Novel 12/15 lipoxygenase inhibitors for the treatment of stroke
Novel 12/15 lipoxygenase inhibitors for the treatment of stroke
批准号:
8684486
负责人:
KLAUS VAN LEYEN
金额:
$30.26万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-05-15 至 2016-04-30
关键词:
ALOX15 geneAdjuvantAffinityAlteplaseAnimalsArachidonate 15-LipoxygenaseBehavioralBiological AssayBlood - brain barrier anatomyBrainBrain InjuriesCYP2D6 geneCYP3A4 geneCause of DeathCell DeathCellsCerebral IschemiaCharacteristicsCultured CellsDoseDrug KineticsEndothelial CellsEnzymesExtravasationFemaleGenderGlutamatesGoalsHemorrhageHippocampus (Brain)HourHumanIn VitroInfarctionIschemiaIschemic StrokeKnock-outLOX geneLaboratoriesLigandsLipoxygenase InhibitorsMetabolicMicrosomesMiddle Cerebral Artery OcclusionModelingMorbidity - disease rateMusNeuronsNeuroprotective AgentsOutcome StudyOxidative StressPTGS2 genePenetrancePharmaceutical ChemistryPharmaceutical PreparationsPharmacodynamicsProcessPropertyProstaglandin-Endoperoxide SynthaseProtein IsoformsSolubilitySourceStrokeSystemTestingTherapeuticThrombosisThrombotic StrokeTimeUnited Statesaqueousbasechemical synthesisclinical applicationcyclooxygenase 1designdisabilitydrug discoveryimprovedin vivoinhibitor/antagonistintravenous administrationmalemortalitymouse modelneuron lossneuroprotectionnewsnovelnovel therapeuticsprotective effectpublic health relevanceresearch studyscreeningstroke therapythrombolysis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal is to develop novel therapeutics effective in stroke. This will be achieved by advancing candidate molecules toward clinical application utilizing our assay cascade to identify novel, selective inhibitors of the 12/15 lipoxygenase that protect against ischemic stroke. Our drug discovery approach will be to synthesize novel ligands based on the LOXBlock inhibitors that are potent inhibitors of the human 12/15 lipoxygenase and that protect neurons against oxidative stress-related cell death. Candidate molecules will undergo profiling to assess criteria specifically related to the physicochemical properties of compounds in a therapeutic setting, including enzyme selectivity and tests to determine potential interactions with key metabolic enzyme systems. Best candidates will be tested for protection against experimental stroke in mice.
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会议论文
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海外基金