Artigos de revistas sobre o tema "Amphidinols"
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Molina-Miras, Alejandro, Alejandro Bueso-Sánchez, María del Carmen Cerón-García, Asterio Sánchez-Mirón, Antonio Contreras-Gómez e Francisco García-Camacho. "Effect of Nitrogen, Phosphorous, and Light Colimitation on Amphidinol Production and Growth in the Marine Dinoflagellate Microalga Amphidinium carterae". Toxins 14, n.º 9 (28 de agosto de 2022): 594. http://dx.doi.org/10.3390/toxins14090594.
Texto completo da fonteOrefice, Ida, Sergio Balzano, Giovanna Romano e Angela Sardo. "Amphidinium spp. as a Source of Antimicrobial, Antifungal, and Anticancer Compounds". Life 13, n.º 11 (4 de novembro de 2023): 2164. http://dx.doi.org/10.3390/life13112164.
Texto completo da fonteMartínez, Kevin A., Chiara Lauritano, Dana Druka, Giovanna Romano, Teresa Grohmann, Marcel Jaspars, Jesús Martín et al. "Amphidinol 22, a New Cytotoxic and Antifungal Amphidinol from the Dinoflagellate Amphidinium carterae". Marine Drugs 17, n.º 7 (27 de junho de 2019): 385. http://dx.doi.org/10.3390/md17070385.
Texto completo da fonteWellkamp, Marvin, Francisco García-Camacho, Lorena M. Durán-Riveroll, Jan Tebben, Urban Tillmann e Bernd Krock. "LC-MS/MS Method Development for the Discovery and Identification of Amphidinols Produced by Amphidinium". Marine Drugs 18, n.º 10 (29 de setembro de 2020): 497. http://dx.doi.org/10.3390/md18100497.
Texto completo da fonteMorsy, Nagy, Keiichi Konoki, Toshihiro Houdai, Nobuaki Matsumori, Tohru Oishi, Michio Murata e Saburo Aimoto. "Roles of integral protein in membrane permeabilization by amphidinols". Biochimica et Biophysica Acta (BBA) - Biomembranes 1778, n.º 6 (junho de 2008): 1453–59. http://dx.doi.org/10.1016/j.bbamem.2008.01.018.
Texto completo da fonteCossy, Janine, Tomoki Tsuchiya, Laurent Ferrié, Sébastien Reymond, Thomas Kreuzer, Françoise Colobert, Pierre Jourdain e István Markó. "Efficient Syntheses of the Polyene Fragments Present in Amphidinols". Synlett 2007, n.º 14 (20 de julho de 2007): 2286–88. http://dx.doi.org/10.1055/s-2007-984910.
Texto completo da fonteMorsy, Nagy, Toshihiro Houdai, Keiichi Konoki, Nobuaki Matsumori, Tohru Oishi e Michio Murata. "Effects of lipid constituents on membrane-permeabilizing activity of amphidinols". Bioorganic & Medicinal Chemistry 16, n.º 6 (15 de março de 2008): 3084–90. http://dx.doi.org/10.1016/j.bmc.2007.12.029.
Texto completo da fonteDurán-Riveroll, Lorena M., Jannik Weber e Bernd Krock. "First Identification of Amphidinols from Mexican Strains and New Analogs". Toxins 15, n.º 2 (16 de fevereiro de 2023): 163. http://dx.doi.org/10.3390/toxins15020163.
Texto completo da fonteHoudai, Toshihiro, Shigeru Matsuoka, Nagy Morsy, Nobuaki Matsumori, Masayuki Satake e Michio Murata. "Hairpin conformation of amphidinols possibly accounting for potent membrane permeabilizing activities". Tetrahedron 61, n.º 11 (março de 2005): 2795–802. http://dx.doi.org/10.1016/j.tet.2005.01.069.
Texto completo da fonteHoudai, Toshihiro, Shigeru Matsuoka, Michio Murata, Masayuki Satake, Sayo Ota, Yasukatsu Oshima e Lesley L. Rhodes. "Acetate labeling patterns of dinoflagellate polyketides, amphidinols 2, 3 and 4". Tetrahedron 57, n.º 26 (junho de 2001): 5551–55. http://dx.doi.org/10.1016/s0040-4020(01)00481-1.
Texto completo da fonteMorsy, Nagy, Toshihiro Houdai, Shigeru Matsuoka, Nobuaki Matsumori, Seiji Adachi, Tohru Oishi, Michio Murata, Takashi Iwashita e Tsuyoshi Fujita. "Structures of new amphidinols with truncated polyhydroxyl chain and their membrane-permeabilizing activities". Bioorganic & Medicinal Chemistry 14, n.º 19 (outubro de 2006): 6548–54. http://dx.doi.org/10.1016/j.bmc.2006.06.012.
Texto completo da fonteLópez-Rodríguez, Mercedes, Lorenzo López-Rosales, Giullia Diletta, María del Carmen Cerón-García, Elvira Navarro-López, Juan José Gallardo-Rodríguez, Ana Isabel Tristán, Ana Cristina Abreu e Francisco García-Camacho. "The Isolation of Specialty Compounds from Amphidinium carterae Biomass by Two-Step Solid-Phase and Liquid-Liquid Extraction". Toxins 14, n.º 9 (28 de agosto de 2022): 593. http://dx.doi.org/10.3390/toxins14090593.
Texto completo da fonteYang, Xiao, Zhi Yan, Jingjing Chen, Derui Wang e Ke Li. "Acute Toxicity of the Dinoflagellate Amphidinium carterae on Early Life Stages of Zebrafish (Danio rerio)". Toxics 11, n.º 4 (13 de abril de 2023): 370. http://dx.doi.org/10.3390/toxics11040370.
Texto completo da fonteMolina-Miras, A., A. Morales-Amador, C. R. de Vera, L. López-Rosales, A. Sánchez-Mirón, M. L. Souto, J. J. Fernández, M. Norte, F. García-Camacho e E. Molina-Grima. "A pilot-scale bioprocess to produce amphidinols from the marine microalga Amphidinium carterae: Isolation of a novel analogue". Algal Research 31 (abril de 2018): 87–98. http://dx.doi.org/10.1016/j.algal.2018.01.010.
Texto completo da fonteCutignano, Adele, Genoveffa Nuzzo, Angela Sardo e Angelo Fontana. "The Missing Piece in Biosynthesis of Amphidinols: First Evidence of Glycolate as a Starter Unit in New Polyketides from Amphidinium carterae". Marine Drugs 15, n.º 6 (31 de maio de 2017): 157. http://dx.doi.org/10.3390/md15060157.
Texto completo da fonteAbreu, Ana Cristina, Alejandro Molina-Miras, Luis M. Aguilera-Sáez, Lorenzo López-Rosales, María del Carmen Cerón-García, Asterio Sánchez-Mirón, Lucía Olmo-García et al. "Production of Amphidinols and Other Bioproducts of Interest by the Marine Microalga Amphidinium carterae Unraveled by Nuclear Magnetic Resonance Metabolomics Approach Coupled to Multivariate Data Analysis". Journal of Agricultural and Food Chemistry 67, n.º 34 (15 de agosto de 2019): 9667–82. http://dx.doi.org/10.1021/acs.jafc.9b02821.
Texto completo da fonteMorales-Amador, Adrián, Alejandro Molina-Miras, Lorenzo López-Rosales, Asterio Sánchez-Mirón, Francisco García-Camacho, María L. Souto e José J. Fernández. "Isolation and Structural Elucidation of New Amphidinol Analogues from Amphidinium carterae Cultivated in a Pilot-Scale Photobioreactor". Marine Drugs 19, n.º 8 (29 de julho de 2021): 432. http://dx.doi.org/10.3390/md19080432.
Texto completo da fonteGrisin, Aleksandr, e P. Andrew Evans. "A highly convergent synthesis of the C1–C31 polyol domain of amphidinol 3 featuring a TST-RCM reaction: confirmation of the revised relative stereochemistry". Chemical Science 6, n.º 11 (2015): 6407–12. http://dx.doi.org/10.1039/c5sc00814j.
Texto completo da fonteWakamiya, Yuma, e Tohru Oishi. "Total Synthesis of Amphidinol 3". Journal of Synthetic Organic Chemistry, Japan 79, n.º 7 (1 de julho de 2021): 664–72. http://dx.doi.org/10.5059/yukigoseikyokaishi.79.664.
Texto completo da fonteHaq, Saddef, Benjamin L. Oyler, Ernest Williams, Mohd M. Khan, David R. Goodlett, Tsvetan Bachvaroff e Allen R. Place. "Investigating A Multi-Domain Polyketide Synthase in Amphidinium carterae". Marine Drugs 21, n.º 8 (27 de julho de 2023): 425. http://dx.doi.org/10.3390/md21080425.
Texto completo da fonteChen, Kai, Zhengshuang Xu e Tao Ye. "Total synthesis of amphidinins E, F and epi-amphidinin F". Organic Chemistry Frontiers 5, n.º 4 (2018): 629–32. http://dx.doi.org/10.1039/c7qo00820a.
Texto completo da fonteFürstner, Alois, Christophe Aïssa, Ricardo Riveiros e Jacques Ragot. "Totalsynthese von Amphidinolid T4". Angewandte Chemie 114, n.º 24 (16 de dezembro de 2002): 4958–60. http://dx.doi.org/10.1002/ange.200290041.
Texto completo da fonteWakamiya, Yuma, Makoto Ebine, Nobuaki Matsumori e Tohru Oishi. "Total Synthesis of Amphidinol 3: A General Strategy for Synthesizing Amphidinol Analogues and Structure–Activity Relationship Study". Journal of the American Chemical Society 142, n.º 7 (27 de janeiro de 2020): 3472–78. http://dx.doi.org/10.1021/jacs.9b11789.
Texto completo da fonteCrimmins, Michael T., Timothy J. Martin e Theodore A. Martinot. "Synthesis of the Bis-tetrahydropyran Core of Amphidinol 3". Organic Letters 12, n.º 17 (3 de setembro de 2010): 3890–93. http://dx.doi.org/10.1021/ol1015898.
Texto completo da fonteBensoussan, Charlélie, Nicolas Rival, Gilles Hanquet, Françoise Colobert, Sébastien Reymond e Janine Cossy. "Isolation, structural determination and synthetic approaches toward amphidinol 3". Natural Product Reports 31, n.º 4 (2014): 468. http://dx.doi.org/10.1039/c3np70062c.
Texto completo da fontede Vicente, Javier, John R. Huckins e Scott D. Rychnovsky. "Synthesis of the C31–C67 Fragment of Amphidinol 3". Angewandte Chemie 118, n.º 43 (6 de novembro de 2006): 7416–20. http://dx.doi.org/10.1002/ange.200602742.
Texto completo da fontede Vicente, Javier, John R. Huckins e Scott D. Rychnovsky. "Synthesis of the C31–C67 Fragment of Amphidinol 3". Angewandte Chemie International Edition 45, n.º 43 (6 de novembro de 2006): 7258–62. http://dx.doi.org/10.1002/anie.200602742.
Texto completo da fonteCossy, Janine, Tomoki Tsuchiya, Sébastien Reymond, Thomas Kreuzer, Françoise Colobert e István Markó. "Convergent Synthesis of the C18-C30 Fragment of Amphidinol 3". Synlett 2009, n.º 16 (3 de setembro de 2009): 2706–10. http://dx.doi.org/10.1055/s-0029-1217754.
Texto completo da fonteTsuruda, Takeshi, Makoto Ebine, Aya Umeda e Tohru Oishi. "Stereoselective Synthesis of the C1–C29 Part of Amphidinol 3". Journal of Organic Chemistry 80, n.º 2 (7 de janeiro de 2015): 859–71. http://dx.doi.org/10.1021/jo502322m.
Texto completo da fonteManabe, Yoshiyuki, Makoto Ebine, Nobuaki Matsumori, Michio Murata e Tohru Oishi. "Confirmation of the Absolute Configuration at C45 of Amphidinol 3". Journal of Natural Products 75, n.º 11 (6 de novembro de 2012): 2003–6. http://dx.doi.org/10.1021/np300604w.
Texto completo da fonteHoudai, Toshihiro, Nobuaki Matsumori e Michio Murata. "Structure of Membrane-Bound Amphidinol 3 in Isotropic Small Bicelles". Organic Letters 10, n.º 19 (2 de outubro de 2008): 4191–94. http://dx.doi.org/10.1021/ol8016337.
Texto completo da fonteRival, Nicolas, Damien Hazelard, Gilles Hanquet, Thomas Kreuzer, Charlelie Bensoussan, Sébastien Reymond, Janine Cossy e Françoise Colobert. "Diastereoselective synthesis of the C17–C30 fragment of amphidinol 3". Organic & Biomolecular Chemistry 10, n.º 47 (2012): 9418. http://dx.doi.org/10.1039/c2ob26641e.
Texto completo da fonteRival, Nicolas, Gilles Hanquet, Charlelie Bensoussan, Sébastien Reymond, Janine Cossy e Françoise Colobert. "Diastereoselective synthesis of the C14–C29 fragment of amphidinol 3". Organic & Biomolecular Chemistry 11, n.º 39 (2013): 6829. http://dx.doi.org/10.1039/c3ob41569d.
Texto completo da fonteMurata, Michio, Respati T. Swasono, Mitsunori Kanemoto e Tohru Oishi. "Structural Reevaluations of Amphidinol 3, a Potent Antifungal Compound from Dinoflagellate". HETEROCYCLES 82, n.º 2 (2010): 1359. http://dx.doi.org/10.3987/com-10-s(e)86.
Texto completo da fonteMeng, Yanhui, Ryan M. Van Wagoner, Ian Misner, Carmelo Tomas e Jeffrey L. C. Wright. "Structure and Biosynthesis of Amphidinol 17, a Hemolytic Compound fromAmphidinium carterae⊥". Journal of Natural Products 73, n.º 3 (26 de março de 2010): 409–15. http://dx.doi.org/10.1021/np900616q.
Texto completo da fonteHicks, Jacqueline D., Eric M. Flamme e William R. Roush. "Synthesis of the C(43)−C(67) Fragment of Amphidinol 3". Organic Letters 7, n.º 24 (novembro de 2005): 5509–12. http://dx.doi.org/10.1021/ol052322j.
Texto completo da fonteBensoussan, Charlelie, Nicolas Rival, Gilles Hanquet, Francoise Colobert, Sebastien Reymond e Janine Cossy. "ChemInform Abstract: Isolation, Structural Determination, and Synthetic Approaches Toward Amphidinol 3". ChemInform 45, n.º 30 (10 de julho de 2014): no. http://dx.doi.org/10.1002/chin.201430244.
Texto completo da fonteMurata, Michio, Shigeru Matsuoka, Nobuaki Matsumori, Gopal K. Paul e Kazuo Tachibana. "Absolute Configuration of Amphidinol 3, the First Complete Structure Determination from Amphidinol Homologues: Application of a New Configuration Analysis Based on Carbon−Hydrogen Spin-Coupling Constants". Journal of the American Chemical Society 121, n.º 4 (fevereiro de 1999): 870–71. http://dx.doi.org/10.1021/ja983655x.
Texto completo da fonteEspiritu, Rafael A. "Membrane permeabilizing action of amphidinol 3 and theonellamide A in raft-forming lipid mixtures". Zeitschrift für Naturforschung C 72, n.º 1-2 (26 de janeiro de 2017): 43–48. http://dx.doi.org/10.1515/znc-2016-0043.
Texto completo da fonteEspiritu, Rafael Atillo, Nobuaki Matsumori, Masashi Tsuda e Michio Murata. "Direct and Stereospecific Interaction of Amphidinol 3 with Sterol in Lipid Bilayers". Biochemistry 53, n.º 20 (12 de maio de 2014): 3287–93. http://dx.doi.org/10.1021/bi5002932.
Texto completo da fonteKanemoto, Mitsunori, Michio Murata e Tohru Oishi. "Stereoselective Synthesis of the C31−C40/C43−C52 Unit of Amphidinol 3". Journal of Organic Chemistry 74, n.º 22 (20 de novembro de 2009): 8810–13. http://dx.doi.org/10.1021/jo901793f.
Texto completo da fonteEbine, Makoto, Mitsunori Kanemoto, Yoshiyuki Manabe, Yosuke Konno, Ken Sakai, Nobuaki Matsumori, Michio Murata e Tohru Oishi. "Synthesis and Structure Revision of the C43–C67 Part of Amphidinol 3". Organic Letters 15, n.º 11 (21 de maio de 2013): 2846–49. http://dx.doi.org/10.1021/ol401176a.
Texto completo da fonteWakamiya, Yuma, Makoto Ebine, Mariko Murayama, Hiroyuki Omizu, Nobuaki Matsumori, Michio Murata e Tohru Oishi. "Synthesis and Stereochemical Revision of the C31-C67 Fragment of Amphidinol 3". Angewandte Chemie 130, n.º 21 (27 de abril de 2018): 6168–72. http://dx.doi.org/10.1002/ange.201712167.
Texto completo da fonteYadav, Jhillu S., Yerragorla Gopalarao, Dandekar Chandrakanth e Basi V. Subba Reddy. "Stereoselective Synthesis of the C(1) - C(28) Fragment of Amphidinol 3". Helvetica Chimica Acta 99, n.º 6 (junho de 2016): 436–46. http://dx.doi.org/10.1002/hlca.201500281.
Texto completo da fonteWakamiya, Yuma, Makoto Ebine, Mariko Murayama, Hiroyuki Omizu, Nobuaki Matsumori, Michio Murata e Tohru Oishi. "Synthesis and Stereochemical Revision of the C31-C67 Fragment of Amphidinol 3". Angewandte Chemie International Edition 57, n.º 21 (27 de abril de 2018): 6060–64. http://dx.doi.org/10.1002/anie.201712167.
Texto completo da fonteMurata, Michio, Shigeru Matsuoka, Nobuaki Matsumori, Gopal K. Paul e Kazuo Tachibana. "ChemInform Abstract: Absolute Configuration of Amphidinol 3 (I), the First Complete Structure Determination from Amphidinol Homologues: Application of a New Configuration Analysis Based on Carbon-Hydrogen Spin-Coupling Constants." ChemInform 30, n.º 25 (15 de junho de 2010): no. http://dx.doi.org/10.1002/chin.199925207.
Texto completo da fonteBarone, Maria Elena, Elliot Murphy, Rachel Parkes, Gerard T. A. Fleming, Floriana Campanile, Olivier P. Thomas e Nicolas Touzet. "Antibacterial Activity and Amphidinol Profiling of the Marine Dinoflagellate Amphidinium carterae (Subclade III)". International Journal of Molecular Sciences 22, n.º 22 (11 de novembro de 2021): 12196. http://dx.doi.org/10.3390/ijms222212196.
Texto completo da fonteOishi, Tohru, Tomoyuki Koge e Makoto Ebine. "Synthesis of an Analog of Amphidinol 3 Corresponding to the C31–C67 Section". HETEROCYCLES 96, n.º 7 (2018): 1197. http://dx.doi.org/10.3987/com-18-13927.
Texto completo da fonteHoudai, Toshihiro, Shigeru Matsuoka, Nobuaki Matsumori e Michio Murata. "Membrane-permeabilizing activities of amphidinol 3, polyene-polyhydroxy antifungal from a marine dinoflagellate". Biochimica et Biophysica Acta (BBA) - Biomembranes 1667, n.º 1 (novembro de 2004): 91–100. http://dx.doi.org/10.1016/j.bbamem.2004.09.002.
Texto completo da fonteColobert, Françoise, Thomas Kreuzer, Janine Cossy, Sébastien Reymond, Tomoki Tsuchiya, Laurent Ferrié, Istvan Marko e Pierre Jourdain. "Stereoselective Synthesis of the C(53)-C(67) Polyene Fragment of Amphidinol 3". Synlett 2007, n.º 15 (setembro de 2007): 2351–54. http://dx.doi.org/10.1055/s-2007-985601.
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