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当前位置: 首页 > 产品中心 > Other_reagents > 脂肪原/鹅去氧胆酸/AG-CN2-0410-M500/500 mg
商品详细脂肪原/鹅去氧胆酸/AG-CN2-0410-M500/500 mg
脂肪原/鹅去氧胆酸/AG-CN2-0410-M500/500 mg
脂肪原/鹅去氧胆酸/AG-CN2-0410-M500/500 mg
商品编号: AG-CN2-0410-M500
品牌: Adipogen Inc
市场价: ¥1200.00
美元价: 720.00
产地: 美国(厂家直采)
公司:
产品分类: 其他试剂
公司分类: Other_reagents
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
MoreInformation
ProductDetails
SynonymsCDCA;Ulmenide;Kebilis;Hekbilin;Fluibil;Chenodiol;Anthropodeoxycholicacid
ProductTypeChemical
Properties
FormulaC24H40O4
MW392.6
MerckIndex14:2054
CAS474-25-9
RTECSFZ1980000
Source/HostChemicalsSynthetic.Originallyisolatedfrombile.
PurityChemicals≥95%(NMR)
AppearanceWhitetooff-whitecrystallinepowder.
SolubilitySolubleinDMSO,ethanolordimethylformamide.Sparinglysolubleinwater.
IdentityDeterminedby1H-NMR.
InChiKeyRUDATBOHQWOJDD-BSWAIDMHSA-N
ShippingandHandling
ShippingAMBIENT
ShortTermStorage+4°C
LongTermStorage-20°C
HandlingAdviceProtectfromlight.
Protectfrommoisture.
Use/StABIlityStableforatleast2yearsafterreceiptwhenstoredat-20°C.
Documents
MSDSDownloadPDF
ProductSpecificationSheet
DatasheetDownloadPDF
  • Cytotoxichydrophobicprimarybileacid[1].
  • ActivatoroffarnesoidXreceptor(FXR),anuclearreceptorthatishepatoprotectiveandregulatesbileacidsynthesis(cholesterol7α-hydroxylase(CYP7A1)suppression),conjugationandtransport,aswellasgenesinvolvedinlipidandglucosemetabolismand[4-6,14].
  • Bileacid-controlledsignalingpathwaysarepromisingnoveltargetstotreatsuchmetabolicdiseasesasobesity,typeIIdiabetes,insulinresistance,hyperlipidemiaandatherosclerosis[1,8,9,12].
  • Inhibitorof5β-reductase(AKR1D1)[10,15].
  • PotentselectiveinhibitorofDD2(AKR1C2)[3].
  • Potentinhibitorof11β-HSD1dehydrogenase[7].
  • ChangestumorcellviabilityviaIL-6pathway[11].
  • Anticancercompound.Apoptosisinducer[13].
  • Immunosuppressiveandanti-inflammatorycompound.Modulatesoxidativestress[2,16].
  • Differentiationregulatorofmouseembryonicstemcells[17].
  • Usedfordissolutionofcholesterolgallstones.
ProductReferences
  1. Bileacidsasdrugs:principles,mechanismsofactionandformulations:A.F.Hofmann;Ital.J.Gastroenterol.27,106(1995)(Review)
  2. S-adenosil-L-methionineisabletoreversetheimmunosuppressiveeffectsofchenodeoxycholicacidinvitro:G.Filaci,etal.;Int.J.Immunopharmacol.19,157(1997)
  3. IdentificationofaminoacidresiduesresponsIBLefordifferencesinsubstratespecificityandinhibitorsensitivitybetweentwohumanliverdihydrodioldehydrogenaseisoenzymesbysite-directedmutagenesis:K.Matsuura,etal.;Biochem.J.323,61(1997)
  4. Identificationofanuclearreceptorforbileacids:M.Makishima,etal.;Science284,1362(1999)
  5. Bileacids:naturalligandsforanorphannuclearreceptor:D.J.Parks,etal.;Science284,1365(1999)(Review)
  6. AnaturalproductthatlowerscholesterolasananatagoNISTligandforFXR:N.L.Urizar,etal.;Science296,1703(2002)
  7. Effectofchenodeoxycholicacidon11beta-hydroxysteroiddehydrogenaseinvarioustargettissues:D.J.Morris,etal.;Metabolism53,811(2004)
  8. TheFarnesoidXReceptor-AMolecularLinkBetweenBileAcidandLipidandGlucoseMetabolism:T.Claudel,etal.;Hepatology48,1632(2008)(Review)
  9. FarnesoidXreceptorantagonizesnuclearfactorkappaBinhepaticinflammatoryresponse:Y.D.Wang,etal.;Hepatology48,1632(2008)(Review)
  10. Bileacidsmodulateglucocorticoidmetabolismandthehypothalamic-pituitary-adrenalaxisinobstructivejaundice:A.D.McNeilly,etal.;J.Hepatol.52,705(2010)
  11. Effectsofbileacidsonexpressionofinterleukin-6andcellviabilityinQBC939cellline:J.Wang,etal.;ZhonghuaWaiKeZaZhi.48,919(2010)
  12. Fastingplasmachenodeoxycholicacidandcholicacidconcentrationsareinverselycorrelatedwithinsulinsensitivityinadults:B.Cariou,etal.;Nutrition&Metabolism8,48(2011)
  13. Deoxycholicandchenodeoxycholicbileacidsinduceapoptosisviaoxidativestressinhumancolonadenocarcinomacells:J.I.Barrasa,etal.;Apoptosis16,1054(2011)
  14. FarnesoidXreceptoractivationbychenodeoxycholicacidinducesdetoxifyingenzymesthroughAMP-activatedproteinkinaseandextracellularsignal-regulatedkinase1/2-mediatedphosphorylationofCCAAT/enhancerbindingproteinβ:K.Noh,etal.;DrugMetab.Dispos.39,1451(2011)
  15. Substratespecificityandinhibitoranalysesofhumansteroid5β-reductase(AKR1D1):M.Chen,etal.;Steroids76,484(2011)
  16. Effectofchenodeoxycholicacidonfibrosis,inflammationandoxidativestressinkidneyinhigh-fructose-fedWistarrats:Z.Hu,etal.;KidneyBloodPressRes.36,85(2012)
  17. Directeffectofchenodeoxycholicacidondifferentiationofmouseembryonicstemcellsculturedunderfeeder-freecultureconditions:S.J.Park,etal.;Biomed.Res.Int.2013,375076(2013)
品牌介绍
Adipogen公司由三个子公司组成,分别是Adipogen,Inc.(韩国),AdipogenSA(瑞士)和 AdipogenCorporation(美国圣地亚哥)。总部设在美国,运营总部在瑞士利斯塔尔。Adipogen公司专门从事生命科学研究试剂的开发,如癌症、免疫、炎症、代谢疾病(糖尿病、肥胖)、干细胞和神经退行性疾病等领域。其重点关注开发创新优质的ELISA试剂盒。另外,也可提供抗体和蛋白产品,Adipogen拥有自己的化学实验室,致力于开发创新型小分子化合物。