Marine Fatty Acids as New Antifungal, Antimycobacterial, and Topo-l Agents

海洋脂肪酸作为新型抗真菌、抗分枝杆菌和拓扑醇药物

基本信息

项目摘要

DESCRIPTION (provided by applicant): Fatty acids play a critical role in human health. Our research group has been active in discovering new fatty acids from marine biota whose structures differ significantly from those of fatty acids normally encountered in terrestrial organisms. It is our aim to study further these novel fatty acids so as to better understand their biochemistry and their potential use in health related problems. In particular, we wish to answer the following questions: 1) Are the structural features of the novel marine fatty acids sufficiently different from those present in common fatty acids so as to significantly alter their biogenesis in prokaryotic and eukaryotic cells? 2) Will the marine fatty acids be sufficiently different from the more common and better studied fatty acids in their toxicity towards pathogenic agents such as fungi and/or mycobacteria? 3) Will the marine fatty acids be useful in helping to prevent and/or control diseases arising from fungi and mycobacteria? If the most unusual marine fatty acids are toxic to the causative agents of infectious diseases, then we can use them in food formulations and supplements that could help in the prevention, reduction, and/or treatment of fungal infections and/or more complex diseases such as tuberculosis. Our long-range goal, therefore, is to identify novel marine fatty acids with the potential of helping in the prevention, reduction, and/or treatment of infectious diseases. The objective of this application, which is the next step toward attainment of our long-range goal, is to explore the chemistry and toxicity of 2-methoxylated 5,9-diunsaturated fatty acids, mid-chain methoxylated fatty acids, and 4,5-methylene fatty acids by: (1) developing the first synthesis for racemic and quiral 2-methoxylated 5,9-diunsaturated fatty acids and determining their antimycobacterial, InhA, and topoisomerase-l inhibitory activities, (2) synthesizing a series of mid-chain methoxylated fatty acids and study their enoyl reductase (EcFabl) inhibitory activity, (3) developing the first synthesis for racemic and optically active 4,5-methylene fatty acids and determining their antifungal and antimycobacterial potential, and (4) carrying out a developmental plan to achieve competitiveness of the PI for non-SCORE support. At the end of this project we will provide new fatty acids that will be made available to biochemists, cell biologists, and pharmacologists to be used against these diseases. The novel antifungal compounds could also be used as yeast and mold inhibitors in food stuffs and as systematic antifungals.
描述(由申请人提供):脂肪酸在人体健康中起着关键作用。我们的研究小组一直在积极地从海洋生物中发现新的脂肪酸,其结构与陆地生物中通常遇到的脂肪酸有显着不同。我们的目标是进一步研究这些新型脂肪酸,以便更好地了解它们的生物化学及其在健康相关问题中的潜在用途。特别是,我们希望回答以下问题:1)新的海洋脂肪酸的结构特征是否与普通脂肪酸中存在的结构特征有足够的不同,从而显着改变它们在原核和真核细胞中的生物合成?2)海洋脂肪酸对病原体(如真菌和/或分枝杆菌)的毒性是否与更常见和更好研究的脂肪酸有足够的不同?3)海洋脂肪酸是否有助于预防和/或控制由真菌和分枝杆菌引起的疾病?如果最不寻常的海洋脂肪酸对传染病的病原体有毒,那么我们可以将它们用于食品配方和补充剂中,有助于预防,减少和/或治疗真菌感染和/或更复杂的疾病,如结核病。因此,我们的长期目标是确定具有帮助预防,减少和/或治疗传染病潜力的新型海洋脂肪酸。本申请的目的是通过以下方式探索2-甲氧基化5,9-二不饱和脂肪酸、中链甲氧基化脂肪酸和4,5-亚甲基脂肪酸的化学和毒性,这是实现我们长期目标的下一步:(1)首次开发了外消旋和喹喔啉2-甲氧基化5,9-二不饱和脂肪酸的合成方法,并测定了它们的抗分枝杆菌活性InhA,和拓扑异构酶-1抑制活性;(2)合成了一系列中链甲氧基化脂肪酸并研究了它们的烯酰还原酶(EcFabl)抑制活性;(3)首次合成了外消旋和光学活性的4,5-亚甲基脂肪酸并测定了它们的抗真菌和抗分枝杆菌潜力,以及(4)实施发展计划,以实现PI对非SCORE支持的竞争力。在这个项目结束时,我们将提供新的脂肪酸,将提供给生物化学家,细胞生物学家和药理学家用于治疗这些疾病。这些新的抗真菌化合物也可用作食品中的酵母和霉菌抑制剂以及系统抗真菌剂。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Nestor Manuel Carballeira其他文献

Nestor Manuel Carballeira的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('Nestor Manuel Carballeira', 18)}}的其他基金

Marine Fatty Acids as New Antifungal, Antimycobacterial, and Topo-l Agents
海洋脂肪酸作为新型抗真菌、抗分枝杆菌和拓扑醇药物
  • 批准号:
    7908886
  • 财政年份:
    2008
  • 资助金额:
    $ 25.64万
  • 项目类别:
Marine Fatty Acids as New Antifungal, Antimycobacterial, and Topo-l Agents
海洋脂肪酸作为新型抗真菌、抗分枝杆菌和拓扑醇药物
  • 批准号:
    8112609
  • 财政年份:
    2008
  • 资助金额:
    $ 25.64万
  • 项目类别:
Marine Fatty Acids as New Antifungal, Antimycobacterial, and Topo-l Agents
海洋脂肪酸作为新型抗真菌、抗分枝杆菌和拓扑醇药物
  • 批准号:
    7491954
  • 财政年份:
    2008
  • 资助金额:
    $ 25.64万
  • 项目类别:
Fatty Acid Analogs to treat Cancer/Infectious Diseases
用于治疗癌症/传染病的脂肪酸类似物
  • 批准号:
    6766332
  • 财政年份:
    2004
  • 资助金额:
    $ 25.64万
  • 项目类别:
NOVEL MARINE ANTIMICROBIAL LIPIDS
新型海洋抗菌脂质
  • 批准号:
    6609864
  • 财政年份:
    2002
  • 资助金额:
    $ 25.64万
  • 项目类别:
NOVEL MARINE ANTIMICROBIAL LIPIDS
新型海洋抗菌脂质
  • 批准号:
    6601188
  • 财政年份:
    2002
  • 资助金额:
    $ 25.64万
  • 项目类别:
NOVEL MARINE ANTIMICROBIAL LIPIDS
新型海洋抗菌脂质
  • 批准号:
    6631255
  • 财政年份:
    2002
  • 资助金额:
    $ 25.64万
  • 项目类别:
NOVEL MARINE ANTIMICROBIAL LIPIDS
新型海洋抗菌脂质
  • 批准号:
    6564516
  • 财政年份:
    2002
  • 资助金额:
    $ 25.64万
  • 项目类别:
NOVEL MARINE ANTIMICROBIAL LIPIDS
新型海洋抗菌脂质
  • 批准号:
    6472792
  • 财政年份:
    2001
  • 资助金额:
    $ 25.64万
  • 项目类别:
Support for University Biomedical Excellence at UPR-RP
UPR-RP 对大学生物医学卓越的支持
  • 批准号:
    10205075
  • 财政年份:
    2001
  • 资助金额:
    $ 25.64万
  • 项目类别:

相似海外基金

Functional Hybrid Natural Product Synthases by Tracking Acyl Carrier Protein Binding and Conformational Dynamics
通过跟踪酰基载体蛋白结合和构象动力学进行功能性杂化天然产物合成
  • 批准号:
    9171419
  • 财政年份:
    2016
  • 资助金额:
    $ 25.64万
  • 项目类别:
Functional Hybrid Natural Product Synthases by Tracking Acyl Carrier Protein Binding and Conformational Dynamics
通过跟踪酰基载体蛋白结合和构象动力学进行功能性杂化天然产物合成
  • 批准号:
    10581893
  • 财政年份:
    2016
  • 资助金额:
    $ 25.64万
  • 项目类别:
Functional Hybrid Natural Product Synthases by Tracking Acyl Carrier Protein Binding and Conformational Dynamics
通过跟踪酰基载体蛋白结合和构象动力学进行功能性杂化天然产物合成
  • 批准号:
    10045624
  • 财政年份:
    2016
  • 资助金额:
    $ 25.64万
  • 项目类别:
Screening of Plasmodium falciparum enoyl-Acyl carrier protein reductase (PfFabI) inhibitors from microbial metabolites for prophylaxis and blocking transmission of malaria
从微生物代谢产物中筛选恶性疟原虫烯酰酰基载体蛋白还原酶 (PfFabI)​​ 抑制剂,用于预防和阻断疟疾传播
  • 批准号:
    26460128
  • 财政年份:
    2014
  • 资助金额:
    $ 25.64万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Mechanism-based crosslinkers of acyl carrier protein dehydratase
基于机制的酰基载体蛋白脱水酶交联剂
  • 批准号:
    24810015
  • 财政年份:
    2012
  • 资助金额:
    $ 25.64万
  • 项目类别:
    Grant-in-Aid for Research Activity Start-up
Structure and function of acyl carrier protein
酰基载体蛋白的结构和功能
  • 批准号:
    155331-2008
  • 财政年份:
    2012
  • 资助金额:
    $ 25.64万
  • 项目类别:
    Discovery Grants Program - Individual
Structure and function of acyl carrier protein
酰基载体蛋白的结构和功能
  • 批准号:
    155331-2008
  • 财政年份:
    2011
  • 资助金额:
    $ 25.64万
  • 项目类别:
    Discovery Grants Program - Individual
Structure and function of acyl carrier protein
酰基载体蛋白的结构和功能
  • 批准号:
    155331-2008
  • 财政年份:
    2010
  • 资助金额:
    $ 25.64万
  • 项目类别:
    Discovery Grants Program - Individual
Structure and function of acyl carrier protein
酰基载体蛋白的结构和功能
  • 批准号:
    155331-2008
  • 财政年份:
    2009
  • 资助金额:
    $ 25.64万
  • 项目类别:
    Discovery Grants Program - Individual
Structure and function of acyl carrier protein
酰基载体蛋白的结构和功能
  • 批准号:
    155331-2008
  • 财政年份:
    2008
  • 资助金额:
    $ 25.64万
  • 项目类别:
    Discovery Grants Program - Individual
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了