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IB1440 BEC Hydrochloride 免疫学/炎

症 索莱宝
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  • ¥350 - 4220
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  • 北京
  • IB1440
  • 2025年07月23日
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    • 详细信息
    • 技术资料
    • 保存条件

      Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 保质期

      Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 英文名

      BEC Hydrochloride

    • 库存

      现询

    • 供应商

      北京索莱宝科技有限公司

    • CAS号

      222638-67-7

    • 规格

      50mg/25mg/10mg/1mg/5mg

    规格:50mg产品价格:¥4220.0
    规格:25mg产品价格:¥2880.0
    规格:10mg产品价格:¥1394.0
    规格:1mg产品价格:¥350.0
    规格:5mg产品价格:¥810.0

    基本信息
    CASNo.222638-67-7
    英文名称BEC Hydrochloride
    别名;BECHCl;S-(2-boronoethyl)-L-cysteine.;Aricept,E-2020DonepezilHCl;
    分子式C5H12BNO4S·HCl
    分子量229.48
    溶解性Soluble in DMSO
    纯度≥98%
    外观(性状)White to off-white Solid
    储存条件Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
    MDLMFCD03453539
    SMILESB(CCSC[C@@H](C(=O)O)N)(O)O.Cl
    靶点Arginase
    通路Metabolic Enzyme&Protease
    背景说明BEC Hydrochloride是一个竞争性的 Arginase II抑制剂。
    生物活性BEC hydrochloride is a slow-binding and competitive Arginase II inhibitor with Ki of 0.31 μM and 30 nM at pH 7.5 and pH 9.5, respectively[1].
    IC50Ki: 0.31μM(BEC hydrochloride,at pH 7.5) and 30nM(BEC hydrochloride,at pH 9.5)[1]
    In VitroThe X-ray crystal structure of the arginase-BEC complex has been determined at 2.3 resolution from crystals perfectly twinned by hemihedry. The structure of the complex reveals that the boronic acid moiety undergoes nucleophilic attack by metal-bridging hydroxide ion to yield a tetrahedral boronate anion that bridges the binuclear manganese cluster,thereby mimicking the tetrahedral intermediate(and its flanking transition states)in the arginine hydrolysis reaction[2].
    细胞实验Administration of the arginase inhibitor BEC decreases arginase activity and causes alterations in NO homeostasis,which are reflected by increases in S-nitrosylated and nitrated proteins in the lungs from inflamed mice. BEC enhances perivascular and peribronchiolar lung inflammation,mucus metaplasia,NF-κB DNA binding,and mRNA expression of the NF-κB-driven chemokine genes CCL20 and KC,and leads to further increases in airways hyperresponsiveness[3].
    数据来源文献[1]. Colleluori DM, et al. Classical and slow-binding inhibitors of human type II arginase. Biochemistry. 2001 Aug 7;40(31):9356-62.
    [2]. Kim NN, et al. Probing erectile function: S-(2-boronoethyl)-L-cysteine binds to arginase as a transition state analogue and enhances smooth muscle relaxation in human penile corpus cavernosum. Biochemistry. 2001 Mar 6;40(9):2678-88.
    [3]. Ckless K, et al. Inhibition of arginase activity enhances inflammation in mice with allergic airway disease, in association with increases in protein S-nitrosylation and tyrosine nitration. J Immunol. 2008 Sep 15;181(6):4255-64.
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