Name | Romifidine Hydrochloride |
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Synonyms | N-(2-bromo-6-fluorophenyl)-4,5-dihydro-1H-imidazol-2-amine,hydrochloride |
Description | Romifidine hydrochloride is an α2 adrenergic receptor agonist. Romifidine hydrochloride shows sedation effects in vivo[1][2]. |
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Related Catalog | |
In Vivo | Romifidine hydrochloride (80 μg/kg; i.v. once) produces sedative effects with significantly greater drooping during the 45-90 min time period in welsh mountain ponies[1]. Romifidine hydrochloride (40, 80 and 120 mg/kg; i.v. at seven-day intervals) shows a shallower and shorter-lived sedation than with detomidine in horses[2]. |
References |
Molecular Formula | C9H10BrClFN3 |
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Molecular Weight | 294.55100 |
Exact Mass | 292.97300 |
PSA | 36.42000 |
LogP | 2.59870 |