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Aryl N-ω-(6-Fluoroindol-1-yl)alkylcarbamates as Inhibitors of Fatty Acid Amide Hydrolase, Monoacylglycerol Lipase, and Butyrylcholinesterase: Structure–Activity Relationships and Hydrolytic Stability

机译：芳基N- ω-（6-氟吲哚-1-基）烷基氨基甲酸酯作为脂肪酸酰胺水解酶，单酰基甘油脂肪酶和丁酰胆碱酯酶的抑制剂：结构 - 活性关系和水解稳定性

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Stefan Rudolph; Helmut Dahlhaus; Walburga Hanekamp; Christian Albers; Maximilian Barth; Giulia Michels; Denise Friedrich; Matthias Lehr;
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1. Structure-activity relationship of a new series of reversible dual monoacylglycerol lipase/fatty acid amide hydrolase inhibitors [J] . Cisneros J.A., Bj?rklund E., González-Gil I., Journal of Medicinal Chemistry . 2012,第2期

机译：新型可逆双单酰基甘油脂肪酶/脂肪酸酰胺水解酶抑制剂系列的构效关系
2. Synthesis and quantitative structure-activity relationship of fatty acid amide hydrolase inhibitors: Modulation at the N-portion of biphenyl-3-yl alkylcarbamates [J] . Mor M, Lodola A, Rivara S, Journal of Medicinal Chemistry . 2008,第12期

机译：脂肪酸酰胺水解酶抑制剂的合成及定量构效关系：联苯-3-基烷基氨基甲酸酯的N部分调节
3. Structure-Activity Relationship of a Series of Inhibitors of Monoacylglycerol Hydrolysis-Comparison with Effects upon Fatty Acid Amide Hydrolase [J] . Jose Antonio Cisneros, Severine Vandevoorde, Silvia Ortega-Gutierrez Journal of Medicinal Chemistry . 2007,第20期

机译：一系列单酰基甘油水解比较抑制剂与脂肪酸酰胺水解酶的构效关系
4. Biological activities and structure-activity relationship of substitution compounds of N-2-(3-mdolyl)ethylsucdnamic acid and N-2-(l-naphthyl)ethylsuccinamic acid, derived from a new category of root-promoting substances, N-(phenethyl)succinamic ac [C] . Mihoko Itagaki, Hiroshi Soejima, Ko Ishii, Symposium of the International Society of Root Research . 2003

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5. I. Optimization and analysis of the central heterocycle of alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase. II. Total synthesis of chloropeptin II (complestatin) and progress towards a second generation total synthesis of chloropeptin I and II. [D] . Garfunkle, Joie. 2009

机译：I.脂肪酸酰胺水解酶的α-酮杂环抑制剂中心杂环的优化和分析。二。氯肽II（complestatin）的全合成，并向第二代氯肽I和II的全合成方向发展。
6. Structure-property relationships of a class of carbamate-based Fatty Acid Amide Hydrolase (FAAH) inhibitors: chemical and biological stability [O] . Dr. Federica Vacondio, Prof. Claudia Silva, Dr. Alessio Lodola, -1

机译：一类基于氨基甲酸酯的脂肪酸酰胺水解酶（FAAH）抑制剂的结构 - 性质关系：化学和生物稳定性
7. Aryl N-(6-Fluoroindol-1-yl)alkylcarbamates as Inhibitors of Fatty Acid Amide Hydrolase, Monoacylglycerol Lipase and Butyrylcholinesterase: StructureActivity Relationships and Hydrolytic Stability [O] . -1

机译：芳基N - （6-氟吲哚-1-基）烷基氨基甲酸酯作为脂肪酸酰胺水解酶，单酰基甘油脂肪酶和丁酰胆碱酯酶的抑制剂：结构性反应关系和水解稳定性

Aryl N-ω-(6-Fluoroindol-1-yl)alkylcarbamates as Inhibitors of Fatty Acid Amide Hydrolase, Monoacylglycerol Lipase, and Butyrylcholinesterase: Structure–Activity Relationships and Hydrolytic Stability

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