Romifidine information

Romifidine
Clinical data
AHFS/Drugs.com	International Drug Names
Routes of; administration	IV
ATCvet code	QN05CM93 (WHO) ;
Legal status
Legal status	Veterinary use only;
Identifiers
	IUPAC name N-(2-bromo-6-fluorophenyl)-4,5-dihydro-1H-imidazol-2-amine;
CAS Number	65896-16-4 ;
PubChem CID	71969;
ChemSpider	64975 ;
UNII	876351L05K;
CompTox Dashboard (EPA)	DTXSID40216103 ;
ECHA InfoCard	100.158.065
Chemical and physical data
Formula	C9H9BrFN3
Molar mass	258.094 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C1CN=C(N1)NC2=C(C=CC=C2Br)F;
	InChI InChI=1S/C9H9BrFN3/c10-6-2-1-3-7(11)8(6)14-9-12-4-5-13-9/h1-3H,4-5H2,(H2,12,13,14) ; Key:KDPNLRQZHDJRFU-UHFFFAOYSA-N ;
	(what is this?) (verify)

Romifidine is a drug that is used in veterinary medicine as a sedative mainly in large animals such as horses,^[1] although it may be used in a wide variety of species.^[2]^[3] It is not used in humans, but is closely related in structure to the commonly used drug clonidine.

Romifidine acts as an agonist at the α₂ adrenergic receptor subtype. Side effects can include bradycardia and respiratory depression. It is often used alongside other sedative or analgesic drugs such as ketamine or butorphanol.^[4]^[5] Yohimbine can be used as an antidote to rapidly reverse the effects.

^ Spadavecchia C, Arendt-Nielsen L, Andersen OK, Spadavecchia L, Schatzmann U (November 2005). "Effect of romifidine on the nociceptive withdrawal reflex and temporal summation in conscious horses". American Journal of Veterinary Research. 66 (11): 1992–8. doi:10.2460/ajvr.2005.66.1992. PMID 16334961.
^ De Lucas JJ, Rodríguez C, Marín M, González F, Ballesteros C, San Andrés MI (February 2007). "Pharmacokinetics of intramuscular ketamine in young ostriches premedicated with romifidine". Journal of Veterinary Medicine. A, Physiology, Pathology, Clinical Medicine. 54 (1): 48–50. doi:10.1111/j.1439-0442.2007.00910.x. PMID 17359455.
^ Belda E, Laredo FG, Escobar M, Soler M, Lucas X, Agut A (January 2008). "Sedative and cardiorespiratory effects of three doses of romifidine in comparison with medetomidine in five cats". The Veterinary Record. 162 (3): 82–7. doi:10.1136/vr.162.3.82. PMID 18204032. S2CID 41300654.
^ Corletto F, Raisis AA, Brearley JC (January 2005). "Comparison of morphine and butorphanol as pre-anaesthetic agents in combination with romifidine for field castration in ponies". Veterinary Anaesthesia and Analgesia. 32 (1): 16–22. doi:10.1111/j.1467-2995.2004.00184.x. PMID 15663735.
^ Kerr CL, McDonell WN, Young SS (October 2004). "Cardiopulmonary effects of romifidine/ketamine or xylazine/ketamine when used for short duration anesthesia in the horse". Canadian Journal of Veterinary Research. 68 (4): 274–82. PMC 1111358. PMID 15581222.

[1] Spadavecchia C, Arendt-Nielsen L, Andersen OK, Spadavecchia L, Schatzmann U (November 2005). "Effect of romifidine on the nociceptive withdrawal reflex and temporal summation in conscious horses". American Journal of Veterinary Research. 66 (11): 1992–8. doi:10.2460/ajvr.2005.66.1992. PMID 16334961.

[2] De Lucas JJ, Rodríguez C, Marín M, González F, Ballesteros C, San Andrés MI (February 2007). "Pharmacokinetics of intramuscular ketamine in young ostriches premedicated with romifidine". Journal of Veterinary Medicine. A, Physiology, Pathology, Clinical Medicine. 54 (1): 48–50. doi:10.1111/j.1439-0442.2007.00910.x. PMID 17359455.

[3] Belda E, Laredo FG, Escobar M, Soler M, Lucas X, Agut A (January 2008). "Sedative and cardiorespiratory effects of three doses of romifidine in comparison with medetomidine in five cats". The Veterinary Record. 162 (3): 82–7. doi:10.1136/vr.162.3.82. PMID 18204032. S2CID 41300654.

[4] Corletto F, Raisis AA, Brearley JC (January 2005). "Comparison of morphine and butorphanol as pre-anaesthetic agents in combination with romifidine for field castration in ponies". Veterinary Anaesthesia and Analgesia. 32 (1): 16–22. doi:10.1111/j.1467-2995.2004.00184.x. PMID 15663735.

[5] Kerr CL, McDonell WN, Young SS (October 2004). "Cardiopulmonary effects of romifidine/ketamine or xylazine/ketamine when used for short duration anesthesia in the horse". Canadian Journal of Veterinary Research. 68 (4): 274–82. PMC 1111358. PMID 15581222.

Romifidine information

and 26 Related for: Romifidine information

Romifidine

LSD

Phenylephrine

Beta blocker

Zolpidem

Aripiprazole

Cannabis

Propranolol

Ethchlorvynol

Cyclobenzaprine

Promethazine

Dimenhydrinate

Psychiatry

Salbutamol

Doxylamine

Tizanidine

Suvorexant

Propofol

Hydroxyzine

Trazodone

Diphenhydramine

Mirtazapine

Zopiclone

Chloral hydrate

Phenobarbital

Xylazine

Clinical data

AHFS/Drugs.com	International Drug Names
Routes of administration	IV
ATCvet code	QN05CM93 (WHO)
Legal status
Legal status	Veterinary use only
Identifiers
IUPAC name N-(2-bromo-6-fluorophenyl)-4,5-dihydro-1H-imidazol-2-amine
CAS Number	65896-16-4^Y
PubChem CID	71969
ChemSpider	64975^N
UNII	876351L05K
CompTox Dashboard (EPA)	DTXSID40216103
ECHA InfoCard	100.158.065
Chemical and physical data
Formula	C₉H₉BrFN₃
Molar mass	258.094 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES C1CN=C(N1)NC2=C(C=CC=C2Br)F
InChI InChI=1S/C9H9BrFN3/c10-6-2-1-3-7(11)8(6)14-9-12-4-5-13-9/h1-3H,4-5H2,(H2,12,13,14)^N Key:KDPNLRQZHDJRFU-UHFFFAOYSA-N^N
^NY (what is this?) (verify)