Design, Total Synthesis & Properties of Novel Chemical Analogs of Human Insulin
Design, Total Synthesis & Properties of Novel Chemical Analogs of Human Insulin
批准号:
8009137
负责人:
STEPHEN B.H. KENT
金额:
$43.61万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-08-01 至 2014-05-31
关键词:
AffinityAmino Acid SubstitutionAmino AcidsAnimal ModelBeta CellBindingBiologicalBiological AssayBiological TestingBiotechnologyChemicalsClinicalCollaborationsCrystallizationCrystallographyCustomDataDiabetes MellitusDisulfidesDrug FormulationsDrug KineticsEdetic AcidElectrostaticsEstersFamily suidaeFunctional RNAGenerationsGoalsHalogensHumanHypoglycemiaIn VitroIndianaInsulinInsulin Infusion SystemsInsulin ReceptorInsulin-Dependent Diabetes MellitusInsulin-Like Growth Factor ReceptorLinkLong-Acting InsulinMeasuresMediatingMethodsModificationMonitorNMR SpectroscopyPatientsPharmaceutical ChemistryPharmacologic SubstancePoisonPredispositionPreparationProinsulinPropertyProteinsProtocols documentationRattusRelative (related person)ResearchRouteSeriesStreptozocinSurrogate MarkersTestingTherapeuticThermodynamicsTimeUniversitiesX-Ray CrystallographyZincabsorptionanalogaryl halidebasechemical stabilitychemical synthesisdesigndiabeticdiabetic ratfrontierglycemic controlimprovedinterestmalenovelpolypeptidepublic health relevancereceptorreceptor bindingthree dimensional structure
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Optimal control of Type I diabetes mellitus (DM) often requires a combination of rapid- acting and long-acting insulin analogs to achieve tight glycemic control. Current rapid- acting analogs, a pioneering triumph of biotechnology 15 years ago, are nonetheless too delayed in absorption for either ideal meal-time glycemic control or the safe and effective use of automated insulin pumps. We therefore seek to develop a second-generation rapid-acting insulin analog with substantially improved properties in order to provide additional benefits to patients. To this end, we first propose to optimize and apply a novel total chemical synthesis of insulin that provides for highly efficient folding/formation of disulfides. Facile chemical synthesis of insulin will enable the incorporation of a wide range of non-coded amino acids in order to systematically tune the properties of the insulin molecule. We will prepare a series of designed chemical analogs of insulin for biophysical characterization, receptor binding assays, and biological testing in animal models of DM. Our design goals for a second-generation insulin analog include: (i) faster onset of action; (ii) briefer duration of action; (iii) enhanced physical stability; (iv) enhanced chemical stability; and (v) enhanced receptor selectivity. Our proposed research promises to expand the chemical space of insulin therapeutics to exploit for the first time the armamentarium of modern medicinal chemistry.
PUBLIC HEALTH RELEVANCE: "Our goal is to develop a second-generation rapid-acting insulin analog with substantially improved properties in order to provide additional benefits to patients. We will prepare a series of designed chemical analogs of insulin for biophysical characterization, receptor binding assays, and biological testing in animal models of diabetes mellitus. Our proposed research promises to expand the chemical space of insulin therapeutics to exploit for the first time the armamentarium of modern medicinal chemistry."
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批准号:8868928
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项目类别:
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资助金额:$19.75万
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财政年份:2014
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负责人:STEPHEN B.H. KENT
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依托单位:
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Design, Total Synthesis & Properties of Novel Chemical Analogs of Human Insulin
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批准号:8113870
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财政年份:2010
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依托单位:
TRAINING IN THE USE OF BRUKER AND VARIAN SPECTROMETERS AND NMR
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批准号:7954645
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资助金额:$0.03万
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财政年份:2009
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依托单位:
PROTONATION STATES OF CATALYTIC ASP25 AND ASP25' IN 13C LABELED HIV-1 PROTEASE
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资助金额:$0.42万
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财政年份:2009
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负责人:STEPHEN B.H. KENT
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依托单位:
NMR DYNAMICS STUDY OF CHEMICAL ANALOGUES OF HIV-1 PROTEASE
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批准号:7954643
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资助金额:$0.47万
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财政年份:2009
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负责人:STEPHEN B.H. KENT
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依托单位:
Systematic Approach to the Chemical Synthesis (RMI)
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批准号:7014822
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资助金额:$28.25万
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财政年份:2005
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负责人:STEPHEN B.H. KENT
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依托单位:
A Systematic Approach to the Chemical Synthesis (RMI)
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批准号:7265325
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项目类别:
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资助金额:$26.78万
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财政年份:2005
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负责人:STEPHEN B.H. KENT
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依托单位:
A Systematic Approach to the Chemical Synthesis of G-Protein Coupled Receptors
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批准号:7124689
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项目类别:
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资助金额:$27.58万
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财政年份:2005
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负责人:STEPHEN B.H. KENT
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依托单位:
A Systematic Approach to the Chemical Synthesis of G-Protein Coupled Receptors
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批准号:7662367
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资助金额:$26.27万
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财政年份:2005
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负责人:STEPHEN B.H. KENT
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依托单位:
A Systematic Approach to the Chemical Synthesis (RMI)
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批准号:7473310
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项目类别:
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资助金额:$26.27万
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财政年份:2005
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负责人:STEPHEN B.H. KENT
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依托单位:
STRUCTURE-FUNCTION STUDIES OF THE HIV PROTEASE
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批准号:2186413
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项目类别:
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资助金额:$24.9万
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财政年份:1993
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负责人:STEPHEN B.H. KENT
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依托单位:
STRUCTURE-FUNCTION STUDIES OF THE HIV PROTEASE
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批准号:3308347
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项目类别:
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资助金额:$24.83万
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财政年份:1993
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负责人:STEPHEN B.H. KENT
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依托单位:
DRUG DESIGN CYCLE TARGETED TO RETROVIRAL PROTEASES
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批准号:3096445
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项目类别:
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资助金额:$26.88万
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财政年份:1993
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负责人:STEPHEN B.H. KENT
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依托单位:
STRUCTURE-FUNCTION STUDIES OF THE HIV1 PROTEASE
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批准号:2331986
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项目类别:
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资助金额:$28.18万
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财政年份:1993
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负责人:STEPHEN B.H. KENT
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依托单位:
STRUCTURE-FUNCTION STUDIES OF THE HIV PROTEASE
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批准号:2186414
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项目类别:
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资助金额:$25.08万
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财政年份:1993
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负责人:STEPHEN B.H. KENT
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依托单位:
DRUG DESIGN CYCLE TARGETED TO RETROVIRAL PROTEASES
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批准号:2186380
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项目类别:
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资助金额:$82.88万
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财政年份:1992
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负责人:STEPHEN B.H. KENT
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依托单位:
DRUG DESIGN CYCLE TARGETED TO RETROVIRAL PROTEASES
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批准号:3096446
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项目类别:
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资助金额:$57.42万
-
财政年份:1992
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负责人:STEPHEN B.H. KENT
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依托单位:
海外基金