Basic Information

Drug ID DDPD00175 ...
Drug Name Pravastatin
Molecular Weight 424.5277
Molecular Formula C23H36O7
CAS Number 81093-37-0
SMILES [H][C@]12[C@H](C[C@H](O)C=C1C=C[C@H](C)[C@@H]2CC[C@@H](O)C[C@@H](O)CC(O)=O)OC(=O)[C@@H](C)CC
External Links
DRUGBANK DB00175
PubChem Compound 54687
PDR 3511
Drugs.com Drugs.com Drug Page

Experimental Physicochemical Property

Property Name Property Value Unit Raw Value Raw Unit Reference
Log P 0.59 - 0.59 - 'MSDS'
Boiling Point 600.0 >600 'MSDS'
Melting Point 172.1 171.2-173 'MSDS'
Water Solubility 10000.0 mg/L 10 mg/ml 'MSDS'
pKa 4.2 - 4.2 - Dinnekere V. et al. 2016. Scientifica.

Pharmacokinetic/ Toxicokinetic Property

Property Name Property Value Unit Raw Value Raw Unit Annotation Factor Reference
AUC 75.0 ng.h/ml 60-90 mcg.h/L PO, oral; DRUGBANK
Bioavailability 17.0 % 17.0 % PO, oral; DRUGBANK
Bioavailability 18.0 % 18±8 % Oral single dose; The Pharmacological Basis of Therapeutics
C Max 42.5 ng/ml 30-55 mcg/L PO, oral; DRUGBANK
C Max 33.0 ng/ml 28-38 ng/ml Oral single dose; The Pharmacological Basis of Therapeutics
T Max 1.3 h 1-1.5 h PO, oral; DRUGBANK
T Max 1.2 h 1-1.4 h Oral single dose; The Pharmacological Basis of Therapeutics
Clearance 0.59 L/h/kg 6.3-13.5 ml/min/kg adults; DRUGBANK
Clearance 450.0 L/h 4.0-11 L/min Children; DRUGBANK
Clearance 0.81 L/h/kg 13.5±2.4 ml/min/kg Elderly → ;Hepatic cirrhosis, cirr ↓ ;RD, renal impairment, Renal disease,including uremia ↓ ; The Pharmacological Basis of Therapeutics
Volume of Distribution 0.50 L/kg 0.5 L/kg DRUGBANK
Volume of Distribution 0.0340 L/kg 31-37 mL/kg Steady state volume of distribution; Children; DRUGBANK
Volume of Distribution 0.46 L/kg 0.46±0.04 L/kg The Pharmacological Basis of Therapeutics
Half-life 1.8 h 1.8 h elimination half-life; DRUGBANK
Half-life 0.80 h 0.8±0.2 h The Pharmacological Basis of Therapeutics
Half-life 1.8 h 1.8±0.8 h PO, oral; RD, renal impairment, Renal disease,including uremia → ;Age → ; The Pharmacological Basis of Therapeutics
Toxicity LD50 8939.0 mg/kg 8939.0 mg/kg PO, oral; mouse; DRUGBANK
Eliminate Route 70.0 % ~70 % Faeces excretion; DRUGBANK
Eliminate Route 20.0 % ~20 % Urinary excretion; DRUGBANK
Eliminate Route 47.0 % ~47 % Urinary excretion; intravenous injection, IV; DRUGBANK
Eliminate Route 53.0 % 53 % Bile excretion; intravenous injection, IV; DRUGBANK
Eliminate Route 47.0 % 47±7 % Urinary excretion; Unchanged drug; The Pharmacological Basis of Therapeutics
Protein Binding 0 % ~43-48 % plasma proteins; DRUGBANK
Protein Binding 45.5 % 43-48 % The Pharmacological Basis of Therapeutics

Maximum Dosage

Property Name Property Value Unit Raw Value Raw Unit Annotation Brand Name Component Reference
Max dose for children 20.0 mg/day 20 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for children 60.0 mg/day 60 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for children 10.0 mg/day 10 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for children 60.0 mg/day 60 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for adolescents 40.0 mg/day 40 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for adolescents 60.0 mg/day 60 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for adolescents 20.0 mg/day 20 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for adolescents 60.0 mg/day 60 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for adults 80.0 mg/day 80 mg/day PO, oral Pravastatin Sodium pravastatin sodium PDR
Max dose for geriatric 80.0 mg/day 80 mg/day PO, oral Pravastatin Sodium pravastatin sodium 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