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[Studies on monoamine oxidase inhibitory action of hydrazines and other compounds].

Xu Fb, Kin Kc, Chen Yl, Zhang Zd

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Abstract

The tyramine colorimetric method was employed for evaluating monoamine oxidase inhibitor (MAOI). Forty-nine compounds (including hydrazines, derivatives of aminoacid and guanidine, and alkaloids of Amaryllidaceae have been examined in vitro and in vivo. It was found that the most promising compound in respect of inhibitory effect on MAO with low toxicity is 4-thiaheptane-1, 7-di-oyl-bis-isopropyl-hydrazine (Tapha, or CH-6). A single administration of 25 mg/kg of Tapha had an inhibitory activity as powerful as that of phenelzine. Its acute LD_(50) in mice was 5170mg/kg, whilst that of phenelzine was 87mg/kg. Thus, Tapha has a much wider therapeutic range than phenelzine. It is suggested that Tapha has a great safety margin and is worth while for clinical trials.

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What this paper is about

The tyramine colorimetric method was employed for evaluating monoamine oxidase inhibitor (MAOI). Forty-nine compounds (including hydrazines, derivatives of aminoacid and guanidine, and alkaloids of Amaryllidaceae have been examined in vitro and in vivo. It was found that the most promising compound in respect of inhibitory effect on MAO with low toxicity is 4-thiaheptane-1, 7-di-oyl-bis-isopropyl-hydrazine (Tapha, or CH-6). A single administration of 25 mg/kg of Tapha had an inhibitory activity as powerful as that of phenelzine. Its acute LD_(50) in mice was 5170mg/kg, whilst that of phenelzine was 87mg/kg. Thus, Tapha has a much wider therapeutic range than phenelzine. It is suggested that Tapha has a great safety margin and is worth while for clinical trials.

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Available abstract

The tyramine colorimetric method was employed for evaluating monoamine oxidase inhibitor (MAOI). Forty-nine compounds (including hydrazines, derivatives of aminoacid and guanidine, and alkaloids of Amaryllidaceae have been examined in vitro and in vivo. It was found that the most promising compound in respect of inhibitory effect on MAO with low toxicity is 4-thiaheptane-1, 7-di-oyl-bis-isopropyl-hydrazine (Tapha, or CH-6). A single administration of 25 mg/kg of Tapha had an inhibitory activity as powerful as that of phenelzine. Its acute LD_(50) in mice was 5170mg/kg, whilst that of phenelzine was 87mg/kg. Thus, Tapha has a much wider therapeutic range than phenelzine. It is suggested that Tapha has a great safety margin and is worth while for clinical trials.

Key concepts: Phenelzine, Monoamine oxidase, Chemistry, Monoamine oxidase inhibitor, Pharmacology, Hydrazine (antidepressant), Tyramine, Acute toxicity

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