oxyphenisatine acetate 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | PK/Tox | Related Drugs | BioActivity |

Stem definitionDrug idCAS RN
2037 115-33-3

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • oxyphenisatine acetate
  • acetphenolisatinum
  • phenlaxinum
  • oxyphenisatin acetate
  • acelax
  • acetalax
  • acetophenolisatin
  • bisatin
  • brocatine
  • diacetyldihydroxydiphenylisatin
  • diacetyldioxyphenylisatin
  • diacetyldiphenolisatin
  • diasatin
  • diasatine
  • diphesatin
  • diphesatine
  • oxyphenisatin diacetate
  • phenlaxine
A laxative that undergoes enterohepatic circulation. It may cause jaundice.
  • Molecular weight: 401.42
  • Formula: C24H19NO5
  • CLOGP: 2.52
  • LIPINSKI: 0
  • HAC: 6
  • HDO: 1
  • TPSA: 81.70
  • ALOGS: -5.91
  • ROTB: 6

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 3.321 High 1
caco2-efflux Caco-2 efflux ratio (BA/AB) 2.985 High 1
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 20.941 10^-6 cm/s High 1
dh-clint Dog hepatocyte intrinsic clearance 149.624 uL/min/10^6 cells High 1
dppb Dog plasma protein binding (% unbound) 1.120 % High 1
fcs-ppb Fetal calf serum protein binding (% unbound) 1.980 % High 1
herg hERG pIC50 5.253 pIC50 High 1
hh-clint Human hepatocyte intrinsic clearance 273.527 uL/min/10^6 cells High 1
hlm-clint Human liver microsomal intrinsic clearance 261.216 uL/min/mg protein High 1
hppb Human plasma protein binding (% unbound) 0.810 % High 1
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 5.929 High 1
mh-clint Mouse hepatocyte intrinsic clearance 267.301 High 1
mppb Mouse plasma protein binding (% unbound) 1.220 High 1
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 15.136 High 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 2.560 % High 1
rh-clint Rat hepatocyte intrinsic clearance 301.995 uL/min/10^6 cells High 1
rh-fuinc Rat hepatocyte fraction unbound in incubation 26.950 % High 1
rppb Rat plasma protein binding (% unbound) 0.730 % High 1
solubility-dd Solubility at pH 7.4 in DMSO 1.197 uM High 1

Approvals:

None

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 D002400 Cathartics
MeSH PA D005765 Gastrointestinal Agents
CHEBI has role CHEBI:50503 laxative

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

DiseaseRelationSNOMED_IDDOID
Constipation indication 14760008 DOID:2089




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 10.07 acidic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
D05320 KEGG_DRUG
C0030080 UMLSCUI
CHEBI:135638 CHEBI
CHEMBL1402684 ChEMBL_ID
8269 PUBCHEM_CID
DB14627 DRUGBANK_ID
8136 RXNORM
004457 NDDF
346604000 SNOMEDCT_US
D010114 MESH_DESCRIPTOR_UI
C0031422 UMLSCUI
DB04823 DRUGBANK_ID
31315 PUBCHEM_CID
U0Y1YAL65X UNII
CHEBI:135358 CHEBI

Pharmaceutical products:

None