Doxylamine Succinate
A succinate salt form of doxylamine used as a sleep aid and to treat pregnancy-related nausea. Like the parent compound, it exerts sedative and antiemetic effects through histamine receptor blockade.
Berat Molekul
388,5000 g/mol
TPSA
100,00 Ų
Area Terapeutik
Mekanisme Kerja
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.
Struktur 2D
Cite this structure
Embed this structure
SMILES
CN(C)CCOC(C)(c1ccccc1)c1ccccn1.O=C(O)CCC(=O)O
InChI
InChI=1S/C17H22N2O.C4H6O4/c1-17(20-14-13-19(2)3,15-9-5-4-6-10-15)16-11-7-8-12-18-16;5-3(6)1-2-4(7)8/h4-12H,13-14H2,1-3H3;1-2H2,(H,5,6)(H,7,8)
Molecular Formula
C21H28N2O5
HBD / HBA
2 / 7
Ikatan yang Dapat Dirotasi
9
Atom Berat
28
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.
Pertanyaan yang Sering Diajukan
A succinate salt form of doxylamine used as a sleep aid and to treat pregnancy-related nausea. Like the parent compound, it exerts sedative and antiemetic effects through histamine receptor blockade.
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, Doxylamine Succinate 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). CHEMBL1200392. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 11224. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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