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Hotline:400-820-3792Inhibitors•ScreeningLibraries•Proteinswww.MedChemEBradykininCat.No.:HY-P0206CASNo.:58-82-2分⼦式:C₅₀H₇₃N₁₅O₁₁分⼦量:1060.21Sequence:Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-ArgSequenceShortening:RPPGFSPFR作⽤靶点:BradykininReceptor;EndogenousMetabolite;Ser/ThrProtease作⽤通路:GPCR/GProtein;MetabolicEnzyme/Protease储存⽅式:Powder-80°C2years-20°C1yearInsolvent-80°C6months-20°C1monthBIOLOGICALACTIVITY⽣物活性Bradykinin由激肽释放酶-激肽系统产⽣的活性肽。它炎症调节因⼦,也被认为⼏种⾎管和肾功能以及神经调节因⼦。IC50&TargetBradykininB2Receptor(B2R)HumanEndogenousMetabolite体外研究BradykininisapotentvasodilatorpeptidethatexertsitsvasodilatoryactionthroughstimulationofspecificendothelialB2receptors,therebycausingthereleaseofprostacyclin,NO,andEDHF[1].Bradykininhasbeenreportedtobeinvolvedintheprogressionofmanytypesofcancer.Bradykinintreatmentpromotestheinvasionandmigrationofcolorectalcancercells.BradykinintreatmentstimulatesERK1/2activationandIL-6production[2].ExogenousbradykininmarkedlyinhibitsTFexpressioninmRNAandproteinlevelinducedbyLPSinadose-dependentmanner.TheNOsynthaseantagonistL-NAMEandPI3KinhibitorLY294002dramaticallyabolishtheinhibitoryeffectsofbradykininontissuefactorexpression[3].体内研究Applicationof1μMbradykinintotheovaryproducessignificantdecreasesinheartrateandmeanarterialpressure.Invagotomizedanimals,applicationof1μMbradykinintotheovaryproducesbradycardiaandhypotensionsimilartotheresponsesevokedwhenvagalinnervationisintact[4].Vascularbradykinincanimprovepancreaticmicrocirculationandhemorheologyinratswithsevereacutepancreatitis.Thepancreatic1/3MasterofBioactiveMolecules—您⾝边的抑制剂⼤师www.MedChemEmicrocirculatorybloodflowvolumeandvelocityinthevascularbradykinintreatmentgroupincreasesgraduallyafter48h[5].PI3K/AktsignalingpathwayactivationinducedbybradykininadministrationreducestheactivityofGSK-3βandMAPK,andreducesNF-x03BA;Blevelinthenucleus,therebyinhibitingTFexpression.Consistentwiththis,intraperitonealinjectionofC57/BL6micewithbradykininalsoinhibitsthethrombusformationinducedbyligationofinferiorvenacava[3].PROTOCOLCellAssay[2]SW480cellsarepretreatedwithdifferentconcentrationsofbradykinin(0,0.1,0.5,1μM),andthensubjectedtoinvasionandmigrationassays[2].MCEhasnotindependentlyconfirmedtheaccuracyofthesemethods.Theyareforreferenceonly.AnimalRats:Bradykininacetateisappliedtopicallytothesurfaceoftheovarywithathinpieceofcotton(7×7mmAdministration[3][4]square)soakedwiththesolution.Afterapplicationfor30s,thecottonisremoved.Eachofthestimuliisdeliveredtotheanimalafterobservingstabilizationofheartrateandmeanarterialpressure[4].Mouse:Micearerandomlydividedinto3groups:Sham,ModelandBradykinin.Beforesurgicalprocedure,themiceofbradykiningroupareintraperitoneallyinjectedwithbradykinin(10mg/kg/d)onceadayforthreedays.Afterligation,themicereceivebradykinininjectionforanothertwodaysandanalgesictherapyisperformedusingbuprenorphineat0.1mg/kgbodyweightfor3days.Themiceinothergroupsreceiveequalsalineascontrol[3].MCEhasnotindependentlyconfirmedtheaccuracyofthesemethods.Theyareforreferenceonly.户使⽤本产品发表的科研⽂献•AnalChem.2022Apr26;94(16):6363-6370.•iScience.21October2022.•ACSChemNeurosci.2021Jun29.•SLASDiscov.2018Nov1:2472555218810323.•JAmSocMassSpectrom.2020Jul5.Seemorecustomervalidationsonwww.MedChemEREFERENCES[1].HornigB,etal.Roleofbradykinininmediatingvasculareffectsofangiotensin-convertingenzymeinhibitorsinhumans.Circulation.1997Mar4;95(5):1115-8.[2].WangG,etal.BradykininstimulatesIL-6productionandcellinvasionincolorectalcancercells.OncolRep.2014Oct;32(4):1709-14.[3].DongR,etal.ExogenousBradykininInhibitsTissueFactorInductionandDeepVeinThrombosisviaActivatingtheeNOS/Phosphoinositide3-Kinase/AktSignalingPathway.CellPhysiolBiochem.2015;37(4):1592-606.[4].UchidaS,etal.Afferentfibersinvolvedinthebradykinin-inducedcardiovascularreflexesfromtheovaryinrats.AutonNeurosci.2015Dec;193:57-62.[5].LiuLT,etal.Effectofvascularbradykininonpancreaticmicrocirculationandhemorheologyinratswithsevereacutepancreatitis.EurRevMedPharmacolSci.2015;19(14):2646-50.2/3MasterofBioactiveMolecules—您⾝边

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