BRD4 Inhibitors as Potential Therapeutics for Oncology
BRD4 抑制剂作为肿瘤学的潜在治疗药物
基本信息
- 批准号:9551899
- 负责人:
- 金额:$ 25.16万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:Antineoplastic AgentsBiologyCellsChemicalsCollaborationsCommunitiesDevelopmentDiseaseExtramural ActivitiesFosteringGeneral PopulationGenomicsGoalsInformaticsLeadModelingPharmaceutical ChemistryPharmaceutical PreparationsPhenotypeProcessProtocols documentationPublicationsResearchResearch PersonnelResourcesSynthesis ChemistryTherapeuticUnited States National Institutes of HealthValidationWorkassay developmentbasedrug developmentdrug discoveryhigh throughput screeninghuman diseaseimprovedinhibitor/antagonistnew technologynovelnovel therapeuticsoncologyscreeningsmall moleculesmall molecule therapeuticstherapeutic developmenttool
项目摘要
During this period, the NCGC has worked to adapt existing cell-based protocols like CETSA to enable characterization of potential BRD4 inhibitors.
As a center, the NCGC has fostered and maintained over 130 active collaborations with both NIH and extramural investigators, facilitating drug discovery efforts across the entire spectrum of human disease. These efforts have led to dozens of high-throughput screens and a number of medicinal chemistry campaigns to further improve on screening hits, providing our collaborators and the general research community with publications and a variety of promising small molecule probes and leads. In addition, the NCGC has worked to advance a number of informatic initiatives to make better use of existing drug and disease target information and provide the general public with easily accessible resources, further catalyzing the development of new therapies for human disease.
在此期间,NCGC致力于调整现有的基于细胞的方案,如CETSA,以表征潜在的BRD4抑制剂。
作为一个中心,NCGC与NIH和校外研究人员建立并保持了130多个积极的合作关系,促进了整个人类疾病领域的药物发现工作。 这些努力已经促成了数十项高通量筛选和许多药物化学活动,以进一步改进筛选结果,为我们的合作者和一般研究界提供出版物和各种有前途的小分子探针和线索。 此外,NCGC还致力于推进多项信息化举措,以更好地利用现有的药物和疾病靶点信息,并为公众提供易于获取的资源,进一步促进人类疾病新疗法的开发。
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)
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Matthew Hall其他文献
Matthew Hall的其他文献
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{{ truncateString('Matthew Hall', 18)}}的其他基金
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