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Climazolam

From Wikipedia, the free encyclopedia
Anesthetic drug
Pharmaceutical compound
Climazolam
Clinical data
Trade namesClimasol
AHFS/Drugs.comInternational Drug Names
ATCvet code
Legal status
Legal status
Identifiers
  • 8-Chloro-6-(2-chlorophenyl)-1-methyl-4H-imidazo[1,5-a][1,4]benzodiazepine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H13Cl2N3
Molar mass342.22 g·mol−1
3D model (JSmol)
  • ClC1=CC=CC=C1C2=NCC3=CN=C(C)N3C4=C2C=C(C=C4)Cl

Climazolam[1] (Ro21-3982) was introduced under licence as a veterinary medicine by the Swiss Pharmaceutical company Gräub under the tradenameClimasol.[2] Climazolam is a benzodiazepine, specifically animidazobenzodiazepinederivative developed byHoffman-LaRoche. It is similar in structure tomidazolam anddiclazepam and is used inveterinary medicine for anesthetizing animals.[3][4]

References

[edit]
  1. ^US 4280957, Walser A, Fryer RI, "Imidazodiazepines and processes therefor", issued 28 July 1981, assigned to Hoffman La Roche 
  2. ^"Climazolam".Drugs.com. Archived fromthe original on 2017-08-01. Retrieved2018-01-23.
  3. ^Ganter M, Kanngiesser M (Aug 1991). "Effect of ketamine and its combinations with xylazine and climazolam on the circulation and respiration in swine".Zentralbl Veterinarmed A (in German).38 (7):501–509.doi:10.1111/j.1439-0442.1991.tb01041.x.PMID 1950241.
  4. ^Bettschart-Wolfensberger R, Taylor PM, Sear JW, Bloomfield MR, Rentsch K, Dawling S (Oct 1996). "Physiologic effects of anesthesia induced and maintained by intravenous administration of a climazolam-ketamine combination in ponies premedicated with acepromazine and xylazine".American Journal of Veterinary Research.57 (10):1472–1477.PMID 8896687.
1,4-Benzodiazepines
1,5-Benzodiazepines
2,3-Benzodiazepines*
Triazolobenzodiazepines
Imidazobenzodiazepines
Oxazolobenzodiazepines
Thienodiazepines
Thienotriazolodiazepines
Thienobenzodiazepines*
Pyridodiazepines
Pyridotriazolodiazepines
Pyrazolodiazepines
Pyrrolodiazepines
Tetrahydroisoquinobenzodiazepines
Pyrrolobenzodiazepines*
Benzodiazepine prodrugs
* atypical activity profile (notGABAA receptor ligands)
Alcohols
Barbiturates
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Flavonoids
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Kava constituents
Monoureides
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Nonbenzodiazepines
Phenols
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