Development of Novel Inhibitors of Glutamate Carboxypeptidase II
Development of Novel Inhibitors of Glutamate Carboxypeptidase II
批准号:
7560216
负责人:
Marc O Anderson
金额:
$13.8万
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:
2009-03-01 至 2012-02-29
关键词:
Active SitesAddressAlzheimer&aposs DiseaseAmidesAppointmentAreaBindingBioavailableBiological AvailabilityBiological ModelsBlood - brain barrier anatomyCCL7 geneChargeChemical StructureChimeric ProteinsClinicalCollaborationsComplementComprehensive Cancer CenterComputersConsultCoupledCrystallographyDevelopmentDiagnostic ImagingDiseaseDockingDrug Delivery SystemsDrug DesignDrug KineticsEducational CurriculumEducational process of instructingEducational workshopEnzymesEventFacultyFeedbackFundingFutureGenerationsGlutamate Carboxypeptidase IIGlutamatesGoalsGrantGrowthHIV Envelope Protein gp41HumanHydrolysisHydroxamic AcidsHydroxylamineImaging TechniquesInsulin-Like Growth Factor ReceptorKnowledgeLabelLaboratoriesLassa FeverLearningLiteratureMalignant neoplasm of prostateManuscriptsMembraneMentorsMetalloproteasesMethodsMolecular GeneticsMotivationNatural SciencesNeurologicNeuroprotective AgentsNordihydroguaiaretic AcidOperative Surgical ProceduresOralOrganic ChemistryOrphan DiseasePaperParkinson DiseasePermeabilityPharmaceutical ChemistryPharmaceutical PreparationsPharmacologic SubstancePhilosophyPositioning AttributePostdoctoral FellowPrimary Lateral SclerosisProcessPropertyProtease InhibitorProteinsProteolysisPublic HealthPublicationsPublishingRadioReactionReceptor Protein-Tyrosine KinasesRecruitment ActivityResearchSan FranciscoScientistSecureStrokeStructureStudentsSulfonamidesTechniquesTraumatic Brain InjuryUniversitiesVariantViral Fusion ProteinsWorkZincabsorptionanalogantitumor drugbasebioimagingcancer therapycarboxyl groupcareercareer developmentdesigndrug developmentexperiencefascinatefunctional groupgraduate studenthydroxamateimprovedin vitro activityin vivoinhibitor/antagonistinstructorlecturesmalignant breast neoplasmmembernext generationnovelprogramsscaffoldskillssmall moleculesymposiumtext searchingtool
中文摘要
描述(由申请人提供):谷氨酸羧肽酶II (GCPII)是治疗许多神经系统疾病以及前列腺癌诊断成像和治疗的重要靶点。该酶是一种膜结合金属肽酶,具有良好的酶活性。GCPII抑制剂的开发是识别神经保护剂的一种很有前途的方法,可以用于治疗许多人类疾病,包括创伤性脑损伤、中风、肌萎缩侧索硬化症(ALS)、阿尔茨海默病、帕金森病和其他疾病。虽然几种抑制剂设计已经获得了有效的体外活性,但由于药代动力学问题,将这些化合物开发成有用的药物是复杂的。特别是,GCPII抑制剂通常是高电荷分子,不能口服生物利用和/或不能通过血脑屏障,限制了它们用于治疗神经系统疾病。这些研究将试图建立新的GCPII抑制剂类别,这些抑制剂有望有效并具有改善的药代动力学特性。这些研究的另一个目标将是检查等压变化对抑制剂效力的影响。具体目标:(1)开发谷氨酸羧肽酶II的新型n -羟谷氨酰基抑制剂(2)利用基于结构的方法开发谷氨酰基磺胺类新型谷氨酸羧肽酶II抑制剂(3)修饰谷氨酸羧肽酶II抑制剂以改善药代动力学。GCPII抑制剂对于许多重要的神经系统疾病是一种很有希望的治疗方法,并且通过它们与这种酶的相互作用,可以作为神经保护药物。此外,由于GCPII在前列腺癌中过度表达,使用小分子抑制剂靶向该蛋白进行生物成像和癌症治疗是一个非常重要的目标。
英文摘要
DESCRIPTION (provided by applicant): Glutamate carboxypeptidase II (GCPII) is an important target for the treatment of a number of neurological conditions, as well as for diagnostic imaging and treatment of prostate cancer. The enzyme is a membrane- bound metallopeptidase with well-characterized enzymatic activities. Development of GCPII inhibitors is a promising approach for the identification of neuroprotective agents that could be useful to treat a number of human ailments, including traumatic brain injury, stroke, amytrophic lateral sclerosis (ALS), Alzheimer's disease, Parkinson's disease, and other diseases. While several inhibitor designs have obtained potent in vitro activity, developing such compounds into useful drugs is complicated by pharmacokinetic issues. Particularly, GCPII inhibitors are often highly charged molecules that are not orally bioavailable and/or do not pass through the blood brain barrier, limiting their use to treat neurological conditions. These studies will attempt to establish new classes of GCPII inhibitors which are expected to be potent and have improved pharmacokinetic properties. Another goal of these studies will be to examine the effect of isosteric variation on inhibitor potency. Specific Aims: (1) Development of novel N-hydroxyglutamyl inhibitors of glutamate carboxypeptidase II (2) Develop novel glutamyl sulfonamides as inhibitors of glutamate carboxypeptidase II using a structure-based approach (3) Modify glutamate carboxypeptidase II inhibitors to improve pharmacokinetics. Project Narrative: Relevance to public health GCPII inhibitors are a promising treatment for a number of significant neurological conditions, and through their interaction with this enzyme, may serve as neuroprotective drugs. Furthermore, as GCPII is over expressed in prostate cancer, the use of small molecule inhibitors to target for this protein for bioimaging and cancer therapy is a very important goal.
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Development of inhibitors of the calcium-activated chloride channel TMEM16a
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批准号:8575042
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项目类别:
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资助金额:$28.4万
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财政年份:2013
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负责人:Marc O Anderson
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依托单位:
Development of Novel Inhibitors of Glutamate Carboxypeptidase II
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批准号:8035988
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项目类别:
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资助金额:$14.81万
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财政年份:2009
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负责人:Marc O Anderson
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依托单位:
Development of Novel Inhibitors of Glutamate Carboxypeptidase II
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批准号:7777336
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项目类别:
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资助金额:$14.84万
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财政年份:2009
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负责人:Marc O Anderson
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依托单位:
海外基金