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当前位置: 首页 > 产品中心 > Other_reagents > Adipogen/Salinosporamide A/AG-CN2-0444-C100/100 µg
商品详细Adipogen/Salinosporamide A/AG-CN2-0444-C100/100 µg
Adipogen/Salinosporamide A/AG-CN2-0444-C100/100 µg
Adipogen/Salinosporamide A/AG-CN2-0444-C100/100 µg
商品编号: AG-CN2-0444-C100
品牌: Adipogen Inc
市场价: ¥3800.00
美元价: 2280.00
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
SynonymsSalA;Marizomib;NPI-0052
ProductTypeChemical
Properties
FormulaC15H20ClNO4
MW313.8
CAS437742-34-2
Source/HostChemicalsIsolatedfromSalinosporatropica.
PurityChemicals≥95%(HPLC)
AppearanceWhitesolid.
SolubilitySolubleinDMSO.Donotdissolveinmethanolorethanol.
OtherProductDataNote:Werecommendtousefreshsolutions.AliquotsshouldbepreparedinDMSOandstoredat-20°C.
InChiKeyNGWSFRIPKNWYAO-SHTIJGAHSA-N
ShippingandHandling
ShippingBLUEICE
ShortTermStorage+4°C
LongTermStorage-20°C
HandlingAdviceKeepunderinertgas.
Protectfromlight.
Protectfrommoistureandoxygen.
Use/StABIlityStableforatleast1yearafterreceiptwhenstoredat-20°C.
Documents
MSDSDownloadPDF
ProductSpecificationSheet
DatasheetDownloadPDF
  • Potent,irreversIBLeinhibitorofallthe3proteolyticactivitiesofthemammalian20Sproteasome.
  • β5subunit:chymotrypsin-like(EC50=3.5nM)
  • β2subunit:trypsin-like(EC50=28nM)
  • β1subunit:caspase-likeorpeptidyl-glutamylpeptide-hydrolyzing(PGPH)(EC50=430nM)
  • Potentanticancercompound.
  • Triggersapoptosis,withdistinctproteasomeactivityandmechanismofactioncomparedtobortezomib(Velcade)(Prod.No.AG-CR1-3602).
  • MostpotentsuppressorofNF-κBactivation,comparedwithbortezomib,MG-132(Prod.No.AG-CP3-0011),N-acetyl-leucyl-leucyl-norleucinal(ALLN)andlactacystin(Prod.No.AG-CN2-0104).
  • InhibitorofTNF-α,IL-1,IL-6,ICAM-1andVEGFsynthesis.
  • Displaysalongerinhibitiondurationthanbortezomib.
  • Potentantileukemicactivityagainstbortezomib-resistantleukemiacells.
ProductReferences
  1. SalinosporamideA:ahighlycytotoxicproteasomeinhibitorfromanovelmicrobialsource,amarinebacteriumofthenewgenussalinospora:R.H.Feling,etal.;Angew.Chem.Int.Ed.Engl.42,355(2003)
  2. Structure-activityrelationshipstudiesofsalinosporamideA(NPI-0052),anovelmarinederivedproteasomeinhibitor:V.R.Macherla,etal.;J.Med.Chem.48,3684(2005)
  3. AnovelorallyactiveproteasomeinhibitorinducesapoptosisinmultiplemyelomacellswithmechanismsdistinctfromBortezomib:D.Chauhan,etal.;CancerCell8,407(2005)
  4. CrystalstructuresofSalinosporamideA(NPI-0052)andB(NPI-0047)incomplexwiththe20Sproteasomerevealimportantconsequencesofbeta-lactoneringopeningandamechanismforirreversiblebinding:M.Groll,etal.;JACS128,5136(2006)
  5. NPI-0052enhancestumoricidalresponsetoconventionalcancertherapyinacoloncancermodel:J.C.Cusack,etal.;Clin.CancerRes.12,6758(2006)
  6. ComparisonofbiochemicalandBIOLOGicaleffectsofML858(salinosporamideA)andbortezomib:M.J.Williamson,etal.;Mol.CancerTher.5,3052(2006)
  7. SalinosporamideA(NPI-0052)potentiatesapoptosis,suppressesosteoclastogenesis,andinhibitsinvasionthroughdown-modulationofNF-κB-regulatedgeneproducts:K.S.Ahn,etal.;Blood110,2286(2007)
  8. AmechaNISTicandkineticstudyofthebeta-lactonehydrolysisofSalinosporamideA(NPI-0052),anovelproteasomeinhibitor:N.Denora,etal.;J.Pharm.Sci.96,2037(2007)
  9. CombinationofproteasomeinhibitorsbortezomibandNPI-0052triggerinvivosynergisticcytotoxicityinmultiplemyeloma:D.Chauhan,etal.;Blood111,1654(2008)
  10. DiscoveryanddevelopmentoftheanticanceragentsalinosporamideA(NPI-0052):W.Fenical,etal.;Bioorg.Med.Chem.17,2175(2009)
  11. Generatingagenerationofproteasomeinhibitors:frommicrobialfermentationtototalsynthesisofsalinosporamidea(marizomib)andothersalinosporamides:B.C.Potts&K.S.Lam;Mar.Drugs8,835(2010)(Review)
  12. Salinosporamidenaturalproducts:Potent20Sproteasomeinhibitorsaspromisingcancerchemotherapeutics:T.A.Gulder&B.S.Moore;Angew.Chem.Int.Ed.Engl.49,9346(2010)(Review)
  13. Marizomib,aproteasomeinhibitorforallseasons:preclinicalprofileandaframeworkforclinicaltrials:B.C.Potts,etal.;Curr.CancerDrugTargets11,254(2011)
  14. Proteasomeregulatormarizomib(NPI-0052)exhibitsprolongedinhibition,attenuatedefflux,andgreatercytotoxicitythanitsreversibleanalogs:A.Obaidat,etal.;J.Pharmacol.Exp.Ther.337,479(2011)
  15. Molecularmechanismsofacquiredproteasomeinhibitorresistance:A.J.Kale&B.S.Moore;J.Med.Chem.55,10317(2012)
  16. AntileukemicactivityandmechanismofdrugresistancetothemarineSalinisporatropicaproteasomeinhibitorsalinosporamideA(Marizomib):D.Niewerth,etal.;Mol.Pharmacol.86,12(2014)
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。