Dipivefrin

CHEMBL1201262 Phase 4 Одобрено Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
351.4 g/mol
LogP
2.9
Phase
4

A prodrug of epinephrine (adrenaline) used as eye drops to lower intraocular pressure in open-angle glaucoma. After penetrating the eye, it is converted to epinephrine, which reduces fluid production and increases drainage within the eye. The prodrug form penetrates the cornea more effectively than epinephrine itself.

Молекулярная масса

351,4000 g/mol

LogP

2,90

TPSA

84,90 Ų

Правило пяти Липинского

Соответствует

Терапевтические области

Механизм действия

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Механизм

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

2D Структура

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SMILES

CNCC(O)c1ccc(OC(=O)C(C)(C)C)c(OC(=O)C(C)(C)C)c1

InChI

InChI=1S/C19H29NO5/c1-18(2,3)16(22)24-14-9-8-12(13(21)11-20-7)10-15(14)25-17(23)19(4,5)6/h8-10,13,20-21H,11H2,1-7H3

Molecular Formula

C19H29NO5

HBD / HBA

2 / 6

Вращаемые Связи

9

Тяжёлые Атомы

25

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

A prodrug of epinephrine (adrenaline) used as eye drops to lower intraocular pressure in open-angle glaucoma. After penetrating the eye, it is converted to epinephrine, which reduces fluid production and increases drainage within the eye. The prodrug form penetrates the cornea more effectively than epinephrine itself.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Dipivefrin 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). CHEMBL1201262. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3105. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

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.