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Discovery Antibodies/Orphenadrine citrate salt/1 g/O-100-1 g

价格
¥600.00
货号:O-100-1g
浏览量:127
品牌:Discovery
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商品描述
Cat#:O-100
AlternativeNameNorflex®,Banflex®,Flexon®,X-Otag®
  • LyophilizedPowder
  • BioassayTested
  • SourceSynthetic
    MW:461.5
    Purity:>96%
    Effectiveconcentration0.3-100µM.
      • Orphenadrine citrate salt
    Chemicalnameβ-Dimethylaminoethyl2-methylbenzhydrylethercitratesalt.
    MolecularformulaC18H23NO●C6H8O7.
    CASNo.:4682-36-4.
    ActivityOrphenadrinewasfoundtoactasmuscarinicreceptorantagoNIST,H1 histaminereceptorantagonist,musclerelaxant,inhibitorofthenoradrenergictransporter,NMDAreceptorantagonistandNaV channelblocker1-4.
      • Brocks,D.R. etal. (1999) J.Pharm.Pharm.Sci. 2, 39.
      • Desaphy,J.F. etal. (2009) Pain 142, 225.
      • Kornhuber,J. etal. (1995) J.Neural.Transm.Gen.Sect. 102, 237.
      • Pubill,D. etal. (1999) J.Pharm.Pharmacol. 51, 307.
    ShippingandstorageShippedatroomtemperature.Productassuppliedcanbestoredintactatroomtemperatureforseveralweeks.Forlongerperiods,itshouldbestoredat-20°C.
    SolubilityDMSO.Centrifugeallproductpreparationsbeforeuse(10000xg5min).
    StorageofsolutionsUptofourweeksat4°Corthreemonthsat-20°C.
      • Orphenadrine citrate salt
        AlomoneLabs Orphenadrinecitratesalt inhibitscharbacol-induced Ca2+ signalin C6cellsexpressingM1muscarinicreceptor.
        ChangesinintracellularCa2+ weredetectedviachangesinFluo-3emissionfollowingapplication.A.Normalizedfluorescencebeforeandafterco-application(at20seconds,seearrow)of10µMcarbacholand0-100µM Orphenadrinecitratesalt (#O-100)asindicated.B.Inhibition(aspercentofcontrol)of10µMcarbacholevokedCa2+ rise,plottedagainstOrphenadrinecitratesaltconcentrations.
    References-Scientificbackground
    • 1.Brocks,D.R. etal. (1999) J.Pharm.Pharm.Sci. 2, 39.
    • 2.Desaphy,J.F. etal. (2009) Pain 142, 225.
    • 3.Kornhuber,J. etal. (1995) J.Neural.Transm.Gen.Sect. 102, 237.
    • 4.Pubill,D. etal. (1999) J.Pharm.Pharmacol. 51, 307.
      • Thegroupofanticholinergicdrugsincludesbenztropine,biperiden,diphenhydramine,ethopropazine,orphenadrine,procyclidineandtrihexyphenidyl.OrphenadrineasthecitratesaltisusedforthetreatmentofParkinson’sdiseaseandinmusculoskeletaldisorders.Itisalsousedasananalgesic,althoughitsmechanismofactionisstillunknown1,2.Orphenadrinebindstoandmodulatestheactivityofmuscarinicreceptorsofratbrain,withIC50of0.37µM1.

        OrphenadrineinhibitsNaVchannelsinaconcentration-,voltage-andfrequency-dependentmannerbybindingtothesamereceptorasthelocalanesthetics2.Orphenadrinewasreportedasamuscarinicreceptorantagonist,H1histaminereceptorantagonist,musclerelaxant,andinhibitsthenoradrenergictransporterandblockstheNMDAreceptorionchannel3,4.

    TargetMuscarinic,H1histamine,NMDAreceptors,NaV Na+ channels
    receivea1gfreetrialsample!
    Lastupdate:26/09/2019

    Orphenadrinecitratesalt(#O-100) isahighlypure,synthetic,andbiologicallyactivecompound.

    Forresearchpurposesonly,notforhumanuse
    Discovery Antibodies的Cyclin dependant kinase 2 (CDK2) is a serine/threonine protein kinase which controls both G1/S and G2/M transitions. CDKs along with cyclins and CDK inhibitors regulate cell cycle progression. Specific cyclins activate different CDKs; in early G1, CDK2 pairs with cyclin E to promote entry into the S phase before switching to partner with cyclin A to drive the cell through S phase. Once activated CDKs phosphorylate downstream proteins to initiate signalling cascades. CDK2 phosphorylates and inactivates the RB1 (pRb) tumour suppressor family of proteins.CDK的活动受到严格控制。CDK2活性可以被包括P21在内的一系列抑制剂抑制。细胞周期失调和增殖控制的丧失与细胞转化和癌症密切相关。CDK2在DNA损伤反应(DDR)中的细胞周期停滞中也似乎起着积极作用,它的抑制作用会阻碍DDR,并使细胞对电离辐射敏感,从而诱导细胞死亡。该抗体与AlexaFluor®488偶联。AlexaFluor®488是一种流行的鲜绿色荧光染料,具有高pH稳定性。
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