Feprazone

drug
On this page

Also known as DA 2370DA-2370FeprazonaSID26758004SID144205761SID170465969

Summary

Feprazone (CHEMBL1452696) is an approved small molecule (ATC M02AA16); indicated across 3 conditions including rheumatic disorder.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: M02AA16 (+2 more)
  • Indications: 3 conditions
  • Chemistry: 320.4 Da · C20H20N2O2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1452696
NameFeprazone
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID35455
ATCM02AA16, M01AX18, M01AX68
Molecular formulaC20H20N2O2
Molecular weight320.4
InChIKeyRBBWCVQDXDFISW-UHFFFAOYSA-N

SMILES: CC(=CCC1C(=O)N(N(C1=O)C2=CC=CC=C2)C3=CC=CC=C3)C

IUPAC name: 4-(3-methylbut-2-enyl)-1,2-diphenylpyrazolidine-3,5-dione

Also known as: DA 2370, DA-2370, Feprazona, Feprazone, SID26758004, SID144205761, FEPRAZONE, SID170465969, feprazone

Patent coverage: 2,428 distinct patent families (9,738 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 4 (assay-derived). Sample: Nuclear receptor ROR-gamma, Prelamin-A/C, Prostaglandin G/H synthase 1, Bile salt export pump.

Bioactivity

ChEMBL activities: 1 potent at pChembl ≥ 5 of 4 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
PTGS16.58AC50260nMCHEMBL_ACT_25205277

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

3 indications (3 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
rheumatic disorder4MONDO:0005554EFO:0005755

2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 0.

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).