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 WebsiteAG14361 is a potent PARP inhibitor, enhanced Temozolomide (TMZ) cytotoxicity in MMR(mismatch repair)-proficient / deficient cells.
More Information Supplier PageAG14361 is a potent PARP inhibitor, enhanced Temozolomide (TMZ) cytotoxicity in MMR(mismatch repair)-proficient / deficient cells.
More Information Supplier PageAG14361 is a potent PARP inhibitor, enhanced Temozolomide (TMZ) cytotoxicity in MMR(mismatch repair)-proficient / deficient cells.
More Information Supplier PageAG14361 is a potent PARP inhibitor, enhanced Temozolomide (TMZ) cytotoxicity in MMR(mismatch repair)-proficient / deficient cells.
More Information Supplier PageAG14361 is a potent PARP inhibitor, enhanced Temozolomide (TMZ) cytotoxicity in MMR(mismatch repair)-proficient / deficient cells.
More Information Supplier PageAGI-5198, also know as IDH-C35, is the a very potent and selective mutant IDH1 inhibitor that was shown to potential anticancer activity.
More Information Supplier PageAGI-5198, also know as IDH-C35, is the a very potent and selective mutant IDH1 inhibitor that was shown to potential anticancer activity.
More Information Supplier PageAGI-5198, also know as IDH-C35, is the a very potent and selective mutant IDH1 inhibitor that was shown to potential anticancer activity.
More Information Supplier PageAGI-5198, also know as IDH-C35, is the a very potent and selective mutant IDH1 inhibitor that was shown to potential anticancer activity.
More Information Supplier PageAGI-5198, also know as IDH-C35, is the a very potent and selective mutant IDH1 inhibitor that was shown to potential anticancer activity.
More Information Supplier PageAGI-6780 is a potent, selective inhibitor of mutant IDH2 with an IC50 value of 23 nM.
More Information Supplier PageAGI-6780 is a potent, selective inhibitor of mutant IDH2 with an IC50 value of 23 nM.
More Information Supplier PageAGI-6780 is a potent, selective inhibitor of mutant IDH2 with an IC50 value of 23 nM.
More Information Supplier PageAGI-6780 is a potent, selective inhibitor of mutant IDH2 with an IC50 value of 23 nM.
More Information Supplier PageAGI-6780 is a potent, selective inhibitor of mutant IDH2 with an IC50 value of 23 nM.
More Information Supplier PageAGK2 is a potent, and selective SIRT2 inhibitor with IC50 of 3.5 ??M.
More Information Supplier PageAGK2 is a potent, and selective SIRT2 inhibitor with IC50 of 3.5 ??M.
More Information Supplier PageAGK2 is a potent, and selective SIRT2 inhibitor with IC50 of 3.5 ??M.
More Information Supplier PageAGK2 is a potent, and selective SIRT2 inhibitor with IC50 of 3.5 ??M.
More Information Supplier PageAgnuside is an known iridoid glycoside found in Vitex herbs or plants. Agnuside exhibits estrogen-like activities as it interacts with estrogen receptors (ER-alpha) and estrogen receptor-regulated pregesterone receptors.
More Information Supplier PageAgnuside is an known iridoid glycoside found in Vitex herbs or plants. Agnuside exhibits estrogen-like activities as it interacts with estrogen receptors (ER-alpha) and estrogen receptor-regulated pregesterone receptors.
More Information Supplier PageAgnuside is an known iridoid glycoside found in Vitex herbs or plants. Agnuside exhibits estrogen-like activities as it interacts with estrogen receptors (ER-alpha) and estrogen receptor-regulated pregesterone receptors.
More Information Supplier PageAgomelatine is a melatonergic agonist (MT1 and MT2 receptors) and 5-HT2C antagonist.
More Information Supplier PageAgomelatine is a melatonergic agonist (MT1 and MT2 receptors) and 5-HT2C antagonist.
More Information Supplier PageAgomelatine is a melatonergic agonist (MT1 and MT2 receptors) and 5-HT2C antagonist.
More Information Supplier PageAgomelatine is a melatonergic agonist (MT1 and MT2 receptors) and 5-HT2C antagonist.
More Information Supplier PageAgomelatine is a melatonergic agonist (MT1 and MT2 receptors) and 5-HT2C antagonist.
More Information Supplier PageAI-10-49 is a protein-protein interaction inhibitor that selectively binds to CBF??-SMMHC and disrupts its binding to RUNX1 with a FRET IC50 of 0.26 uM,
More Information Supplier PageAI-10-49 is a protein-protein interaction inhibitor that selectively binds to CBF??-SMMHC and disrupts its binding to RUNX1 with a FRET IC50 of 0.26 uM,
More Information Supplier PageAI-10-49 is a protein-protein interaction inhibitor that selectively binds to CBF??-SMMHC and disrupts its binding to RUNX1 with a FRET IC50 of 0.26 uM,
More Information Supplier PageAK-7 is a cell- and brain-permeable inhibitor of SIRT2 (IC50 = 15.5 ??M).
More Information Supplier PageAK-7 is a cell- and brain-permeable inhibitor of SIRT2 (IC50 = 15.5 ??M).
More Information Supplier PageAK-7 is a cell- and brain-permeable inhibitor of SIRT2 (IC50 = 15.5 ??M).
More Information Supplier PageAK-7 is a cell- and brain-permeable inhibitor of SIRT2 (IC50 = 15.5 ??M).
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