dexbrompheniramine

CHEBI:CHEBI_59269

Definition

The (pharmacologically active) (S)-(+)-enantiomer of brompheniramine. A histamine H1 receptor antagonist, it is used (commonly as its maleate salt) for the symptomatic relief of allergic conditions, including rhinitis and conjunctivitis.

Chemical Information

Molecular Formula
C16H19BrN2
Molecular Mass
319.23900
Charge
0
SMILES
CN(C)CC[C@@H](c1ccc(Br)cc1)c1ccccn1
InChI
InChI=1S/C16H19BrN2/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13/h3-9,11,15H,10,12H2,1-2H3/t15-/m0/s1
InChIKey
ZDIGNSYAACHWNL-HNNXBMFYSA-N

Alternative Names

  • (+)-brompheniraminum
  • (3S)-3-(4-bromophenyl)-N,N-dimethyl-3-(pyridin-2-yl)propan-1-amine
  • (S)-(+)-brompheniramine
  • (S)-brompheniramine
  • d-brompheniramine
  • dexbromfeniramina
  • dexbrompheniramine
  • dexbrompheniraminum

Drug Classification

Important Medical Information

⚕️ This information is sourced from ChEBI (Chemical Entities of Biological Interest) database and is intended for educational purposes only.

  • Always consult with a healthcare professional before starting, stopping, or modifying any medication.
  • Side effects may vary and this list may not be comprehensive.
  • Drug interactions may occur with other medications.

Additional Identifiers

oboInOwl#hasDbXref
Wikipedia:Dexbrompheniramine
DRON_00010000
22696
core#notation
CHEBI:59269

Additional References

Wikipedia:Dexbrompheniramine

🔍 Click on any linked disease name to learn more about the conditions this medication is used to treat, or explore related drug classifications for more information about similar medications.

Additional Attributes

oboInOwl#hasOBONamespace
chebi_ontology
oboInOwl#hasDbXref
Wikipedia:Dexbrompheniramine
DRON_00010000
22696
oboInOwl#id
CHEBI:59269
core#notation
CHEBI:59269
oboInOwl#inSubset
http://purl.obolibrary.org/obo/chebi#3_STAR
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class
rdf-schema#domain
https://w3id.org/def/predibionto#has_side_effect29311
owl#annotatedSource
t252652
owl#someValuesFrom
t3003632