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

Stem definitionDrug idCAS RN
prostaglandins 2538 60325-46-4

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • sulproston
  • sulprostone
  • Molecular weight: 465.56
  • Formula: C23H31NO7S
  • CLOGP: 0.18
  • LIPINSKI: 0
  • HAC: 8
  • HDO: 3
  • TPSA: 130
  • ALOGS: -4.20
  • ROTB: 11

Drug dosage:

DoseUnitRoute
0.50 mg P

ADMET properties:

None

Approvals:

None

FDA Adverse Event Reporting System (Female)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Renal cortical necrosis 101.83 94.33 10 63 120 63488829

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC G02AD05 GENITO URINARY SYSTEM AND SEX HORMONES
OTHER GYNECOLOGICALS
UTEROTONICS
Prostaglandins
MeSH PA D000019 Abortifacient Agents
MeSH PA D000020 Abortifacient Agents, Nonsteroidal
MeSH PA D003270 Contraceptive Agents
MeSH PA D003271 Contraceptive Agents, Female
MeSH PA D000080066 Contraceptive Agents, Hormonal
MeSH PA D008600 Menstruation-Inducing Agents
MeSH PA D012102 Reproductive Control Agents

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

None




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 4.5 acidic

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 EP1 subtype GPCR AGONIST Ki 7 IUPHAR
Prostaglandin E2 receptor EP3 subtype GPCR AGONIST Ki 9.46 IUPHAR
Prostaglandin E2 receptor EP4 subtype GPCR Ki 5.11 PDSP
Prostaglandin F2-alpha receptor GPCR AGONIST Ki 6.70 IUPHAR
Prostaglandin E2 receptor EP1 subtype GPCR AGONIST Ki 7.70 IUPHAR
Prostaglandin E2 receptor EP3 subtype GPCR AGONIST Ki 9.20 IUPHAR
Prostaglandin E2 receptor EP3 subtype GPCR AGONIST EC50 9.38 IUPHAR
Prostaglandin E2 receptor EP1 subtype GPCR AGONIST Ki 7 IUPHAR

External reference:

IDSource
D02725 KEGG_DRUG
C0075628 UMLSCUI
CHEBI:135755 CHEBI
CHEMBL1472830 ChEMBL_ID
DB12708 DRUGBANK_ID
C016767 MESH_SUPPLEMENTAL_RECORD_UI
1919 IUPHAR_LIGAND_ID
4243 INN_ID
501Q5EQ1GM UNII
5312153 PUBCHEM_CID
005342 NDDF
713461008 SNOMEDCT_US

Pharmaceutical products:

None