PKC抑制剂(CGP60474)
CGP60474
CAS: 164658-13-3
Molecular Formula: C18H18ClN5O
PKC抑制剂(CGP60474) - Names and Identifiers
PKC抑制剂(CGP60474) - Physico-chemical Properties
| Molecular Formula | C18H18ClN5O |
| Molar Mass | 355.82 |
| Density | 1.356 |
| Melting Point | 144-147℃ |
| Boling Point | 630.6±65.0 °C(Predicted) |
| pKa | 14.93±0.10(Predicted) |
| Storage Condition | 2-8°C(protect from light) |
| In vitro study | CGP60474 (Compound A) is a potent VEGFR-2 inhibitor, with an IC 50 of 84 nM. CGP60474 is also a PKC inhibitor, with competitive kinetics relative to ATP. |
| In vivo study | CGP-60474 (10 mg/kg; i.p.) inhibits the IL-6 level and increases the survival rate in the LPS endotoxemia model. Animal Model: C57Bl/6 mice (LPS endotoxemia model) Dosage: 10 mg/kg Administration: I.p. Result: Had a higher survival rate. |
PKC抑制剂(CGP60474) - Preparation solution concentration reference
| 1mg | 5mg | 10mg | |
|---|---|---|---|
| 1 mM | 2.81 ml | 14.052 ml | 28.104 ml |
| 5 mM | 0.562 ml | 2.81 ml | 5.621 ml |
| 10 mM | 0.281 ml | 1.405 ml | 2.81 ml |
| 5 mM | 0.056 ml | 0.281 ml | 0.562 ml |
Last Update：2024-01-02 23:10:35
PKC抑制剂(CGP60474) - Reference Information
| biological activity | CGP60474 is an efficient anti-endotoxin drug, it is a potent cyclin-dependent kinase (CDK) inhibitor (IC50 values for CDK1/B, CDK2/E, CDK2/a, CDK4/D, CDK5/p25, CDK7/H, and CDK9/T are 26, 3, 4, 216, 10, 200, and 13 nM, respectively). CGP60474 is a selective and ATP competitive PKC inhibitor. |
| target | CDK1-Cyclin B 26 nM (IC 50 ) CDK2/cyclinE 3 nM (IC 50 ) cdk2/cyclin A 4 nM (IC 50 ) CDK4/cyclin D 216 nM (IC 50) Cdk5/P25 10 nM (IC 50 ) CDK7/cyclin H 200 nM (IC 50 ) CDK9/cycT 13 nM (IC 50 ) PKC |
| in vitro study | CGP60474 (Compound a) is a potent VEGFR-2 inhibitor, with an IC 50 of 84 nM. CGP60474 is also a PKC inhibitor, with competitive kinetics relative to ATP. |
| in vivo study | CGP-60474 (10 mg/kg; I.p.) inhibits the IL-6 level and increases the survival rate in the LPS endotoxemia model. Animal Model: C57Bl/6 MICE (LPS endotoxemia model) Dosage: 10 mg/kg Administration: I.p. Result: had a higher survival rate. |
| Animal Model: | C57Bl/6 mice (LPS endotoxemia model) |
| Dosage: | 10 mg/kg |
| Administration: | I .p. |
| Result: | Had a higher survival rate. |
Last Update：2024-04-09 21:49:45
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Product Name: CGP60474 Visit Supplier Webpage Request for quotationCAS: 164658-13-3
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QQ: 2881950922
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Mobile: +86-18821248368
QQ: 495145328
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Product Name: CGP60474 Visit Supplier Webpage Request for quotation
CAS: 164658-13-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 164658-13-3
Tel: 18301782025
Email: 3008007409@qq.com
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View History
PKC抑制剂(CGP60474)
3-methylaminopropionic acid ethyl ester
n-tridecyl-2,6-dimethylmorpholine
十二烷基2-(二甲基氨基)丙酸酯盐酸盐
2-碘-4,6-二甲基苯胺
1,2-DIPALMITOYL-GLYCERO-2-PHOSPHOCHOLINE MONOHYDRATE
Tricyclo[3.3.1.13,7]decane-1-a acid, alpha-[[(1,1-dimethyleth no]-3-hydroxy-, (alphaS)-
7BETA-羟基蟾毒灵
2-[2-(methylthio)benzimidazol-1-yl]propionic acid
4-[(2,6-DIMORPHOLINOPYRIMIDIN-4-YL)CARBONYL]MORPHOLINE
3-methylaminopropionic acid ethyl ester
n-tridecyl-2,6-dimethylmorpholine
十二烷基2-(二甲基氨基)丙酸酯盐酸盐
2-碘-4,6-二甲基苯胺
1,2-DIPALMITOYL-GLYCERO-2-PHOSPHOCHOLINE MONOHYDRATE
Tricyclo[3.3.1.13,7]decane-1-a acid, alpha-[[(1,1-dimethyleth no]-3-hydroxy-, (alphaS)-
7BETA-羟基蟾毒灵
2-[2-(methylthio)benzimidazol-1-yl]propionic acid
4-[(2,6-DIMORPHOLINOPYRIMIDIN-4-YL)CARBONYL]MORPHOLINE