Lisinopril Anhydrous

CHEMBL1237 Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
405.5 g/mol
LogP
-2.9
Phase
4

An anhydrous form of lisinopril, an ACE inhibitor used for hypertension and heart failure. It shares the same cardiovascular and renal protective properties as the standard form.

น้ำหนักโมเลกุล

405.5000 g/mol

LogP

-2.90

TPSA

133.00 Ų

Lipinski RO5

ผ่าน

กลไกการออกฤทธิ์

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)

กลไก

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.

โครงสร้าง 2 มิติ

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SMILES

NCCCC[C@H](N[C@@H](CCc1ccccc1)C(=O)O)C(=O)N1CCC[C@H]1C(=O)O

InChI

InChI=1S/C21H31N3O5/c22-13-5-4-9-16(19(25)24-14-6-10-18(24)21(28)29)23-17(20(26)27)12-11-15-7-2-1-3-8-15/h1-3,7-8,16-18,23H,4-6,9-14,22H2,(H,26,27)(H,28,29)/t16-,17-,18-/m0/s1

Molecular Formula

C21H31N3O5

HBD / HBA

4 / 7

พันธะที่หมุนได้

12

อะตอมหนัก

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.

คำถามที่พบบ่อย

An anhydrous form of lisinopril, an ACE inhibitor used for hypertension and heart failure. It shares the same cardiovascular and renal protective properties as the standard form.

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, Lisinopril Anhydrous 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). CHEMBL1237. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5362119. Chemical information database.

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

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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.