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 WebsiteGW 5074 is a potent, selective and cell-permeable c-Raf1 kinase inhibitor
More Information Supplier PageGW 5074 is a potent, selective and cell-permeable c-Raf1 kinase inhibitor
More Information Supplier PageGW 5074 is a potent, selective and cell-permeable c-Raf1 kinase inhibitor
More Information Supplier PageGW 542573X is an activator of small-conductance Ca2+-activated K+ channels (KCa2).
More Information Supplier PageGW 542573X is an activator of small-conductance Ca2+-activated K+ channels (KCa2).
More Information Supplier PageGW 542573X is an activator of small-conductance Ca2+-activated K+ channels (KCa2).
More Information Supplier PageGW 7647 is a potent and highly selective PPAR?? agonist (EC50 values are 6, 1100 and 6200 nM for human PPAR??, PPAR?? and PPAR?? receptors respectively).
More Information Supplier PageGW 7647 is a potent and highly selective PPAR?? agonist (EC50 values are 6, 1100 and 6200 nM for human PPAR??, PPAR?? and PPAR?? receptors respectively).
More Information Supplier PageGW 7647 is a potent and highly selective PPAR?? agonist (EC50 values are 6, 1100 and 6200 nM for human PPAR??, PPAR?? and PPAR?? receptors respectively).
More Information Supplier PageGW 7647 is a potent and highly selective PPAR?? agonist (EC50 values are 6, 1100 and 6200 nM for human PPAR??, PPAR?? and PPAR?? receptors respectively).
More Information Supplier PageGW 9662 is a selective PPAR?? antagonist (IC50 values are 3.3, 32 and 2000 nM for PPAR??, PPAR?? and PPAR?? respectively).
More Information Supplier PageGW 9662 is a selective PPAR?? antagonist (IC50 values are 3.3, 32 and 2000 nM for PPAR??, PPAR?? and PPAR?? respectively).
More Information Supplier PageGW 9662 is a selective PPAR?? antagonist (IC50 values are 3.3, 32 and 2000 nM for PPAR??, PPAR?? and PPAR?? respectively).
More Information Supplier PageGW 9662 is a selective PPAR?? antagonist (IC50 values are 3.3, 32 and 2000 nM for PPAR??, PPAR?? and PPAR?? respectively).
More Information Supplier PageGW 9662 is a selective PPAR?? antagonist (IC50 values are 3.3, 32 and 2000 nM for PPAR??, PPAR?? and PPAR?? respectively).
More Information Supplier PageGW1929 is a synthetic peroxisome proliferator-activated receptor-?? (PPAR??) agonist with IC50 of 6.2 nM and 13 nM for human and mouse, respectively.
More Information Supplier PageGW1929 is a synthetic peroxisome proliferator-activated receptor-?? (PPAR??) agonist with IC50 of 6.2 nM and 13 nM for human and mouse, respectively.
More Information Supplier PageGW1929 is a synthetic peroxisome proliferator-activated receptor-?? (PPAR??) agonist with IC50 of 6.2 nM and 13 nM for human and mouse, respectively.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageGW3965 is a potent, selective LXR agonist for hLXR?? and hLXR?? with EC50 of 190 and 30 nM, respectively.
More Information Supplier PageGW3965 is a potent, selective LXR agonist for hLXR?? and hLXR?? with EC50 of 190 and 30 nM, respectively.
More Information Supplier PageGW3965 is a potent, selective LXR agonist for hLXR?? and hLXR?? with EC50 of 190 and 30 nM, respectively.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW4064 is a selective, non-steroidal farnesoid X receptor (FXR) agonist (EC50 = 15 nM).
More Information Supplier PageGW4064 is a selective, non-steroidal farnesoid X receptor (FXR) agonist (EC50 = 15 nM).
More Information Supplier PageGW4064 is a selective, non-steroidal farnesoid X receptor (FXR) agonist (EC50 = 15 nM).
More Information Supplier PageGW4064 is a selective, non-steroidal farnesoid X receptor (FXR) agonist (EC50 = 15 nM).
More Information Supplier PageGW4064 is a selective, non-steroidal farnesoid X receptor (FXR) agonist (EC50 = 15 nM).
More Information Supplier PageGW438014A is a potent and selective neuropeptide Y Y5 receptor antagonist.
More Information Supplier PageGW438014A is a potent and selective neuropeptide Y Y5 receptor antagonist.
More Information Supplier PageGW438014A is a potent and selective neuropeptide Y Y5 receptor antagonist.
More Information Supplier PageGW627368 is a novel, potent and selective competitive antagonist of prostanoid EP4 receptor(Ki= 100 nM) with additional human TP receptor affinity(Ki= 150 nM).
More Information Supplier PageGW627368 is a novel, potent and selective competitive antagonist of prostanoid EP4 receptor(Ki= 100 nM) with additional human TP receptor affinity(Ki= 150 nM).
More Information Supplier PageGW6471 is a PPAR?? antagonist, shown to completely inhibit GW409544-induced activation of PPAR??.
More Information Supplier PageGW6471 is a PPAR?? antagonist, shown to completely inhibit GW409544-induced activation of PPAR??.
More Information Supplier PageGW6471 is a PPAR?? antagonist, shown to completely inhibit GW409544-induced activation of PPAR??.
More Information Supplier PageGW6471 is a PPAR?? antagonist, shown to completely inhibit GW409544-induced activation of PPAR??.
More Information Supplier PageCasopitant mesylate is the mesylate salt of a centrally-acting neurokinin 1 (NK1) receptor antagonist with antidepressant and antiemetic activities.
More Information Supplier PageCasopitant mesylate is the mesylate salt of a centrally-acting neurokinin 1 (NK1) receptor antagonist with antidepressant and antiemetic activities.
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