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动物保健制剂中L-648,548的二级降解产物鉴定。

Identification of the secondary degradates of L-648,548 in an animal health formulation.

作者信息

Wang Q, Stong J D, Demontigny P, Ballard J M, Murphy J S, Shim J S, Faulkner A J

机构信息

Merck Research Laboratories, West Point, PA 19486, USA.

出版信息

J Pharm Sci. 1996 Apr;85(4):446-50. doi: 10.1021/js950483i.

Abstract

L-648,548 is a semisynthetic analog of avermectin. During stability investigations of this compound in an animal health formulation, two new degradates were discovered. These degradates (L-648,548 phenol and its 8,9-Z isomer) were identified as the reaction products of 5-oxo-L-648,548 formed by oxidation of L-648,548. Addition of base to the reaction medium containing 5-oxo-L-648,548 was found to catalyze the formation of L-648,548 phenol via a postulated dehydration by an E1cb elimination followed by the rapid tautomerization of the C5 carbonyl. Photolysis of L-648,548 phenol with visible light (including ambient laboratory lighting) was found to readily produce 8,9-Z-L-648,548 phenol. This transformation was confirmed to be exclusively a photoinduced process.

摘要

L-648,548是阿维菌素的一种半合成类似物。在该化合物于动物保健制剂中的稳定性研究期间,发现了两种新的降解产物。这些降解产物(L-648,548苯酚及其8,9-Z异构体)被鉴定为L-648,548氧化形成的5-氧代-L-648,548的反应产物。发现在含有5-氧代-L-648,548的反应介质中加入碱可通过假定的E1cb消除脱水,随后C5羰基快速互变异构来催化L-648,548苯酚的形成。发现L-648,548苯酚在可见光(包括实验室环境光)下光解容易产生8,9-Z-L-648,548苯酚。这种转化被确认为完全是光诱导过程。

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