首页> 美国卫生研究院文献>Marine Drugs >Subereamolline A as a Potent Breast Cancer Migration Invasion and Proliferation Inhibitor and Bioactive Dibrominated Alkaloids from the Red Sea Sponge Pseudoceratina arabica
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Subereamolline A as a Potent Breast Cancer Migration Invasion and Proliferation Inhibitor and Bioactive Dibrominated Alkaloids from the Red Sea Sponge Pseudoceratina arabica

机译:Subereamolline A作为一种有效的乳腺癌迁移侵袭和增殖抑制剂以及来自阿拉伯红海海绵的生物活性二溴化生物碱。

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摘要

A new collection of several Red Sea sponges was investigated for the discovery of potential breast cancer migration inhibitors. Extracts of the Verongid sponges Pseudoceratina arabica and Suberea mollis were selected. Bioassay-directed fractionation of both sponges, using the wound-healing assay, resulted into the isolation of several new and known brominated alkaloids. Active fractions of the sponge Pseudoceratina arabica afforded five new alkaloids, ceratinines A–E (>2–>6), together with the known alkaloids moloka’iamine (>1), hydroxymoloka’iamine (>7) and moloka’iakitamide (>8). The active fraction of the sponge Suberea mollis afforded the three known alkaloids subereamolline A (>9), aerothionin (>10) and homoaerothionin (>11). Ceratinine B (>3) possesses an unprecedented 5,7-dibrominated dihydroindole moiety with an epoxy ring on the side chain of a fully substituted aromatic moiety. Ceratinines D (>5) and E (>6) possess a terminal formamide moiety at the ethylamine side chain. Subereamolline A (>9) potently inhibited the migration and invasion of the highly metastatic human breast cancer cells MDA-MB-231 at the nanomolar doses. Subereamolline A and related brominated alkaloids are novel scaffolds appropriate for further future use for the control of metastatic breast cancer.
机译:研究了几种新的红海海绵,以发现潜在的乳腺癌迁移抑制剂。选择Verongid海绵阿拉伯假单胞菌和软体动物的提取物。使用伤口愈合测定法对两种海绵进行生物测定指导的分级分离,结果分离出了几种新的和已知的溴化生物碱。海绵阿拉伯假单胞菌的活性级分提供了五种新生物碱,角蛋白碱A–E(> 2 – > 6 ),以及已知的生物碱莫洛卡胺(> 1 < / strong>),羟基茂胺(> 7 )和莫洛卡胺基酰胺(> 8 )。海绵亚甲脲活性成分提供了三种已知的生物碱亚甲酚A(> 9 ),Aerothionin(> 10 )和homoaerothionin(> 11 )。角蛋白B(> 3 )具有空前的5,7-二溴二氢吲哚部分,在完全取代的芳族部分的侧链上带有环氧环。角蛋白D(> 5 )和E(> 6 )在乙胺侧链上具有末端甲酰胺部分。亚氨基苯甲酸A(> 9 )以纳摩尔剂量有效抑制高度转移性人乳腺癌细胞MDA-MB-231的迁移和侵袭。亚甲氨蝶呤A和相关的溴化生物碱是适用于将来进一步用于控制转移性乳腺癌的新型支架。

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