Candesartan

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

An angiotensin II receptor blocker used to treat high blood pressure and heart failure. By blocking the angiotensin II receptor, it dilates blood vessels and reduces the workload on the heart. It is also used to protect kidney function in patients with type 2 diabetes and high blood pressure.

Khối lượng phân tử

610,6640 g/mol

LogP

4,10

TPSA

119,00 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Phân loại thuốc

Cơ chế tác dụng

Prodrug hydrolyzed to active form; selective angiotensin II type 1 receptor blocker.

Pharmacokinetics (PK)

Half-Life 9 hours

Pharmacodynamics (PD)

Cơ chế

Prodrug hydrolyzed to active form; selective angiotensin II type 1 receptor blocker.

Cấu trúc 2D

SVG PNG

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SMILES

CCOC1=NC2=CC=CC(=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)C(=O)O

InChI

InChI=1S/C24H20N6O3/c1-2-33-24-25-20-9-5-8-19(23(31)32)21(20)30(24)14-15-10-12-16(13-11-15)17-6-3-4-7-18(17)22-26-28-29-27-22/h3-13H,2,14H2,1H3,(H,31,32)(H,26,27,28,29)

Molecular Formula

C33H34N6O6

HBD / HBA

2 / 7

Liên kết có thể quay

7

Nguyên tử nặng

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.

Câu hỏi thường gặp

An angiotensin II receptor blocker used to treat high blood pressure and heart failure. By blocking the angiotensin II receptor, it dilates blood vessels and reduces the workload on the heart. It is also used to protect kidney function in patients with type 2 diabetes and high blood pressure.

Prodrug hydrolyzed to active form; selective angiotensin II type 1 receptor blocker.

Key pharmacokinetic parameters for Candesartan: Half-life: 9 hours.

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

Related Drugs

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References & Data Sources

  • PubChem — National Center for Biotechnology Information (NCBI). CID 2541. Chemical information database.

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

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.