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 WebsiteJNJ-42041935 is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and selective inhibitor of PHD enzymes.
More Information Supplier PageJNJ-42041935 is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and selective inhibitor of PHD enzymes.
More Information Supplier PageJNJ-42041935 is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and selective inhibitor of PHD enzymes.
More Information Supplier PageJNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.
More Information Supplier PageJNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.
More Information Supplier PageJNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.
More Information Supplier PageJNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.
More Information Supplier PageJNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependent kinases (CDK) and Aurora kinases.
More Information Supplier PageJNJ7777120 is a potent, selective non-imidazole H4?histamine receptor antagonist.
More Information Supplier PageJNJ7777120 is a potent, selective non-imidazole H4?histamine receptor antagonist.
More Information Supplier PageJNJ7777120 is a potent, selective non-imidazole H4?histamine receptor antagonist.
More Information Supplier PageJNJ7777120 is a potent, selective non-imidazole H4?histamine receptor antagonist.
More Information Supplier PageJNJ7777120 is a potent, selective non-imidazole H4?histamine receptor antagonist.
More Information Supplier PageJNK-IN-7 is a relatively selective JNKs inhibitor(IC50= 1.54/1.99/0.75 for JNK1/2/3); also bound to IRAK1, PIK3C3, PIP5K3 and PIP4K2C.
More Information Supplier PageJNK-IN-7 is a relatively selective JNKs inhibitor(IC50= 1.54/1.99/0.75 for JNK1/2/3); also bound to IRAK1, PIK3C3, PIP5K3 and PIP4K2C.
More Information Supplier PageJNK-IN-7 is a relatively selective JNKs inhibitor(IC50= 1.54/1.99/0.75 for JNK1/2/3); also bound to IRAK1, PIK3C3, PIP5K3 and PIP4K2C.
More Information Supplier PageJNK-IN-8 is the first irreversible JNK inhibitor for JNK1, JNK2 and JNK4 with IC50 of 4.7 nM, 18.7 nM and 1 nM, respectively
More Information Supplier PageJNK-IN-8 is the first irreversible JNK inhibitor for JNK1, JNK2 and JNK4 with IC50 of 4.7 nM, 18.7 nM and 1 nM, respectively
More Information Supplier PageJNK-IN-8 is the first irreversible JNK inhibitor for JNK1, JNK2 and JNK4 with IC50 of 4.7 nM, 18.7 nM and 1 nM, respectively
More Information Supplier PageJNK-IN-8 is the first irreversible JNK inhibitor for JNK1, JNK2 and JNK4 with IC50 of 4.7 nM, 18.7 nM and 1 nM, respectively
More Information Supplier PageJNK-IN-8 is the first irreversible JNK inhibitor for JNK1, JNK2 and JNK4 with IC50 of 4.7 nM, 18.7 nM and 1 nM, respectively
More Information Supplier PageJolkinolide B, a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud, has various biological and pharmacological properties.
More Information Supplier PageJolkinolide B, a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud, has various biological and pharmacological properties.
More Information Supplier PageJolkinolide B, a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud, has various biological and pharmacological properties.
More Information Supplier PageJSH 23 is an inhibitor of NF-??B, blocking its translocation into the nucleus (IC50 = 7.1 ?M)
More Information Supplier PageJSH 23 is an inhibitor of NF-??B, blocking its translocation into the nucleus (IC50 = 7.1 ?M)
More Information Supplier PageJSH 23 is an inhibitor of NF-??B, blocking its translocation into the nucleus (IC50 = 7.1 ?M)
More Information Supplier PageJSH 23 is an inhibitor of NF-??B, blocking its translocation into the nucleus (IC50 = 7.1 ?M)
More Information Supplier PageJTC-801 is a selective antagonist for the nociceptin receptor, also known as the ORL-1 receptor.
More Information Supplier PageJTC-801 is a selective antagonist for the nociceptin receptor, also known as the ORL-1 receptor.
More Information Supplier PageJTC-801 is a selective antagonist for the nociceptin receptor, also known as the ORL-1 receptor.
More Information Supplier PageJTC-801 is a selective antagonist for the nociceptin receptor, also known as the ORL-1 receptor.
More Information Supplier PageJTC-801 is a selective antagonist for the nociceptin receptor, also known as the ORL-1 receptor.
More Information Supplier PageJTT-705 (Dalcetrapib) is a CETP inhibitor.Inhibition of CETP is a target to increase HDL-cholesterol and potentially reduce atherosclerosis.
More Information Supplier PageJTT-705 (Dalcetrapib) is a CETP inhibitor.Inhibition of CETP is a target to increase HDL-cholesterol and potentially reduce atherosclerosis.
More Information Supplier PageJTT-705 (Dalcetrapib) is a CETP inhibitor.Inhibition of CETP is a target to increase HDL-cholesterol and potentially reduce atherosclerosis.
More Information Supplier PageJTT-705 (Dalcetrapib) is a CETP inhibitor.Inhibition of CETP is a target to increase HDL-cholesterol and potentially reduce atherosclerosis.
More Information Supplier PageJTT-705 (Dalcetrapib) is a CETP inhibitor.Inhibition of CETP is a target to increase HDL-cholesterol and potentially reduce atherosclerosis.
More Information Supplier PageJujuboside A, a neuroprotective agent from semen Ziziphi Spinosae ameliorates behavioral disorders of the dementia mouse model.
More Information Supplier PageJujuboside A, a neuroprotective agent from semen Ziziphi Spinosae ameliorates behavioral disorders of the dementia mouse model.
More Information Supplier PageJujuboside A, a neuroprotective agent from semen Ziziphi Spinosae ameliorates behavioral disorders of the dementia mouse model.
More Information Supplier PageJujuboside B is a main bioactive saponin constituent of Ziziphi Spinosae Semen, which is a traditional herb for the treatment of insomnia and anxiety.
More Information Supplier PageJujuboside B is a main bioactive saponin constituent of Ziziphi Spinosae Semen, which is a traditional herb for the treatment of insomnia and anxiety.
More Information Supplier PageJujuboside B is a main bioactive saponin constituent of Ziziphi Spinosae Semen, which is a traditional herb for the treatment of insomnia and anxiety.
More Information Supplier PageJW 55 is an inhibitor of the PARP domain of tankyrase 1 and 2 (TNKS1/2).
More Information Supplier PageJW 55 is an inhibitor of the PARP domain of tankyrase 1 and 2 (TNKS1/2).
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