Ganodermanondiol (Synonyms: 灵芝酮二醇)

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Ganodermanondiol  (Synonyms: 灵芝酮二醇)

Ganodermanondiol 是从灵芝中分离出的一种促黑素生成抑制剂。Ganodermanondiol 对叔丁基过氧化氢诱导的肝毒性具有高效的细胞保护作用。Ganodermanondiol 具有抗 HIV-1 protease 活性，其 IC50 值为 90 μM。Ganodermanondiol 具有很强的抗补体活性，对经典补体途径作用的 IC50 值为 41.7 μM。

Ganodermanondiol (Synonyms: 灵芝酮二醇)

Ganodermanondiol Chemical Structure

CAS No. : 107900-76-5

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生物活性

Ganodermanondiol is a melanogenesis inhibitor isolated from the Ganoderma lucidum[1].Ganodermanondiol exhibits potent cytoprotective effects on tert-butyl hydroperoxide-induced hepatotoxicity[2]. Ganodermanondiol shows significant anti-HIV-1 protease activity with an IC50 of 90 μM[3]. Ganodermanondiol exhibits a strong anticomplement activity against the classical pathway of the complement system with an IC50 of 41.7μM[4].

IC50 & Target

IC50: 90μM (HIV-1 protease)[3]
分子量

456.70

Formula

C30H48O3
CAS 号

107900-76-5
中文名称

灵芝酮二醇
结构分类
  • Terpenoids
  • Triterpenes
初始来源
  • 植物
  • 多孔菌科
  • 微生物
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.
纯度 & 产品资料
Data Sheet (531 KB) 产品使用指南 (1538 KB)

参考文献

  • [1]. Kim JW, et al. Effects of Ganodermanondiol, a New Melanogenesis Inhibitor from the Medicinal Mushroom Ganoderma lucidum. Int J Mol Sci. 2016 Oct 27;17(11).  [Content Brief]

    [2]. Li B, et al. Protective effect of ganodermanondiol isolated from the Lingzhi mushroom against tert-butyl hydroperoxide-induced hepatotoxicity through Nrf2-mediated antioxidant enzymes. Food Chem Toxicol. 2013 Mar;53:317-24.  [Content Brief]

    [3]. Min BS, et al. Triterpenes from the spores of Ganoderma lucidum and their inhibitory activity against HIV-1 protease. Chem Pharm Bull (Tokyo). 1998 Oct;46(10):1607-12.  [Content Brief]

    [4]. Min BS, et al. Anticomplement activity of terpenoids from the spores of Ganoderma lucidum. Planta Med. 2001 Dec;67(9):811-4.  [Content Brief]

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