Selective LPA1 receptor antagonists as agents in prevention of renal fibrosis
Selective LPA1 receptor antagonists as agents in prevention of renal fibrosis
批准号:
8251867
负责人:
ANIL K KARIHALOO
金额:
$38.96万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-03-01 至 2013-08-28
关键词:
ActinsAnimal ModelApoptosisAreaBiochemicalBiologicalBiological AssayCYP2D6 geneCYP3A4 geneCell ProliferationCellsCharacteristicsChemicalsChemistryChronic Kidney FailureDNA Sequence RearrangementDataDevelopmentDoseDrug InteractionsEffectivenessEnd stage renal failureEnsureEnzymesEpithelial CellsFibrosisGoalsHigh Pressure Liquid ChromatographyHumanHuman CloningIn VitroIsoxazolesKidneyLeadLegal patentLibrariesLifeLigandsLysophosphatidic Acid ReceptorsLysophospholipidsMAPK1 geneMAPK3 geneMinorModelingModificationMusOutcomePathway interactionsPermeabilityPharmaceutical PreparationsPhasePhosphorylationPreparationPreventionPropertyRenal Replacement TherapyReportingResearch DesignResearch MethodologyRiskSeriesSignal TransductionStructureSystemTestingTubular formationUreteral obstructionWorkanalogbasedrug discoveryepithelial to mesenchymal transitionhigh throughput screeningin vitro Assayin vitro activityin vivolysophosphatidic acidmeetingsmortalitynovelnovel therapeuticsphase 1 studyphase 2 studypreventprogramsreceptorresponsevzg-1 Receptor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The ultimate goal of our project is to develop novel therapeutics effective in chronic kidney diseases that normally develop fibrosis, lead to end stage renal disease and require renal replacement therapy. This will be achieved by identifying novel selective functional antagonists for the lysophosphatidic acid (LPA) type 1 receptor. Our drug discovery approach will synthesize novel compounds free of drug-drug interaction risks that demonstrate selective, functional antagonism of the LPA-1 receptor. Their effectiveness will be confirmed using a series of high throughput cell-based assays. Candidate molecules will then be evaluated for their ability to prevent the progression of renal fibrosis in a unilateral ureteral obstruction (UUO) animal model. The intent of this Phase 1 study is to identify at least one novel series of molecules for lead optimization in a Phase 2 program.
PUBLIC HEALTH RELEVANCE: The objective is to discover and develop new drugs for treating chronic kidney diseases that involve renal fibrosis, a significant cause of mortality.
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Development of novel agents for the treatment of renal fibrosis
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批准号:8780197
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项目类别:
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资助金额:$61.63万
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财政年份:2012
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负责人:ANIL K KARIHALOO
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依托单位:
Role of Glypicans in HGF Mediated Cell Morphogenesis
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批准号:7279669
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项目类别:
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资助金额:$0.1万
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财政年份:2003
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负责人:ANIL K KARIHALOO
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依托单位:
Role of Glypicans in HGF Mediated Cell Morphogenesis
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批准号:6892388
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项目类别:
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资助金额:$11.83万
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财政年份:2003
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负责人:ANIL K KARIHALOO
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依托单位:
Role of Glypicans in HGF Mediated Cell Morphogenesis
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批准号:6744097
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项目类别:
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资助金额:$11.56万
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财政年份:2003
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负责人:ANIL K KARIHALOO
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依托单位:
Role of Glypicans in HGF Mediated Cell Morphogenesis
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批准号:6602379
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项目类别:
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资助金额:$11.31万
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财政年份:2003
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负责人:ANIL K KARIHALOO
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依托单位:
EPITHELIAL BRANCHING MORPHOGENESIS AND ENDOSTATIN
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批准号:6554742
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项目类别:
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资助金额:$5.44万
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财政年份:2002
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负责人:ANIL K KARIHALOO
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依托单位:
EPITHELIAL BRANCHING MORPHOGENESIS AND ENDOSTATIN
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批准号:6447271
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项目类别:
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资助金额:$4.73万
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财政年份:2001
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负责人:ANIL K KARIHALOO
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依托单位:
海外基金