Enalapril Maleate

CHEMBL1200659 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
492.5 g/mol
LogP
Phase
4

The maleate salt form of enalapril, this blood pressure medication relaxes blood vessels by blocking the enzyme that produces the vessel-constricting hormone angiotensin II. The maleate salt form is the standard oral formulation.

Khối lượng phân tử

492,5000 g/mol

TPSA

171,00 Ų

Lĩnh vực điều trị

Cơ chế tác dụng

Prodrug converted to enalaprilat; inhibits ACE preventing angiotensin I to II conversion.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Prodrug converted to enalaprilat; inhibits ACE preventing angiotensin I to II conversion.

Cấu trúc 2D

SVG PNG

Cite this structure


                        

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SMILES

CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)O.O=C(O)/C=C\C(=O)O

InChI

InChI=1S/C20H28N2O5.C4H4O4/c1-3-27-20(26)16(12-11-15-8-5-4-6-9-15)21-14(2)18(23)22-13-7-10-17(22)19(24)25;5-3(6)1-2-4(7)8/h4-6,8-9,14,16-17,21H,3,7,10-13H2,1-2H3,(H,24,25);1-2H,(H,5,6)(H,7,8)/b;2-1-/t14-,16-,17-;/m0./s1

Molecular Formula

C24H32N2O9

HBD / HBA

4 / 10

Liên kết có thể quay

12

Nguyên tử nặng

35

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

The maleate salt form of enalapril, this blood pressure medication relaxes blood vessels by blocking the enzyme that produces the vessel-constricting hormone angiotensin II. The maleate salt form is the standard oral formulation.

Prodrug converted to enalaprilat; inhibits ACE preventing angiotensin I to II conversion.

Yes, Enalapril Maleate 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). CHEMBL1200659. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5388961. 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.