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 WebsiteAMG 900 is a novel potent and highly selective pan-aurora kinase inhibitor with activity in taxane-resistant tumor cell lines.
More Information Supplier PageAMG-073 HCl (Cinacalcet HCl) represents a new class of compounds for the treatment of hyperparathyroidism known as calcimimetics, which reduce parathyroid hormone (PTH) synthesis and secretion by increasing the sensitivity of the parathyroid calcium-sensing receptor (CaR) to extracellular calcium.
More Information Supplier PageAMG-073 HCl (Cinacalcet HCl) represents a new class of compounds for the treatment of hyperparathyroidism known as calcimimetics, which reduce parathyroid hormone (PTH) synthesis and secretion by increasing the sensitivity of the parathyroid calcium-sensing receptor (CaR) to extracellular calcium.
More Information Supplier PageAMG-073 HCl (Cinacalcet HCl) represents a new class of compounds for the treatment of hyperparathyroidism known as calcimimetics, which reduce parathyroid hormone (PTH) synthesis and secretion by increasing the sensitivity of the parathyroid calcium-sensing receptor (CaR) to extracellular calcium.
More Information Supplier PageAMG-073 HCl (Cinacalcet HCl) represents a new class of compounds for the treatment of hyperparathyroidism known as calcimimetics, which reduce parathyroid hormone (PTH) synthesis and secretion by increasing the sensitivity of the parathyroid calcium-sensing receptor (CaR) to extracellular calcium.
More Information Supplier PageAMG-458 is a potent inhibitor of c-Met with an IC50 value of 60nM and displays selectivity against VEGFR2.
More Information Supplier PageAMG-458 is a potent inhibitor of c-Met with an IC50 value of 60nM and displays selectivity against VEGFR2.
More Information Supplier PageAMG-458 is a potent inhibitor of c-Met with an IC50 value of 60nM and displays selectivity against VEGFR2.
More Information Supplier PageAMG-458 is a potent inhibitor of c-Met with an IC50 value of 60nM and displays selectivity against VEGFR2.
More Information Supplier PageAMG-458 is a potent inhibitor of c-Met with an IC50 value of 60nM and displays selectivity against VEGFR2.
More Information Supplier PageAMG-47a is an orally bioavailable potent inhibitor of Lck and T cell proliferation. It exhibits anti-inflammatory activity (ED50 11 mg/kg) in the anti-CD3 induced production of IL-2 in mice.
More Information Supplier PageAMG-47a is an orally bioavailable potent inhibitor of Lck and T cell proliferation. It exhibits anti-inflammatory activity (ED50 11 mg/kg) in the anti-CD3 induced production of IL-2 in mice.
More Information Supplier PageAMG-47a is an orally bioavailable potent inhibitor of Lck and T cell proliferation. It exhibits anti-inflammatory activity (ED50 11 mg/kg) in the anti-CD3 induced production of IL-2 in mice.
More Information Supplier PageAMG-47a is an orally bioavailable potent inhibitor of Lck and T cell proliferation. It exhibits anti-inflammatory activity (ED50 11 mg/kg) in the anti-CD3 induced production of IL-2 in mice.
More Information Supplier PageAMG-925 is a potent, selective, and bioavailable FLT3/cyclin-dependent kinase 4 (CDK4) dual kinase inhibitor.
More Information Supplier PageAMG-925 is a potent, selective, and bioavailable FLT3/cyclin-dependent kinase 4 (CDK4) dual kinase inhibitor.
More Information Supplier PageAMG-925 is a potent, selective, and bioavailable FLT3/cyclin-dependent kinase 4 (CDK4) dual kinase inhibitor.
More Information Supplier PageAMG-Tie2-1 is a highly potent, non-selective inhibitor of Tie-2 (IC50
More Information Supplier PageAMG-Tie2-1 is a highly potent, non-selective inhibitor of Tie-2 (IC50
More Information Supplier PageAMG-Tie2-1 is a highly potent, non-selective inhibitor of Tie-2 (IC50
More Information Supplier PageAMG-Tie2-1 is a highly potent, non-selective inhibitor of Tie-2 (IC50
More Information Supplier PageAMG 232 is a highly potent, selective and orally bioavailable piperidinone inhibitor of the MDM2-p53 interaction((SPR KD= 0.045 nM, SJSA-1 EdU IC50=9.1 nM).
More Information Supplier PageAMG 232 is a highly potent, selective and orally bioavailable piperidinone inhibitor of the MDM2-p53 interaction((SPR KD= 0.045 nM, SJSA-1 EdU IC50=9.1 nM).
More Information Supplier PageAMG 232 is a highly potent, selective and orally bioavailable piperidinone inhibitor of the MDM2-p53 interaction((SPR KD= 0.045 nM, SJSA-1 EdU IC50=9.1 nM).
More Information Supplier PageAmidopyrine is white crystalline substance used as an analgesic and antipyretic.
More Information Supplier PageAmidopyrine is white crystalline substance used as an analgesic and antipyretic.
More Information Supplier PageAmidopyrine is white crystalline substance used as an analgesic and antipyretic.
More Information Supplier PageAmidopyrine is white crystalline substance used as an analgesic and antipyretic.
More Information Supplier PageAmidopyrine is white crystalline substance used as an analgesic and antipyretic.
More Information Supplier PageAmifostine is the first approved radioprotective drug, used to decrease the risk of kidney problems caused by treatment with cisplatin.
More Information Supplier PageAmifostine is the first approved radioprotective drug, used to decrease the risk of kidney problems caused by treatment with cisplatin.
More Information Supplier PageAmifostine is the first approved radioprotective drug, used to decrease the risk of kidney problems caused by treatment with cisplatin.
More Information Supplier PageAmifostine is the first approved radioprotective drug, used to decrease the risk of kidney problems caused by treatment with cisplatin.
More Information Supplier PageAmiloride hydrochloride dihydrate is a potent epithelial sodium channel blocker and selective low threshold (T-type) calcium channel protein inhibitor (KD=30??M).
More Information Supplier PageAmiloride hydrochloride is a Na+ channel blocker, also inhibits TRPP3 channels and Na+/H+ exchanger (NHE).
More Information Supplier PageAmiloride hydrochloride is a Na+ channel blocker, also inhibits TRPP3 channels and Na+/H+ exchanger (NHE).
More Information Supplier PageAmiloride hydrochloride is a Na+ channel blocker, also inhibits TRPP3 channels and Na+/H+ exchanger (NHE).
More Information Supplier PageAmiloride hydrochloride dihydrate is a potent epithelial sodium channel blocker and selective low threshold (T-type) calcium channel protein inhibitor (KD=30??M).
More Information Supplier PageAmineptine is a tricyclic antidepressant drug selectively blocking dopamine uptake, on 3H-imipramine binding, which was investigated in platelets of major depressed patients in conjunction with changes in clinical state.
More Information Supplier PageAmineptine is a tricyclic antidepressant drug selectively blocking dopamine uptake, on 3H-imipramine binding, which was investigated in platelets of major depressed patients in conjunction with changes in clinical state.
More Information Supplier PageAmineptine is a tricyclic antidepressant drug selectively blocking dopamine uptake, on 3H-imipramine binding, which was investigated in platelets of major depressed patients in conjunction with changes in clinical state.
More Information Supplier PageAminocaproic acid is used to treat excessive postoperative bleeding, especially after procedures in which a great amount of bleeding is expected,
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