Dexchlorpheniramine
The pharmacologically active dextrorotatory isomer of chlorpheniramine, an antihistamine used to relieve symptoms of allergic rhinitis and urticaria. It has greater antihistamine potency than the racemate.
分子量
274.7900 g/mol
LogP
3.40
TPSA
16.10 Ų
Lipinski 五规则
符合
治疗领域
作用机制
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.
二维结构
Cite this structure
Embed this structure
SMILES
CN(C)CC[C@@H](c1ccc(Cl)cc1)c1ccccn1
InChI
InChI=1S/C16H19ClN2/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
Molecular Formula
C16H19ClN2
HBD / HBA
- / 2
可旋转键数
5
重原子数
19
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.
常见问题
The pharmacologically active dextrorotatory isomer of chlorpheniramine, an antihistamine used to relieve symptoms of allergic rhinitis and urticaria. It has greater antihistamine potency than the racemate.
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, Dexchlorpheniramine 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). CHEMBL1201353. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 33036. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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