Phenoxypropazine
drugOn this page
Also known as FenoxipropazinaFenoxypropazineFENOXYPROPAZONESID144206870
Summary
Phenoxypropazine (CHEMBL1909286) is an approved small molecule.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Chemistry: 166.22 Da · C9H14N2O
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1909286 |
| Name | Phenoxypropazine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 71467 |
| Molecular formula | C9H14N2O |
| Molecular weight | 166.22 |
| InChIKey | QNEXFJFTGQBXBJ-UHFFFAOYSA-N |
SMILES: CC(COC1=CC=CC=C1)NN
IUPAC name: 1-phenoxypropan-2-ylhydrazine
Also known as: Fenoxipropazina, Fenoxypropazine, Phenoxypropazine, phenoxypropazine, FENOXYPROPAZONE, SID144206870, PHENOXYPROPAZINE, fenoxypropazine
Parent form; salt/anhydrous children: CHEMBL4303424
Patent coverage: 218 distinct patent families (602 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: 2 (assay-derived). Sample: Amine oxidase [flavin-containing] A, Prostaglandin G/H synthase 1.
Bioactivity
ChEMBL activities: 2 potent at pChembl ≥ 5 of 3 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| PTGS1 | 6.43 | AC50 | 371.3 | nM | CHEMBL_ACT_25206419 |
| PTGS1 | 6.4 | AC50 | 395.3 | nM | CHEMBL_ACT_25205489 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
0 indications (0 at ChEMBL trial phase 4).
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.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.