Sumatriptan

CHEMBL128 Phase 4 Approuvé Small molecule
Half-Life
2.5 hours
Bioavailability
Protein Binding
Molecular Weight
295.4 g/mol
LogP
0.9
Phase
4

Designed specifically for migraine attacks, this triptan medication works by activating serotonin receptors in the brain and blood vessels, causing the swollen blood vessels responsible for migraine pain to constrict back to normal size. Available in tablet, nasal spray, and injectable forms, it is most effective when taken at the first sign of a migraine.

Masse moléculaire

295,4020 g/mol

LogP

0,90

TPSA

73,60 Ų

Règle des 5 de Lipinski

Conforme

Aires thérapeutiques

Classes de médicaments

Mécanisme d'action

Selective 5-HT1B/1D receptor agonist.

Pharmacokinetics (PK)

Half-Life 2.5 hours

Pharmacodynamics (PD)

Mécanisme

Selective 5-HT1B/1D receptor agonist.

Structure 2D

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

CNS(=O)(=O)Cc1ccc2[nH]cc(CCN(C)C)c2c1

InChI

InChI=1S/C14H21N3O2S/c1-15-20(18,19)10-11-4-5-14-13(8-11)12(9-16-14)6-7-17(2)3/h4-5,8-9,15-16H,6-7,10H2,1-3H3

Molecular Formula

C14H21N3O2S

HBD / HBA

2 / 4

Liaisons Rotatives

6

Atomes Lourds

20

No side effects recorded

Side effect data is not yet available for this drug.

Foire aux questions

Designed specifically for migraine attacks, this triptan medication works by activating serotonin receptors in the brain and blood vessels, causing the swollen blood vessels responsible for migraine pain to constrict back to normal size. Available in tablet, nasal spray, and injectable forms, it is most effective when taken at the first sign of a migraine.

Selective 5-HT1B/1D receptor agonist.

Key pharmacokinetic parameters for Sumatriptan: Half-life: 2.5 hours.

Yes, Sumatriptan is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

Related Drugs

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL128. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5358. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Avertissement médical

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.