-immune conditions.
More Information Supplier PagePrednisolone is a synthetic glucocorticoid, a derivative of cortisol, which is used to treat a variety of inflammatory and auto-immune conditions.
More Information Supplier PagePrednisone reduces mucosal TNF-a production, intestinal permeability and levels of NF-kB expression.
More Information Supplier PagePrednisone reduces mucosal TNF-a production, intestinal permeability and levels of NF-kB expression.
More Information Supplier PagePrednisone reduces mucosal TNF-a production, intestinal permeability and levels of NF-kB expression.
More Information Supplier PagePrednisone reduces mucosal TNF-a production, intestinal permeability and levels of NF-kB expression.
More Information Supplier PagePrednisone reduces mucosal TNF-a production, intestinal permeability and levels of NF-kB expression.
More Information Supplier PagePregnenolone is an endogenous steroid hormone for inhibition of M1 receptor- and M3 receptor-mediated currents with IC5N/A of 11.4 ?M and 6.N/A ?M, respectively.
More Information Supplier PagePregnenolone is an endogenous steroid hormone for inhibition of M1 receptor- and M3 receptor-mediated currents with IC5N/A of 11.4 ?M and 6.N/A ?M, respectively.
More Information Supplier PagePregnenolone is an endogenous steroid hormone for inhibition of M1 receptor- and M3 receptor-mediated currents with IC5N/A of 11.4 ?M and 6.N/A ?M, respectively.
More Information Supplier PagePregnenolone is an endogenous steroid hormone for inhibition of M1 receptor- and M3 receptor-mediated currents with IC5N/A of 11.4 ?M and 6.N/A ?M, respectively.
More Information Supplier PagePregnenolone is an endogenous steroid hormone for inhibition of M1 receptor- and M3 receptor-mediated currents with IC5N/A of 11.4 ?M and 6.N/A ?M, respectively.
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