Chemical Component Summary

Name2-BROMO-2-CHLORO-1,1,1-TRIFLUOROETHANE
Identifiers(2R)-2-bromo-2-chloro-1,1,1-trifluoro-ethane
FormulaC2 H Br Cl F3
Molecular Weight197.382
TypeNON-POLYMER
Isomeric SMILES[C@@H](C(F)(F)F)(Cl)Br
InChIInChI=1S/C2HBrClF3/c3-1(4)2(5,6)7/h1H/t1-/m0/s1
InChIKeyBCQZXOMGPXTTIC-SFOWXEAESA-N

Chemical Details

Formal Charge0
Atom Count8
Chiral Atom Count1
Bond Count7
Aromatic Bond Count0

Drug Info: DrugBank

DrugBank IDDB01159 
NameHalothane
Groups
  • approved
  • vet_approved
DescriptionA nonflammable, halogenated, hydrocarbon anesthetic that provides relatively rapid induction with little or no excitement. Analgesia may not be adequate. nitrous oxide is often given concomitantly. Because halothane may not produce sufficient muscle relaxation, supplemental neuromuscular blocking agents may be required. (From AMA Drug Evaluations Annual, 1994, p178)
Synonyms
  • 2-bromo-2-chloro-1,1,1-trifluoroethane
  • 1-bromo-1-chloro-2,2,2-trifluoroethane
  • 1,1,1-trifluoro-2-chloro-2-bromoethane
  • Alotano
  • Halothanum
Brand Names
  • Fluothane Liq Inh 1000mg/gm
  • Halothane Liq 99.9%
  • Halothane
  • Fluothane Anesthetic
IndicationFor the induction and maintenance of general anesthesia
Categories
  • Agents that produce hypertension
  • Anesthetics
  • Anesthetics, General
  • Anesthetics, Inhalation
  • Central Nervous System Agents
ATC-CodeN01AB01
CAS number151-67-7

Drug Targets

NameTarget SequencePharmacological ActionActions
Potassium channel subfamily K member 3MKRQNVRTLALIVCTFTYLLVGAAVFDALESEPELIERQRLELRQQELRA...unknownbinder
Potassium channel subfamily K member 9MKRQNVRTLSLIVCTFTYLLVGAAVFDALESDHEMREEEKLKAEEIRIKG...unknownbinder
GABA(A) ReceptorMRKSPGLSDCLWAWILLLSTLTGRSYGQPSLQDELKDNTTVFTRILDRLL...unknownpositive allosteric modulator
Plasma membrane calcium-transporting ATPaseMGDMANNSVAYSGVKNSLKEANHDGDFGITLAELRALMELRSTDALRKIQ...unknowninhibitor
Calcium-activated potassium channel subunit alpha-1MANGGGGGGGSSGGGGGGGGSSLRMSSNIHANHLSLDASSSSSSSSSSSS...unknowninhibitor
View More
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
PubChem 445258
ChEBI CHEBI:49646