Basic Information

Drug ID DDPD01211 ...
Drug Name Clarithromycin
Molecular Weight 747.9534
Molecular Formula C38H69NO13
CAS Number 81103-11-9
SMILES [H][C@@]1(C[C@@](C)(OC)[C@@H](O)[C@H](C)O1)O[C@H]1[C@H](C)[C@@H](O[C@]2([H])O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@@](C)(C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@](C)(O)[C@@H](CC)OC(=O)[C@@H]1C)OC
External Links
DRUGBANK DB01211
PubChem Compound 84029
PDR 6
Drugs.com Drugs.com Drug Page

Experimental Physicochemical Property

Property Name Property Value Unit Raw Value Raw Unit Reference
Log P 3.16 - 3.16 - MCFARLAND,JW ET AL. (1997)
Melting Point 220.0 220 PhysProp
Water Solubility 0.33 mg/L 0.33 mg/L DRUGBANK
pKa 8.99 - 8.99 - MCFARLAND,JW ET AL. (1997)

Pharmacokinetic/ Toxicokinetic Property

Property Name Property Value Unit Raw Value Raw Unit Annotation Factor Reference
Bioavailability 55.0 % 55±8 % PO, oral; The Pharmacological Basis of Therapeutics
C Max 2400.0 ng/ml 2.4 mcg/ml PO, oral; adults; normal,healthy; The Pharmacological Basis of Therapeutics
C Max 700.0 ng/ml 0.7 mcg/ml PO, oral; Derivative; adults; normal,healthy; The Pharmacological Basis of Therapeutics
T Max 2.8 h 2.8 h PO, oral; adults; normal,healthy; The Pharmacological Basis of Therapeutics
T Max 3.0 h 3.0 h PO, oral; Derivative; adults; normal,healthy; The Pharmacological Basis of Therapeutics
Clearance 0.44 L/h/kg 7.3±1.9 ml/min/kg PO, oral; Elderly ↓ ;Hepatitis, Hep → ;RD, renal impairment, Renal disease,including uremia ↓ ; The Pharmacological Basis of Therapeutics
Clearance 0.44 L/h/kg 7.3 ml/min/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Volume of Distribution 2.6 L/kg 2.6±0.5 L/kg Elderly → ;Hepatitis, Hep ↑ ; The Pharmacological Basis of Therapeutics
Volume of Distribution 1.5 L/kg 1.5 L/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Half-life 3.5 h 3-4 h DRUGBANK
Half-life 3.3 h 3.3±0.5 h PO, oral; RD, renal impairment, Renal disease,including uremia ↑ ;Hepatic cirrhosis, cirr ↑ ;increasing doses ↑ ;Age ↑ ; The Pharmacological Basis of Therapeutics
Half-life 2.8 h 2.8 h intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Eliminate Route 36.0 % 36±7 % Urinary excretion; Oral single dose; Unchanged drug; Elderly → ; The Pharmacological Basis of Therapeutics
Protein Binding 70.0 % ~70 % DRUGBANK
Protein Binding 46.0 % 42-50 % The Pharmacological Basis of Therapeutics

Maximum Dosage

Property Name Property Value Unit Raw Value Raw Unit Annotation Brand Name Component Reference
Max dose for infants 15.0 mg/kg/day 15 mg/kg/day PO, oral Biaxin clarithromycin PDR
Max dose for infants 15.0 mg/kg/day 15 mg/kg/day PO, oral Biaxin clarithromycin PDR
Max dose for children 15.0 mg/kg/day 15 mg/kg/day PO, oral Biaxin clarithromycin PDR
Max dose for children 30.0 mg/kg/day 30 mg/kg/day PO, oral Biaxin clarithromycin PDR
Max dose for children 1000.0 mg/day 1 g/day PO, oral Biaxin clarithromycin PDR
Max dose for adolescents 15.0 mg/kg/day 15 mg/kg/day PO, oral Biaxin clarithromycin PDR
Max dose for adolescents 30.0 mg/kg/day 30 mg/kg/day PO, oral Biaxin clarithromycin PDR
Max dose for adolescents 1000.0 mg/day 1 g/day PO, oral Biaxin clarithromycin PDR
Max dose for adults 1500.0 mg/day 1.5 g/day PO, oral Biaxin clarithromycin PDR
Max dose for adults 1000.0 mg/day 1 g/day PO, oral Biaxin clarithromycin PDR
Max dose for geriatric 1500.0 mg/day 1.5 g/day PO, oral Biaxin clarithromycin PDR
Max dose for geriatric 1000.0 mg/day 1 g/day PO, oral Biaxin clarithromycin 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