Literature DB >> 17166530

Phenanthrenes and a dihydrophenanthrene from Tamus communis and their cytotoxic activity.

Adriána Kovács1, Peter Forgo, István Zupkó, Borbála Réthy, György Falkay, Pál Szabó, Judit Hohmann.   

Abstract

From the petroleum ether extract of the rhizomes of Tamus communis, the 7-hydroxy-2,3,4,8-tetramethoxyphenanthrene (1) was isolated, together with the known 2,3,4-trimethoxy-7,8-methylenedioxyphenanthrene (2), 3-hydroxy-2,4,-dimethoxy-7,8-methylenedioxyphenanthrene (3), 2-hydroxy-3,5,7-trimethoxyphenanthrene (4) and 2-hydroxy-3,5,7-trimethoxy-9,10-dihydrophenanthrene (5), through cytotoxic assay guidance. The structures were determined by means of HREIMS, (1)H NMR, JMOD and NOESY experiments. The cytotoxic effects of the isolated compounds were tested on cervix adenocarcinoma (HeLa) cells, with the MTT assay. The results demonstrated that, with the exception of 2, all these compounds displayed pronounced cytotoxic activity; especially 1 and 3 exhibited significant cell growth inhibitory effects, with IC(50)=8.52+/-0.70 and 3.64+/-0.12 microM, respectively.

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Year:  2006        PMID: 17166530     DOI: 10.1016/j.phytochem.2006.10.028

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  3 in total

1.  Synthesis of 9-fluorenylidenes and 9,10-phenanthrenes through palladium-catalyzed aryne annulation by o-halostyrenes and o-halo allylic benzenes.

Authors:  Shilpa A Worlikar; Richard C Larock
Journal:  J Org Chem       Date:  2009-12-04       Impact factor: 4.354

2.  An efficient approach to the synthesis of highly congested 9,10-dihydrophenanthrene-2,4-dicarbonitriles and their biological evaluation as antimicrobial agents.

Authors:  Hassan M Faidallah; Khalid M A Al-Shaikh; Tariq R Sobahi; Khalid A Khan; Abdullah M Asiri
Journal:  Molecules       Date:  2013-12-16       Impact factor: 4.411

Review 3.  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

  3 in total

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