Belinostat
A histone deacetylase (HDAC) inhibitor that alters gene expression in cancer cells by preventing the removal of acetyl groups from histones, reactivating tumor suppressor genes and promoting cancer cell death. It is approved for relapsed or refractory peripheral T-cell lymphoma.
分子量
318.3000 g/mol
LogP
1.70
TPSA
104.00 Ų
Lipinski 五规则
符合
治疗领域
Pharmacokinetics (PK)
Pharmacodynamics (PD)
二维结构
Cite this structure
Embed this structure
SMILES
O=C(/C=C/c1cccc(S(=O)(=O)Nc2ccccc2)c1)NO
InChI
InChI=1S/C15H14N2O4S/c18-15(16-19)10-9-12-5-4-8-14(11-12)22(20,21)17-13-6-2-1-3-7-13/h1-11,17,19H,(H,16,18)/b10-9+
Molecular Formula
C15H14N2O4S
HBD / HBA
3 / 5
可旋转键数
5
重原子数
22
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.
常见问题
A histone deacetylase (HDAC) inhibitor that alters gene expression in cancer cells by preventing the removal of acetyl groups from histones, reactivating tumor suppressor genes and promoting cancer cell death. It is approved for relapsed or refractory peripheral T-cell lymphoma.
Yes, Belinostat is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL408513. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6918638. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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