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Adipogen/Luteolin/AGCN20098M005/5 mg

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ProductDetails
Synonyms3,4,5,7-Tetrahydroxyflavone;Luteolol;BRN0292084;C.I.NaturalYellow2;Digitoflavone;Flacitran;Flavopurpol;Daphneflavonol;Argemexitin
ProductTypeChemical
Properties
FormulaC15H10O6
MW286.2
CAS491-70-3
RTECSLK9275210
Source/HostChemicalsSynthetic.
PurityChemicals≥98%(HPLC)
AppearanceYellowsolid.
SolubilitySolubleinDMSO,DMF,methanolorethanol.Slightlysolubleinwater.
InChiKeyIQPNAANSBPBGFQ-UHFFFAOYSA-N
ShippingandHandling
ShippingAMBIENT
ShortTermStorage+4°C
LongTermStorage-20°C
Use/StABIlityStableforatleast2yearsafterreceiptwhenstoredat-20°C.
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ProductSpecificationSheet
DatasheetDownloadPDF
  • Anticancerandantimetastatic[1,3,8].
  • α-Glucosidaseinhibitor[2].
  • TopoisomeraseIInhibitor[3].
  • Apoptosisinducer[7,8].
  • Anti-inflammatory[4,5].
  • 15-Lipoxygenase(15-LOX)inhibitor[6].
  • IL-6productioninhibitor[9].
  • Fattyacidsynthase(FAS)inhibitor[10].
  • Antioxidant.FreerADIcalscavenger[11].
  • AntiAdipogenic.PPAR-γinhibitor[12].
  • Neuroprotective.Monoaminetransporteractivator[13].
  • Inhibitorofphosphodiesterases1-5(PDE1-5)[14].
  • PKC(ε)andSrckinaseinhibitor[15].
  • HDACinhibitor[16].
  • Autophagymodulator[17]
  • Phosphatidylinositol3-kinase(PI3K)/Aktsignalinginhibitor[18].
  • p90ribosomalS6kinase(RSK1/RSK2)kinaseactivityinhibitor[19].
ProductReferences
  1. Effectsofluteolinandquercetin,inhibitorsoftyrosinekinase,oncellgrowthandmetastasis-associatedpropertiesinA431cellsoverexpressingepidermalgrowthfactorreceptor:Y.T.Huang,etal.;Br.J.Pharmacol.128,999(1999)
  2. Inhibitionofalpha-glucosidaseandamylasebyluteolin,aflavonoid:J.S.Kim,etal.;Biosci.Biotechnol.Biochem.64,2458(2000)
  3. Luteolin,anemerginganti-cancerflavonoid,poisonseukaryoticDNAtopoisomeraseI:A.R.Chowdhury,etal.;Biochem.J.366,653(2002)
  4. Inhibitionofmatrix-proteasesbypolyphenols:Chemicalinsightsforanti-inflammatoryandanti-invasiondrugdesign:L.Sartor,etal.;Biochem.Pharmacol.64, 229(2002)
  5. Luteolininhibitsthenuclearfactor-kappaBtranscriptionalactivityinRat-1fibroblasts:S.H.Kim,etal.;Biochem.Pharmacol.66,955(2003)
  6. Inhibitionof15-lipoxygenasesbyflavonoids:Structure-activityrelationsandmodeofaction:C.D.Sadik,etal.;Biochem.Pharmacol.65,773(2003)
  7. InductionofapoptosisbyluteolinthroughcleavageofBcl-2familyinhumanleukemiaHL-60cells:A.C.Cheng,etal.;Eur.J.Pharmacol.509,1(2005)
  8. Luteolininhibitsinsulin-likegrowthfactor1receptorsignalinginprostatecancercells:J.Fang,etal.;Carcinogenesis28,713(2007)
  9. LuteolinreducesIL-6productioninmicrogliabyinhibitingJNKphosphorylationandactivationofAP-1:S.Jang,etal.;PNAS105,7534(2008)
  10. Inhibitionoffattyacidsynthasebyluteolinpost-transcriptionallydown-regulatesc-Metexpressionindependentofproteosomal/lysosomaldegradation:D.T.Coleman,etal.;Mol.CancerTher.8,214(2009)
  11. Physicochemicalpropertiesandantioxidantactivitiesofluteolin-phospholipidcomplex:K.Xu,etal.;Molecules14,3486(2009)
  12. LuteolininhibitsadipogenicdifferentiationbyregulatingPPARgammaactivation:H.S.Park,etal.;Biofactors35,373(2009)
  13. FunctionalactivationofmonoaminetransportersbyluteolinandapigeninisolatedfromthefruitofPerillafrutescens:G.Zhao,etal.;NeuRochem.Int.56,168(2010)
  14. Luteolin,anon-selectivecompetitiveinhibitorofphosphodiesterases1-5,displaced[3H]-rolipramfromhigh-affinityroliprambindingsitesandreversedxylazine/ketamine-inducedanesthesia:M.C.Yu,etal.;Pulmon.Gastrointest.Urogen.Pharmacol.627,269(2010)
  15. LuteolininhibitsproteinkinaseC(epsilon)andc-SrcactivitiesandUVB-inducedskincancer:S.Byun,etal.;CancerRes.70,2415(2010)
  16. Inhibitionofcellsurvival,invasion,tumorgrowthandhistonedeacetylaseactivitybythedietaryflavonoidluteolininhumanepithelioidcancercells:S.Attoub,etal.;Eur.J.Pharmacol.651,18(2011)
  17. Autophagyinhibitorchloroquineenhancedthecelldeathinducingeffectoftheflavonoidluteolininmetastaticsquamouscellcarcinomacells:L.Verschooten,etal.;PLoSOne7,e48264
  18. RafandPI3Karethemoleculartargetsfortheanti-metastaticeffectofLuteolin:H.Y.Kim,etal.;Phytother.Res.27,1481(2013)
  19. Luteolinisanovelp90ribosomalS6kinase(RSK)inhibitorthatsuppressesNotch4signalingbyblockingtheactivationofY-boxbindingprotein-1(YB-1):K.M.Reipas,etal.;Oncotarget4,329(2013)

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