Lasmiditan
This selective serotonin 5-HT1F receptor agonist treats acute migraine without vasoconstriction, safe for cardiovascular patients.
分子量
377.4000 g/mol
LogP
2.80
TPSA
62.30 Ų
リピンスキーの五則
適合
治療領域
作用機序
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
2D構造
Cite this structure
Embed this structure
SMILES
CN1CCC(C(=O)c2cccc(NC(=O)c3c(F)cc(F)cc3F)n2)CC1
InChI
InChI=1S/C19H18F3N3O2/c1-25-7-5-11(6-8-25)18(26)15-3-2-4-16(23-15)24-19(27)17-13(21)9-12(20)10-14(17)22/h2-4,9-11H,5-8H2,1H3,(H,23,24,27)
Molecular Formula
C19H18F3N3O2
HBD / HBA
1 / 7
回転可能結合数
4
重原子数
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.
よくある質問
This selective serotonin 5-HT1F receptor agonist treats acute migraine without vasoconstriction, safe for cardiovascular patients.
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
Yes, Lasmiditan 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). CHEMBL3039520. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 11610526. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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