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

Stem definitionDrug idCAS RN
193 75558-90-6

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • amperozide
  • Molecular weight: 401.50
  • Formula: C23H29F2N3O
  • CLOGP: 5.37
  • LIPINSKI: 1
  • HAC: 4
  • HDO: 1
  • TPSA: 35.58
  • ALOGS: -4.49
  • ROTB: 7

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 4.123 Moderate 0.66
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.867 Moderate 0.66
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 32.211 10^-6 cm/s Moderate 0.66
dh-clint Dog hepatocyte intrinsic clearance 14.125 uL/min/10^6 cells Moderate 0.66
dppb Dog plasma protein binding (% unbound) 1.080 % Moderate 0.66
fcs-ppb Fetal calf serum protein binding (% unbound) 4.150 % Moderate 0.66
herg hERG pIC50 6.067 pIC50 Moderate 0.66
hh-clint Human hepatocyte intrinsic clearance 7.464 uL/min/10^6 cells Moderate 0.66
hlm-clint Human liver microsomal intrinsic clearance 82.414 uL/min/mg protein Moderate 0.66
hppb Human plasma protein binding (% unbound) 1.180 % Moderate 0.66
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 0.998 Moderate 0.66
mh-clint Mouse hepatocyte intrinsic clearance 45.186 Moderate 0.66
mppb Mouse plasma protein binding (% unbound) 1.120 Moderate 0.66
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 4.989 Moderate 0.66
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 3.030 % Moderate 0.66
rh-clint Rat hepatocyte intrinsic clearance 102.565 uL/min/10^6 cells Moderate 0.66
rh-fuinc Rat hepatocyte fraction unbound in incubation 12.630 % Moderate 0.66
rppb Rat plasma protein binding (% unbound) 0.900 % Moderate 0.66
solubility-dd Solubility at pH 7.4 in DMSO 21.184 uM Moderate 0.66

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 D002491 Central Nervous System Agents
MeSH PA D002492 Central Nervous System Depressants
MeSH PA D011619 Psychotropic Drugs
MeSH PA D012702 Serotonin Antagonists
MeSH PA D014149 Tranquilizing Agents
MeSH PA D014150 Antipsychotic Agents
MeSH PA D018377 Neurotransmitter Agents
MeSH PA D018490 Serotonin Agents
CHEBI has role CHEBI:35474 anxiolytic drug
CHEBI has role CHEBI:48279 serotonergic antagonist
CHEBI has role CHEBI:51039 dopamine uptake inhibitor
CHEBI has role CHEBI:65191 second generation antipsychotic
CHEBI has role CHEBI:176497 geroprotector

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 12.94 acidic
pKa2 8.09 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
Fatty-acid amide hydrolase 1 Enzyme IC50 6.34 CHEMBL
5-hydroxytryptamine receptor 6 GPCR Ki 5.80 PDSP

External reference:

IDSource
C0051747 UMLSCUI
CHEBI:180480 CHEBI
CHEMBL1079935 ChEMBL_ID
DB08927 DRUGBANK_ID
C049058 MESH_SUPPLEMENTAL_RECORD_UI
73333 PUBCHEM_CID
5033 INN_ID
0M2W3TAG39 UNII
0M2W3TAG39 INXIGHT DRUGS

Pharmaceutical products:

None