Marine natural products
Identifieur interne : 001A94 ( Main/Exploration ); précédent : 001A93; suivant : 001A95Marine natural products
Auteurs : John W. Blunt [Nouvelle-Zélande] ; Brent R. Copp [Nouvelle-Zélande] ; Wan-Ping Hu [Nouvelle-Zélande] ; Murray H. G. Munro [Nouvelle-Zélande] ; Peter T. Northcote [Nouvelle-Zélande] ; Michle R. Prinsep [Nouvelle-Zélande]Source :
- Natural Product Reports [ 0265-0568 ] ; 2009.
English descriptors
- Teeft :
- Acta, Agelas, Ahmed, Alkaloid, Analogue, Angew, Antibacterial, Antibiot, Antifungal, Antimicrobial, Apoptosis, Appl, Ascidian, Aspergillus, Aureus, Berlinck, Biochem, Biol, Bioorg, Biosynthetic, Brominated, Bryozoan, Chem, Chim, Choi, Ciavatta, Cimino, Clardy, Commun, Compd, Curr, Cyclic, Cytotoxic, Cytotoxicity, Deng, Diene, Ding, Diterpene, Diterpenes, Dmitrenok, Ecol, Enantioselective, Ester, Fang, Fattorusso, Feng, Fenical, Food chem, Fromont, Fujita, Fusetani, Gavagnin, Gerwick, Glycoside, Grube, Hainan, Hamann, Helv, Heterocycle, Higuchi, Huang, Inhibitor, Jiang, Jung, Kalinovsky, Kashman, Kawabata, Kinase, Kita, Kobayashi, Kock, Konig, Kubota, Laatsch, Laurencia, Lett, Lipid, Lyngbya, Macrolide, Mangrove, Marine source, Masuda, Matsunaga, Methyl, Microbiol, Miyamoto, Molinski, Mollo, Mollusc, Munro, Nakao, Namikoshi, Natural product, Natural products, Numata, Ohta, Olivera, Papua, Peng, Penicillium, Peptide, Pharm, Pharmacol, Physiol, Phytochemistry, Polyketide, Polyketides, Proksch, Qingdao, Racemic, Receptor, Rinehart, Roberge, Royal society, Rus, Sanya, Scheuer, Sesquiterpene, Sesquiterpenes, Shen, Sheu, Shizuri, Soest, Stereochemistry, Sterol, Stonik, Streptomyces, Stylissa, Synlett, Takahashi, Tanaka, Tenney, Tetrahedron, Tetrahedron lett, Total synthesis, Toxicon, Tsuda, Tumour, Uemura, Urchin, Valeriote, Wang, Xiao, Yamada, Yoshida, Zhang, Zhao, Zhou.
Abstract
Covering: 2007. Previous review: Nat. Prod. Rep., 2008, 25, 35 This review covers the literature published in 2007 for marine natural products, with 948 citations (627 for the period January to December 2007) referring to compounds isolated from marine microorganisms and phytoplankton, green algae, brown algae, red algae, sponges, cnidarians, bryozoans, molluscs, tunicates, echinoderms and true mangrove plants. The emphasis is on new compounds (961 for 2007), together with the relevant biological activities, source organisms and country of origin. Biosynthetic studies, first syntheses, and syntheses that lead to the revision of structures or stereochemistries, have been included.
Url:
DOI: 10.1039/b805113p
Affiliations:
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Le document en format XML
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<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acta</term>
<term>Agelas</term>
<term>Ahmed</term>
<term>Alkaloid</term>
<term>Analogue</term>
<term>Angew</term>
<term>Antibacterial</term>
<term>Antibiot</term>
<term>Antifungal</term>
<term>Antimicrobial</term>
<term>Apoptosis</term>
<term>Appl</term>
<term>Ascidian</term>
<term>Aspergillus</term>
<term>Aureus</term>
<term>Berlinck</term>
<term>Biochem</term>
<term>Biol</term>
<term>Bioorg</term>
<term>Biosynthetic</term>
<term>Brominated</term>
<term>Bryozoan</term>
<term>Chem</term>
<term>Chim</term>
<term>Choi</term>
<term>Ciavatta</term>
<term>Cimino</term>
<term>Clardy</term>
<term>Commun</term>
<term>Compd</term>
<term>Curr</term>
<term>Cyclic</term>
<term>Cytotoxic</term>
<term>Cytotoxicity</term>
<term>Deng</term>
<term>Diene</term>
<term>Ding</term>
<term>Diterpene</term>
<term>Diterpenes</term>
<term>Dmitrenok</term>
<term>Ecol</term>
<term>Enantioselective</term>
<term>Ester</term>
<term>Fang</term>
<term>Fattorusso</term>
<term>Feng</term>
<term>Fenical</term>
<term>Food chem</term>
<term>Fromont</term>
<term>Fujita</term>
<term>Fusetani</term>
<term>Gavagnin</term>
<term>Gerwick</term>
<term>Glycoside</term>
<term>Grube</term>
<term>Hainan</term>
<term>Hamann</term>
<term>Helv</term>
<term>Heterocycle</term>
<term>Higuchi</term>
<term>Huang</term>
<term>Inhibitor</term>
<term>Jiang</term>
<term>Jung</term>
<term>Kalinovsky</term>
<term>Kashman</term>
<term>Kawabata</term>
<term>Kinase</term>
<term>Kita</term>
<term>Kobayashi</term>
<term>Kock</term>
<term>Konig</term>
<term>Kubota</term>
<term>Laatsch</term>
<term>Laurencia</term>
<term>Lett</term>
<term>Lipid</term>
<term>Lyngbya</term>
<term>Macrolide</term>
<term>Mangrove</term>
<term>Marine source</term>
<term>Masuda</term>
<term>Matsunaga</term>
<term>Methyl</term>
<term>Microbiol</term>
<term>Miyamoto</term>
<term>Molinski</term>
<term>Mollo</term>
<term>Mollusc</term>
<term>Munro</term>
<term>Nakao</term>
<term>Namikoshi</term>
<term>Natural product</term>
<term>Natural products</term>
<term>Numata</term>
<term>Ohta</term>
<term>Olivera</term>
<term>Papua</term>
<term>Peng</term>
<term>Penicillium</term>
<term>Peptide</term>
<term>Pharm</term>
<term>Pharmacol</term>
<term>Physiol</term>
<term>Phytochemistry</term>
<term>Polyketide</term>
<term>Polyketides</term>
<term>Proksch</term>
<term>Qingdao</term>
<term>Racemic</term>
<term>Receptor</term>
<term>Rinehart</term>
<term>Roberge</term>
<term>Royal society</term>
<term>Rus</term>
<term>Sanya</term>
<term>Scheuer</term>
<term>Sesquiterpene</term>
<term>Sesquiterpenes</term>
<term>Shen</term>
<term>Sheu</term>
<term>Shizuri</term>
<term>Soest</term>
<term>Stereochemistry</term>
<term>Sterol</term>
<term>Stonik</term>
<term>Streptomyces</term>
<term>Stylissa</term>
<term>Synlett</term>
<term>Takahashi</term>
<term>Tanaka</term>
<term>Tenney</term>
<term>Tetrahedron</term>
<term>Tetrahedron lett</term>
<term>Total synthesis</term>
<term>Toxicon</term>
<term>Tsuda</term>
<term>Tumour</term>
<term>Uemura</term>
<term>Urchin</term>
<term>Valeriote</term>
<term>Wang</term>
<term>Xiao</term>
<term>Yamada</term>
<term>Yoshida</term>
<term>Zhang</term>
<term>Zhao</term>
<term>Zhou</term>
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<front><div type="abstract">Covering: 2007. Previous review: Nat. Prod. Rep., 2008, 25, 35 This review covers the literature published in 2007 for marine natural products, with 948 citations (627 for the period January to December 2007) referring to compounds isolated from marine microorganisms and phytoplankton, green algae, brown algae, red algae, sponges, cnidarians, bryozoans, molluscs, tunicates, echinoderms and true mangrove plants. The emphasis is on new compounds (961 for 2007), together with the relevant biological activities, source organisms and country of origin. Biosynthetic studies, first syntheses, and syntheses that lead to the revision of structures or stereochemistries, have been included.</div>
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