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新型降血糖药物米格列唑在犬体内的代谢产物鉴定

Identification of the metabolites of a new hypoglycaemic agent, midaglizole, in dogs.

作者信息

Nakaoka M, Hakusui H

机构信息

Drug Metabolism Research Center, Daiichi Seiyaku Co., Ltd, Tokyo, Japan.

出版信息

Xenobiotica. 1987 Nov;17(11):1329-39. doi: 10.3109/00498258709047163.

Abstract
  1. The metabolism of a new hypoglycaemic agent, midaglizole, was studied. Six major metabolites were isolated from the urine of dogs dosed with 14C-midaglizole. The structures of these metabolites were elucidated by n.m.r., i.r., u.v. and mass spectrometry, and confirmed by comparison with synthesized authentic samples. 2. For midaglizole, oxidation on the imidazoline ring and subsequent ring-opening were the major metabolic pathways in dogs. 3. Two metabolites, namely, the imidazole analogue (M-I) and amidine analogue (M-III), had hypoglycaemic activity.
摘要
  1. 对一种新型降血糖药物米格列唑的代谢进行了研究。从给予14C-米格列唑的犬尿液中分离出六种主要代谢物。通过核磁共振、红外光谱、紫外光谱和质谱对这些代谢物的结构进行了阐明,并与合成的标准样品进行比较得以确认。2. 对于米格列唑而言,咪唑啉环上的氧化及随后的开环是犬体内的主要代谢途径。3. 两种代谢物,即咪唑类似物(M-I)和脒类似物(M-III)具有降血糖活性。

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