首页> 外国专利> STREPTOMYCES SP., NERVE CELL PROTECTING COMPOUND DERIVED FROM STREPTOMYCES SP. AND PROCESS FOR PREPARING THEREOF

STREPTOMYCES SP., NERVE CELL PROTECTING COMPOUND DERIVED FROM STREPTOMYCES SP. AND PROCESS FOR PREPARING THEREOF

机译:STREPTOMYCES SP。,来自STREPTOMYCES SP的神经细胞保护化合物。及其准备的过程

摘要

PURPOSE: Provided are the nerve cell protectants produced from Streptomyces sp. and preparation method thereof. In vitro test, their pharmaceutically acceptable organic and inorganic salts, hydrates and isomers show strong inhibition of the cell toxicity and thereby protect the nerve cells. CONSTITUTION: The derivatives isolated from the growth medium of Streptomyces sp. genus 833 (KCTC 8796 P), are represented by the chemical structure 1, 2, 3. These phenazostatin structures are identified by the instrumental analysis. These compounds are separated from the organic solvents extracts of the growth medium through column chromatography and final 3 active fractions are recrystallized from methanol. In screening, N18-RE-105 cell has been used as the vitro model to examine the compounds. In the test, the compounds show inhibitory activity against the active oxygens such as superoxide, hydrogen peroxide and hydroxyl radical. These phenazostatin compounds show strong inhibition activity of L-glutamate cell toxicity of the above model cell.
机译:目的:提供由链霉菌属产生的神经细胞保护剂。及其制备方法。在体外试验中,它们的可药用有机和无机盐,水合物和异构体对细胞毒性具有很强的抑制作用,从而保护了神经细胞。组成:从链霉菌的生长培养基分离的衍生物。属833(KCTC 8796 P)由化学结构1、2、3表示。这些吩唑他汀结构通过仪器分析鉴定。通过柱色谱法将这些化合物与生长培养基的有机溶剂提取物分离,并从甲醇中重结晶最终的3个活性级分。在筛选中,N18-RE-105细胞已用作体外模型来检查化合物。在测试中,这些化合物对活性氧(如超氧化物,过氧化氢和羟​​基自由基)表现出抑制活性。这些吩唑他汀化合物显示出对上述模型细胞的L-谷氨酸细胞毒性的强抑制活性。

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