Naftopidil

CHEMBL142635 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
392.5 g/mol
LogP
4.1
Phase
4

An alpha-1 adrenergic receptor blocker used in Japan and other Asian countries to treat benign prostatic hyperplasia, relieving urinary symptoms by relaxing smooth muscle in the prostate and bladder neck. It may also have benefits for sexual function.

Khối lượng phân tử

392,5000 g/mol

LogP

4,10

TPSA

45,20 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cấu trúc 2D

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SMILES

COc1ccccc1N1CCN(CC(O)COc2cccc3ccccc23)CC1

InChI

InChI=1S/C24H28N2O3/c1-28-24-11-5-4-10-22(24)26-15-13-25(14-16-26)17-20(27)18-29-23-12-6-8-19-7-2-3-9-21(19)23/h2-12,20,27H,13-18H2,1H3

Molecular Formula

C24H28N2O3

HBD / HBA

1 / 5

Liên kết có thể quay

7

Nguyên tử nặng

29

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.

Câu hỏi thường gặp

An alpha-1 adrenergic receptor blocker used in Japan and other Asian countries to treat benign prostatic hyperplasia, relieving urinary symptoms by relaxing smooth muscle in the prostate and bladder neck. It may also have benefits for sexual function.

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

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL142635. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 4418. Chemical information database.

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

Tuyên bố miễn trách y tế

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.