Results 21 to 30 of about 175 (106)

Synthesis and Stereochemical Revision of the C31–C67 Fragment of Amphidinol 3

Angewandte Chemie, 2018
AbstractAmphidinol 3 (AM3) is a marine natural product produced by the dinoflagellate Amphidinium klebsii. Although the absolute configuration of AM3 was determined in 1999 by extensive NMR analysis and degradation of the natural product, it was a daunting task because of the presence of numerous stereogenic centers on the acyclic carbon chain and the ...
Yuma Wakamiya, Makoto Ebine, Mariko Murayama, Hiroyuki Omizu, Nobuaki Matsumori, Michio Murata, Tohru Oishi   +6 more
openaire   +3 more sources

Algal amphidinols, an alternative to sulfites in the fight against Brettanomyces bruxellensis

LWT
This study evaluated the biocidal activity of a microalgal extract from Amphidinium carterae under oenological conditions to limit Brettanomyces bruxellensis development in red wines over 150 days. Viable and culturable cell concentrations were analyzed during this period.
Abry, Chloé, Bauvois, Charlotte, de Crasto, Laurent, Tourbier, Erick, Lecourt, Julien, Alexandre, Hervé   +5 more
openaire   +1 more source

Unlocking the Health Potential of Microalgae as Sustainable Sources of Bioactive Compounds. [PDF]

Int J Mol Sci, 2021
Saide A, Martínez KA, Ianora A, Lauritano C.   +3 more
europepmc   +1 more source

Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review. [PDF]

Molecules, 2023
Mushtaq A, Zahoor AF, Bilal M, Hussain SM, Irfan M, Akhtar R, Irfan A, Kotwica-Mojzych K, Mojzych M.   +8 more
europepmc   +1 more source

Synthetic Studies of Amphidinol 3

Synthetic Studies of Amphidinol 3
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Towards the total synthesis of the amphidinol-3

, 2012
Les amphidinols sont une nouvelle classe de molécules naturelles de type polycétide dont l’amphidinol-3 est la seule molécule possédant sa structure entièrement établie. L’amphidinol-3 exhibe les meilleures activités biologiques de cette famille, principalement antifongique ethémolytique. La synthèse du fragment C17-C30 a été le premier objectif de ces
openaire   +1 more source

Rapid Screening of Polyol Polyketides from Marine Dinoflagellates. [PDF]

Anal Chem, 2022
Morales-Amador A, Souto ML, Hertweck C, Fernández JJ, García-Altares M.   +4 more
europepmc   +1 more source

Extraction, Isolation, Characterization, and Bioactivity of Polypropionates and Related Polyketide Metabolites from the Caribbean Region. [PDF]

Antibiotics (Basel), 2023
Rodríguez-Berríos RR, Ríos-Delgado AM, Perdomo-Lizardo AP, Cardona-Rivera AE, Vidal-Rosado ÁG, Narváez-Lozano GA, Nieves-Quiñones IA, Rodríguez-Vargas JA, Álamo-Diverse KY, Lebrón-Acosta N, Medina-Berríos N, Rivera-Lugo PS, Avellanet-Crespo YA, Ortiz-Colón YW.   +13 more
europepmc   +1 more source

Phytoplankton Toxins and Their Potential Therapeutic Applications: A Journey toward the Quest for Potent Pharmaceuticals. [PDF]

Mar Drugs, 2022
Pradhan B, Ki JS.
europepmc   +1 more source

Genomic and Targeted Approaches Unveil the Cell Membrane as a Major Target of the Antifungal Cytotoxin Amantelide A. [PDF]

Chembiochem, 2021
Elsadek LA, Matthews JH, Nishimura S, Nakatani T, Ito A, Gu T, Luo D, Salvador-Reyes LA, Paul VJ, Kakeya H, Luesch H.   +10 more
europepmc   +1 more source