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首页> 外文期刊>Folia Microbiologica >Characterization and antimicrobial activity of 4-(β-d-glucopyranosyl-1→4-α-l-rhamnopyranosyloxy)-benzyl thiocarboxamide; a novel bioactive compound from Moringa oleifera seed extract
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Characterization and antimicrobial activity of 4-(β-d-glucopyranosyl-1→4-α-l-rhamnopyranosyloxy)-benzyl thiocarboxamide; a novel bioactive compound from Moringa oleifera seed extract

机译:4-(β-d-吡喃吡喃糖基-1→4-α-1-鼠李糖吡喃糖基氧基)-苄基硫代羧酰胺的表征和抗菌活性;辣木种子提取物的新型生物活性化合物

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Antimicrobial activity of crude seed extract of Moringa oleifera was investigated by thin layer chromatography bioassay against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Cladosporium cladosporioides, and Penicillium sclerotigenum; most of them were prominently inhibited by an isolate with R F 0.92–0.96. Characterization and identification of the extract revealed the occurrence of three bioactive compounds: 4-(α-l-rhamnopyranosyloxy)benzyl isothiocyanate, methyl N-4-(α-l-rhamnopyranosyloxy) benzyl carbamate (both known compounds), and 4-(β-d-glucopyranosyl-1→4-α-l-rhamnopyranosyloxy)-benzyl thiocarboxamide, existence of which in any Moringa spp. or plant is reported for the first time. The UV spectrum of the novel compound showed maximum absorption at 273 and 225 nm in MeOH while the IR spectrum revealed several characteristic bands at 3100, 2900, 1700, 1500, 1300, 1100 and 1000 cm−1. The 1H-NMR showed signals at 1.2 and 3.77 ppm and the 13C-NMR presented signals at 155, 122, 91.7 and 98.4 ppm. All the compounds at 5 mg/L had very high bactericidal activity against some of test pathogens even at contact period 1–2 h. 4-(β-d-Glucopyranosyl-1→4-α-l-rhamnopyranosyloxy)benzyl thiocarboxamide was the most potent, with 99.2 % inhibition toward Shigella dysenteriae and 100 % toward Bacillus cereus, E. coli and Salmonella typhi within 4 h of contact.
机译:通过薄层色谱生物测定法对辣木的粗制种子提取物的抗微生物活性进行了研究,该生物测定法对大肠杆菌,铜绿假单胞菌,金黄色葡萄球菌,cladosporium cladosporioides和Spenicillium sclerotigenum具有抗药性。其中大多数被R F 0.92-0.96的分离株显着抑制。提取物的表征和鉴定表明存在三种生物活性化合物:异硫氰酸4-(α-1-rhamnopyranosyloxy)苄基氰酸酯,氨基甲酸N-4-(α-1-rhamnopyranosyloxy)苄基甲基酯(均为已知化合物)和4-( β-d-吡喃吡喃糖基-1→4-α-1-鼠李糖吡喃糖基氧基)-苄基硫代羧酰胺,在任何辣木中都存在。或植物是首次报告。该新化合物的紫外光谱在MeOH的273和225 nm处显示最大吸收,而红外光谱显示在3100、2900、1700、1500、1300、1100和1000 cm -1 处的几个特征带。 1 H-NMR信号在1.2和3.77 ppm,而 13 C-NMR信号在155、122、91.7和98.4 ppm。所有浓度为5 mg / L的化合物,即使在接触期1-2小时,对某些测试病原体也具有很高的杀菌活性。最有效的是4-(β-d-Glucopyranosyl-1→4-α-1-rhamnopyranosyloxy)苄基硫代羧酰胺,对痢疾志贺氏菌的抑制率为99.2%,对蜡状芽孢杆菌,大肠杆菌和伤寒沙门氏菌的抑制率为100%联系。

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