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

Stem definitionDrug idCAS RN
68 5355-48-6

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • acetyldigoxin
  • novodigal
  • beta-Acetyldigoxin
  • beta acetyldigoxin
Alpha- or beta-acetyl derivatives of DIGOXIN or lanatoside C from Digitalis lanata. They are better absorbed and longer acting than digoxin and are used in congestive heart failure.
  • Molecular weight: 822.99
  • Formula: C43H66O15
  • CLOGP: 1.99
  • LIPINSKI: 2
  • HAC: 15
  • HDO: 5
  • TPSA: 209.13
  • ALOGS: -4.08
  • ROTB: 9

Drug dosage:

DoseUnitRoute
0.50 mg O

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 1.606 High 0.88
caco2-efflux Caco-2 efflux ratio (BA/AB) 22.646 High 0.88
herg hERG pIC50 4.417 pIC50 High 0.88
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 11.324 10^-6 cm/s High 0.88
dh-clint Dog hepatocyte intrinsic clearance 3.206 uL/min/10^6 cells High 0.88
dppb Dog plasma protein binding (% unbound) 47.180 % High 0.88
fcs-ppb Fetal calf serum protein binding (% unbound) 41.230 % High 0.88
hh-clint Human hepatocyte intrinsic clearance 1.706 uL/min/10^6 cells High 0.88
hlm-clint Human liver microsomal intrinsic clearance 5.794 uL/min/mg protein High 0.88
hppb Human plasma protein binding (% unbound) 49.710 % High 0.88
kinase-safety-class ACVR2B,CDK5,EIF2AK3,GRK2,ITK,PDK1,PDK2,PRKDC 8
mdck-mdr1-bcrp-efflux MDCK-MDR1-BCRP efflux ratio 9.550 High 0.84
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 27.040 High 0.88
mh-clint Mouse hepatocyte intrinsic clearance 7.079 High 0.88
mppb Mouse plasma protein binding (% unbound) 34.110 High 0.88
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 39.537 High 0.88
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pld-class Phospholipidosis risk class (1 = positive, 0 = negative) 1 High 0.84
pppb Pig plasma protein binding (% unbound) 43.080 % High 0.88
rat-kpuu-brain Rat brain Kpuu 0.011 % High 0.84
rh-clint Rat hepatocyte intrinsic clearance 3.281 uL/min/10^6 cells High 0.88
rh-fuinc Rat hepatocyte fraction unbound in incubation 71.570 % High 0.88
rppb Rat plasma protein binding (% unbound) 41.060 % High 0.88
solubility-dd Solubility at pH 7.4 in DMSO 770.903 uM High 0.88

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
ATC C01AA02 CARDIOVASCULAR SYSTEM
CARDIAC THERAPY
CARDIAC GLYCOSIDES
Digitalis glycosides
ATC C01AA52 CARDIOVASCULAR SYSTEM
CARDIAC THERAPY
CARDIAC GLYCOSIDES
Digitalis glycosides
MeSH PA D000889 Anti-Arrhythmia Agents
MeSH PA D002316 Cardiotonic Agents
MeSH PA D002317 Cardiovascular Agents
MeSH PA D004791 Enzyme Inhibitors
MeSH PA D020011 Protective Agents

Related Drugs by ATC class:

C01AA Digitalis glycosides 7 drugs

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

None

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
N0000168451 NUI
199 RXNORM
C0001050 UMLSCUI
CHEMBL2074725 ChEMBL_ID
DB13691 DRUGBANK_ID
11765960 PUBCHEM_CID
D000113 MESH_DESCRIPTOR_UI
CHEBI:135892 CHEBI
P7K44M64CW UNII
007426 NDDF

Pharmaceutical products:

None