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 WebsiteNU6102 is selective for CDK1 and CDK2 compared to CDK4/D1 (IC50=1.6 ??M), DYRK1A (IC50=0.9 ??M), PDK1 (IC50=0.8 ??M) and ROCKII (IC50=0.6 ??M).
More Information Supplier PageNU-7441 (KU-57788) is a potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor. The IC50 values are 14, 1700, 5000, >100000 and >100000 nM for DNA-PK, mTOR, PI 3-K, ATM and ATR respectively.
More Information Supplier PageNU-7441 (KU-57788) is a potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor. The IC50 values are 14, 1700, 5000, >100000 and >100000 nM for DNA-PK, mTOR, PI 3-K, ATM and ATR respectively.
More Information Supplier PageNU-7441 (KU-57788) is a potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor. The IC50 values are 14, 1700, 5000, >100000 and >100000 nM for DNA-PK, mTOR, PI 3-K, ATM and ATR respectively.
More Information Supplier PageNU-7441 (KU-57788) is a potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor. The IC50 values are 14, 1700, 5000, >100000 and >100000 nM for DNA-PK, mTOR, PI 3-K, ATM and ATR respectively.
More Information Supplier PageNU2058 is a guanine-based CDK inhibitor with IC50 of 17 uM and 26 uM for CDK2 and CDK1.
More Information Supplier PageNU2058 is a guanine-based CDK inhibitor with IC50 of 17 uM and 26 uM for CDK2 and CDK1.
More Information Supplier PageNU2058 is a guanine-based CDK inhibitor with IC50 of 17 uM and 26 uM for CDK2 and CDK1.
More Information Supplier PageNU6027 is a potent inhibitor of cellular ATR activity (IC(50)=6.7 ??M) and enhanced hydroxyurea and cisplatin cytotoxicity in an ATR-dependent manner.
More Information Supplier PageNU6027 is a potent inhibitor of cellular ATR activity (IC(50)=6.7 ??M) and enhanced hydroxyurea and cisplatin cytotoxicity in an ATR-dependent manner.
More Information Supplier PageNU6027 is a potent inhibitor of cellular ATR activity (IC(50)=6.7 ??M) and enhanced hydroxyurea and cisplatin cytotoxicity in an ATR-dependent manner.
More Information Supplier PageNU6027 is a potent inhibitor of cellular ATR activity (IC(50)=6.7 ??M) and enhanced hydroxyurea and cisplatin cytotoxicity in an ATR-dependent manner.
More Information Supplier PageNU7026 is a novel DNA-dependent protein kinase inhibitor that potentiates the cytotoxicity of topoisomerase II poisons used in the treatment of leukemia.
More Information Supplier PageNU7026 is a novel DNA-dependent protein kinase inhibitor that potentiates the cytotoxicity of topoisomerase II poisons used in the treatment of leukemia.
More Information Supplier PageNU7026 is a novel DNA-dependent protein kinase inhibitor that potentiates the cytotoxicity of topoisomerase II poisons used in the treatment of leukemia.
More Information Supplier PageNU7026 is a novel DNA-dependent protein kinase inhibitor that potentiates the cytotoxicity of topoisomerase II poisons used in the treatment of leukemia.
More Information Supplier PageNuciferine is an alkaloid found within the plants Nymphaea caerulea and Nelumbo nucifera.
More Information Supplier PageNuciferine is an alkaloid found within the plants Nymphaea caerulea and Nelumbo nucifera.
More Information Supplier PageNuciferine is an alkaloid found within the plants Nymphaea caerulea and Nelumbo nucifera.
More Information Supplier PageNuclear yellow exhibits excitation/emission maxima ~335/495 nm when bound to DNA.
More Information Supplier PageNuclear yellow exhibits excitation/emission maxima ~335/495 nm when bound to DNA.
More Information Supplier PageNuclear yellow exhibits excitation/emission maxima ~335/495 nm when bound to DNA.
More Information Supplier PageNutlin 3a is a potent inhibitor of MDM2 (mouse double minute 2) binding to p53 that induces the expression of p53 regulated genes, and shows potent antiproliferative activity in cells expressing functional p53.
More Information Supplier PageNutlin 3a is a potent inhibitor of MDM2 (mouse double minute 2) binding to p53 that induces the expression of p53 regulated genes, and shows potent antiproliferative activity in cells expressing functional p53.
More Information Supplier PageNutlin 3a is a potent inhibitor of MDM2 (mouse double minute 2) binding to p53 that induces the expression of p53 regulated genes, and shows potent antiproliferative activity in cells expressing functional p53.
More Information Supplier PageNutlin 3a is a potent inhibitor of MDM2 (mouse double minute 2) binding to p53 that induces the expression of p53 regulated genes, and shows potent antiproliferative activity in cells expressing functional p53.
More Information Supplier PageNutlin 3a is a potent inhibitor of MDM2 (mouse double minute 2) binding to p53 that induces the expression of p53 regulated genes, and shows potent antiproliferative activity in cells expressing functional p53.
More Information Supplier PageNutlin 3b is a p53/MDM2 antagonist or inhibitor with IC50 value of 13.6 uM, 150-fold less potent (+)-enantiomer of Nutlin-3 as in comparison with opposite (-)-enantiomer Nutlin-3a.
More Information Supplier PageNutlin 3b is a p53/MDM2 antagonist or inhibitor with IC50 value of 13.6 uM, 150-fold less potent (+)-enantiomer of Nutlin-3 as in comparison with opposite (-)-enantiomer Nutlin-3a.
More Information Supplier PageNutlin 3b is a p53/MDM2 antagonist or inhibitor with IC50 value of 13.6 uM, 150-fold less potent (+)-enantiomer of Nutlin-3 as in comparison with opposite (-)-enantiomer Nutlin-3a.
More Information Supplier PageNutlin 3b is a p53/MDM2 antagonist or inhibitor with IC50 value of 13.6 uM, 150-fold less potent (+)-enantiomer of Nutlin-3 as in comparison with opposite (-)-enantiomer Nutlin-3a.
More Information Supplier PageNutlin 3b is a p53/MDM2 antagonist or inhibitor with IC50 value of 13.6 uM, 150-fold less potent (+)-enantiomer of Nutlin-3 as in comparison with opposite (-)-enantiomer Nutlin-3a.
More Information Supplier PageNVP DPP 728 dihydrochloride is a potent and orally active inhibitor of dipeptidyl peptidase (DPP)-IV with Ki and IC50 values of 11 nM and 14 nM, respectively.
More Information Supplier PageNVP DPP 728 dihydrochloride is a potent and orally active inhibitor of dipeptidyl peptidase (DPP)-IV with Ki and IC50 values of 11 nM and 14 nM, respectively.
More Information Supplier PageNVP-231 is a potent, specific, and reversible CerK inhibitor that competitively inhibits binding of ceramide to CerK.
More Information Supplier PageNVP-231 is a potent, specific, and reversible CerK inhibitor that competitively inhibits binding of ceramide to CerK.
More Information Supplier PageNVP-231 is a potent, specific, and reversible CerK inhibitor that competitively inhibits binding of ceramide to CerK.
More Information Supplier PageNVP-231 is a potent, specific, and reversible CerK inhibitor that competitively inhibits binding of ceramide to CerK.
More Information Supplier PageNVP-AAM077 inhibited progenitor cells proliferation in the subventricular zone and dentate gyrus and reduced the survival of newborn cells in the dentate gyrus in the adult mice.
More Information Supplier PageNVP-AAM077 inhibited progenitor cells proliferation in the subventricular zone and dentate gyrus and reduced the survival of newborn cells in the dentate gyrus in the adult mice.
More Information Supplier PageNVP-AAM077 inhibited progenitor cells proliferation in the subventricular zone and dentate gyrus and reduced the survival of newborn cells in the dentate gyrus in the adult mice.
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