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海洋 α-甲氧基脂肪酸类似物的合成,有效抑制拓扑异构酶 IB 从利什曼原虫与喜树碱不同的机制。

Synthesis of marine α-methoxylated fatty acid analogs that effectively inhibit the topoisomerase IB from Leishmania donovani with a mechanism different from that of camptothecin.

机构信息

Department of Chemistry, University of Puerto Rico, PO Box 23346, San Juan 00931-3346, Puerto Rico.

出版信息

Mar Drugs. 2013 Sep 30;11(10):3661-75. doi: 10.3390/md11103661.

DOI:10.3390/md11103661
PMID:24084785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3826128/
Abstract

Sponges biosynthesize α-methoxylated fatty acids with unusual biophysical and biological properties and in some cases they display enhanced anticancer activities. However, the antiprotozoal properties of the α-methoxylated fatty acids have been less studied. In this work, we describe the total synthesis of (5Z,9Z)-(±)-2-methoxy-5, 9-eicosadienoic acid (1) and its acetylenic analog (±)-2-methoxy-5,9-eicosadiynoic acid (2), and report that they inhibit (EC₅₀ values between 31 and 22 µM) the Leishmania donovani DNA topoisomerase IB enzyme (LdTopIB). The inhibition of LdTopIB (EC₅₀ = 53 µM) by the acid (±)-2-methoxy-6-icosynoic acid (12) was studied as well. The potency of LdTopIB inhibition followed the trend 2 > 1 > 12, indicating that the effectiveness of inhibition depends on the degree of unsaturation. All of the studied α-methoxylated fatty acids failed to inhibit the human topoisomerase IB enzyme (hTopIB) at 100 µM. However, the α-methoxylated fatty acids were capable of inhibiting an active but truncated LdTopIB with which camptothecin (CPT) cannot interact suggesting that the methoxylated fatty acids inhibit LdTopIB with a mechanism different from that of CPT. The diunsaturated fatty acids displayed low cytotoxicity towards Leishmania infantum promastigotes (EC₅₀ values between 260 and 240 µM), but 12 displayed a better cytotoxicity towards Leishmania donovani promastigotes (EC₅₀ = 100 µM) and a better therapeutic index.

摘要

海绵生物合成具有不寻常的物理化学和生物学特性的α-甲氧基脂肪酸,在某些情况下它们显示出增强的抗癌活性。然而,α-甲氧基脂肪酸的抗原生动物特性研究较少。在这项工作中,我们描述了(5Z,9Z)-(±)-2-甲氧基-5,9-二十碳二烯酸(1)及其炔属类似物(±)-2-甲氧基-5,9-二十碳二炔酸(2)的全合成,并报告它们抑制(EC₅₀ 值在 31 和 22 μM 之间)利什曼原虫 DNA 拓扑异构酶 IB 酶(LdTopIB)。还研究了酸(±)-2-甲氧基-6-二十碳炔酸(12)对 LdTopIB 的抑制作用。LdTopIB 抑制的效力遵循趋势 2 > 1 > 12,表明抑制的有效性取决于不饱和程度。所有研究的α-甲氧基脂肪酸在 100 μM 时均不能抑制人拓扑异构酶 IB 酶(hTopIB)。然而,α-甲氧基脂肪酸能够抑制与喜树碱(CPT)不能相互作用的活性但截断的 LdTopIB,这表明甲氧基脂肪酸以不同于 CPT 的机制抑制 LdTopIB。二不饱和脂肪酸对利什曼原虫前鞭毛体显示出低细胞毒性(EC₅₀ 值在 260 和 240 μM 之间),但 12 对利什曼原虫前鞭毛体显示出更好的细胞毒性(EC₅₀ = 100 μM)和更好的治疗指数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/a93b2366e05f/marinedrugs-11-03661-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/8d4b4212b2df/marinedrugs-11-03661-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/91c43600572c/marinedrugs-11-03661-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/ea5bc9ec6348/marinedrugs-11-03661-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/79632da53dad/marinedrugs-11-03661-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/a93b2366e05f/marinedrugs-11-03661-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/8d4b4212b2df/marinedrugs-11-03661-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/91c43600572c/marinedrugs-11-03661-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/ea5bc9ec6348/marinedrugs-11-03661-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/79632da53dad/marinedrugs-11-03661-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e796/3826128/a93b2366e05f/marinedrugs-11-03661-g004.jpg

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3
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4
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