Vibegron

CHEMBL2107826 Phase 4 Одобрено Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
444.5 g/mol
LogP
1.8
Phase
4

Vibegron is a selective beta-3 adrenergic receptor agonist that activates β3 receptors in bladder smooth muscle (detrusor), causing relaxation and increasing bladder capacity while reducing urinary urgency and frequency without affecting bladder contractility during voiding. It is approved for overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency in adults. As a β3 agonist, it offers an alternative mechanism to antimuscarinics with potentially fewer systemic anticholinergic side effects.

Молекулярная масса

444,5000 g/mol

LogP

1,80

TPSA

94,00 Ų

Правило пяти Липинского

Соответствует

Терапевтические области

Механизм действия

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Механизм

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

2D Структура

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SMILES

O=C(Nc1ccc(C[C@@H]2CC[C@H]([C@H](O)c3ccccc3)N2)cc1)[C@@H]1CCc2nccc(=O)n21

InChI

InChI=1S/C26H28N4O3/c31-24-14-15-27-23-13-12-22(30(23)24)26(33)29-19-8-6-17(7-9-19)16-20-10-11-21(28-20)25(32)18-4-2-1-3-5-18/h1-9,14-15,20-22,25,28,32H,10-13,16H2,(H,29,33)/t20-,21+,22-,25+/m0/s1

Molecular Formula

C26H28N4O3

HBD / HBA

3 / 5

Вращаемые Связи

6

Тяжёлые Атомы

33

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.

Часто задаваемые вопросы

Vibegron is a selective beta-3 adrenergic receptor agonist that activates β3 receptors in bladder smooth muscle (detrusor), causing relaxation and increasing bladder capacity while reducing urinary urgency and frequency without affecting bladder contractility during voiding. It is approved for overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency in adults. As a β3 agonist, it offers an alternative mechanism to antimuscarinics with potentially fewer systemic anticholinergic side effects.

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Yes, Vibegron 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). CHEMBL2107826. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 44472635. Chemical information database.

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

Медицинский отказ от ответственности

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.