Secondary Metabolites of Medicinal Plants. Bharat Singh

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Secondary Metabolites of Medicinal Plants - Bharat Singh

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al. 2017; Zhang et al. 2018). Similarly, 3-O-[2′-O-β-D-glucopyranosyl-3′-O-(2″-hydroxy-1″-carboxyethoxycarboxypropyl)]-β-D-glucuropyranosyl oleanolic acid 28-O-β-D-glucopyranoside (achyranthoside I) and oleanolic acid 3-O-[3′-O-(2″-hydroxy-1″-carboxyethoxycarboxypropyl)] β-D-glucuropyranoside (achyranthoside II) were identified from A. bidentata (Guangshu et al. 2004). The chikusetsusaponins IVa and V, achyranthosides B, C, D, E, and G, sulfachyranthosides B and D, and betavulgarosides II and IV were identified by LC–MS determination from Achyranthes root (Kawahara et al. 2016). The structures of isolated compounds from A. bidentata was established by spectral data analysis as β-ecdysterone, (25R)-inokosterone, (25S)-inokosterone, zingibroside R1, and ginsenoside Ro (Jiang et al. 2017). Achyranthoside C, achyranthoside C 6′-methyl ester, achyranthoside C 1‴-methyl ester, achyranthoside C methyl ester, achyranthoside G, and achyranthoside H methyl ester were reported to be from the roots of Achyranthes fauriei (Ando et al. 2008; Fukumura et al. 2009).

      The ethanolic extract of A. bidentata was showed hepatoprotective (Dange and Phadke 1989), antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH) model (Suresh Kumar et al. 2008; Edwin et al. 2008; Nehete et al. 2009; Upadhya et al. 2015), hemolytic activity (Sun 2006), and treatment of arthritis in traditional Chinese medicine and possesses anti-inflammatory properties (Xu et al. 2017). A. bidentata root extract treatment improves bone biomechanical quality and shows osteoprotective effects (He et al. 2010; Zhang et al. 2012; Wang et al. 2017) and metastatic chemoprevention property (Jiang et al. 2017).

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      5 Ando, H., Fukumura, M., Hori, Y. et al. (2008). Two new glucuronide saponins,

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