Basic Information

Drug ID DDPD00758 ...
Drug Name Clopidogrel
Molecular Weight 321.822
Molecular Formula C16H16ClNO2S
CAS Number 113665-84-2
SMILES [H][C@@](N1CCC2=C(C1)C=CS2)(C(=O)OC)C1=CC=CC=C1Cl
External Links
DRUGBANK DB00758
PubChem Compound 60606
PDR 525
Drugs.com Drugs.com Drug Page

Experimental Physicochemical Property

Property Name Property Value Unit Raw Value Raw Unit Reference
Melting Point 158.0 ℃ 158 ℃ http://www.chemspider.com/Chemical-Structure.54632.html?rid=9b9b483b-9db2-454c-a1be-2494307b6b23&page_num=0

Pharmacokinetic/ Toxicokinetic Property

Property Name Property Value Unit Raw Value Raw Unit Annotation Reference
Absorption 50.0 % 50 % PO, oral; DRUGBANK
AUC 45.1 ng.h/ml 45.1±16.2 ng.h/ml PO, oral; poor metabolizers, PM; DRUGBANK
AUC 104.3 ng.h/ml 104.3±57.3 ng.h/ml PO, oral; high-fat meal; DRUGBANK
C Max 2.0 ng/ml 2.01±2.0 ng/ml PO, oral; DRUGBANK
C Max 31.3 ng/ml 31.3±13 ng/ml PO, oral; poor metabolizers, PM; DRUGBANK
C Max 60.8 ng/ml 60.8±34.3 ng/ml PO, oral; high-fat meal; DRUGBANK
T Max 0.75 h 0.5-1 h PO, oral; Active metabolite; DRUGBANK
T Max 1.4 h 1.40±1.07 h PO, oral; DRUGBANK
Metabolic 85.0 % 80-90 % Liver metabolism; PO, oral; Inactive metabolite; DRUGBANK
Clearance 18960.0 L/h 18960±15890 L/h PO, oral; DRUGBANK
Clearance 16980.0 L/h 16980±10410 L/h PO, oral; DRUGBANK
Clearance 1.4 L/h/kg 23.65 ml/min/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Volume of Distribution 39240.0 L 39240±33520 L Apparent volume of distribution; DRUGBANK
Volume of Distribution 2.0 L/kg 2.01 L/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Half-life 6.0 h ~6 h PO, oral; DRUGBANK
Half-life 0.50 h ~30 min Active metabolite; DRUGBANK
Half-life 5.1 h 5.06 h intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Toxicity Lethal Dose 1750.0 mg/kg 1500-2000 mg/kg Single dose; mouse; Rattus, Rat; DRUGBANK
Toxicity Lethal Dose 3000.0 mg/kg 3000.0 mg/kg Single dose; non-human primate; DRUGBANK
Eliminate Route 50.0 % 50 % Urinary excretion; PO, oral; DRUGBANK
Eliminate Route 46.0 % 46 % Faeces excretion; PO, oral; DRUGBANK
Protein Binding 98.0 % 98 % plasma proteins; DRUGBANK
Protein Binding 78.3 % 71-85.5 % cow; DRUGBANK

Maximum Dosage

Property Name Property Value Unit Raw Value Raw Unit Annotation Brand Name Component Reference
Max dose for neonates 0.2 mg/kg/day 0.2 mg/kg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for infants 0.2 mg/kg/day 0.2 mg/kg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for children 6.0 mg/kg/day 6 mg/kg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for children 75.0 mg/day 75 mg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for children 0.2 mg/kg/day 0.2 mg/kg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for adolescents 6.0 mg/kg/day 6 mg/kg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for adolescents 75.0 mg/day 75 mg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for adults 75.0 mg/day 75 mg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for adults 600.0 mg 600 mg PO, oral Plavix clopidogrel bisulfate PDR
Max dose for geriatric 75.0 mg/day 75 mg/day PO, oral Plavix clopidogrel bisulfate PDR
Max dose for geriatric 600.0 mg 600 mg PO, oral Plavix clopidogrel bisulfate PDR

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