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New Marine Antifouling Compounds from the Red Alga Laurencia sp.
Oguri, Yuko; Watanabe, Mami; Ishikawa, Takafumi; Kamada, Takashi; Vairappan, Charles S; Matsuura, Hiroshi; Kaneko, Kensuke; Ishii, Takahiro; Suzuki, Minoru; Yoshimura, Erina; Nogata, Yasuyuki; Okino, Tatsufumi.
Afiliação
  • Oguri Y; Graduate School of Environmental Science, Hokkaido University, Sapporo 060-0810, Japan. oguri-yuu@awi.co.jp.
  • Watanabe M; Graduate School of Environmental Science, Hokkaido University, Sapporo 060-0810, Japan. watamatsu@ees.hokudai.ac.jp.
  • Ishikawa T; Graduate School of Environmental Science, Hokkaido University, Sapporo 060-0810, Japan. tishikawa947@gmail.com.
  • Kamada T; Institute for Tropical Biology and Conservation, Universiti Malaysia Sabah, Kota Kinabalu, Sabah 88400, Malaysia. takashi.kamada@ums.edu.my.
  • Vairappan CS; Institute for Tropical Biology and Conservation, Universiti Malaysia Sabah, Kota Kinabalu, Sabah 88400, Malaysia. csv@mes.edu.my.
  • Matsuura H; National Institute of Technology, Asahikawa College, Asahikawa 071-8142, Japan. matsuura@asahikawa-nct.ac.jp.
  • Kaneko K; Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan. kaneko.kensuke.6a@kyoto-u.ac.jp.
  • Ishii T; Faculty of Agriculture, University of the Ryukyus, Senbaru 1, Nishihara, Okinawa 903-0213, Japan. ishiit@agr.u-ryukyu.ac.jp.
  • Suzuki M; Coastal Branch of Natural History Museum and Institute, Chiba, 123 Yoshio, Katsuura, Chiba 299-5242, Japan. reiboku1965@yahoo.co.jp.
  • Yoshimura E; CERES, Inc., 1-4-5 Midori, Abiko, Chiba 270-1153, Japan. erinamusi@yahoo.co.jp.
  • Nogata Y; Environmental Science Research Laboratory, Central Research Institute of Electric Power Industry, 1646 Abiko, Abiko, Chiba 270-1194, Japan. noga@criepi.denken.or.jp.
  • Okino T; Graduate School of Environmental Science, Hokkaido University, Sapporo 060-0810, Japan. okino@ees.hokudai.ac.jp.
Mar Drugs ; 15(9)2017 Aug 28.
Article em En | MEDLINE | ID: mdl-28846653
Six new compounds, omaezol, intricatriol, hachijojimallenes A and B, debromoaplysinal, and 11,12-dihydro-3-hydroxyretinol have been isolated from four collections of Laurencia sp. These structures were determined by MS and NMR analyses. Their antifouling activities were evaluated together with eight previously known compounds isolated from the same samples. In particular, omaezol and hachijojimallene A showed potent activities (EC50 = 0.15-0.23 µg/mL) against larvae of the barnacle Amphibalanus amphitrite.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sesquiterpenos / Thoracica / Omeprazol / Laurencia / Diterpenos / Incrustação Biológica / Larva Limite: Animals País/Região como assunto: Asia Idioma: En Revista: Mar Drugs Assunto da revista: BIOLOGIA / FARMACOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sesquiterpenos / Thoracica / Omeprazol / Laurencia / Diterpenos / Incrustação Biológica / Larva Limite: Animals País/Região como assunto: Asia Idioma: En Revista: Mar Drugs Assunto da revista: BIOLOGIA / FARMACOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão