Cathepsin L-IN-2(Synonyms: Z-Phe-Phe-FMK)

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上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白，专注于信号通路和疾病研究领域。

Cathepsin L-IN-2 (Synonyms: Z-Phe-Phe-FMK)

Cathepsin L-IN-2 (Z-Phe-Phe-FMK) 是一种有效且不可逆的组织蛋白酶 L (cathepsin L) 和组织蛋白酶 B (cathepsin B) 抑制剂。

Cathepsin L-IN-2(Synonyms: Z-Phe-Phe-FMK)

Cathepsin L-IN-2 Chemical Structure

CAS No. : 108005-94-3

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生物活性

Cathepsin L-IN-2 (Z-Phe-Phe-FMK) is a potent and irreversible cathepsin L and cathepsin B inhibitor[1][2].

分子量

462.51

Formula

C27H27FN2O4
CAS 号

108005-94-3
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献

  • [1]. Jonathan Frew, et al. Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiency. Mol Neurodegener. 2020 Mar 16;15(1):21.

    [2]. Kirsi Ravanko, et al. Cysteine cathepsins are central contributors of invasion by cultured adenosylmethionine decarboxylase-transformed rodent fibroblasts. Cancer Res. 2004 Dec 15;64(24):8831-8.

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