Levocabastine
A selective H1 antihistamine available as eye drops or nasal spray for treating allergic conjunctivitis and rhinitis. It provides rapid and long-lasting relief from itching, redness, and other allergy symptoms.
Khối lượng phân tử
420,5000 g/mol
LogP
2,50
TPSA
64,30 Ų
Lipinski RO5
Đạt
Cơ chế tác dụng
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.
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
C[C@@H]1CN([C@H]2CC[C@](C#N)(c3ccc(F)cc3)CC2)CC[C@]1(C(=O)O)c1ccccc1
InChI
InChI=1S/C26H29FN2O2/c1-19-17-29(16-15-26(19,24(30)31)21-5-3-2-4-6-21)23-11-13-25(18-28,14-12-23)20-7-9-22(27)10-8-20/h2-10,19,23H,11-17H2,1H3,(H,30,31)/t19-,23-,25-,26-/m1/s1
Molecular Formula
C26H29FN2O2
HBD / HBA
1 / 5
Liên kết có thể quay
4
Nguyên tử nặng
31
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.
Câu hỏi thường gặp
A selective H1 antihistamine available as eye drops or nasal spray for treating allergic conjunctivitis and rhinitis. It provides rapid and long-lasting relief from itching, redness, and other allergy symptoms.
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, Levocabastine 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). CHEMBL1615438. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 54385. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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