. . . . . . . . . . . . . . . . "4-\u7F9F\u57FA-2-\u58EC\u70EF\u919B\uFF08\u82F1\u8A9E\uFF1A4-hydroxy-2-nonenal\uFF0C\u62164-Hydroxynonenal\uFF0C\u7F29\u51994-HNE\u6216HNE\uFF09\u662F\u4E00\u79CD\u03B1,\u03B2-\u4E0D\u9971\u548C\u70EF\u919B\uFF0C\u662F\u7EC6\u80DE\u8102\u8D28\u8FC7\u6C27\u5316\u7684\u4E3B\u8981\u4E0D\u9971\u548C\u70EF\u919B\u4EA7\u7269\uFF0C1991\u5E74\u7531Esterbauer\u53D1\u73B0\u3002"@zh . . . . . "4-\u7F9F\u57FA-2-\u58EC\u70EF\u919B"@zh . . . "Skeletal formula of 4-hydroxynonenal"@en . . . . . "changed"@en . . . . . . . . . . "4-Hydroxynonenal, ist ein reaktiver, \u03B1,\u03B2-unges\u00E4ttigter Aldehyd, der aus der Lipidperoxidation mehrfach unges\u00E4ttigter Fetts\u00E4uren (engl. polyunsaturated fatty acids - PUFAs) entsteht. Bei diesem Vorgang werden wiederum Proteine unter Bedingungen des oxidativen Stresses modifiziert, d. h. gesch\u00E4digt."@de . . . "4-Hydroxynonenal, or 4-hydroxy-2-nonenal or 4-HNE or HNE, (C9H16O2), is an \u03B1,\u03B2-unsaturated hydroxyalkenal that is produced by lipid peroxidation in cells. 4-HNE is the primary \u03B1,\u03B2-unsaturated hydroxyalkenal formed in this process. It is a colorless oil. It is found throughout animal tissues, and in higher quantities during oxidative stress due to the increase in the lipid peroxidation chain reaction, due to the increase in stress events. 4-HNE has been hypothesized to play a key role in cell signal transduction, in a variety of pathways from cell cycle events to cellular adhesion."@en . . . . "La 4-idrossinonenale \u00E8 un composto organico, precisamente un \u0251,\u03B2 insaturo che viene prodotto attraverso perossidazione lipidica nelle cellule."@it . . . . "4"^^ . . . . . "1235987"^^ . . . . . . . . . . . . . . . . . . . "La 4-idrossinonenale \u00E8 un composto organico, precisamente un \u0251,\u03B2 insaturo che viene prodotto attraverso perossidazione lipidica nelle cellule."@it . . . . . . . . . . . . . . . . . . . . . . . . . . . . . "250"^^ . . . "4"^^ . . . "4-\u7F9F\u57FA-2-\u58EC\u70EF\u919B\uFF08\u82F1\u8A9E\uFF1A4-hydroxy-2-nonenal\uFF0C\u62164-Hydroxynonenal\uFF0C\u7F29\u51994-HNE\u6216HNE\uFF09\u662F\u4E00\u79CD\u03B1,\u03B2-\u4E0D\u9971\u548C\u70EF\u919B\uFF0C\u662F\u7EC6\u80DE\u8102\u8D28\u8FC7\u6C27\u5316\u7684\u4E3B\u8981\u4E0D\u9971\u548C\u70EF\u919B\u4EA7\u7269\uFF0C1991\u5E74\u7531Esterbauer\u53D1\u73B0\u3002"@zh . . . "4-Hydroxynonenal"@en . . . "4-Hydroxynonenal"@de . . . . . . . . . . . . . . . . . "1116078280"^^ . . . . . . . . . . . . . . . . "4-idrossinonenale"@it . . . . . . . . . . . . . . "4-Hydroxy-2-nonenal"@en . . . "300"^^ . . . . . . "477222328"^^ . . . . . "4-Hydroxynonenal, or 4-hydroxy-2-nonenal or 4-HNE or HNE, (C9H16O2), is an \u03B1,\u03B2-unsaturated hydroxyalkenal that is produced by lipid peroxidation in cells. 4-HNE is the primary \u03B1,\u03B2-unsaturated hydroxyalkenal formed in this process. It is a colorless oil. It is found throughout animal tissues, and in higher quantities during oxidative stress due to the increase in the lipid peroxidation chain reaction, due to the increase in stress events. 4-HNE has been hypothesized to play a key role in cell signal transduction, in a variety of pathways from cell cycle events to cellular adhesion. Early identification and characterization of 4-hydroxynonenal was reported by Esterbauer, et al., who also obtained the same compound synthetically. The topic has since been often reviewed."@en . . . "4-Hydroxynonenal, ist ein reaktiver, \u03B1,\u03B2-unges\u00E4ttigter Aldehyd, der aus der Lipidperoxidation mehrfach unges\u00E4ttigter Fetts\u00E4uren (engl. polyunsaturated fatty acids - PUFAs) entsteht. Bei diesem Vorgang werden wiederum Proteine unter Bedingungen des oxidativen Stresses modifiziert, d. h. gesch\u00E4digt."@de . . . . "4"^^ . . "16566"^^ . "changed"@en . . . . . . . . . "4-Hydroxynon-2-enal"@en .