Results 121 to 130 of about 206 (130)
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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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Synthesis of an Analog of Amphidinol 3 Corresponding to the C31–C67 Section
HETEROCYCLES, 2018Tohru Oishi, Tomoyuki Koge, Makoto Ebine
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Syntheses of C22–C29 and C20–C29 Sections of Amphidinol 3
Tetrahedron LettersYuki Yamashita +4 more
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Stereoselective Synthesis of the C(1) - C(28) Fragment of Amphidinol 3
Helvetica Chimica Acta, 2016Jhillu S. Yadav +3 more
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