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KN-62
- английское имяKN-62
- CAS №127191-97-3
- CBNumberCB8443368
- ФормулаC38H35N5O6S2
- мольный вес721.84
- номер MDLMFCD00083180
- файл Mol127191-97-3.mol
химическое свойство
Температура плавления | 92-94°C |
Температура кипения | 964.7±75.0 °C(Predicted) |
плотность | 1.388 |
температура хранения | -20°C |
растворимость | 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 0.93 mg/mL |
пка | 4.07±0.13(Predicted) |
форма | solid |
цвет | white |
Биологические источники | synthetic (organic) |
Справочник по базе данных CAS | 127191-97-3(CAS DataBase Reference) |
FDA UNII | 63HM46XPOW |
UNSPSC Code | 12352200 |
NACRES | NA.77 |
Заявления о безопасности | 24/25 |
WGK Германия | 3 |
кода HS | 29339980 |
KN-62 химические свойства, назначение, производство
Химические свойства
Yellow SolidИспользование
It is used as a potent and selective inhibitor of CaMKII. KN-62 has demonstrated potent and selective inhibition of Ca2+/calmodulin-dependent protein kinase II (CaMKII; Ki=0.9 ?M) which causes cells to arrest in the S phase. In HEK-293 cells expressing type III adenylyl cyclase (III-AC), 10 ?M of KN-62 blocked CaMKII phosphorylation of III-AC, and inhibited hormone-stimulated Ca2+ oscillations. Additionally, KN-62 is a potent non-competitive antagonist at the P2X7 receptor (IC50 = 15 nM).Общее описание
A cell-permeable, reversible, and selective inhibitor of CaM kinase II (Ki = 900 nM for rat brain CaM kinase II) that binds directly to the calmodulin binding site of the enzyme. Also inhibits the growth of K562 cells in a dose-dependent manner.Биологическая активность
Selective, cell-permeable inhibitor of CaM kinase II (IC 50 = 0.9 μ M). Binds directly to the calmodulin binding site of the enzyme. Potent non-competitive antagonist at the P2X 7 receptor (IC 50 = 15 nM). Also available as part of the Mixed Kinase Inhibitor Tocriset™ .KN-62 поставщик
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