Sacubitril-Valsartan

Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
11.5 hours
Bioavailability
Protein Binding
Molecular Weight
414.5 g/mol
LogP
Phase
4

Sacubitril-valsartan is a first-in-class angiotensin receptor-neprilysin inhibitor (ARNI) combining sacubitril (a neprilysin inhibitor prodrug) and valsartan (an angiotensin II receptor blocker) for heart failure treatment. Sacubitril inhibits neprilysin-mediated breakdown of natriuretic peptides, bradykinin, and other vasoactive substances, while valsartan blocks AT1 receptors, producing complementary vasodilatory and cardioprotective effects. It has demonstrated superior outcomes to ACE inhibitors in patients with heart failure with reduced ejection fraction.

น้ำหนักโมเลกุล

414.5010 g/mol

TPSA

205.00 Ų

ด้านการรักษา

หมวดหมู่ยา

กลไกการออกฤทธิ์

Angiotensin receptor-neprilysin inhibitor (ARNI) combining neprilysin inhibition with AT1 receptor blockade.

Pharmacokinetics (PK)

Half-Life 11.5 hours

Pharmacodynamics (PD)

กลไก

Angiotensin receptor-neprilysin inhibitor (ARNI) combining neprilysin inhibition with AT1 receptor blockade.

SMILES

CCCCC(=O)N(CC1=CC=C(C=C1)C2=CC=CC=C2C3=NNN=N3)[C@@H](C(C)C)C(=O)O.CCOC(=O)[C@H](C)C[C@@H](CC1=CC=C(C=C1)C2=CC=CC=C2)NC(=O)CCC(=O)O

InChI

InChI=1S/C24H29N5O3.C24H29NO5/c1-4-5-10-21(30)29(22(16(2)3)24(31)32)15-17-11-13-18(14-12-17)19-8-6-7-9-20(19)23-25-27-28-26-23;1-3-30-24(29)17(2)15-21(25-22(26)13-14-23(27)28)16-18-9-11-20(12-10-18)19-7-5-4-6-8-19/h6-9,11-14,16,22H,4-5,10,15H2,1-3H3,(H,31,32)(H,25,26,27,28);4-12,17,21H,3,13-16H2,1-2H3,(H,25,26)(H,27,28)/t22-;17-,21+/m01/s1

Molecular Formula

C24H29N2O5

HBD / HBA

4 / 11

พันธะที่หมุนได้

22

อะตอมหนัก

62

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

Sacubitril-valsartan is a first-in-class angiotensin receptor-neprilysin inhibitor (ARNI) combining sacubitril (a neprilysin inhibitor prodrug) and valsartan (an angiotensin II receptor blocker) for heart failure treatment. Sacubitril inhibits neprilysin-mediated breakdown of natriuretic peptides, bradykinin, and other vasoactive substances, while valsartan blocks AT1 receptors, producing complementary vasodilatory and cardioprotective effects. It has demonstrated superior outcomes to ACE inhibitors in patients with heart failure with reduced ejection fraction.

Angiotensin receptor-neprilysin inhibitor (ARNI) combining neprilysin inhibition with AT1 receptor blockade.

Key pharmacokinetic parameters for Sacubitril-Valsartan: Half-life: 11.5 hours.

Yes, Sacubitril-Valsartan 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 24755620. Chemical information database.

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

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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.