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Motualevic acids A-F, antimicrobial acids from the sponge Siliquariaspongia sp.莫图莱维酸 A-F,来自海绵 Siliquaria sp. 的抗菌酸
Org Lett. 2009 Mar 5;11(5):1087-90. doi: 10.1021/ol802890b.
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J Med Chem. 2008 Apr 10;51(7):1981-90. doi: 10.1021/jm800038g. Epub 2008 Mar 14.
3
Drugs for bad bugs: confronting the challenges of antibacterial discovery.对抗耐药菌的药物:应对抗菌药物研发的挑战
Nat Rev Drug Discov. 2007 Jan;6(1):29-40. doi: 10.1038/nrd2201. Epub 2006 Dec 8.
4
Antibacterial natural products in medicinal chemistry--exodus or revival?药物化学中的抗菌天然产物——是衰落还是复兴?
Angew Chem Int Ed Engl. 2006 Aug 4;45(31):5072-129. doi: 10.1002/anie.200600350.
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Synthesis of marine polyacetylenes callyberynes A-C by transition-metal-catalyzed cross-coupling reactions to sp centers.通过过渡金属催化的交叉偶联反应合成海洋聚乙炔类化合物卡利贝炔A - C至sp中心。
J Org Chem. 2006 Mar 31;71(7):2802-10. doi: 10.1021/jo052609u.
6
Development of a concise and diversity-oriented approach for the synthesis of plecomacrolides via the diene-ene RCM.通过双烯-烯复分解反应合成多球壳菌素的简洁且注重多样性方法的开发。
Org Lett. 2006 Mar 16;8(6):1193-6. doi: 10.1021/ol060221v.
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Empirical antibacterial drug discovery--foundation in natural products.经验性抗菌药物发现——基于天然产物
Biochem Pharmacol. 2006 Mar 30;71(7):1006-15. doi: 10.1016/j.bcp.2005.12.016. Epub 2006 Jan 19.
8
Daptomycin: a new drug class for the treatment of Gram-positive infections.达托霉素:用于治疗革兰氏阳性菌感染的新型药物类别。
Drugs Today (Barc). 2005 Feb;41(2):81-90. doi: 10.1358/dot.2005.41.2.882660.
9
Introduction: antibiotic resistance.引言:抗生素耐药性。
Chem Rev. 2005 Feb;105(2):391-4. doi: 10.1021/cr030100y.
10
Antibacterial resistance worldwide: causes, challenges and responses.全球抗菌药物耐药性:原因、挑战及应对措施
Nat Med. 2004 Dec;10(12 Suppl):S122-9. doi: 10.1038/nm1145.

莫图拉维酸及其类似物的合成及抗菌构效关系。

Motualevic acids and analogs: synthesis and antimicrobial structure-activity relationships.

机构信息

Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Bioorg Med Chem Lett. 2010 Jul 15;20(14):4108-11. doi: 10.1016/j.bmcl.2010.05.073. Epub 2010 Jun 9.

DOI:10.1016/j.bmcl.2010.05.073
PMID:20538459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2900419/
Abstract

Synthesis of the marine natural products motualevic acids A, E, and analogs in which modifications have been made to the omega-brominated lipid (E)-14,14-dibromotetra-deca-2,13-dienoic acid or amino acid unit are reported, together with antimicrobial activities against Staphylococcus aureus, methicillin-resistant S. aureus, Enterococcus faecium, and vancomycin-resistant Enterococcus.

摘要

报道了海洋天然产物莫特乌列维酸 A、E 及其类似物的合成,这些类似物对ω-溴化脂质(E)-14,14-二溴十四碳-2,13-二烯酸或氨基酸单元进行了修饰,同时还具有抗金黄色葡萄球菌、耐甲氧西林金黄色葡萄球菌、屎肠球菌和万古霉素耐药肠球菌的抗菌活性。