Sparsentan

CHEMBL539423 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
592.8 g/mol
LogP
5.0
Phase
4

Sparsentan is a dual angiotensin II AT1 receptor and endothelin A receptor antagonist developed for the treatment of IgA nephropathy (IgAN) and focal segmental glomerulosclerosis (FSGS). By simultaneously blocking both the renin-angiotensin and endothelin pathways contributing to glomerular hypertension, proteinuria, and progressive renal fibrosis, it provides complementary nephroprotective effects beyond what is achievable with either pathway blockade alone. It has demonstrated significant reductions in proteinuria in clinical trials.

Moleküler Ağırlık

592,8000 g/mol

LogP

5,00

TPSA

122,00 Ų

Lipinski RO5

Geçer

Terapötik Alanlar

Etki Mekanizması

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanizma

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

2D Yapı

SVG PNG

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SMILES

CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(-c2ccccc2S(=O)(=O)Nc2noc(C)c2C)c(COCC)c1

InChI

InChI=1S/C32H40N4O5S/c1-5-7-14-29-33-32(17-10-11-18-32)31(37)36(29)20-24-15-16-26(25(19-24)21-40-6-2)27-12-8-9-13-28(27)42(38,39)35-30-22(3)23(4)41-34-30/h8-9,12-13,15-16,19H,5-7,10-11,14,17-18,20-21H2,1-4H3,(H,34,35)

Molecular Formula

C32H40N4O5S

HBD / HBA

1 / 8

Döndürülebilir Bağlar

12

Ağır Atomlar

42

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.

Sıkça Sorulan Sorular

Sparsentan is a dual angiotensin II AT1 receptor and endothelin A receptor antagonist developed for the treatment of IgA nephropathy (IgAN) and focal segmental glomerulosclerosis (FSGS). By simultaneously blocking both the renin-angiotensin and endothelin pathways contributing to glomerular hypertension, proteinuria, and progressive renal fibrosis, it provides complementary nephroprotective effects beyond what is achievable with either pathway blockade alone. It has demonstrated significant reductions in proteinuria in clinical trials.

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Yes, Sparsentan 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). CHEMBL539423. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 10257882. Chemical information database.

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

Tıbbi Sorumluluk Reddi

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.