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DeoxycytidineanalogthatinhibitsDNAsynthesis.MetabolizedtoformgemcitABInetriphosphate(dFdCTP)andgemcitabinediphosphate(dFdCDP).dFdCTDinhibitsribonucleotidereductasecausingareductionincellularnucleotides.dFdCTPisincorporatedinDNAresultinginDNAstrandtermination.Displaysantitumoractivityinvitroandinvivo.
GemcitabinehydrochlorideisalsoofferedaspartoftheTocriscreenPlusandTocriscreenLibraryofFDA-ApprovedCompounds.FindoutmoreaboutcompoundlibrariesavailablefromTocris.
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight299.66.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Herteletal(1990)EvaluationoftheantitumoractivityofGemcitabine(2',2'-Difluoro-2'-deoxycytidine).CancerRes.504417PMID:2364394
Heinemannetal(1995)Gemcitabine:amodulatorofintracellularnucleotideanddeoxynucleotidemetabolism.Semin.Oncol.2211PMID:7481839
Plunkettetal(1995)Preclinicalcharacteristicsofgemcitabine.AnticancerDrugs67PMID:8718419
Keywords:Gemcitabinehydrochloride,supplier,DNA,synthesis,inhibitors,inhibits,Ribonucleotide,reductases,chemotherapeutics,DNA,,RNA,and,Protein,Synthesis,Ribonucleotide,Reductase,DNA,,RNA,and,Protein,Synthesis,TocrisBioscience
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