Basic Information

Drug ID DDPD00246 ...
Drug Name Ziprasidone
Molecular Weight 412.936
Molecular Formula C21H21ClN4OS
CAS Number 146939-27-7
SMILES ClC1=C(CCN2CCN(CC2)C2=NSC3=CC=CC=C23)C=C2CC(=O)NC2=C1
External Links
DRUGBANK DB00246
PubChem Compound 60854
PDR 2532
Drugs.com Drugs.com Drug Page

Experimental Physicochemical Property

Property Name Property Value Unit Raw Value Raw Unit Reference
Log P 3.8 - 3.8 - DRUGBANK
Melting Point 276.0 >276 https://www.trc-canada.com/product-detail/?CatNum=Z485000

Pharmacokinetic/ Toxicokinetic Property

Property Name Property Value Unit Raw Value Raw Unit Annotation Factor Reference
Absorption 100.0 % 100.0 % DRUGBANK
Bioavailability 60.0 % 60.0 % DRUGBANK
Bioavailability 100.0 % 100.0 % PO, oral; food; food ↑ ; DRUGBANK
Bioavailability 59.0 % 59.0 % PO, oral; The Pharmacological Basis of Therapeutics
Bioavailability 100.0 % 100.0 % IM,intramuscular injection; The Pharmacological Basis of Therapeutics
C Max 68.0 ng/ml 68±20 ng/ml PO, oral; The Pharmacological Basis of Therapeutics
C Max 156.0 ng/ml 156.0 ng/ml The Pharmacological Basis of Therapeutics
T Max 4.0 h 4±1 h PO, oral; The Pharmacological Basis of Therapeutics
T Max 0.70 h 0.7 h The Pharmacological Basis of Therapeutics
Clearance 0.45 L/h/kg 7.5 ml/min/kg Average clearance; DRUGBANK
Clearance 0.70 L/h/kg 11.7 ml/min/kg The Pharmacological Basis of Therapeutics
Clearance 0.31 L/h/kg 5.1 ml/min/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Volume of Distribution 1.5 L/kg 1.5 L/kg Apparent volume of distribution; DRUGBANK
Volume of Distribution 2.3 L/kg 2.3 L/kg The Pharmacological Basis of Therapeutics
Volume of Distribution 1.0 L/kg 1 L/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Half-life 6.5 h 6-7 h DRUGBANK
Half-life 2.9 h 2.9 h Elderly ↑ ;food ↓ ; The Pharmacological Basis of Therapeutics
Half-life 3.1 h 3.1 h intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Eliminate Route 1.0 % <1 % Urinary excretion; PO, oral; Unchanged drug; DRUGBANK
Eliminate Route 4.0 % <4 % Faeces excretion; PO, oral; Unchanged drug; DRUGBANK
Eliminate Route 1.0 % <1 % Urinary excretion; PO, oral; Unchanged drug; The Pharmacological Basis of Therapeutics
Protein Binding 99.0 % >99 % plasma proteins; DRUGBANK
Protein Binding 99.9 % 99.9±0.08 % 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 40.0 mg/day 40 mg/day PO, oral Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for children 10.0 mg/dose 10 mg/dose IM,intramuscular injection Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for children 40.0 mg/day 40 mg/day PO, oral Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for adolescents 40.0 mg/day 40 mg/day PO, oral Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for adolescents 20.0 mg/dose 20 mg/dose IM,intramuscular injection Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for adolescents 40.0 mg/day 40 mg/day PO, oral Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for adolescents 10.0 mg/dose 10 mg/dose IM,intramuscular injection Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for adults 160.0 mg/day 160 mg/day PO, oral Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for adults 40.0 mg/day 40 mg/day IM,intramuscular injection Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for geriatric 160.0 mg/day 160 mg/day PO, oral Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) PDR
Max dose for geriatric 40.0 mg/day 40 mg/day IM,intramuscular injection Geodon (ziprasidone hydrochloride); (ziprasidone mesylate) 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