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      Juncaceae Species as Promising Sources of Phenanthrenes: Antiproliferative Compounds from Juncus maritimus Lam

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          Abstract

          Juncaceae family represents an abundant source of phenanthrenes. In continuation of our work aiming at the isolation of biologically active compounds from Juncaceae species, Juncus maritimus Lam. was subjected to phytochemical and pharmacological investigations. The isolation process was carried out by using combined extraction and chromatographic methods. The structures of the obtained chemical compounds were elucidated by spectroscopic analysis, including HRESIMS, 1D ( 1H, 13C-JMOD), and 2D ( 1H- 1H-COSY, HSQC, HMBC, NOESY) NMR spectra. Four new [maritins A–D ( 14)] and seven known phenanthrenes ( 511) were isolated from the plant, of which two ( 4 and 11) are phenanthrene dimers composed of effusol monomers. Maritin C ( 3) has an unusual 4,5-ethanophenanthrene skeleton most likely produced by biosynthetic incorporation of a vinyl group into a cyclohexadiene ring. Compounds 111 were tested for their antiproliferative activity on seven human tumor cell lines (HeLa, HTM-26, T-47D, A2780, A2780cis, MCF-7, KCR) and one normal cell line (MRC-5) using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The dimeric phenanthrenes showed strong antiproliferative activity against T-47D cells with IC 50 values of 9.1 and 6.2 µM, respectively.

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          Most cited references14

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          Phenanthrenes: A Promising Group of Plant Secondary Metabolites

          Although phenanthrenes are considered to constitute a relatively small group of natural products, discovering new phenanthrene derivatives and evaluating their prospective biological activities have become of great interest to many research groups worldwide. Based on 160 references, this review covers the phytochemistry and pharmacology of 213 naturally occurring phenanthrenes that have been isolated between 2008 and 2016. More than 40% of the 450 currently known naturally occurring phenanthrenes were identified during this period. The family Orchidaceae is the most abundant source of these compounds, although several new plant families and genera have been involved in the search for phenanthrenes. The presence of certain substituent patterns may be restricted to specific families; vinyl-substituted phenanthrenes were reported only from Juncaceae plants, and prenylated derivatives occur mainly in Euphorbiaceae species. Therefore, these compounds also can serve as chemotaxonomic markers. Almost all of the newly isolated compounds have been studied for their biological activities (e.g., potential cytotoxic, antimicrobial, anti-inflammatory, and antioxidant effects), and many of them showed multiple activities. According to the accumulated data, denbinobin, with a novel mechanism of action, has great potential as a lead compound for the development of a new anticancer agent.
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            Phenanthrenes from Juncus inflexus with Antimicrobial Activity against Methicillin-Resistant Staphylococcus aureus

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              Phenanthrenes fromJuncus effususwith anxiolytic and sedative activities

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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                13 February 2021
                February 2021
                : 26
                : 4
                : 999
                Affiliations
                [1 ]Department of Pharmacognosy, University of Szeged, 6720 Szeged, Hungary; kusznorbert@ 123456gmail.com (N.K.); stefko.dori@ 123456gmail.com (D.S.); bartaanita96@ 123456gmail.com (A.B.); hohmann.judit@ 123456szte.hu (J.H.)
                [2 ]Department of Medical Microbiology and Immunobiology, University of Szeged, Dóm tér 10, 6720 Szeged, Hungary; kincses.annamaria90@ 123456gmail.com (A.K.); szemeredi.nikoletta@ 123456med.u-szeged.hu (N.S.); spengler.gabriella@ 123456med.u-szeged.hu (G.S.)
                [3 ]Interdisciplinary Centre of Natural Products, University of Szeged, Eötvös u. 6, 6720 Szeged, Hungary
                Author notes
                [* ]Correspondence: vasasa@ 123456pharmacognosy.hu ; Tel.: +36-62-546-451
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-9973-6442
                https://orcid.org/0000-0002-1591-1419
                https://orcid.org/0000-0002-8638-5815
                https://orcid.org/0000-0001-8085-0950
                https://orcid.org/0000-0002-2887-6392
                https://orcid.org/0000-0002-1818-7702
                Article
                molecules-26-00999
                10.3390/molecules26040999
                7918049
                b845a176-c615-4bb7-9b49-ec8c3b977d9d
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 20 January 2021
                : 08 February 2021
                Categories
                Article

                juncus maritimus,maritins a–d,phenanthrene dimers,dihydrophenanthrene

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