Name | Ro 41-3290 |
---|---|
Synonyms |
4H-Benzo[a]quinolizin-4-one, 10-chloro-6,7-dihydro-1-[[(3S)-3-hydroxy-1-pyrrolidinyl]carbonyl]-3-phenyl-
EIR1Q66583 10-Chloro-1-{[(3S)-3-hydroxy-1-pyrrolidinyl]carbonyl}-3-phenyl-6,7-dihydro-4H-pyrido[2,1-a]isoquinolin-4-one RO-41-3290 |
Description | Ro 41-3290 is the desethylated derivative of Ro 41-3696, which is a nonbenzodiazepine partial agonist at the benzodiazepine receptor. Ro 41-3290 is an investigational hypnotic. |
---|---|
Related Catalog | |
Target |
Benzodiazepine receptor[1] |
In Vivo | At all times plasma levels of Ro 41-3290, the desethylated derivative of Ro 41-3696, are higher than those of the parent drug (tmax and t1/2 values=~2 and 8 hours, respectively)[1]. Pharmacokinetics of both Ro 41-3696 and its O-desethyl metabolite Ro 41-3290 are dose proportional and time independent. Ro 41-3696 is absorbed and eliminates rapidly (time of maximum plasma concentration, approximately 1 hour; elimination half-life, approximately 2 hours). Plasma levels of Ro 41-3290 are higher than those of the parent drug, and it is more slowly eliminated (values for time of maximum plasma concentration and elimination half-life, approximately 2 and approximately 7 hours, respectively)[2]. |
References |
Density | 1.4±0.1 g/cm3 |
---|---|
Boiling Point | 723.3±60.0 °C at 760 mmHg |
Molecular Formula | C24H21ClN2O3 |
Molecular Weight | 420.888 |
Flash Point | 391.2±32.9 °C |
Exact Mass | 420.124084 |
LogP | 3.00 |
Vapour Pressure | 0.0±2.5 mmHg at 25°C |
Index of Refraction | 1.717 |