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当前位置: 首页 > 产品中心 > Small_molecule > Medchemexpress/(R)-(+)-依托莫西钠盐(同义词:(+)-依托莫西钠盐)/HY-50202A/50mg
商品详细Medchemexpress/(R)-(+)-依托莫西钠盐(同义词:(+)-依托莫西钠盐)/HY-50202A/50mg
Medchemexpress/(R)-(+)-依托莫西钠盐(同义词:(+)-依托莫西钠盐)/HY-50202A/50mg
Medchemexpress/(R)-(+)-依托莫西钠盐(同义词:(+)-依托莫西钠盐)/HY-50202A/50mg
商品编号: HY-50202A-10mM*1mLinWater
品牌: MedChemExp
市场价: ¥1840.00
美元价: 1104.00
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
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商品介绍
(R)-(+)-EtomoxirsodiumsaltisR-formofEtomoxirsodiumsalt.Etomoxirisapotentinhibitorofcarnitinepalmitoyltransferase-I(CPT-1).
Description

(R)-(+)-EtomoxirsodiumsaltisR-formofEtomoxirsodiumsalt.Etomoxirisapotentinhibitorofcarnitinepalmitoyltransferase-I(CPT-1).

IC50&Target

CPT-1[1]

InVitro

(R)-(+)-EtomoxirsodiumsaltisR-formofEtomoxirsodiumsalt.EtomoxirbindsirreversIBLytothecatalyticsiteofCPT-1inhibitingitsactivity,butalsoupregulatesfattyacidoxidationenzymes.Etomoxirisdevelopedasaninhibitorofthemitochondrialcarnitinepalmitoyltransferase-1(CPT-1)locatedontheoutermitochondrialmembrane.Etomoxir,inthelivercanactasperoxisomalproliferator,increasingDNAsynthesisandlivergrowth.Thus,etomoxir,inadditionofbeingaCPT1inhibitorcouldbeconsideredasaPPARalphaagoNIST[1].EtomoxirisamemberoftheoxiranecarboxylicacidcarnitinepalmitoyltransferaseIinhibitorsandhasbeensuggestedasatherapeuticagentforthetreatmentofheartfailure.AcuteEtomoxirtreatmentirreversiblyinhibitstheactivityofcarnitinepalmitoyltransferaseI.Asaresult,fattyacidimportintothemitochondriaandβ-oxidationisreduced,whereascytosolicfattyacidaccumulatesandglucoseoxidationiselevated.Prolongedincubation(24h)withEtomoxirproducesdiverseeffectsontheexpressionofseveralmetabolicenzyme[2].

InVivo

(R)-(+)-EtomoxirsodiumsaltisR-formofEtomoxirsodiumsalt.Etomoxirisaninhibitoroffreefattyacid(FFA)oxidation-relatedkeyenzymeCPT1.P53interactsdirectlywithBax,whichisinhibitedbyEtomoxir,furtherconfirmingthedirectinteractionofP53andBax,andtheinvolvementofFAO-mediatedmitochondrialROSgenerationindb/dbmice[3].RatsareinjecteddailywithEtomoxir,aspecificCPT-Iinhibitor,for8daysat20mg/kgofbodymass.Etomoxir-treatedratsdisplaya44%reducedcardiacCPT-Iactivity.ThetreatmentofLewisratsfor8dayswith20mg/kgEtomoxirdoesnotalterbloodglucose,whichisinlinewithcomparableetomoxir-feedingstudies.Similarly,Etomoxirfeedingdoesnotaffectgeneralgrowthcharacteristicssuchasgaininbodymass,nordoesitaffecthindlimbmusclemass.However,heartmassandlivermassarebothsignificantlyincreasedby11%inEtomoxir-treatedrats[4].

References
  • [1].RuppH,etal.Theuseofpartialfattyacidoxidationinhibitorsformetabolictherapyofanginapectorisandheartfailure.Herz.2002Nov;27(7):621-36.

    [2].XuFY,etal.EtomoxirmediatesdifferentialmetabolicchannelingoffattyacidandglycerolprecursorsintocardiolipininH9c2cells.JLipidRes.2003Feb;44(2):415-23.

    [3].LiJ,etal.FFA-ROS-P53-mediatedmitochondrialapoptosiscontributestoreductionofosteoblastogenesisandbonemassintype2diabetesmellitus.SciRep.2015Jul31;5:12724.

    [4].LuikenJJ,etal.Etomoxir-inducedpartialcarnitinepalmitoyltransferase-I(CPT-I)inhibitioninvivodoesnotaltercardiaclong-chainfattyaciduptakeandoxidationrates.BiochemJ.2009Apr15;419(2):447-55.

CellAssay
[2]

EtomoxirisdissolvedinDMSOandstored,andthendilutedwithappropriatemediumbeforeuse[2].

RatheartH9c2myoblasticcellsareincubatedinDMEMcontaining10%fetalbovineserumuntilnearconfluence.Insomeexperiments,cellsarepreincubatedfor2hwithDMEM(serum-free)intheabsenceorpresenceof1-80μMEtomoxirandthenincubatedfor2hwith0.1mM[1-14C]oleicacid(10μCi/dish,bindstoBSAina1:1molarratio).Inotherexperiments,cellsarepreincubatedfor2hplusorminus40μMEtomoxirandthenincubatedfor2hwith0.1μMor0.1mM[1,3-3H]glycerol(10μCi/dish),0.1mM[1-14C]oleicacid(2μCi/dish,bindstoBSAina1:1molarratio),0.1mM[1-14C]palmiticacid(2μCi/dish,bindstoBSAina1:1molarratio),28μM[3H]ethanolamine(2μCi/dish),28μM[methyl-3H]choline(2μCi/dish),0.4mM[3H]serine(20μCi/dish),or40μMmyo-[3H]inositol(10μCi/dish).Themediumisremovedandthecellswashedtwicewithice-coldsalineandthenharvestedfromthedishwith2mLmethanol-water(1:1,v/v)forlipidextraction.AnaliquotofthehomogenateistakenforthedeterminationoftotaluptakeofrADIoactivityintocells.Phospholipidsarethenisolatedandradioactivityinthesedetermined[2].MCEhasnotindependentlyconfirmedtheaccuracyofthesemethods.Theyareforreferenceonly.

AnimalAdministration
[3][4]

Etomoxirisdissolvedin0.9%(w/v)NaCl(Rat)[4].

Mice[3]
80maleC57BLKS/Jlar-Leprdb/dbmiceand20wildtypelittermates(8week)areused.db/dbmicearerandomlydividedintofourgroups:db/dbgroup,Etomoxirgroup,MitoQgroup,andPFT-αgroup.IntheEtomoxirgroup,miceareintraperitoneallyinjectedwith1mg/kgEtomoxirtwiceeveryweek.IntheMitoQgroup,50μMMitoQisgiventothemiceinwater.Waterbottles,containingeitherMitoQ,arecoveredwithaluminumfoil,andallbottlesarerefilledevery3days.InthePFT-αgroup,miceareintraperitoneallyinjectedwith1mg/kgPFT-αtwiceeveryweek.WTmiceareadministratedwithvehicleinstead.Theexperimentalperiodis8weeks.Attheend,peripheralbloodsamplesandbonemarrowcellsareharvestedfortheassays.
Rat[4]
MaleLewisrats,weighing150-200g,areusedinthepresentstudy.Animalsarekeptona12h:12hlight/darkcycleandfedaPurinaChowdietandwateradlibitum.Theratsaredividedintotwogroups:(1)controland(2)Etomoxir.Etomoxir(20mg/kgofbodyweight)isdissolvedin0.9%(w/v)NaClandadministeredintraperitoneallyfor8days.Controlratsreceivesaline.Thelastinjectionisgiven24hbeforetheexperiment.Animalsareanaesthetizedwithanintraperitonealinjectionofanembutalandheparin(3:1)mixture.Subsequently,theheartisremovedforLCFAuptakestudiesandforanalysesoftransporterproteincontents.MCEhasnotindependentlyconfirmedtheaccuracyofthesemethods.Theyareforreferenceonly.

References
  • [1].RuppH,etal.Theuseofpartialfattyacidoxidationinhibitorsformetabolictherapyofanginapectorisandheartfailure.Herz.2002Nov;27(7):621-36.

    [2].XuFY,etal.EtomoxirmediatesdifferentialmetabolicchannelingoffattyacidandglycerolprecursorsintocardiolipininH9c2cells.JLipidRes.2003Feb;44(2):415-23.

    [3].LiJ,etal.FFA-ROS-P53-mediatedmitochondrialapoptosiscontributestoreductionofosteoblastogenesisandbonemassintype2diabetesmellitus.SciRep.2015Jul31;5:12724.

    [4].LuikenJJ,etal.Etomoxir-inducedpartialcarnitinepalmitoyltransferase-I(CPT-I)inhibitioninvivodoesnotaltercardiaclong-chainfattyaciduptakeandoxidationrates.BiochemJ.2009Apr15;419(2):447-55.

MolecularWeight

320.74

Formula

C₁₅H₁₈ClNaO₄

CASNo.

828934-41-4

Storage

4°C,storedundernitrogen

Shipping

RoomtemperatureincontinentalUS;mayvaryelsewhere

Solvent&Solubility

H2O:80mg/mL(Needwarming)

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

Purity:99.94%