Basic Information

Drug ID DDPD01171 ...
Drug Name Moclobemide
Molecular Weight 268.739
Molecular Formula C13H17ClN2O2
CAS Number 71320-77-9
SMILES [H]C1COCCN1CCNC(=O)C1=CC=C(Cl)C=C1
External Links
DRUGBANK DB01171
T3DB T3D3004
PubChem Compound 4235

Experimental Physicochemical Property

Property Name Property Value Unit Raw Value Raw Unit Reference
Log P 10.6 - 10.6 - DRUGBANK
Boiling Point 377.0 377 DRUGBANK
Melting Point 132.0 132 DRUGBANK
Water Solubility 0.000352 mg/L 0.000352 mg/L DRUGBANK
pKa 10.6 - 10.6 - DRUGBANK

Pharmacokinetic/ Toxicokinetic Property

Property Name Property Value Unit Raw Value Raw Unit Annotation Reference
Absorption 95.0 % >95 % PO, oral; DRUGBANK
Bioavailability 56.0 % 56 % PO, oral; DRUGBANK
Bioavailability 90.0 % 90 % PO, oral; increasing doses; DRUGBANK
T Max 0.65 h 0.3-1 h PO, oral; DRUGBANK
Metabolic 100.0 % ~100 % Liver metabolism; DRUGBANK
Clearance 54.0 L/h 30-78 L/h Urinary excretion; DRUGBANK
Clearance 0.60 L/h/kg 10 ml/min/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Volume of Distribution 1.3 L/kg 1-1.5 L/kg DRUGBANK
Volume of Distribution 1.1 L/kg 1.1 L/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Half-life 1.5 h 1-2 h DRUGBANK
Half-life 4.0 h 4 h Hepatitis, Hep; DRUGBANK
Half-life 1.5 h 1.5 h intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Toxicity LD50 730.0 mg/kg 730.0 mg/kg mouse; DRUGBANK
Toxicity LD50 1300.0 mg/kg 1300.0 mg/kg Rattus, Rat; DRUGBANK
Toxicity LD50 730.0 mg/kg 730.0 mg/kg mouse; T3DB
Toxicity LD50 1300.0 mg/kg 1300.0 mg/kg Rattus, Rat; T3DB
Eliminate Route 100.0 % ~100 % Urinary excretion; DRUGBANK
Protein Binding 50.0 % ~50 % DRUGBANK

Maximum Dosage

Not Available

Drug Property Radar Chart

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Note: Center: Q1-1.5*IQR, Edge: Q3+1.5*IQR; Q1: Quantile 1, Q3: Quantile 3, IQR: Q3-Q1