Mitapivat

CHEMBL4299940 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
450.6 g/mol
LogP
1.8
Phase
4

This oral activator of the red blood cell enzyme pyruvate kinase (PKR) is used to treat hemolytic anemia in adults with pyruvate kinase deficiency, a rare inherited condition where red blood cells break down prematurely. By restoring PKR activity, it helps red blood cells survive longer and improves anemia.

Peso Molecular

450,6000 g/mol

LogP

1,80

TPSA

91,00 Ų

Regra dos 5 de Lipinski

Aprovado

Mecanismo de Ação

Absorbs, reflects, or scatters ultraviolet radiation before it reaches the skin, protecting against UV-induced DNA damage and sunburn.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Absorbs, reflects, or scatters ultraviolet radiation before it reaches the skin, protecting against UV-induced DNA damage and sunburn.

Estrutura 2D

SVG PNG

Cite this structure


                        

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SMILES

O=C(c1ccc(NS(=O)(=O)c2cccc3cccnc23)cc1)N1CCN(CC2CC2)CC1

InChI

InChI=1S/C24H26N4O3S/c29-24(28-15-13-27(14-16-28)17-18-6-7-18)20-8-10-21(11-9-20)26-32(30,31)22-5-1-3-19-4-2-12-25-23(19)22/h1-5,8-12,18,26H,6-7,13-17H2

Molecular Formula

C24H26N4O3S

HBD / HBA

1 / 6

Ligações Rotacionáveis

6

Átomos Pesados

32

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.

Perguntas frequentes

This oral activator of the red blood cell enzyme pyruvate kinase (PKR) is used to treat hemolytic anemia in adults with pyruvate kinase deficiency, a rare inherited condition where red blood cells break down prematurely. By restoring PKR activity, it helps red blood cells survive longer and improves anemia.

Absorbs, reflects, or scatters ultraviolet radiation before it reaches the skin, protecting against UV-induced DNA damage and sunburn.

Yes, Mitapivat 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). CHEMBL4299940. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 59634741. Chemical information database.

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

Aviso Médico

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.