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 WebsiteTyrphostin AG 879 is an inhibitor of the tyrosine kinase activity of nerve growth factor (NGF) TrkA.
More Information Supplier PageTyrphostin AG 879 is an inhibitor of the tyrosine kinase activity of nerve growth factor (NGF) TrkA.
More Information Supplier PageTyrphostin AG 879 is an inhibitor of the tyrosine kinase activity of nerve growth factor (NGF) TrkA.
More Information Supplier PageTyrphostin AG 879 is an inhibitor of the tyrosine kinase activity of nerve growth factor (NGF) TrkA.
More Information Supplier PageU 73122 is a phospholipase C inhibitor. It inhibits agonist-induced platelet aggregation with IC50 values of 1-5 ??M.
More Information Supplier PageU 73122 is a phospholipase C inhibitor. It inhibits agonist-induced platelet aggregation with IC50 values of 1-5 ??M.
More Information Supplier PageU 73122 is a phospholipase C inhibitor. It inhibits agonist-induced platelet aggregation with IC50 values of 1-5 ??M.
More Information Supplier PageU-95666E is a D2 selective dopamine agonist with an ED50 of about 46 nM, was investigated for its effect on rat striatal acetylcholine (ACh) concentration
More Information Supplier PageU-95666E is a D2 selective dopamine agonist with an ED50 of about 46 nM, was investigated for its effect on rat striatal acetylcholine (ACh) concentration
More Information Supplier PageU-95666E is a D2 selective dopamine agonist with an ED50 of about 46 nM, was investigated for its effect on rat striatal acetylcholine (ACh) concentration
More Information Supplier PageU-95666E is a D2 selective dopamine agonist with an ED50 of about 46 nM, was investigated for its effect on rat striatal acetylcholine (ACh) concentration
More Information Supplier PageU-104 is a novel ureido-sulfonamide inhibitor of Carbonic Anhydrase IX (CAIX).
More Information Supplier PageU-104 is a novel ureido-sulfonamide inhibitor of Carbonic Anhydrase IX (CAIX).
More Information Supplier PageU-104 is a novel ureido-sulfonamide inhibitor of Carbonic Anhydrase IX (CAIX).
More Information Supplier PageU0126-EtOH is an inhibitor of both MEK1 and MEK2 with an IC50 of 72 nM and 58 nM respectively.
More Information Supplier PageU0126-EtOH is an inhibitor of both MEK1 and MEK2 with an IC50 of 72 nM and 58 nM respectively.
More Information Supplier PageU0126-EtOH is an inhibitor of both MEK1 and MEK2 with an IC50 of 72 nM and 58 nM respectively.
More Information Supplier PageU0126-EtOH is an inhibitor of both MEK1 and MEK2 with an IC50 of 72 nM and 58 nM respectively.
More Information Supplier PageU0126-EtOH is an inhibitor of both MEK1 and MEK2 with an IC50 of 72 nM and 58 nM respectively.
More Information Supplier PageUCPH 101 is a selective non-substrate inhibitor of EAAT1 (IC50 values are 660, >300000 and >300000 nM for EAAT1, EAAT2 and EAAT3 respectively).
More Information Supplier PageUCPH 101 is a selective non-substrate inhibitor of EAAT1 (IC50 values are 660, >300000 and >300000 nM for EAAT1, EAAT2 and EAAT3 respectively).
More Information Supplier PageUCPH 101 is a selective non-substrate inhibitor of EAAT1 (IC50 values are 660, >300000 and >300000 nM for EAAT1, EAAT2 and EAAT3 respectively).
More Information Supplier PageUCPH 101 is a selective non-substrate inhibitor of EAAT1 (IC50 values are 660, >300000 and >300000 nM for EAAT1, EAAT2 and EAAT3 respectively).
More Information Supplier PageUF010 is a potent and selective HADC inhibitor with IC50 ~0.06 ??M, 0.1 ??M, 0.5 ??M and 1.5 ??M for HDACs 3, 2, 1 and 8, respectively. It has > 6-fold selectivity over other HDACs.
More Information Supplier PageUF010 is a potent and selective HADC inhibitor with IC50 ~0.06 ??M, 0.1 ??M, 0.5 ??M and 1.5 ??M for HDACs 3, 2, 1 and 8, respectively. It has > 6-fold selectivity over other HDACs.
More Information Supplier PageUF010 is a potent and selective HADC inhibitor with IC50 ~0.06 ??M, 0.1 ??M, 0.5 ??M and 1.5 ??M for HDACs 3, 2, 1 and 8, respectively. It has > 6-fold selectivity over other HDACs.
More Information Supplier PageUK 14,304 tartrate is a water-soluble form UK 14,304. It is a full α2 adrenergic agonist.
More Information Supplier PageUK 14,304 tartrate is a water-soluble form UK 14,304. It is a full α2 adrenergic agonist.
More Information Supplier PageUK 14,304 tartrate is a water-soluble form UK 14,304. It is a full α2 adrenergic agonist.
More Information Supplier PageUK 356618 is a selective and potent inhibitor of MMP-3 that shows selectivity over a range of MMPs.
More Information Supplier PageUK 356618 is a selective and potent inhibitor of MMP-3 that shows selectivity over a range of MMPs.
More Information Supplier PageUmbelliferone is a widespread natural product of the coumarin family. It absorbs ultraviolet light strongly at several wavelengths.
More Information Supplier PageUmbelliferone is a widespread natural product of the coumarin family. It absorbs ultraviolet light strongly at several wavelengths.
More Information Supplier PageUmbelliferone is a widespread natural product of the coumarin family. It absorbs ultraviolet light strongly at several wavelengths.
More Information Supplier PageUmeclidinium bromide(GSK573719A) is a muscarinic receptor antagonist which is useful in treatment of chronic obstructive pulmonary disease (COPD).
More Information Supplier PageUmeclidinium bromide(GSK573719A) is a muscarinic receptor antagonist which is useful in treatment of chronic obstructive pulmonary disease (COPD).
More Information Supplier PageUmeclidinium bromide(GSK573719A) is a muscarinic receptor antagonist which is useful in treatment of chronic obstructive pulmonary disease (COPD).
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