Literature DB >> 16783700

Cytotoxic phenanthrenes from the rhizomes of Tamus communis.

Borbála Réthy1, Adriána Kovács, István Zupkó, Peter Forgo, Andrea Vasas, György Falkay, Judit Hohmann.   

Abstract

From the fresh rhizomes of Tamus communis five phenanthrenes (1 - 5) were isolated under the guidance of cytotoxic assays in HeLa cells. The compounds were obtained from the highly active CHCl (3) fraction of the MeOH extract by using multistep chromatographic purifications, including VLC, preparative TLC, HPLC and gel filtration. The compounds were identified by means of EI-mass, UV and NMR spectroscopy as 7-hydroxy-2,3,4-trimethoxyphenanthrene (1), 2,7-dihydroxy-3,4-dimethoxyphenanthrene (nudol) (2), 2,7-dihydroxy-3,4,8-trimethoxyphenanthrene (3), 3,7-dihydroxy-2,4,8-trimethoxyphenanthrene (confusarin) (4), and 3,7-dihydroxy-2,4-dimethoxyphenanthrene (5). Compound 1 is a new natural product, and 2 - 4 were isolated for the first time from T. communis. In the cytotoxic assays, compounds 1 - 3 and 5 significantly inhibited the growth of HeLa cells (IC (50) = 0.97 - 20.18 microM). Compound 3, with an IC (50) value of 0.97 microM, is of special interest because of its high activity.

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Year:  2006        PMID: 16783700     DOI: 10.1055/s-2006-941505

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  8 in total

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7.  Nudol, a phenanthrene derivative from Dendrobium nobile, induces cell cycle arrest and apoptosis and inhibits migration in osteosarcoma cells.

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Review 8.  Phytochemical Constituents and Pharmacological Potential of Tamus communis Rhizomes.

Authors:  Iva Slavova; Teodora Tomova; Slavena Kusovska; Yoana Chukova; Mariana Argirova
Journal:  Molecules       Date:  2022-03-12       Impact factor: 4.411

  8 in total

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