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首页> 外文期刊>Helvetica chimica acta >Synthesis and Glycosidase Inhibitory Activities of 5-(1',4'-Dideoxy-1',4'-imino-D-erythrosyl)-2-methyl-3-furonic Acid (=5-[(3S,4R)-3,4-Dihydroxypyrrolidin-2-yl]-2-methylfuran-3-carboxylic Acid) Derivatives: New Leads as Selective alpha-L-Fucosidase a
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Synthesis and Glycosidase Inhibitory Activities of 5-(1',4'-Dideoxy-1',4'-imino-D-erythrosyl)-2-methyl-3-furonic Acid (=5-[(3S,4R)-3,4-Dihydroxypyrrolidin-2-yl]-2-methylfuran-3-carboxylic Acid) Derivatives: New Leads as Selective alpha-L-Fucosidase a

机译:5-(1',4'-Dideoxy-1',4'-亚氨基-D-赤藓糖基)-2-甲基-3-呋喃糖酸(= 5-[(3S,4R)-3)的合成和糖苷酶抑制活性,4-二羟基吡咯烷-2-基] -2-甲基呋喃-3-羧酸)衍生物:新的潜在的选择性α-L-岩藻糖苷酶a

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摘要

The Garcia-Gonzalez reaction of D-glucose and ethyl acetoacetate generated ethyl 5-[(1'S)-D-erythrosyl]-2-methyl-3-furoate (5), which was converted to ethyl 5-[(1'R)-1',4'-dideoxy-1',4'-imino-D-erythrosyl]-2-methyl-3-furoate (3c) and to ethyl 5-[(1'S)-1',4'-dideoxy-1',4'-imino-D-erythrosyl]-2-methyl-3-furoate (4c). Similar methods were developed to generate other carboxylic acid derivatives such as methyl (see 3e and 4e), isopropyl (see 3f), and butyl esters (see 3g), S-phenyl (see 3a) and S-ethyl thioesters (see 3m), N-benzylcarboxamides 3b and 4b, glycine-derived amide 3h, and N-phenyl (see 3i), N-isopropyl (see 3j and 4j), N,N-diethyl-(see 3k and 4k), and N-ethyl-carboxamides (see 3I). All the new 5-(1',4'-dideoxy-1',4'-imino-D-erythrosyl)-3-furoic acid (=5-[(3S,4R)-3,4-dihydroxypyrrolidin-2-yl) furan-3-carboxylic acid) derivatives 3 and 4 were assayed for inhibitory activity towards 25 commercially available glycosiases. Derivative 3a with a S-phenyl thioester group is a good and selective alpha-L-fucosidase inhibitor (K_i = 2-4muM), whereas 4b (with a N-benzylcarboxamide group) is a good beta-galactosidase inhibitor.
机译:D-葡萄糖与乙酰乙酸乙酯的Garcia-Gonzalez反应生成5-[((1'S)-D-赤藓糖基] -2-甲基-3-糠酸乙酯(5),将其转化为5-[(1'R)乙基-1',4'-二甲氧基-1',4'-亚氨基-D-赤藓基] -2-甲基-3-糠酸酯(3c)和5-[(1'S)-1',4'-二甲氧基-乙基1',4'-亚氨基-D-赤藓基] -2-甲基-3-糠酸酯(4c)。开发了类似的方法来生成其他羧酸衍生物,例如甲基(参见3e和4e),异丙基(参见3f)和丁酯(参见3g),S-苯基(参见3a)和S-乙基硫代酯(参见3m) ,N-苄基羧酰胺3b和4b,甘氨酸衍生的酰胺3h和N-苯基(请参见3i),N-异丙基(请参见3j和4j),N,N-二乙基-(请参见3k和4k)和N-乙基-羧酰胺(参见3I)。所有新的5-(1',4'-二脱氧-1',4'-亚氨基-D-赤藓糖基)-3-糠酸(= 5-[(3S,4R)-3,4-dihydroxypyrrolidin-2-测定了yl)呋喃-3-羧酸)衍生物3和4对25种市售糖基化酶的抑制活性。具有S-苯基硫酯基团的衍生物3a是良好的选择性α-L-岩藻糖苷酶抑制剂(K_i =2-4μM),而具有4b(具有N-苄基羧酰胺基团)是良好的β-半乳糖苷酶抑制剂。

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