Ritlecitinib

CHEMBL4085457 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
285.3 g/mol
LogP
2.1
Phase
4

Ritlecitinib is an irreversible covalent inhibitor of JAK3 and the TEC family of kinases (including ITK, RLK, BTK, BMX, and TXK) that blocks signaling from multiple pro-inflammatory cytokines through the JAK3/STAT pathway and T-cell receptor signaling through the TEC kinase pathway. It is approved for the treatment of alopecia areata in adults and adolescents, and is under investigation in other immune-mediated inflammatory conditions.

Peso Molecular

285,3400 g/mol

LogP

2,10

TPSA

73,90 Ų

Regra dos 5 de Lipinski

Aprovado

Áreas Terapêuticas

Mecanismo de Ação

Irreversibly inhibits Bruton's tyrosine kinase (BTK), a key enzyme in the B-cell receptor signaling pathway that drives the survival and proliferation of malignant B cells.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Irreversibly inhibits Bruton's tyrosine kinase (BTK), a key enzyme in the B-cell receptor signaling pathway that drives the survival and proliferation of malignant B cells.

Estrutura 2D

SVG PNG

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SMILES

C=CC(=O)N1C[C@H](Nc2ncnc3[nH]ccc23)CC[C@@H]1C

InChI

InChI=1S/C15H19N5O/c1-3-13(21)20-8-11(5-4-10(20)2)19-15-12-6-7-16-14(12)17-9-18-15/h3,6-7,9-11H,1,4-5,8H2,2H3,(H2,16,17,18,19)/t10-,11+/m0/s1

Molecular Formula

C15H19N5O

HBD / HBA

2 / 4

Ligações Rotacionáveis

3

Átomos Pesados

21

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

Ritlecitinib is an irreversible covalent inhibitor of JAK3 and the TEC family of kinases (including ITK, RLK, BTK, BMX, and TXK) that blocks signaling from multiple pro-inflammatory cytokines through the JAK3/STAT pathway and T-cell receptor signaling through the TEC kinase pathway. It is approved for the treatment of alopecia areata in adults and adolescents, and is under investigation in other immune-mediated inflammatory conditions.

Irreversibly inhibits Bruton's tyrosine kinase (BTK), a key enzyme in the B-cell receptor signaling pathway that drives the survival and proliferation of malignant B cells.

Yes, Ritlecitinib 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). CHEMBL4085457. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 118115473. 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.