Procaterol-DataSheet-生命科學(xué)試劑-MCE_第1頁(yè)
Procaterol-DataSheet-生命科學(xué)試劑-MCE_第2頁(yè)
Procaterol-DataSheet-生命科學(xué)試劑-MCE_第3頁(yè)
全文預(yù)覽已結(jié)束

下載本文檔

版權(quán)說(shuō)明:本文檔由用戶提供并上傳,收益歸屬內(nèi)容提供方,若內(nèi)容存在侵權(quán),請(qǐng)進(jìn)行舉報(bào)或認(rèn)領(lǐng)

文檔簡(jiǎn)介

Hotline:400-820-3792Inhibitors ? ScreeningLibraries ? Proteinswww.MedChemEProcaterolCat.No.:HY-114732CASNo.:72332-33-3分子式:C??H??N?O?分子量:290.36作用靶點(diǎn):AdrenergicReceptor作用通路:GPCR/GProtein;NeuronalSignaling儲(chǔ)存方式:PleasestoretheproductundertherecommendedconditionsintheCertificateofAnalysis.BIOLOGICALACTIVITY生物活性Procaterol是一種可口服的選擇性β2adrenergicreceptor激動(dòng)劑。Procaterol可通過(guò)環(huán)磷酸腺苷依賴性機(jī)制直接抑制嗜酸性粒細(xì)胞遷移和BEAS-2B細(xì)胞釋放嗜酸性粒細(xì)胞趨化活性因子。Procaterol對(duì)大鼠的支氣管擴(kuò)張作用和代謝作用存在較大的劑量差,可用于運(yùn)動(dòng)員哮喘研究[1]。IC50&Targetβ2adrenoceptor體外研究Procaterol(10-1000ng/mL,12,24,48h,BEAS-2B)directlyinhibitseosinophilmigrationandthereleaseofeosinophilchemotacticfactorfromBEAS-2BcellsthroughacyclicAMP-dependentmechanism[3].Procaterol(10-1000ng/mL,12,24,48h,BEAS-2B)Dose-dependentinhibitionofRANTESreleaseinresponsetoIL-1bandTNF-ainBEAS-2Bcellmonolayers,andenhancementofGM-CSFmRNAexpressioninresponsetoIL-1b[3].Procaterol(0.1μM,72h,Humantrachealsurfaceepithelialcells)reducerhinovirustitersandRNA,cytokineconcentrations,susceptibilitytorhinovirusinfection,andtheexpressionofintercellularadhesionmolecule-1(ICAM-1),thereceptorfortype14rhinovirus,andthenumberofacidicendosomesinthecellsfromwhichrhinovirusRNAentersintothecytoplasm[4].Procaterol(10nM,onetime,Lungepithelialcells)increasedciliarybendamplitude(CBA)andciliarybeatingfrequency(CBF)inadosedependentmannerviacAMP[5].CellMigrationAssay[3]CellLine:eosinophilConcentration:10,100,1000ng/mL1/3 MasterofBioactiveMolecules—您身邊的抑制劑大師www.MedChemEIncubationTime:24hResult:Attenuatedtheeosinophilmigratoryresponseinadose-dependent.體內(nèi)研究Procaterol(0.03-1mg/kg,inhalation3timesaday,14days)hasnosignificantchangesinweightorbodyweightgaininratgastrocnemiusmuscle[1].Procaterol(1mg/kg,inhalation3timesaday,14days)significantlyincreasesweightofthelevatoranimusclewithanaboliceffects[1].Procaterol(1mg/kg,inhalation3timesaday,14days)increasesventralprostateweightisassociatedwithdrugstimulationofb2adrenergicreceptorsintissues[1].Procaterol(0.03-1mg/kg,inhalation3timesaday,14days)differentdosebetweenbronchodilatorandanaboliceffects>30-fold,[1].Procaterol(0.1,1,10mg/kg,orally,beforeovalbumin(HY-W250978)(OVA)inhalation)inhalerdoesnotenhanceairwayhyperresponsiveness,airwaywallinflammation,orairwaywallthickening,anddecreaseseosinophilnumber[2].AnimalModel:Six-week-oldratswerecastratedonDay–5,exceptforanormalgroupof6rats[1]Dosage:0.03,0.1,0.3,1mg/mLAdministration:in-halation3timesaday(09:00,12:00,16:00)for14daysfromDay0toDay13.Result:Nosignificantchangedinweightorbodyweightgaininratgastrocnemiusmuscle.Significantlyincreasedtheweightofthelevatoranimuscle.Increasdinventralprostateweight.AnimalModel:Miceimmunizedwithovalbumin(HY-W250978)(OVA,inhalationof20mg/mLOVAfor10minuteseveryotherday,total7times)+alum[2]Dosage:0.1,1,10mg/kgAdministration:orally,beforeovalbumin(HY-W250978)(OVA)inhalationResult:Inhalationdidnotenhanceairwayhyperresponsiveness,airwaywallinflammation,orairwaywallthickeningafterOVAinhalation.ReducedthenumberofeosinophilsinBALFmice.REFERENCESIkezonoK,etal.Bronchodilatingeffectandanaboliceffectofinhaledprocaterol.IntJSportsMed.2008Nov;29(11):888-94.TashimoH,etal.Effectofprocaterol,abeta(2)selectiveadrenergicreceptoragonist,onairwayinflammationandhyperresponsiveness.AllergolInt.2007Sep;56(3):241-7.KoyamaS,etal.ProcaterolinhibitsIL-1beta-andTNF-alpha-mediatedepithelialcelleosinophilchemotacticactivity.EurRespirJ.19992/3 MasterofBioactiveMolecules—您身邊的抑制劑大師www.MedChemEOct;14(4):767-75.YamayaM,etal.Procaterolinhibitsrhinovirusinfectioninprimaryculturesofhumantrachealepithelialcells.EurJPharmacol.2011Jan10;650(1):431-44.Komatani-TamiyaN,etal.Procaterol-stimulatedincreasesinciliarybendamplitudeandciliarybeatfrequencyinmousebronchioles.CellPhysiolBiochem.2012;29(3-4):511-22.M

溫馨提示

  • 1. 本站所有資源如無(wú)特殊說(shuō)明,都需要本地電腦安裝OFFICE2007和PDF閱讀器。圖紙軟件為CAD,CAXA,PROE,UG,SolidWorks等.壓縮文件請(qǐng)下載最新的WinRAR軟件解壓。
  • 2. 本站的文檔不包含任何第三方提供的附件圖紙等,如果需要附件,請(qǐng)聯(lián)系上傳者。文件的所有權(quán)益歸上傳用戶所有。
  • 3. 本站RAR壓縮包中若帶圖紙,網(wǎng)頁(yè)內(nèi)容里面會(huì)有圖紙預(yù)覽,若沒(méi)有圖紙預(yù)覽就沒(méi)有圖紙。
  • 4. 未經(jīng)權(quán)益所有人同意不得將文件中的內(nèi)容挪作商業(yè)或盈利用途。
  • 5. 人人文庫(kù)網(wǎng)僅提供信息存儲(chǔ)空間,僅對(duì)用戶上傳內(nèi)容的表現(xiàn)方式做保護(hù)處理,對(duì)用戶上傳分享的文檔內(nèi)容本身不做任何修改或編輯,并不能對(duì)任何下載內(nèi)容負(fù)責(zé)。
  • 6. 下載文件中如有侵權(quán)或不適當(dāng)內(nèi)容,請(qǐng)與我們聯(lián)系,我們立即糾正。
  • 7. 本站不保證下載資源的準(zhǔn)確性、安全性和完整性, 同時(shí)也不承擔(dān)用戶因使用這些下載資源對(duì)自己和他人造成任何形式的傷害或損失。

評(píng)論

0/150

提交評(píng)論