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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >Formation of 3,4,5,6-tetrahydro-7-hydroxy-6-methyl-1H-azepino[5,4,3-cd]indole in the reaction of serotonin with acetaldehyde in water in the presence of either L-amino acid, nicotine or fluoride
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Formation of 3,4,5,6-tetrahydro-7-hydroxy-6-methyl-1H-azepino[5,4,3-cd]indole in the reaction of serotonin with acetaldehyde in water in the presence of either L-amino acid, nicotine or fluoride

机译:在5-羟色胺与乙醛在水中存在的情况下,在任一L-氨基存在下,形成3,4,5,6-四氢-7-羟基-6-甲基-1H-氮杂环庚烷[5,4,3-cd]吲哚酸,尼古丁或氟化物

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摘要

Possible formation of a new compound, 3,4,5,6-tetrahydro-7-hydroxy-6-methyl-1H-azepino[5,4,3-cd]indole (4a), in serotonergic neuron after drinking ethanol is chemically suggested by reacting serotonin with acetaldehyde in water in the presence of either L-amino acid, nicotine or fluoride.
机译:喝乙醇后在血清素能神经元中可能形成新化合物3,4,5,6-四氢-7-羟基-6-甲基-1H-阿斯匹诺[5,4,3-cd]吲哚(4a)建议在5-氨基酸,尼古丁或氟化物存在下使5-羟色胺与乙醛在水中反应。

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