Zanubrutinib

CHEMBL3936761 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
471.5 g/mol
LogP
3.5
Phase
4

This oral BTK (Bruton's tyrosine kinase) inhibitor is used to treat certain types of blood cancers including chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), Waldenström's macroglobulinemia, and mantle cell lymphoma. It works by blocking the BTK enzyme that B-cell cancers depend on for their growth and survival signals. Compared to earlier BTK inhibitors, it is designed to be more selective in order to reduce off-target side effects.

Peso Molecular

471,5000 g/mol

LogP

3,50

TPSA

102,00 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

Cite this structure


                        

Embed this structure


                        

SMILES

C=CC(=O)N1CCC([C@@H]2CCNc3c(C(N)=O)c(-c4ccc(Oc5ccccc5)cc4)nn32)CC1

InChI

InChI=1S/C27H29N5O3/c1-2-23(33)31-16-13-18(14-17-31)22-12-15-29-27-24(26(28)34)25(30-32(22)27)19-8-10-21(11-9-19)35-20-6-4-3-5-7-20/h2-11,18,22,29H,1,12-17H2,(H2,28,34)/t22-/m0/s1

Molecular Formula

C27H29N5O3

HBD / HBA

2 / 5

Ligações Rotacionáveis

6

Átomos Pesados

35

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 BTK (Bruton's tyrosine kinase) inhibitor is used to treat certain types of blood cancers including chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), Waldenström's macroglobulinemia, and mantle cell lymphoma. It works by blocking the BTK enzyme that B-cell cancers depend on for their growth and survival signals. Compared to earlier BTK inhibitors, it is designed to be more selective in order to reduce off-target side effects.

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, Zanubrutinib 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). CHEMBL3936761. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 135565884. 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.