fluprostenol 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
prostaglandins 5546 40666-16-8

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • fluprostenol
  • fluoprostenol
  • ICI-81008
  • fluprostenol sodium
Synthetic prostaglandin alpha analog used as an abortifacient
  • Molecular weight: 458.47
  • Formula: C23H29F3O6
  • CLOGP: 2.71
  • LIPINSKI: 0
  • HAC: 6
  • HDO: 4
  • TPSA: 107.22
  • ALOGS: -4.45
  • ROTB: 12

Drug dosage:

None

ADMET properties:

None

Approvals:

DateAgencyCompanyOrphan
None FDA

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
MeSH PA D003270 Contraceptive Agents
MeSH PA D003271 Contraceptive Agents, Female
MeSH PA D000080066 Contraceptive Agents, Hormonal
MeSH PA D008186 Luteolytic Agents
MeSH PA D012102 Reproductive Control Agents
CHEBI has role CHEBI:35674 antihypertensive drugs
CHEBI has role CHEBI:39456 antiglaucoma agent
CHEBI has role CHEBI:49324 female contraceptive drugs
CHEBI has role CHEBI:50691 abortifacient drug
CHEBI has role CHEBI:66900 prostaglandin receptor agonists

Drug Use | Suggest Off label Use Form| |View source of the data|

None




🐶 Veterinary Drug Use

SpeciesUseRelation
Horses Control the timing of estrus in estrous cycling and in clinically anestrous mares that have a corpus luteum Indication

🐶 Veterinary products

ProductApplicantIngredients
Equimate Elanco US Inc. 1

Acid dissociation constants calculated using MoKa v3.0.0

None

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Prostaglandin E2 receptor EP3 subtype GPCR AGONIST Ki 6.15 IUPHAR
Prostaglandin F2-alpha receptor GPCR AGONIST Ki 8.60 IUPHAR

External reference:

IDSource
CHEBI:60782 CHEBI
CHEMBL1201379 ChEMBL_ID
C006326 MESH_SUPPLEMENTAL_RECORD_UI
1940 IUPHAR_LIGAND_ID
DB11519 DRUGBANK_ID
C0060587 UMLSCUI
CHEMBL2107435 ChEMBL_ID
3794 INN_ID
96354004 SNOMEDCT_US
55028-71-2 SECONDARY_CAS_RN
KEGG_DRUG
5311100 PUBCHEM_CID
358S7VUE5N UNII

Pharmaceutical products:

None