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L-Leucine 4-methoxy-β-naphthylamide (hydrochloride)

产品信息
  • 规格: 100mg 产品价格: ¥702.0
    规格: 250mg 产品价格: ¥1664.0
    规格: 1g 产品价格: ¥5616.0

    产品说明氨基肽酶M和亮氨酸氨基肽酶的底物
    该产品包含在以下化合物库中:
      质量控制
      • 纯度 = 98.00%
      化学性质
      CAS号 4467-68-9    
      别名 Leu-MNA
      分子式 C17H22N2O2 • HCl 分子量 322.8
      溶解性 Soluble in DMSO 储存条件 Store at -20°
       实验操作
      细胞实验[2]:

      细胞系

      溶解方法

      反应时间

      应用

      动物实验[3]:

      动物模型

      剂量

      注意事项

      References:

      产品描述

      L-Leucine 4-methoxy-β-naphthylamide is a substrate for aminopeptidase M and leucine aminopeptidase.

      Aminopeptidases are enzymes catalyzing the cleavage of amino acids from the amino terminus (N-terminus) of proteins or peptides. Aminopeptidases are distributed widely throughout the animal and plant kingdoms and are present in various subcellular organelles, in cytosol, as well as membrane components.

      In vitro: L-Leucine 4-methoxy-β-naphthylamide was identified as a cell-permeable substrate for aminopeptidase M and leucine aminopeptidase that was developed for intracellular analysis of protease activities [1]. In a previous method-developing study, peptide derivatives of 4-methoxy-β-naphthylamine including L-leucine 4-methoxy-β-naphthylamide were incubated in microtiter plates together with nitrosalicylaldehyde. Selectivity was achieved by running parallel assays containing inhibitors partially selective for each of peptide derivatives. This method was successfully validated by measurements in cells isolated from cathepsin B-/--, K-/--, and L-/-- mice [2].

      In vivo: Up to now, there is no animal in vivo data reported.

      Clinical trial: So far, no clinical study has been conducted.

      References:
      [1] Monis, B. ,Wasserkrug, H. and Seligman, A.M. Comparison of fixatives and substrates for aminopeptidase. Journal of Histochemistry and Cytochemistry 13(6), 503-509 (1965).
      [2] Rüttger, A. ,Mollenhauer, J.,Lser, R., et al. Microplate assay for quantitative determination of cathepsin activities in viable cells using derivatives of 4-methoxy-β-naphthylamide. Biotechniques 41(4), 469-473 (2006).

      温馨提示:不可用于临床ZL。
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