Dexbrompheniramine Maleate
The maleate salt of dexbrompheniramine, an antihistamine used for allergic rhinitis and urticaria. It is often found in combination cold and allergy preparations.
Peso Molecular
435,3000 g/mol
TPSA
90,70 Ų
Mecanismo de Ação
Competitively blocks histamine H1 receptors on effector cells, preventing histamine-mediated vasodilation, increased vascular permeability, bronchoconstriction, and pruritus. First-generation agents also cross the blood-brain barrier, causing sedation.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Competitively blocks histamine H1 receptors on effector cells, preventing histamine-mediated vasodilation, increased vascular permeability, bronchoconstriction, and pruritus. First-generation agents also cross the blood-brain barrier, causing sedation.
Estrutura 2D
Cite this structure
Embed this structure
SMILES
CN(C)CC[C@@H](c1ccc(Br)cc1)c1ccccn1.O=C(O)/C=C\C(=O)O
InChI
InChI=1S/C16H19BrN2.C4H4O4/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13;5-3(6)1-2-4(7)8/h3-9,11,15H,10,12H2,1-2H3;1-2H,(H,5,6)(H,7,8)/b;2-1-/t15-;/m0./s1
Molecular Formula
C20H23BrN2O4
HBD / HBA
2 / 6
Ligações Rotacionáveis
7
Átomos Pesados
27
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Perguntas frequentes
The maleate salt of dexbrompheniramine, an antihistamine used for allergic rhinitis and urticaria. It is often found in combination cold and allergy preparations.
Competitively blocks histamine H1 receptors on effector cells, preventing histamine-mediated vasodilation, increased vascular permeability, bronchoconstriction, and pruritus. First-generation agents also cross the blood-brain barrier, causing sedation.
Yes, Dexbrompheniramine Maleate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200638. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6433334. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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