Results 91 to 100 of about 175 (106)
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Tetrahedron, 2005
Amphidinols are a unique dinoflagellate metabolite with potent antifungal activity. We examined membrane permeabilizing action by amphidinol analogues with structural variations in polyhydroxy and polyene moieties. Consequently, the polyene and polyhydroxy moieties turned out to play important roles in binding to lipid bilayer membrane and in forming ...
Toshihiro Houdai +5 more
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Amphidinols are a unique dinoflagellate metabolite with potent antifungal activity. We examined membrane permeabilizing action by amphidinol analogues with structural variations in polyhydroxy and polyene moieties. Consequently, the polyene and polyhydroxy moieties turned out to play important roles in binding to lipid bilayer membrane and in forming ...
Toshihiro Houdai +5 more
openaire +1 more source
Membrane permeabilizing action of amphidinol 3 and theonellamide A in raft-forming lipid mixtures
Zeitschrift für Naturforschung C, 2016Abstract Amphidinol 3 (AM3) and theonellamide A (TNM-A) are potent antifungal compounds produced by the dinoflagellate Amphidinium klebsii and the sponge Theonella spp., respectively. Both of these metabolites have been demonstrated to interact with membrane lipids ultimately resulting in a compromised bilayer integrity.
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Chemistry – An Asian Journal
Abstract Structure–activity relationship studies of artificial analogues of amphidinol 3 (AM3) were conducted. Based on the truncated molecule corresponding to the C21–C67 section of AM3, which elicited comparable antifungal activity to the parent compound, its stereoisomers were synthesized from polyol, bis‐THP, and polyene units via
Yoko Yasuno +5 more
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Abstract Structure–activity relationship studies of artificial analogues of amphidinol 3 (AM3) were conducted. Based on the truncated molecule corresponding to the C21–C67 section of AM3, which elicited comparable antifungal activity to the parent compound, its stereoisomers were synthesized from polyol, bis‐THP, and polyene units via
Yoko Yasuno +5 more
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Stereoselective Synthesis of the C(53)-C(67) Polyene Fragment of Amphidinol 3
Synlett, 2007Janine Cossy
exaly
Synthesis of a Truncated Analog of Amphidinol 3 Corresponding to the C21–C39/C52–C67 Section
Chemistry Letters, 2017Tohru Oishi +2 more
exaly
Synthesis of an Analog of Amphidinol 3 Corresponding to the C31–C67 Section
HETEROCYCLES, 2018Tohru Oishi, Tomoyuki Koge, Makoto Ebine
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