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首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >Synthesis, characterization and biological activity of triazolothiadiazines bearing 2H-1,4-benzothiazin-3(4H)-onemoiety
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Synthesis, characterization and biological activity of triazolothiadiazines bearing 2H-1,4-benzothiazin-3(4H)-onemoiety

机译:具有2H-1,4-苯并噻嗪-3(4H)-单原子的三唑并噻二嗪的合成,表征和生物活性

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摘要

A new series of [1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives (7) of 4-[(4-amino-5-sulfanyl-4H-1,2,4-triazol- 3-yl)methyl]-2H-1,4-benzothiazin-3(4H)-one (4), were synthesized from (3-oxo-2,3-dihydro-4H-1,4-benzothiazin-4- yl)acetic acid (3). The structures of all newly synthesized compounds were elucidated by elemental analysis, FT-IR, 1H-NMR and mass spectral data. Synthesized compounds were screened for their antioxidant and antibacterial activity and a few of them exhibited significant activity. Among the tested compounds, (3-oxo-2,3-dihydro-4H-1,4- benzothiazin-4-yl)acetic acid (3) posssess antibacterial activity comparable to that of streptomycin. However the activity decreased on derivatization of the acid group.
机译:4-[(4-氨基-5-硫烷基-4H-1,2,]的[1,2,4]三唑并[3,4-b] [1,3,4]噻二嗪衍生物(7)系列由(3-氧代-2,3-二氢-4H-1,4-苯并噻嗪合成)4-(三唑-3-基)甲基] -2H-1,4-苯并噻嗪-3(4H)-一(4) -4-基)乙酸(3)。通过元素分析,FT-IR,1H-NMR和质谱数据阐明了所有新合成化合物的结构。筛选合成的化合物的抗氧化和抗菌活性,其中一些具有显着活性。在测试的化合物中,(3-氧代-2,3-二氢-4H-1,4-苯并噻嗪-4-基)乙酸(3)具有与链霉素相当的抗菌活性。然而,在酸基团衍生时活性降低。

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