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Neosiphoniamolide A, a Novel Cyclodepsipeptide, with Antifungal Activity from the Marine Sponge Neosiphonia superstes

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    Neosiphoniamolide A, a Novel Cyclodepsipeptide, with Antifungal Activity from the Marine Sponge Neosiphonia superstes
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    Journal of Natural Products

    Cite this: J. Nat. Prod. 1995, 58, 1, 121–123
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    https://doi.org/10.1021/np50115a017
    Published January 1, 1995
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    This article is cited by 34 publications.

    1. A Z M Mofasser, Md Imran Howlader, Md Mahbubul Alam, Nadim Ibn Sayed, Rony Mia. Cyclic Peptides and Betalains. 2025, 305-343. https://doi.org/10.1002/9781394287888.ch14
    2. Sophie Liuu, Annelaure Damont, Alain Perret, Olivier Firmesse, François Becher, Gwenaëlle Lavison‐Bompard, Amandine Hueber, Amina S. Woods, Ekaterina Darii, François Fenaille, Jean‐Claude Tabet. Origin and characterization of cyclodepsipeptides: Comprehensive structural approaches with focus on mass spectrometry analysis of alkali‐cationized molecular species. Mass Spectrometry Reviews 2024, 22 https://doi.org/10.1002/mas.21904
    3. M.S. Aishwarya, R.S. Rachanamol, A.R. Sarika, J. Selvin, A.P. Lipton. Antimicrobial peptides from marine environment. 2023, 197-217. https://doi.org/10.1016/B978-0-323-85682-9.00008-8
    4. Ricardo Ribeiro, Eugénia Pinto, Carla Fernandes, Emília Sousa. Marine Cyclic Peptides: Antimicrobial Activity and Synthetic Strategies. Marine Drugs 2022, 20 (6) , 397. https://doi.org/10.3390/md20060397
    5. Veselin Nasufović, Florian Küllmer, Johanna Bößneck, Hans‐Martin Dahse, Helmar Görls, Peter Bellstedt, Pierre Stallforth, Hans‐Dieter Arndt. Total Synthesis and Bioactivity Mapping of Geodiamolide H. Chemistry – A European Journal 2021, 27 (45) , 11633-11642. https://doi.org/10.1002/chem.202100989
    6. Bing-Nan Han, Li-Li Hong, Bin-Bin Gu, Yang-Ting Sun, Jie Wang, Jin-Tang Liu, Hou-Wen Lin. Natural Products from Sponges. 2019, 329-463. https://doi.org/10.1007/978-94-024-1612-1_15
    7. Sofia-Eléna Motuhi, Mohamed Mehiri, Claude Payri, Stéphane La Barre, Stéphane Bach. Marine Natural Products from New Caledonia—A Review. Marine Drugs 2016, 14 (3) , 58. https://doi.org/10.3390/md14030058
    8. Suraksha Gahalawat, Satyendra Kumar Pandey. Total synthesis of haliclamide. Organic & Biomolecular Chemistry 2016, 14 (39) , 9287-9293. https://doi.org/10.1039/C6OB01775D
    9. Jean Fotie. The Potential of Peptides and Depsipeptides from Terrestrial and Marine Organisms in the Fight against Human Protozoan Diseases. 2014, 279-320. https://doi.org/10.1002/9783527684403.ch10
    10. Liling Jin, Fang Liu, Wei Sun, Fengli Zhang, Valliappan Karuppiah, Zhiyong Li. Pezizomycotina dominates the fungal communities of South China Sea Sponges Theonella swinhoei and Xestospongia testudinaria. FEMS Microbiology Ecology 2014, 90 (3) , 935-945. https://doi.org/10.1111/1574-6941.12446
    11. Jean‐Michel Kornprobst. Porifera (Sponges)–2. 2014, 703-792. https://doi.org/10.1002/9783527335855.marprod192
    12. Jean‐Michel Kornprobst. Porifera (Sponges)–5. 2014, 951-1086. https://doi.org/10.1002/9783527335855.marprod195
    13. Lishu Wang, Xuefeng Zhou, Mangaladoss Fredimoses, Shengrong Liao, Yonghong Liu. Naturally occurring organoiodines. RSC Adv. 2014, 4 (101) , 57350-57376. https://doi.org/10.1039/C4RA09833A
    14. Florie Desriac, Camille Jégou, Eric Balnois, Benjamin Brillet, Patrick Chevalier, Yannick Fleury. Antimicrobial Peptides from Marine Proteobacteria. Marine Drugs 2013, 11 (10) , 3632-3660. https://doi.org/10.3390/md11103632
    15. Sherif S. Ebada, Peter Proksch. The Chemistry of Marine Sponges∗. 2012, 191-293. https://doi.org/10.1007/978-90-481-3834-0_4
    16. Vangelis Smyrniotopoulos, Constantinos Vagias, Mukhlesur M. Rahman, Simon Gibbons, Vassilios Roussis. Ioniols I and II, Tetracyclic Diterpenes with Antibacterial Activity, from Sphaerococcus coronopifolius. Chemistry & Biodiversity 2010, 7 (3) , 666-676. https://doi.org/10.1002/cbdv.200900026
    17. Vangelis Smyrniotopoulos, Constantinos Vagias, Mukhlesur M. Rahman, Simon Gibbons, Vassilios Roussis. Structure and Antibacterial Activity of Brominated Diterpenes from the Red Alga Sphaerococcus coronopifolius. Chemistry & Biodiversity 2010, 7 (1) , 186-195. https://doi.org/10.1002/cbdv.200800309
    18. Silke C. Wenzel, Rolf Müller. Myxobacteria – Unique Microbial Secondary Metabolite Factories. 2010, 189-222. https://doi.org/10.1016/B978-008045382-8.00645-6
    19. Fulvio Gala, Maria Valeria D'Auria, Simona De Marino, Valentina Sepe, Franco Zollo, Charles D. Smith, Staci N. Keller, Angela Zampella. Jaspamides M–P: new tryptophan modified jaspamide derivatives from the sponge Jaspis splendans. Tetrahedron 2009, 65 (1) , 51-56. https://doi.org/10.1016/j.tet.2008.10.076
    20. Fulvio Gala, Maria Valeria D'Auria, Simona De Marino, Valentina Sepe, Franco Zollo, Charles D. Smith, Jean E. Copper, Angela Zampella. Jaspamides H–L, new actin-targeting depsipeptides from the sponge Jaspis splendans. Tetrahedron 2008, 64 (30-31) , 7127-7130. https://doi.org/10.1016/j.tet.2008.05.037
    21. Anke Schmauder, Sven Müller, Martin E. Maier. Concise route to defined stereoisomers of the hydroxy acid of the chondramides. Tetrahedron 2008, 64 (27) , 6263-6269. https://doi.org/10.1016/j.tet.2008.04.109
    22. Danielle Skropeta. Deep-sea natural products. Natural Product Reports 2008, 25 (6) , 1131. https://doi.org/10.1039/b808743a
    23. Fulvio Gala, Maria Valeria D'Auria, Simona De Marino, Franco Zollo, Charles D. Smith, Jean E. Copper, Angela Zampella. New jaspamide derivatives with antimicrofilament activity from the sponge Jaspis splendans. Tetrahedron 2007, 63 (24) , 5212-5219. https://doi.org/10.1016/j.tet.2007.03.162
    24. Silke Christine Wenzel, Rolf Müller. Myxobacterial natural product assembly lines: fascinating examples of curious biochemistry. Natural Product Reports 2007, 24 (6) , 1211. https://doi.org/10.1039/b706416k
    25. Shwan Rachid, Daniel Krug, Brigitte Kunze, Irene Kochems, Maren Scharfe, T. Mark Zabriskie, Helmut Blöcker, Rolf Müller. Molecular and Biochemical Studies of Chondramide Formation—Highly Cytotoxic Natural Products from Chondromyces crocatus Cm c5. Chemistry & Biology 2006, 13 (6) , 667-681. https://doi.org/10.1016/j.chembiol.2006.06.002
    26. Valery M Dembitsky. Biogenic Iodine and Iodine-Containing Metabolites. Natural Product Communications 2006, 1 (2) https://doi.org/10.1177/1934578X0600100210
    27. Jiangnan Peng, Jing Li, Mark T. Hamann. The Marine Bromotyrosine Derivatives. 2005, 59-262. https://doi.org/10.1016/S1099-4831(05)61002-4
    28. Dominique Laurent, Francesco Pietra. Natural‐Product Diversity of the New Caledonian Marine Ecosystem Compared to Other Ecosystems: A Pharmacologically Oriented View. Chemistry & Biodiversity 2004, 1 (4) , 539-594. https://doi.org/10.1002/cbdv.200490048
    29. M. Valeria D'Auria, Angela Zampella, Franco Zollo. The chemistry of lithistid sponge: A spectacular source of new metabolites. 2002, 1175-1258. https://doi.org/10.1016/S1572-5995(02)80027-8
    30. Winston F. Tinto, Alan J. Lough, Stewart McLean, William F. Reynolds, Margaret Yu, Wilfred R. Chan. Geodiamolides H and I, further cyclodepsipeptides from the marine sponge Geodia sp. Tetrahedron 1998, 54 (18) , 4451-4458. https://doi.org/10.1016/S0040-4020(98)00157-4
    31. J. Buckingham. N. 1998, 234-241. https://doi.org/10.1007/978-1-4899-3314-0_14
    32. John R. Lewis. Muscarine, imidazole, oxazole, thiazole and peptide alkaloids, and other miscellaneous alkaloids. Natural Product Reports 1998, 15 (5) , 417. https://doi.org/10.1039/a815417y
    33. D. John Faulkner. Marine natural products. Natural Product Reports 1997, 14 (3) , 259. https://doi.org/10.1039/np9971400259
    34. Rolf Jansen, Brigitte Kunze, Hans Reichenbach, Gerhard Höfle. Antibiotics from Gliding Bacteria, LXX Chondramides A–D, New Cytostatic and Antifungal Cyclodepsipeptides from Chondromyces crocatus (Myxobacteria): Isolation and Structure Elucidation. Liebigs Annalen 1996, 1996 (2) , 285-290. https://doi.org/10.1002/jlac.199619960220
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    Journal of Natural Products

    Cite this: J. Nat. Prod. 1995, 58, 1, 121–123
    Click to copy citationCitation copied!
    https://doi.org/10.1021/np50115a017
    Published January 1, 1995
    Request reuse permissions

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