In vivo Evaluation of Substituted 3-Amino-1,4-benzodiazepines as Anti-depressant, Anxiolytic and Anti-nociceptive Agents

Eric Lattmann; Pornthip Lattmann; Yodchai Boonprakob; Wanchai Airarat; Harjit Singh; Michael Offel; Jintana Sattayasai

doi:10.1055/s-0031-1296366

Arzneimittelforschung, Table of Contents

Arzneimittelforschung 2009; 59(2): 61-71
DOI: 10.1055/s-0031-1296366

CNS-active Drugs · Hypnotics · Psychotropics · Sedatives

Editio Cantor Verlag Aulendorf (Germany)

In vivo Evaluation of Substituted 3-Amino-1,4-benzodiazepines as Anti-depressant, Anxiolytic and Anti-nociceptive Agents

Authors

Eric Lattmann

¹The School of Pharmacy, Aston University, Birmingham, England
Pornthip Lattmann

¹The School of Pharmacy, Aston University, Birmingham, England
Yodchai Boonprakob

²Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
Wanchai Airarat

²Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
Harjit Singh

¹The School of Pharmacy, Aston University, Birmingham, England
Michael Offel

¹The School of Pharmacy, Aston University, Birmingham, England
Jintana Sattayasai

²Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Abstract

Oxazepam (CAS 604-75-1) 4a served as building block in the synthesis of substituted 3-amino-1,4-benzodiazepines, which were subsequently tested in various CNS animal models. The hydroxy group of oxazepam was either activated as a chloride (Method A) or as a phosphor-oxy derivative (Method B) giving the desired 3-amino-1,4-benzodiapines 6a–6r in high yields with primary and secondary amines in a typical nucleophilic substitution reaction. Eighteen 3-substituted 1,4-benzodiazepines were prepared and served as new chemical entities and for lead structure discovery. The mixed cholecystokinin (CCK) antagonist 6e showed anxiolytic and antidepressant effects from 10 μg/kg in mice in the elevated x-maze test and the forced swimming test. The CCK₁ antagonist 6 g has shown antidepressant effects from the same dose, but lacked anxiolytic properties. Both compounds potentiated at a dose of 0.5 mg/kg morphine antinociception with a maximum possible effect (MPE) about 35%. By assessing initially the MPE of antinocipection for the 18 newly synthesised benzodiazepines in the tail-flick test, 4 other benzodiazepines were found active. In further in vivo evaluation the cyclohexyl derivative 6i displayed anxiolytic, antidepressant and antinociceptive properties as single agent at a dose of 5 mg/kg without toxicity. The benzodiazepines 6i and 6p, which initially showed a higher MPE in terms of morphine potentiation (43/44%) showed analgesic effects as single agents, without having anxiolytic or antidepressant properties.

The amino-piperidinyl derivative 6p displayed a similar dose-response relationship to morphine, but was 3 times more potent.

Key words

3-Amino-5-phenyl-l,4-benzodiazepinone - Antidepressants - Antinociceptives - Anxiolytics - 1,4-Benzodiazepines, template - CAS 604-75-1 - Cholecystokinin antagonists - Oxazepam

Full Text

References

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