Acalabrutinib Maleate

CHEMBL4594293 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
581.6 g/mol
LogP
Phase
4

The maleate salt formulation of acalabrutinib, a BTK inhibitor used to treat B-cell blood cancers with the same mechanism of action and safety profile as acalabrutinib. It is taken orally twice daily and should not be combined with strong acid-reducing agents that can impair its absorption. Monitoring for cardiac rhythm disturbances and bleeding is recommended throughout therapy.

Peso Molecular

581,6000 g/mol

TPSA

193,00 Ų

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

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SMILES

CC#CC(=O)N1CCC[C@H]1c1nc(-c2ccc(C(=O)Nc3ccccn3)cc2)c2c(N)nccn12.O=C(O)/C=C\C(=O)O

InChI

InChI=1S/C26H23N7O2.C4H4O4/c1-2-6-21(34)32-15-5-7-19(32)25-31-22(23-24(27)29-14-16-33(23)25)17-9-11-18(12-10-17)26(35)30-20-8-3-4-13-28-20;5-3(6)1-2-4(7)8/h3-4,8-14,16,19H,5,7,15H2,1H3,(H2,27,29)(H,28,30,35);1-2H,(H,5,6)(H,7,8)/b;2-1-/t19-;/m0./s1

Molecular Formula

C30H27N7O6

HBD / HBA

4 / 10

Ligações Rotacionáveis

6

Átomos Pesados

43

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

The maleate salt formulation of acalabrutinib, a BTK inhibitor used to treat B-cell blood cancers with the same mechanism of action and safety profile as acalabrutinib. It is taken orally twice daily and should not be combined with strong acid-reducing agents that can impair its absorption. Monitoring for cardiac rhythm disturbances and bleeding is recommended throughout therapy.

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, Acalabrutinib Maleate 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). CHEMBL4594293. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 126506029. Chemical information database.

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

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.