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当前位置: 首页 > 产品中心 > Small_molecule > Medchemexpress/Empagliflozin(同义词:BI 10773)/HY-15409/100mg
商品详细Medchemexpress/Empagliflozin(同义词:BI 10773)/HY-15409/100mg
Medchemexpress/Empagliflozin(同义词:BI 10773)/HY-15409/100mg
Medchemexpress/Empagliflozin(同义词:BI 10773)/HY-15409/100mg
商品编号: HY-15409-10mM*1mLinDMSO
品牌: MedChemExp
市场价: ¥1100.00
美元价: 660.00
产地: 美国(厂家直采)
公司:
产品分类: 小分子
公司分类: Small_molecule
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
Empagliflozinisaselectivesodiumglucosecotransporter-2(SGLT-2)inhibitorwithanIC50of3.1nMforhSGLT-2.

CustomerValidation

  • Diabetologia.2017Mar;60(3):568-573.
  • JChromatogrBAnalytTechnolBiomedLifeSci.2016Aug1;1027:227-33.
  • JChromatogrBAnalytTechnolBiomedLifeSci.2015Jul14;1000:22-28.
  • BiomedChromatogr.2016Oct;30(10):1549-55.
  • JACCBasicTranslSci.2017Aug;2(3):347-354.
Description

Empagliflozinisaselectivesodiumglucosecotransporter-2(SGLT-2)inhibitorwithanIC50of3.1nMforhSGLT-2.

IC50&Target

IC50:3.1nM(SGLT-2),1.1μM(SGLT-5),2μM(SGLT-6),8.3μM(SGLT-1),11μM(SGLT-4)[1]

InVitro

EmpagliflozinisapotentandcompetitiveSGLT-2inhibitorwithanexcellentselectivityprofileandthehighestselectivitywindowofthetestedSGLT-2inhibitorsoverhSGLT-1.Empagliflozininhibitstheuptakeof[14C]-alpha-methylglucopyranoside(AMG)viahSGLT-2inadose-dependentmannerwithanIC50of3.1nM,butislesspotentforotherSGLTs(IC50range:1100-11000nM).[3H]-EmpagliflozindisplaysahighaffinityforSGLT-2withameanKdof57±37nMintheabsenceofglucoseinkineticbindingexperiments[1].

InVivo

Glucoseintoleranceissignificantlyimprovedafter8daysofEmpagliflozintreatmentateitherdose(3mg/kgEmpagliflozin3058±180vs10mg/kgEmpagliflozin3090±219).Therefore,acutetreatmentwithEmpagliflozinhasabeneficialeffectonhyperglycemiaandglucoseintolerance.SincetherearenosignificantdifferencesinbloodglucosehomeostasiswiththetwodifferentdosesofEmpagliflozin,andrandombloodglucoselevelsofT1DMmicearesignificantlyimprovedby3mg/kgofEmpagliflozin,theeffectofthelowerdoseofEmpagliflozin(3mg/kg)isinvestigatedonpreservingβ-cellmassandfunction[2].

References
  • [1].GremplerR,etal.Empagliflozin,anovelselectivesodiumglucosecotransporter-2(SGLT-2)inhibitor:characterisationandcomparisonwithotherSGLT-2inhibitors.DiabetesObesMetab.2012Jan;14(1):83-90.

    [2].ChengST,etal.TheEffectsofEmpagliflozin,anSGLT2Inhibitor,onPancreaticβ-CellMassandGlucoseHomeostasisinType1Diabetes.PLoSOne.2016Jan25;11(1):e0147391.

    [3].NikoleJ.ByrNEBSc,etal.EmpagliflozinPreventsWorseningofCardiacFunctioninanExperimentalModelofPressureOverload-InducedHeartFailure.JACCBasicTranslSci.2017Aug;2(4):347-354.

PreparingStockSolutions
ConcentrationVolumeMass1mg5mg10mg
1mM2.2177mL11.0887mL22.1774mL
5mM0.4435mL2.2177mL4.4355mL
10mM0.2218mL1.1089mL2.2177mL
Pleaserefertothesolubilityinformationtoselecttheappropriatesolvent.
KinaseAssay
[1]

Membranes(60μg/well)areassayedina10mM4-(2-hydroxyethyl)-1-piperazineethanesulfonicacid(HEPES)buffer(pH7.4)containing137mMNaClinthepresenceorabsenceof20mMglucoseandindicatedconcentrationsof[3H]-Empagliflozinin96-wellplatesatroomtemperaturefor2h.IncubationsarestoppedbyrapidfiltrationthroughGF/BFilterplatesimpregnatedwithpolyethyleneimine0.5%andprewettedwith0.9%NaClsolution,andwashedfourtimeswith0.9%NaClsolution(4°C)usingaHarvesterFiltermate96.Filterplatesaredriedfor2hand50μLofMicroscint20isaddedtoeachwell.RADIoactivityretainedonthefiltersismeasuredusingtheTopCountNXT.Inparallel,theactualamountofactivityusedintheassaysisdeterminedbyaddingthesameamountof[3H]-Empagliflozinthatisaddedperwellintheradioligandbindingstudiesand4mLUltimaGoldScintilatorinto5mLvialsandmeasuringusingaTricarb2900TR.Non-specific[3H]-Empagliflozin-bindingisdeterminedinthepresenceof30μMdapagliflozin[1].MCEhasnotindependentlyconfirmedtheaccuracyofthesemethods.Theyareforreferenceonly.

AnimalAdmiNISTration
[2]

Empagliflozinisdissolvedinhydroxyethylcellulose(HEC)(Mice)[2].

Mice[2]
MaleC57BL/6Jmice(10weeksofage)areused.Empagliflozinisdissolvedinhydroxyethylcellulose(HEC)andadministeredtomiceintheexperimentalgroup(3or10mg/kg)byoralgavageoncedailyfor8days,whereasthevehiclegroupisgivensamevolumeofHECalone.MCEhasnotindependentlyconfirmedtheaccuracyofthesemethods.Theyareforreferenceonly.

References
  • [1].GremplerR,etal.Empagliflozin,anovelselectivesodiumglucosecotransporter-2(SGLT-2)inhibitor:characterisationandcomparisonwithotherSGLT-2inhibitors.DiabetesObesMetab.2012Jan;14(1):83-90.

    [2].ChengST,etal.TheEffectsofEmpagliflozin,anSGLT2Inhibitor,onPancreaticβ-CellMassandGlucoseHomeostasisinType1Diabetes.PLoSOne.2016Jan25;11(1):e0147391.

    [3].NikoleJ.ByrneBSc,etal.EmpagliflozinPreventsWorseningofCardiacFunctioninanExperimentalModelofPressureOverload-InducedHeartFailure.JACCBasicTranslSci.2017Aug;2(4):347-354.

MolecularWeight

450.91

Formula

C₂₃H₂₇ClO₇

CASNo.

864070-44-0

Storage
Powder-20°C3years
 4°C2years
Insolvent-80°C6months
 -20°C1month
Shipping

RoomtemperatureincontinentalUS;mayvaryelsewhere

Solvent&Solubility

10mMinDMSO

Empagliflozinisprepparedin0.5%hydroxyethylcellulose[3].

*"<1 mg/ml"="" means="" slightly="" soluble="" or="" insoluble.="" "≥"="" means="" soluble,="" but="" saturation="">

References
  • [1].GremplerR,etal.Empagliflozin,anovelselectivesodiumglucosecotransporter-2(SGLT-2)inhibitor:characterisationandcomparisonwithotherSGLT-2inhibitors.DiabetesObesMetab.2012Jan;14(1):83-90.

    [2].ChengST,etal.TheEffectsofEmpagliflozin,anSGLT2Inhibitor,onPancreaticβ-CellMassandGlucoseHomeostasisinType1Diabetes.PLoSOne.2016Jan25;11(1):e0147391.

    [3].NikoleJ.ByrneBSc,etal.EmpagliflozinPreventsWorseningofCardiacFunctioninanExperimentalModelofPressureOverload-InducedHeartFailure.JACCBasicTranslSci.2017Aug;2(4):347-354.

Purity:99.91%ee.:98.83%