Fospropofol

drug
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Summary

Fospropofol (CHEMBL1201766) is an approved small molecule; indicated across 38 conditions including atrial fibrillation and hypertensive disorder.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Indications: 38 conditions
  • Clinical trials: 7
  • Chemistry: 288.28 Da · C13H21O5P

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1201766
NameFospropofol
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID3038498
Molecular formulaC13H21O5P
Molecular weight288.28
InChIKeyQVNNONOFASOXQV-UHFFFAOYSA-N

SMILES: CC(C)C1=C(C(=CC=C1)C(C)C)OCOP(=O)(O)O

IUPAC name: [2,6-di(propan-2-yl)phenoxy]methyl dihydrogen phosphate

Also known as: Fospropofol, FOSPROPOFOL

Parent form; salt/anhydrous children: CHEMBL2021422

Patent coverage: 78 distinct patent families (175 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

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

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

Indications & clinical

Indications

38 indications (0 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
atrial fibrillation3MONDO:0004981EFO:0000275
hypertensive disorder3MONDO:0005044EFO:0000537
severe acute respiratory syndrome3MONDO:0005091EFO:0000694
stroke disorder3MONDO:0005098EFO:0000712
subarachnoid hemorrhage3MONDO:0005099EFO:0000713
obesity disorder3MONDO:0011122EFO:0001073
cirrhosis of liver3MONDO:0005155EFO:0001422
ischemia reperfusion injury3MONDO:0005203EFO:0002687
heart disorder3MONDO:0005267EFO:0003777
male reproductive organ cancer3MONDO:0005836EFO:0007355
delirium3MONDO:0045057EFO:0009267
acute respiratory distress syndrome3MONDO:0006502EFO:1000637
respiratory failure3MONDO:0021113HP:0002093
brain injury3MONDO:0043510MONDO:0043510
coronary artery disorder2MONDO:0005010EFO:0001645
injury2MONDO:0021178EFO:0000546
leukemia2MONDO:0005059EFO:0000565
hypotensive disorder2MONDO:0005468EFO:0005251
colon adenocarcinoma2MONDO:0002271EFO:1001949
tonsillitis2MONDO:0001039MONDO:0001039
neoplasm2MONDO:0005070MONDO:0004992
migraine disorder2MONDO:0005277MONDO:0005277
morbid obesity1MONDO:0005139EFO:0001074
chronic kidney disease1MONDO:0005300EFO:0003884
tethered spinal cord syndrome1MONDO:0006995EFO:1001210
kidney failure1MONDO:0001106EFO:1002048
colorectal neoplasm1MONDO:0005335MONDO:0005575
depressive disorder0MONDO:0002050MONDO:0002050

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

Clinical trials

Total trials: 7.

Phase distribution

PhaseTrials
PHASE44
Not specified2
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06251999PHASE4NOT_YET_RECRUITINGEfficacy and Safety of Fospropofol for Same-day Bidirectional Endoscopy in Elderly Patients
NCT06573489PHASE4RECRUITINGEfficacy and Safety of Fospropofol in Adult Laparoscopic Surgery: A Clinical Trial
NCT01401049PHASE4COMPLETEDPreventing Propofol Injection Pain: Prospective Randomized Trial Comparing Propofol Versus Fospropofol
NCT06344325PHASE4COMPLETEDED90 of Fospropofol Disodium in Induction and Maintenance of Anesthesia
NCT00209521PHASE2COMPLETEDComparison of AQUAVAN® Injection to DISOPRIVAN® Injectable Emulsion for Anesthesia During Coronary Artery Surgery
NCT01289483Not specifiedWITHDRAWNFospropofol for Sedation During Elective Awake Intubation
NCT06261996Not specifiedCOMPLETEDSafety and Efficacy of Fospropofol vs Propofol During Invasive Mechanical Ventilation.

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).