Name | 2-(4-methoxyphenyl)-1,6,7,8,9,10-hexahydrocyclohepta[b]pyrazolo[3,4-d]pyridin-3(2h)-one |
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Description | CGS 20625 is a potent, selective and orally active partial agonist for the central benzodiazepine receptor. CGS 20625 inhibits [3H]-flunitrazepam binding to central benzodiazepine receptors with an IC50 of 1.3 nM. CGS 20625 can be used for the research of pentylenetetrazol-induced seizures[1]. |
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Related Catalog | |
Target |
IC50: 1.3 nM ([3H]-flunitrazepam binding to central benzodiazepine receptors)[1] |
References |
Density | 1.246g/cm3 |
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Boiling Point | 503.8ºC at 760mmHg |
Molecular Formula | C18H19N3O2 |
Molecular Weight | 309.36 |
Flash Point | 258.5ºC |
Exact Mass | 309.14800 |
PSA | 59.91000 |
LogP | 2.99130 |
Vapour Pressure | 2.82E-10mmHg at 25°C |
Index of Refraction | 1.617 |