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

Stem definitionDrug idCAS RN
3747 522-24-7

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • fenethazine
  • phenetazine
  • phenethazine
  • phenethazinum
  • rutergan
  • Molecular weight: 270.39
  • Formula: C16H18N2S
  • CLOGP: 4.29
  • LIPINSKI: 0
  • HAC: 2
  • HDO: 0
  • TPSA: 6.48
  • ALOGS: -3.78
  • ROTB: 3

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 3.038 High 0.81
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.310 High 0.81
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 29.923 10^-6 cm/s High 0.81
dh-clint Dog hepatocyte intrinsic clearance 79.250 uL/min/10^6 cells High 0.81
dppb Dog plasma protein binding (% unbound) 6.630 % High 0.81
fcs-ppb Fetal calf serum protein binding (% unbound) 11.980 % High 0.81
herg hERG pIC50 5.554 pIC50 High 0.81
hh-clint Human hepatocyte intrinsic clearance 12.764 uL/min/10^6 cells High 0.81
hlm-clint Human liver microsomal intrinsic clearance 29.854 uL/min/mg protein High 0.81
hppb Human plasma protein binding (% unbound) 6.010 % High 0.81
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 0.209 High 0.81
mh-clint Mouse hepatocyte intrinsic clearance 278.612 High 0.81
mppb Mouse plasma protein binding (% unbound) 6.670 High 0.81
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 0.794 High 0.81
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 17.580 % High 0.81
rh-clint Rat hepatocyte intrinsic clearance 307.610 uL/min/10^6 cells High 0.81
rh-fuinc Rat hepatocyte fraction unbound in incubation 47.300 % High 0.81
rppb Rat plasma protein binding (% unbound) 6.260 % High 0.81
solubility-dd Solubility at pH 7.4 in DMSO 622.300 uM High 0.81

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:

None

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 9.04 Basic
pKa2 3.55 Basic

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
Lysine-specific histone demethylase 1A Enzyme IC50 5.48 CHEMBL

External reference:

IDSource
D02602 KEGG_DRUG
C0060166 UMLSCUI
CHEBI:135112 CHEBI
CHEMBL2106299 ChEMBL_ID
C014551 MESH_SUPPLEMENTAL_RECORD_UI
68223 PUBCHEM_CID
1860 INN_ID
8J97CUZ4HX UNII

Pharmaceutical products:

None