The next generation of synthetically-accessible anticancer drugs exist at minor c
The next generation of synthetically-accessible anticancer drugs exist at minor c
批准号:
7747814
负责人:
GARY R ELDRIDGE
金额:
$12.06万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-08-01 至 2010-07-31
关键词:
AgingAntineoplastic AgentsApoptosisBiological AssayBiological FactorsBreathingChemical StructureChemicalsClinicalCollectionDataDevelopmentDiagnosisDolastatin CompoundDrug DesignEducational process of instructingExhibitsFailureGenomicsGoalsGrowthHigh Pressure Liquid ChromatographyHumanIndividualIonsLeadLibrariesMCF7 cellMalignant NeoplasmsMammary NeoplasmsMinorNational Cancer InstituteNatural Products ChemistryNaturePhasePlantsPopulationProcessPublishingResearchResearch MethodologyScienceScreening procedureSequoiaSmall Business Innovation Research GrantSourceStilbenesStructureStudy SectionTechnologyTestingTimeTumor Cell LineUnited StatesWorkbasebryostatincombinatorial chemistrydrug discoveryexpectationexperienceindexinginnovationinsightmacrophagemeetingsnew technologynext generationnovelphenanthrenepublic health relevancescaffold
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Treating cancer is clearly a very difficult process, and while progress has been made, much work remains to be done. The failures of many seemingly promising compounds to meet expectations have taught us that we must aggressively continue to develop new, innovative research methods to discover new anticancer agents. The objective of this Phase 1 SBIR project is to identify novel anticancer compounds existing at minor concentrations in unstudied plants, so that they can inspire the next generation of anticancer drugs. Sequoia Sciences is a recognized leader in natural products chemistry. Sequoia's published and unpublished data overwhelmingly suggest that new chemical diversity exists at minor concentrations in plants, and that some of these compounds are readily synthetically attainable. In this Phase 1 SBIR proposal, Sequoia presents compelling data on extensively purified and dereplicated chromatographic fractions that inhibit the growth of human tumor cell lines. These data suggest that compounds with novel chemical structures and novel inhibitory activities will be identified during this Phase 1 SBIR. In the era of combinatorial chemistry, genomics, and structure-aided drug design, it is tempting to think that the structural diversity evolved in nature is no longer needed; it has become resoundingly clear, however, that these new technologies alone will not meet the needs of the rapidly aging US population. Medicinal chemists immediately require new structural inspiration from the distinct chemical space occupied by natural products. This Phase 1 SBIR proposes a detailed plan to provide this new structural inspiration for medicinal chemists. PUBLIC HEALTH RELEVANCE: According to the NCI, 565,560 people will die from cancer in 2008 the United States alone. Based on rates from 2003-2005, it is likely that 43% of all people born today will be diagnosed with some form of cancer. Treating cancer is clearly a very difficult process, and while progress has been made, much work remains to be done. It has become resoundingly clear, however, that current technologies alone will not meet the needs of the rapidly aging US population. The objective of this Phase 1 SBIR project is to identify novel anticancer compounds existing at minor concentrations in unstudied plants, so that they can inspire the next generation of anticancer drugs. Medicinal chemists immediately require new structural inspiration from the distinct chemical space occupied by natural products.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1055/s-0031-1280293
发表时间:
2012
期刊:
Planta medica
影响因子:
2.7
作者:
[Russell B Williams;Steven M Martin;Jin-Feng Hu;E. Garo;S. M. Rice;Vanessa L. Norman;Julie A. Lawrence;Grayson W. Hough;M. Goering;M. O’Neil-Johnson;G. Eldridge;C. Starks]
通讯作者:
Russell B Williams;Steven M Martin;Jin-Feng Hu;E. Garo;S. M. Rice;Vanessa L. Norman;Julie A. Lawrence;Grayson W. Hough;M. Goering;M. O’Neil-Johnson;G. Eldridge;C. Starks
Abronione, a rotenoid from the desert annual Abronia villosa.
Abronione,一种来自沙漠一年生 Abronia villosa 的鱼藤素。
DOI:
10.1016/j.phytol.2010.08.004
发表时间:
2011
期刊:
Phytochemistry letters
影响因子:
1.7
作者:
[Starks,CourtneyM, Williams,RussellB, Norman,VanessaL, Lawrence,JulieA, Goering,MattG, O'Neil-Johnson,Mark, Hu,Jin-Feng, Rice,StephanieM, Eldridge,GaryR]
通讯作者:
Eldridge,GaryR
Phenylpropanoids from Phragmipedium calurum and their antiproliferative activity.
Phragmipedium calurum 中的苯丙素及其抗增殖活性。
DOI:
10.1016/j.phytochem.2012.06.017
发表时间:
2012
期刊:
Phytochemistry
影响因子:
3.8
作者:
[Starks,CourtneyM, Williams,RussellB, Norman,VanessaL, Lawrence,JulieA, O'Neil-Johnson,Mark, Eldridge,GaryR]
通讯作者:
Eldridge,GaryR
海外基金