Ubrogepant

CHEMBL2364638 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
549.5 g/mol
LogP
3.1
Phase
4

Ubrogepant is a small molecule calcitonin gene-related peptide (CGRP) receptor antagonist (gepant) that blocks CGRP-mediated vasodilation and neurogenic inflammation implicated in migraine pathophysiology. It is approved for acute treatment of migraine attacks with or without aura in adults. Unlike triptans, it does not cause vasoconstriction, making it potentially safer for patients with cardiovascular risk factors.

Moleküler Ağırlık

549,5000 g/mol

LogP

3,10

TPSA

104,00 Ų

Lipinski RO5

Geçer

Terapötik Alanlar

Etki Mekanizması

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanizma

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

2D Yapı

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

C[C@@H]1[C@H](c2ccccc2)C[C@H](NC(=O)c2cnc3c(c2)C[C@@]2(C3)C(=O)Nc3ncccc32)C(=O)N1CC(F)(F)F

InChI

InChI=1S/C29H26F3N5O3/c1-16-20(17-6-3-2-4-7-17)11-22(26(39)37(16)15-29(30,31)32)35-25(38)19-10-18-12-28(13-23(18)34-14-19)21-8-5-9-33-24(21)36-27(28)40/h2-10,14,16,20,22H,11-13,15H2,1H3,(H,35,38)(H,33,36,40)/t16-,20-,22+,28+/m1/s1

Molecular Formula

C29H26F3N5O3

HBD / HBA

2 / 8

Döndürülebilir Bağlar

4

Ağır Atomlar

40

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.

Sıkça Sorulan Sorular

Ubrogepant is a small molecule calcitonin gene-related peptide (CGRP) receptor antagonist (gepant) that blocks CGRP-mediated vasodilation and neurogenic inflammation implicated in migraine pathophysiology. It is approved for acute treatment of migraine attacks with or without aura in adults. Unlike triptans, it does not cause vasoconstriction, making it potentially safer for patients with cardiovascular risk factors.

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

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

{# 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). CHEMBL2364638. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 68748835. Chemical information database.

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

Tıbbi Sorumluluk Reddi

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.