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      Induced Marine Fungus Chondrostereum sp. as a Means of Producing New Sesquiterpenoids Chondrosterins I and J by Using Glycerol as the Carbon Source

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          Abstract

          Chondrostereum sp., a marine fungus isolated from a soft coral Sarcophyton tortuosum, can yield hirsutane framework sesquiterpenoids. However, the metabolites profiles vary dramatically with the composition change of the culture media. This fungus was cultured in a liquid medium containing glycerol as the carbon source, and two new metabolites, chondrosterins I and J ( 1 and 2), were obtained. Their structures were elucidated primarily based on MS, NMR and X-ray single-crystal diffraction data. By comparison with the known hirsutane sesquiterpenoids, chondrosterins I and J have unique structural features, including a methyl was migrated from C-2 to C-6, and the methyl at C-3 was carboxylated. Compound 2 exhibited potent cytotoxic activities against the cancer cell lines CNE-1 and CNE-2 with the IC 50 values of 1.32 and 0.56 μM.

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          Most cited references14

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          Hirsutane sesquiterpenoids from the marine-derived fungus Chondrostereum sp.

          A new hirsutane sesquiterpenoid, hirsutanol E (1), together with the known compounds hirsutanol A (2) and hirsutanol F (3; gloeosteretriol) were obtained from AcOEt extract of the marine fungus Chondrostereum sp., which was isolated from the soft coral Sarcophyton tortuosum. The structures were elucidated mainly on the basis of the NMR, MS, and X-ray single-crystal diffraction data. Hirsutanol A (2) exhibited potent cytotoxic activities against various cancer cell lines. Copyright © 2011 Verlag Helvetica Chimica Acta AG, Zürich.
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            SADABS: Program for Empirical Absorption Correction of Area Detector Data

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              Isolation and Structural Elucidation of Chondrosterins F–H from the Marine Fungus Chondrostereum sp

              The marine fungus Chondrostereum sp. was collected from a soft coral of the species Sarcophyton tortuosum from the South China Sea. Three new compounds, chondrosterins F–H (1, 4 and 5), together with three known compounds, incarnal (2), arthrosporone (3), and (2E)-decene-4,6,8-triyn-1-ol (6), were isolated. Their structures were elucidated primarily based on NMR and MS data. Incarnal (2) exhibited potent cytotoxic activity against various cancer cell lines.
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                Author and article information

                Journal
                Mar Drugs
                Mar Drugs
                marinedrugs
                Marine Drugs
                MDPI
                1660-3397
                07 January 2014
                January 2014
                : 12
                : 1
                : 167-175
                Affiliations
                [1 ]School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China; E-Mails: ceslhj@ 123456mail.sysu.edu.cn (H.-J.L.); natprodjwh@ 123456gmail.com (W.-H.J.); natprodhjx1@ 123456gmail.com (J.-X.H.); cklam@ 123456mail.sysu.edu.cn (C.-K.L.)
                [2 ]School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China; E-Mails: natprodlwl@ 123456gmail.com (W.-L.L.); marinemyf@ 123456yahoo.com (Y.-F.M.); marinedyq@ 123456gmail.com (Y.-Q.D.)
                [3 ]State Key Laboratory of Oncology in South China, Cancer Center, Sun Yat-Sen University, Guangzhou 510060, China; E-Mails: marineqxj@ 123456gmail.com (X.-J.Q.); zhuxfeng@ 123456mail.sysu.edu.cn (X.-F.Z.)
                [4 ]Guangdong Technology Research Center for Advanced Chinese Medicine, Guangzhou 510006, China
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: lanwj@ 123456mail.sysu.edu.cn ; Tel.: +86-20-39943042; Fax: +86-20-39943000.
                Article
                marinedrugs-12-00167
                10.3390/md12010167
                3917267
                24402176
                75ee26d1-333e-49f3-bb7d-a911bacb777d
                © 2014 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 license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 01 November 2013
                : 02 December 2013
                : 12 December 2013
                Categories
                Communication

                Pharmacology & Pharmaceutical medicine
                chondrosterins,marine fungus,chondrostereum sp.,sesquiterpenoids,cytotoxic activity

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