Design and Study of New Nicotinic Analogs for Use in Depression
Design and Study of New Nicotinic Analogs for Use in Depression
批准号:
8547822
负责人:
alan P. kozikowski
金额:
$81.94万
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:
2009-08-10 至 2016-05-31
关键词:
AdolescenceAdverse effectsAffectAffinityAgonistAlgorithmsAlzheimer&aposs DiseaseAntidepressive AgentsAreaBackBehaviorBehavior assessmentBehavioralBehavioral AssayBiological AssayBiological AvailabilityCellsChemical AgentsChicagoCytochrome P450CytosineDatabasesDevelopmentDrug DesignElectrodesEmotionsEnsureEvaluationExhibitsFamilyFingerprintGoalsGrantHumanIllinoisIn VitroIncidenceIndustryInstitutesInstructionIonsLeadLigandsMalignant neoplasm of prostateMammalian CellMarketingMeasuresMecamylamineMedicalMental DepressionMethodsMolecular ModelsMoodsMuscleNeurologicNeurosciencesNicotineNicotine DependenceNicotinic AgentsNicotinic ReceptorsPainPathway interactionsPharmaceutical ChemistryPharmaceutical PreparationsPositron-Emission TomographyPropertyRecording of previous eventsRelative (related person)ResearchResearch DesignResolutionRiskRodentRoentgen RaysSchizophreniaScopolamineSelf MedicationSeriesSexual DysfunctionSystemTechniquesTestingTherapeuticTobaccoToxic effectToxicologyUniversitiesWorkXenopus oocyteanalogbasebehavior testchannel blockerscholinergicclinical applicationdata miningdesigndrug discoveryexperiencehigh throughput screeningin vivoin vivo Modelinnovationinterestmeetingsmetabolic abnormality assessmentmolecular modelingnovelpatch clamppreclinical evaluationprogramsresearch clinical testingstable cell linesuicidalvoltage clamp
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of this NCDDDG research program is to identify new nicotinic agents that can be used in the treatment of depression. The lead compounds in this endeavor belong to the AMOP-H-OH (6-[5-(azetidin-2-ylmethoxy)-pyridin-3-yl]-hex-5-yn-1-ol) family of products. Preliminary studies show high affinities and selectivities of some of these agents for specific nicotinic acetylcholine receptor (nAChR) subtypes that correlate very well with drug antidepressant signatures as assessed by behavioral studies. Our working hypothesis is that drugs having high potency as partial agonists and that are truly selective for nAChRs composed of a4 and -32 subunits (a4p2-nAChRs) will have desired antidepressant activities. The research program is constructed around three, interlacing projects and supported by an administrative core. In the medicinal chemistry Project 1, we will design and synthesize new AMOP-H-OH analogs by varying their steric and stereoelectroman nAChR subtypes naturally or heterologously expressed in mammalian cells or Xenopus oocytes. This work will define whether new ligands act as full or partial agonists, as competitive or non-competitive antagonists, as open or closed channel blockers, or as positive or negative allosteric modulators at functional nAChRs based on established electrophysiological recording techniques and higher-throughput isotopic ion flux assays when possible. In Project 3, behavioral profiles for new ligands also will be determined using the innovative, powerful and high-throughput SmartCube?1/2 system, augmented by more classical methods, to assess drug activities as antidepressants. The studies will be conducted in a series of iterations, with in vitro nAChR subtype pharmacological profiling, modeling, and in vivo behavioral testing serving to inform synthetic strategies toward compounds that are optimized to have progressively superior nAChR subtype selectivity and behavioral activity The bestrs related to emotion and mood. However, the major focus of the work is to develop new antidepressant medications.
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Pharmacokinetics and brain penetration of LF-3-88, (2-[5-[5-(2(S)-azetidinylmethoxyl)-3-pyridyl]-3-isoxazolyl]ethanol), a selective α4β2-nAChR partial agonist and promising antidepressant.
LF-3-88(2-[5-[5-(2(S)-azetidinylmethoxyl)-3-pyridyl]-3-isoxazolyl]ethanol)的药代动力学和脑渗透性,选择性α4β2-nAChR部分激动剂
DOI:
10.1016/j.jchromb.2012.11.011
发表时间:
2013
期刊:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
影响因子:
--
作者:
[Yuan,Yang, Yu,Li-Fang, Qiu,Xi, Kozikowski,AlanP, vanBreemen,RichardB]
通讯作者:
vanBreemen,RichardB
DOI:
10.1021/ml3002715
发表时间:
2012-12-13
期刊:
ACS MEDICINAL CHEMISTRY LETTERS
影响因子:
4.2
作者:
[Yu, Li-Fang, Zhang, Han-Kun, Gunosewoyo, Hendra, Kozikowski, Alan P.]
通讯作者:
Kozikowski, Alan P.
Discovery of highly potent and selective α4β2-nicotinic acetylcholine receptor (nAChR) partial agonists containing an isoxazolylpyridine ether scaffold that demonstrate antidepressant-like activity. Part II.
发现高效和选择性α4β2-烟碱乙酰胆碱受体(nAChR) 部分激动剂,含有异恶唑基吡啶醚支架,具有抗抑郁样活性。
DOI:
10.1021/jm301177j
发表时间:
2012
期刊:
Journal of medicinal chemistry
影响因子:
7.3
作者:
[Yu,Li-Fang, Eaton,JBrek, Fedolak,Allison, Zhang,Han-Kun, Hanania,Taleen, Brunner,Dani, Lukas,RonaldJ, Kozikowski,AlanP]
通讯作者:
Kozikowski,AlanP
DOI:
10.1021/jm400510u
发表时间:
2013-07-11
期刊:
Journal of medicinal chemistry
影响因子:
7.3
作者:
[Zhang HK, Yu LF, Eaton JB, Whiteaker P, Onajole OK, Hanania T, Brunner D, Lukas RJ, Kozikowski AP]
通讯作者:
Kozikowski AP
DOI:
10.1021/jm200855b
发表时间:
2011-10-27
期刊:
JOURNAL OF MEDICINAL CHEMISTRY
影响因子:
7.3
作者:
[Liu, Jianhua, Yu, Li-Fang, Eaton, J. Brek, Caldarone, Barbara, Cavino, Katie, Ruiz, Christina, Terry, Matthew, Fedolak, Allison, Wang, Daguang, Ghavami, Afshin, Lowe, David A., Brunner, Dani, Lukas, Ronald J., Kozikowski, Alan P.]
通讯作者:
Kozikowski, Alan P.
共 7 条
Design and Study of New Nicotinic Analogs for Use in Depression
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批准号:8321085
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项目类别:
-
资助金额:$86.18万
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财政年份:2009
-
负责人:alan P. kozikowski
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依托单位:
Design and Study of New Nicotinic Analogs for Use in Depression
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批准号:8110539
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项目类别:
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资助金额:$91.81万
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财政年份:2009
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负责人:alan P. kozikowski
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依托单位:
Design and Study of New Nicotinic Analogs for Use in Depression
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批准号:7697562
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项目类别:
-
资助金额:$96.42万
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财政年份:2009
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负责人:alan P. kozikowski
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依托单位:
Design and Study of New Nicotinic Analogs for Use in Depression
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批准号:7910616
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项目类别:
-
资助金额:$93.56万
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财政年份:2009
-
负责人:alan P. kozikowski
-
依托单位:
Chemistry and Biology of 5-HT2C Receptor Ligands for Drug Abuse
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批准号:7883679
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项目类别:
-
资助金额:$57.89万
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财政年份:2007
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负责人:alan P. kozikowski
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依托单位:
Chemistry and Biology of 5-HT2C Receptor Ligands for Drug Abuse
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批准号:7649438
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项目类别:
-
资助金额:$54.17万
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财政年份:2007
-
负责人:alan P. kozikowski
-
依托单位:
Chemistry and Biology of 5-HT2C Receptor Ligands for Drug Abuse
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批准号:7501965
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项目类别:
-
资助金额:$52.32万
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财政年份:2007
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负责人:alan P. kozikowski
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依托单位:
Molecular Interventions for Bipolar Disorder
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批准号:7528127
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项目类别:
-
资助金额:$43.89万
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财政年份:2006
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负责人:alan P. kozikowski
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依托单位:
Molecular Interventions for Bipolar Disorder
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批准号:7738531
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项目类别:
-
资助金额:$44.53万
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财政年份:2006
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负责人:alan P. kozikowski
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依托单位:
Molecular Interventions for Bipolar Disorder
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批准号:8010220
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项目类别:
-
资助金额:$44.09万
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财政年份:2006
-
负责人:alan P. kozikowski
-
依托单位:
PKC Modulators for the Treatment of Alzheimer's disease
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批准号:7455260
-
项目类别:
-
资助金额:$32.19万
-
财政年份:2005
-
负责人:alan P. kozikowski
-
依托单位:
海外基金