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10-吲哚细胞松弛素chaetoglobosinF的NMR解析 Title:NMRAnalysisofChaetoglobosinF:AStudyonIndoleCellRelaxant Introduction: Naturalproductsderivedfromfungihavebeenarichsourceofvaluablecompoundswithdiversebiologicalactivities.ChaetoglobosinF,asecondarymetaboliteproducedbyvariousfungi,hasattractedsignificantattentionduetoitspotentialasatherapeuticagent.Thiscompoundexhibitspromisingcellrelaxantproperties,particularlyinthecontextofcardiovasculardiseases.Understandingitsstructuralfeaturesandmodeofactionisthereforeofgreatimportance.NuclearMagneticResonance(NMR)spectroscopyisapowerfulanalyticaltechniquethatcanprovidedetailedinsightsintothestructureandpropertiesoforganicmolecules.Inthisstudy,weaimtoperformacomprehensiveanalysisofChaetoglobosinFusingNMRtechniquestogainabetterunderstandingofitsmolecularstructureanddynamics. Methods: ChaetoglobosinFwasisolatedfromthefungalstrainusingstandardextractionandpurificationtechniques.TheisolatedcompoundwasthensubjectedtoNMRspectralmeasurementsusinghigh-fieldNMRspectrometersequippedwithcryogenicprobes.Various1Dand2DNMRexperiments,including^1H,^13C,COSY,TOCSY,HSQC,andHMBC,werecarriedouttoassignthesignalsandestablishtheconnectivitybetweendifferentatomsinthemolecule.TheNMRdataweresubsequentlyanalyzedtodeterminethechemicalshiftvalues,couplingconstants,andspatialrelationshipsbetweentheatoms. ResultsandDiscussion: TheNMRanalysisofChaetoglobosinFprovidedvaluableinsightsintoitsstructuralfeaturesandmoleculardynamics.The^1HNMRspectrumrevealedthepresenceofcharacteristicprotonsignals,enablingustoidentifythedifferentfunctionalgroupsandtheirconnectivityinthemolecule.The^13CNMRspectrumallowedustodeterminethecarbonresonancefrequencies,whichfurthersupportedthestructuralassignmentsmadebasedonthe^1HNMRdata. ThroughCOSY,TOCSY,andHSQCexperiments,wewereabletoestablishthecorrelationsbetweenprotonsandcarbonatoms,therebyconstructingthescalarcouplingnetwork.Thisinformationwascrucialinelucidatingtheconnectivityofthevarioussubunitswithinthemolecule.TheHMBCexperimenthelpedindeter