DRUG DISCOVERY FROM PLANTS OF VIETNAM AND LAOS FOR AIDS AND MALARIA THERAPIES
从越南和老挝植物中发现的治疗艾滋病和疟疾的药物
基本信息
- 批准号:6663463
- 负责人:
- 金额:$ 13.47万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2002
- 资助国家:美国
- 起止时间:2002-09-30 至 2003-09-29
- 项目状态:已结题
- 来源:
- 关键词:AIDS therapy Plasmodium falciparum antiAIDS agent antimalarial agents bioassay chemical structure chromatography cooperative study cytotoxicity drug discovery /isolation drug screening /evaluation green fluorescent proteins lymphocyte macrophage mass spectrometry medicinal plants nuclear magnetic resonance spectroscopy plant extracts southeast Asia tissue /cell culture virus replication
项目摘要
The major objective of Associate Project-3 (AP-3) is to isolate and
identify specific inhibitors of HIV replication and agents active against
chloroquine-resistant Plasmodium falciparum. It will provide bioassay
support for the discovery of natural products effective against malaria
and AIDS through the screening of approximately 500 plant extracts
annually followed by bioactivity fractionation procedures. Source
materials for evaluation will be selected and collected under and Lao
People's Democratic Republic. A primarily biodiversity-based selection
approach will be adopted, although ethnobotanical inquiry may be employed
to a limited extent. This project will also perform initial extraction of
plant materials and scale-up isolation of confirmed active phytochemicals.
Spectroscopic and chemical methods will be used to determine the
structures of pure bioactive compounds. Efforts will be made to minimize
the re-isolation of compounds with known anti-HIV or anti-malarial
properties through literature (NAPRALERT) and LC/MS/MS dereplication
techniques. Additionally, several inhibitors of HIV-1 reverse
transcriptase (RT) and numerous promising anti-malarial compounds and
extracts have been identified through ongoing collaborative drug discovery
efforts with researchers in Vietnam. These biologically active natural
products will be re-isolated and evaluated in more physiologically complex
bioassay systems and relevant mechanistic assays in order to prioritize
them for more advanced in vivo studies. In concert with Glaxo Wellcome,
active compounds will be evaluated as candidates for development as drugs.
Alternatively, novel isolates may be considered as new leads for the
development of selective inhibitors.
联合项目3 (AP-3)的主要目标是分离和
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 }}
John M. Pezzuto其他文献
Botanicals in Cancer Chemoprevention
- DOI:
10.1023/a:1021254725842 - 发表时间:
2002-12-01 - 期刊:
- 影响因子:8.700
- 作者:
Eun Jung Park;John M. Pezzuto - 通讯作者:
John M. Pezzuto
Synthesis, molecular docking and anticancer studies of peptides and <em>iso</em>-peptides
- DOI:
10.1016/j.bmcl.2015.05.020 - 发表时间:
2015-08-01 - 期刊:
- 影响因子:
- 作者:
Farukh Jabeen;Siva S. Panda;Tamara P. Kondratyuk;Eun-Jung Park;John M. Pezzuto;C. Dennis Ihsan-ul-haq;Alan R. Hall; Katritzky - 通讯作者:
Katritzky
Natural modulators of estrogen biosynthesis and function as chemopreventive agents
- DOI:
10.1007/bf02975150 - 发表时间:
2001-12-01 - 期刊:
- 影响因子:7.500
- 作者:
Krishna P. L. Bhat;John M. Pezzuto - 通讯作者:
John M. Pezzuto
Anti-inflammatory Quinoline Alkaloids from the Roots of Waltheria indica
来自 Waltheria indica 根的抗炎喹啉生物碱
- DOI:
10.1021/acs.jnatprod.2c00861 - 发表时间:
- 期刊:
- 影响因子:5.1
- 作者:
Feifei Liu;Timothy J. O’Donnell;Eun-Jung Park;Sasha Kovacs;Kenzo Nakamura;Asim Dave;Yuheng Luo;Rui Sun;Marisa Wall;Supakit Wongwiwatthananukit;Dane Kaohelani Silva;Philip G. Williams;John M. Pezzuto;Leng Chee Chang - 通讯作者:
Leng Chee Chang
Analysis of Gossypol and Gossypol-Acetic Acid by High-Performance Liquid Chromatography
- DOI:
10.1002/jps.2600730328 - 发表时间:
1984-03-01 - 期刊:
- 影响因子:
- 作者:
Guido B. Marcelle;John M. Pezzuto;Donald P. Waller;D.D. Soejarto;H.H.S. Fong;Mohamed S. Ahmed;Geoffrey A. Cordell - 通讯作者:
Geoffrey A. Cordell
John M. Pezzuto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('John M. Pezzuto', 18)}}的其他基金
COLLEGE OF PHARMACY RESEARCH INNOVATION (COPRI) CORE
药学院研究创新(COPRI)核心
- 批准号:
8360711 - 财政年份:2011
- 资助金额:
$ 13.47万 - 项目类别:
Nutritional Supplements and Cancer Chemoprevention
营养补充剂和癌症化学预防
- 批准号:
6559789 - 财政年份:2002
- 资助金额:
$ 13.47万 - 项目类别:
DRUG DISCOVERY FROM PLANTS OF VIETNAM AND LAOS FOR AIDS AND MALARIA THERAPIES
从越南和老挝植物中发现的治疗艾滋病和疟疾的药物
- 批准号:
6504593 - 财政年份:2001
- 资助金额:
$ 13.47万 - 项目类别:
SCREENING OF VARIOUS CHEMOPREVENTIVE AGENTS IN THE MNU-I
MNU-I 中各种化学预防药物的筛选
- 批准号:
6358327 - 财政年份:2000
- 资助金额:
$ 13.47万 - 项目类别:
SCREENING EMPLOYING A TRANSGENIC MOUSE MODEL WHICH YIELD
使用产生的转基因小鼠模型进行筛选
- 批准号:
6358333 - 财政年份:2000
- 资助金额:
$ 13.47万 - 项目类别:
相似海外基金
Genomics and sero-epidemiology of Plasmodium falciparum malaria in a pre-elimination setting
消灭前环境中恶性疟原虫疟疾的基因组学和血清流行病学
- 批准号:
10666280 - 财政年份:2023
- 资助金额:
$ 13.47万 - 项目类别:
Elucidating mechanisms for artemisinin-induced dormancy in Plasmodium falciparum
阐明青蒿素诱导恶性疟原虫休眠的机制
- 批准号:
10742385 - 财政年份:2023
- 资助金额:
$ 13.47万 - 项目类别:
Investigating the role of SCF ubiquitin ligases during sexual development of Plasmodium falciparum
研究 SCF 泛素连接酶在恶性疟原虫性发育过程中的作用
- 批准号:
MR/W025566/1 - 财政年份:2023
- 资助金额:
$ 13.47万 - 项目类别:
Research Grant
Rotation 1: Investigating the role(s) of the putative FANCJ helicase in the malaria parasite Plasmodium falciparum
第 1 轮:研究假定的 FANCJ 解旋酶在疟原虫恶性疟原虫中的作用
- 批准号:
2886902 - 财政年份:2023
- 资助金额:
$ 13.47万 - 项目类别:
Studentship
Exploring the role of phosphoinositides in the trafficking of proteins to the apical complex in the malaria parasite Plasmodium falciparum.
探索磷酸肌醇在疟原虫恶性疟原虫顶复合体蛋白质运输中的作用。
- 批准号:
495093 - 财政年份:2023
- 资助金额:
$ 13.47万 - 项目类别:
Operating Grants
DDT-BMQ-0000100 Qualification of the Plasmodium falciparum 18S rRNA biomarker for malaria-endemic controlled human malaria infection studies
DDT-BMQ-0000100 疟疾流行控制人类疟疾感染研究中恶性疟原虫 18S rRNA 生物标志物的鉴定
- 批准号:
10836140 - 财政年份:2023
- 资助金额:
$ 13.47万 - 项目类别:
Defining molecular determinants of Plasmodium falciparum hematopoietic infection using single cell profiling and genetics
使用单细胞分析和遗传学定义恶性疟原虫造血系统感染的分子决定因素
- 批准号:
EP/Y003705/1 - 财政年份:2023
- 资助金额:
$ 13.47万 - 项目类别:
Fellowship
Detailed mechanism of trafficking proteins involved in the virulence of Plasmodium falciparum
恶性疟原虫毒力中涉及的运输蛋白的详细机制
- 批准号:
22KF0032 - 财政年份:2023
- 资助金额:
$ 13.47万 - 项目类别:
Grant-in-Aid for JSPS Fellows
Étude du rôle de la phosphatase de phosphoinositides SAC1 dans le trafic de protéines au complexe apical chez le parasite de la malaria Plasmodium falciparum
疟疾疟原虫顶端寄生虫复合物中磷酸肌醇磷酸酶 SAC1 的研究
- 批准号:
486094 - 财政年份:2022
- 资助金额:
$ 13.47万 - 项目类别:
Studentship Programs
In vitro bioreactor production of a genetically modified late liver stage-arresting replication competent Plasmodium falciparum sporozoite vaccine
体外生物反应器生产具有复制能力的转基因晚期肝阶段恶性疟原虫子孢子疫苗
- 批准号:
10547414 - 财政年份:2022
- 资助金额:
$ 13.47万 - 项目类别: