Quantitative structure-activity relationship (QSAR) methodology in forensic toxicology: Modeling postmortem redistribution of structurally diverse drugs using multivariate statistics

Forensic Science International

Volumn 190, Issue 1-3, 2009, Pages 9-15

  Giaginis, Costas ^a,b   Tsantili Kakoulidou, Anna ^b   Theocharis, Stamatios ^a  

^a UNIVERSITY OF ATHENS MEDICAL SCHOOL   (Greece)

^b UNIVERSITY OF ATHENS   (Greece)

Author keywords

Forensic toxicology; Molecular properties; Multivariate data analysis; Physicochemical properties; Postmortem redistribution; QSAR

Indexed keywords

ALPRAZOLAM; AMANTADINE; AMFEBUTAMONE; AMITRIPTYLINE; AMOXAPINE; AMPHETAMINE; AMPHETAMINE DERIVATIVE; BARBITURIC ACID DERIVATIVE; BENZATROPINE; BENZODIAZEPINE DERIVATIVE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CHLOROQUINE; CHLORPHENIRAMINE; CHLORPROMAZINE; CLOMIPRAMINE; CLONAZEPAM; CLOZAPINE; CODEINE; CYCLOBENZAPRINE; DESIPRAMINE; DEXTROMETHORPHAN; DIAZEPAM; DILTIAZEM; HALOGEN; NONSTEROID ANTIINFLAMMATORY AGENT; OPIATE; PHENOTHIAZINE DERIVATIVE; SEROTONIN NORADRENALIN REUPTAKE INHIBITOR; TRICYCLIC ANTIDEPRESSANT AGENT; UNINDEXED DRUG;

ARTICLE; AUTOPSY; DRUG STRUCTURE; DRUG TISSUE LEVEL; FORENSIC TOXICOLOGY; LIPOPHILICITY; MATHEMATICAL MODEL; MOLECULAR MECHANICS; MOLECULAR SIZE; MULTIVARIATE ANALYSIS; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; STRUCTURE ACTIVITY RELATION;

EID: 67650995779     PISSN: 03790738     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.forsciint.2009.05.003     Document Type: Article

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