简介:Thesynthesisofporphyrinnitrogenmustardsfromdeuteroporphyrinand3,8dialkyloxyhematoporphyrinmethylestersthroughreduction,bro...
简介:3α-bromo-epipicropodophyllinwaspreparedanditsinhibitionactivitiesagainstKBcellsandL1210leukemiacellsinvitroarehigherthanthoseofVP-16,awidelyuseddruginclinicatpresent.ThisisthefirsttimetointroducesubstitutionatC-3ofring-Cintheworkofmodifyingstructureofpodophyllotoxin.Itcanbetransformedeasilyto4β-hydroxy-2,3-ene-apopicropodophyllinunderbasiccondition,sothat,correspondingderivativesof2,3-ene-apopicropodophyllinwithsubstitutiononcarbon-4couldbesynthesized.Thiscompoundcanberegardednotonlyasaleadingcompoundtobemodifiedbecauseofitsantitumoractivities,butalsoasanintermediateforthestructuretransformation.
简介:AIMThepreviousworkhasdemonstratedthatthepolysaccharidesofAngelicasinensis(Oliv.)Dielshavesignificantlyantitumoractivityandindicatedthattheactivityisstronglydependentontheirstructures.However,therelationshipsbetweenthestructureandtheactivitiesarestillambiguous.Thus,atpresent,moreeffortsarebeingexpendedinseekingtoisolatethepolysaccharidesfromAngelicasinensis(Oliv.)Diels,measuretheirstructuralfeaturesandantitumoractivities,andelucidatestructure-activityrelationshipsofpolysaccharides.METHODSTherootsofAngelicasinensis(Oliv.)DielswereextractedWithwater,separatedbySephacrylS-400andDEAE-sephadexA-25columnsandfurtherpurifledonSephadexG-100column.
简介:Lactivicin,anovelinhibitorofbacterialcellwallsynthesis,wasisolatedfromtheculturefil-tratesofmicroorganismYK-258andYK-422.Itexhibitsbiologicalactivitiessimilartothoseoftheβ-lactamantibiotics,althoughitdoesnothaveaβ-lactamringinitsmolecule.Sincethediscoveryoflactivicin,hundredsofitsderivativeshavebeensynthesized.Most