2. GPCR/G Protein Neuronal Signaling
  3. Adrenergic Receptor
  4. Romifidine hydrochloride

Romifidine hydrochloride is an α2 adrenergic receptor agonist. Romifidine hydrochloride shows sedation effects in vivo.

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Romifidine hydrochloride Chemical Structure

Romifidine hydrochloride Chemical Structure

CAS No. : 65896-14-2

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Description

Romifidine hydrochloride is an α2 adrenergic receptor agonist. Romifidine hydrochloride shows sedation effects in vivo[1][2].

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].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Molecular Weight

294.55

Formula

C9H10BrClFN3
CAS No.
SMILES

FC1=C(NC2=NCCN2)C(Br)=CC=C1.[H]Cl
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Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
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Romifidine hydrochloride Related Classifications

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Romifidine65896-14-2Adrenergic ReceptorBeta ReceptordetomidinexylazinesedationponyhorseInhibitorinhibitorinhibit

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Romifidine hydrochloride
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