首页> 外文会议>IUPAC World Congress on Chemistry >First total synthesis of the (±)-2-methoxy-6-heptadecynoic acid and related 2-methoxylated analogs as effective inhibitors of the Leishmania topoisomerase IB enzyme*
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First total synthesis of the (±)-2-methoxy-6-heptadecynoic acid and related 2-methoxylated analogs as effective inhibitors of the Leishmania topoisomerase IB enzyme*

机译:(±)-2-甲氧基-6-庚二甲酸和相关的2-甲氧基化类似物作为Leishmania Topoisomerase IB酶的有效抑制剂的第一次合成

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摘要

The fatty acids (±)-2-methoxy-6Z-heptadecenoic acid, (±)-2-methoxy-6-hepta-decynoic acid, and (±)-2-methoxyheptadecanoic acid were synthesized and their inhibitory activity against the Leishmania DNA topoisomerase IB enzyme (LdTopIB) determined. Both 2-OMe-17:1 fatty acids were synthesized from 4-bromo-1-pentanol, the olefinic fatty acid in 10 steps and in 7 % overall yield, while the acetylenic fatty acid in 7 steps and in 14 % overall yield. The 2-OMe-17:0 acid was prepared in 6 steps and in 42 % yield from 1-hexadecanol. The 2-OMe-17:l acids inhibited LdTopIB, with the acetylenic acid displaying an EC_(50) = 16.6 ± 1.1 μM, but the 2-OMe-17:0 acid did not inhibit LdTopIB. The (±)-2-methoxy-6Z-heptadecenoic acid preferentially inhibited LdTopIB over the human TopIB enzyme.
机译:脂肪酸(±)-2-甲氧基-6Z-庚二烯酸,(±)-2-甲氧基-6-庚基 - 癸酸和(±)-2-甲氧基甲基甲酸是合成的,并对Leishmania DNA的抑制活性 测定拓扑异构酶IB酶(LDTOPIB)。 2-OME-17:1脂肪酸两步合成10步,烯烃脂肪酸在10步和7%的总收率中合成,同时乙炔脂肪酸在7步和14%的总收率中。 在6步骤中制备2-OME-17:0酸,并从1-十六甲醇中产生42%的产率。 2-OME-17:L酸抑制LDTOPIB,乙炔酸显示EC_(50)= 16.6±1.1μm,但2-OME-17:0酸不抑制LDTOPIB。 (±)-2-甲氧基-6Z-庚二烯酸优先抑制人机TOPIB酶的LDTOPIB。

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