Moexipril

CHEMBL1165 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
498.6 g/mol
LogP
1.2
Phase
4

This ACE inhibitor lowers blood pressure by blocking the enzyme that converts angiotensin I to the potent vasoconstrictor angiotensin II, causing blood vessels to relax and the kidneys to excrete more sodium and water. It is used to treat high blood pressure and may have additional cardiovascular protective effects.

分子量

498.6000 g/mol

LogP

1.20

TPSA

114.00 Ų

リピンスキーの五則

適合

治療領域

作用機序

Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.

2D構造

SVG PNG

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SMILES

CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N1Cc2cc(OC)c(OC)cc2C[C@H]1C(=O)O

InChI

InChI=1S/C27H34N2O7/c1-5-36-27(33)21(12-11-18-9-7-6-8-10-18)28-17(2)25(30)29-16-20-15-24(35-4)23(34-3)14-19(20)13-22(29)26(31)32/h6-10,14-15,17,21-22,28H,5,11-13,16H2,1-4H3,(H,31,32)/t17-,21-,22-/m0/s1

Molecular Formula

C27H34N2O7

HBD / HBA

2 / 8

回転可能結合数

12

重原子数

36

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.

よくある質問

This ACE inhibitor lowers blood pressure by blocking the enzyme that converts angiotensin I to the potent vasoconstrictor angiotensin II, causing blood vessels to relax and the kidneys to excrete more sodium and water. It is used to treat high blood pressure and may have additional cardiovascular protective effects.

Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.

Yes, Moexipril 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). CHEMBL1165. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 91270. Chemical information database.

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

医学的免責事項

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.