Fasudil-hydrochloride-semihydrate-HA-1077-hydrochloride-semihydrate-DataSheet-生命科学试剂-MedChemExpress

Hotline:400-820-3792Inhibitors•ScreeningLibraries•Proteinswww.MedChemEFasudilhydrochloridesemihydrateCat.No.:HY-10341BCASNo.:186694-02-0Synonyms:HA-1077hydrochloridesemihydrate;AT877hydrochloridesemihydrate分⼦式:C₁₄H₁₇N₃O₂S.ClH.₁/₂H₂O分⼦量:673.68作⽤靶点:ROCK;CalciumChannel;Autophagy;HIV;PKA;PKC作⽤通路:CellCycle/DNADamage;Cytoskeleton;StemCell/Wnt;TGF-

beta/Smad;MembraneTransporter/IonChannel;Neuronal

Signaling;Autophagy;Anti-infection;Epigenetics储存⽅式:PleasestoretheproductundertherecommendedconditionsintheCertificateofAnalysis.BIOLOGICALACTIVITY⽣物活性Fasudil(HA-1077;AT877)hydrochloridesemihydrate⼀种⾮特异性RhoA/ROCK抑制剂，并抑制蛋⽩激酶。Fasudilhydrochloridesemihydrate抑制ROCK1的Ki为0.33μM，抑制ROCK2，PKA，PKC，PKG的IC50分别为0.158μM和4.58μM，12.30μM，1.650μM。Fasudilhydrochloridesemihydrate也⼀种有效的Ca2+通道拮抗剂和⾎管扩张剂。IC50&TargetPKAp160ROCKROCK2PKC4.58μM(IC50)0.33μM(Ki)0.158μM(IC50)12.3μM(IC50)PKG1.65μM(IC50)体外研究Fasudilhydrochloridesemihydrate(100μM)inhibitscellspreading,theformationofstressfibers,andexpressionofα-SMAwithconcomitantsuppressionofcellgrowthinratHSCs(hepaticstellatecells)andhumanHSC-derivedTWNT-4cells[4].Fasudilhydrochloridesemihydrate(50-100μM;24hours)inhibitstheLPA(lysophoaphatidicacid)-inducedphosphorylationofERK1/2,JNK,andp38detectedbywesternblottinginratHSCsandhumanHSC-derivedTWNT-4cells[4].Fasudilhydrochloridesemihydrate(25-100μM;24hours)suppressestranscriptionofcollagenandTIMP,stimulatestranscriptionofMMP-1inhumanHSC-derivedTWNT-4cells[4].WesternBlotAnalysis[4]1/3MasterofBioactiveMolecules—您⾝边的抑制剂⼤师www.MedChemECellLine:RatHSCsandhumanHSC-derivedTWNT-4cellsConcentration:50μM;100μMIncubationTime:24hoursResult:SuppressedtheLPA-inducedphosphorylationofERK1/2,JNKandp38MAPKby60%,70%,and90%,respectively.RT-PCR[4]CellLine:RatHSCsandhumanHSC-derivedTWNT-4cellsConcentration:25μM;50μM;100μMIncubationTime:24hoursResult:ReducedtheexpressionoftypeIcollagen,a-SMA,andTIMP-1.体内研究Fasudilhydrochloridesemihydrate(10mg/kg;i.v.;1hbeforeoperation)exhibitsprotectableeffectsoncardiovasculardiseaseandreducestheactivationofJNKandattenuatesmitochondrial-nucleartranslocationofAIFunderischemicinjury[5].Fasudilhydrochloridesemihydrate(50mg/kg/d;i.p.)inhibitsacuteandrelapsingEAE(experimentalautoimmuneencephalomyelitis)inducedbyproteolipidproteinPLPp139-151,reduceslymphocytesproliferation,resultsdownregulationofinterleukin(IL)-17andamarkeddecreaseoftheIFN-γ/IL-4ratio[6].Fasudilhydrochloridesemihydrate(100mg/kg/d;p.o.)significantlyreducesincidenceandpathologicalexaminationscoreofEAE(experimentalautoimmuneencephalomyelitis)inSJL/Jmice,decreasesinflammation,demyelination,axonallossandAPPpositiveinspinalcordinmice[6].AnimalModel:Myocardialischemiaandreperfusioninrat(250-300g)[5]Dosage:10mg/kgAdministration:Intravenousinjection;1hbeforeoperationResult:ActivatedtheRho-kinase,JNK,andresultedAIFtranslocatedtothenucleus.InhibitedRho-kinaseactivity,andreducedmyocardialinfarctsizeandheartcellapoptosis.户使⽤本产品发表的科研⽂献•SciTranslMed.2018Jul18;10(450).pii:eaaq1093.•JExpClinCancerRes.2020Jun16;39(1):113.•ClinTranslMed.2022Jul;12(7):e961.•NeuralRegenRes.2021Dec;16(12):2512-2520.•JPharmPharmacol.2021Mar29;rgab033.2/3MasterofBioactiveMolecules—您⾝边的抑制剂⼤师www.MedChemESeemorecustomervalidationsonwww.MedChemEREFERENCES[1].ChenM,etal.Fasudilanditsanalogs:anewpowerfulweaponinthelongwaragainstcentralnervoussystemdisorders?ExpertOpinInvestigDrugs.2013Apr;22(4):537-50.[2].HuangXN,etal.Theeffectsoffasudilonthepermeabilityoftheratblood-brainbarrierandblood-spinalcordbarrierfollowingexperimentalautoimmuneencephalomyelitis.JNeuroimmunol.2011Oct28;239(1-2):61-7.[3].UehataM,etal.CalciumsensitizationofsmoothmusclemediatedbyaRho-associatedproteinkinaseinhypertension.Nature.1997Oct30;389(6654):990-4.[4].FukushimaM,etal.Fasudilhydrochloridehydrate,aRho-kinase(ROCK)inhibitor,suppressescollagenproductionandenhancescollagenaseactivityinhepaticstellatecells.LiverInt.2005Aug;25(4):829-38.[5].ZhangJ,etal.InhibitionoftheactivityofRho-kinasereducescardiomyocyteapoptosisinheartischemia/reperfusionviasuppressingJNK-mediatedAIFtranslocation.ClinChimActa.2009Mar;401(1-2):76-80.[6].SunX,etal.TheselectiveRho-kinaseinhibitorFasudilisprotectiveandtherapeuticinexperimentalautoimmuneencephalomyelitis.JNeuroimmunol.2006Nov;180(