Drugs Information:
Belinostat
Basic Information
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ID | DDInter174 | |
Drug Type | small molecule | |
Molecular Formula | C15H14N2O4S | |
Molecular Weight | 318.350 | |
CAS Number | 866323-14-0 | |
Description | Belinostat is a novel agent that inhibits the enzyme histone deacetylase (HDAC) with a sulfonamide-hydroxamide structure. It was developed as an orphan drug to target hematological malignancies and solid tumors by TopoTarget. The safety and efficacy of belinostat is currently being evaluated for use in combination with traditional front-line therapies for the treatment of PTCL. Intravenous administration of the agent is available as Beleodaq as monotherapy and the dosing regimen involves a 21-day cycle. It was US-approved in July 2014 as a therapeutic agent for relapsed or refractory peripheral T-cell lymphoma. | |
ATC Classification | L01XH04 | |
IUPAC Name | (2E)-N-hydroxy-3-[3-(phenylsulfamoyl)phenyl]prop-2-enamide | |
InChI | NCNRHFGMJRPRSK-MDZDMXLPSA-N | |
Canonical SMILES | ONC(=O)\C=C\C1=CC=CC(=C1)S(=O)(=O)NC1=CC=CC=C1 | |
Useful Links | DrugBank ChEBI PubChem Substance ChemSpider BindingDB Wikipedia ChEMBL ZINC |
Interactions with
Belinostat
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