Natural acetogenins from annonaceae, synthesis and mechanisms of action (Q104914441)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900917-5

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(2S)-4-[(8R,13R)-8,13-dihydroxy-13-[(2R,5S)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(13R)-13-[(2S,5R)-5-[(2R,5R)-5-[(1R,5S)-1,5-dihydroxyundecyl]oxolan-2-yl]oxolan-2-yl]-13-hydroxytridecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(4S,11R)-4,11-dihydroxy-11-[(2R,5R)-5-[(2R,5R)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

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(2R)-4-[(2S)-2-hydroxy-7-[(2S,5S)-5-[(1R,4S,5R,10R)-1,4,5,10-tetrahydroxynonadecyl]oxolan-2-yl]heptyl]-2-methyl-2H-furan-5-one

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(2R)-2-methyl-4-[(2R,10R,13R)-2,10,13-trihydroxy-13-[(2R,5R)-5-[(Z,1R)-1-hydroxypentadec-4-enyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(3R,5S)-5-[(6R,11S)-6,11-dihydroxy-11-[(2R,5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]undecyl]-3-(2-oxopropyl)oxolan-2-one

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(3R,5R)-5-[(11R)-11-hydroxy-11-[(2R,5R)-5-[(Z,1R)-1-hydroxypentadec-4-enyl]oxolan-2-yl]-5-oxoundecyl]-3-(2-oxopropyl)oxolan-2-one

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(2S)-2-methyl-4-[(2R,8R,10S,13S)-2,8,10,13-tetrahydroxy-13-[(2S,5S)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2S)-4-[(2R,8R)-2,8-dihydroxy-9-[(2R,5S)-5-[(1S,4R,5S)-1,4,5-trihydroxyheptadecyl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(2R)-2-methyl-4-[12-[(2R,3R)-3-[2-[(2R,3S)-3-[(E)-tetradec-3-enyl]oxiran-2-yl]ethyl]oxiran-2-yl]dodecyl]-2H-furan-5-one

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(5S)-3-[(2R)-2-Hydroxy-9-[(2S,2'S,5R,5'R)-octahydro-5'-[(1R,4R,5R)-1,4,5-trihydroxypentadecyl][2,2'-bifuran]-5-yl]nonyl]-5-methyl-2(5H)-furanone

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(2R)-4-[(13R)-13-[(2R,5R)-5-[(2R,5R)-5-[(1S,6R)-1,6-dihydroxyundecyl]oxolan-2-yl]oxolan-2-yl]-13-hydroxytridecyl]-2-methyl-2H-furan-5-one

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(2R)-4-[16-[(2R,3R)-3-[2-[(2R,3R)-3-decyloxiran-2-yl]ethyl]oxiran-2-yl]hexadecyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[(2S,10R,13R)-2,10,13-trihydroxy-13-[(2S,5S)-5-[(2R,5S)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(5S)-5-methyl-4-(12-oxononacosyl)-5H-furan-2-one

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4-Deoxyannonacin 10-ketone

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(2S)-4-[(11R)-11-[(2S,5R)-5-[(2R,5R)-5-[(1S,5S)-1,5-dihydroxyundecyl]oxolan-2-yl]oxolan-2-yl]-11-hydroxyundecyl]-2-methyl-2H-furan-5-one

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(2R)-4-[(2S,13R)-13-[(2R,5S)-5-[(2R,5S)-5-[(1R,5S)-1,5-dihydroxyundecyl]oxolan-2-yl]oxolan-2-yl]-2,13-dihydroxytridecyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[(2R,5S,6S)-2,5,6-trihydroxy-9-[(2R,5S)-5-[(1S,4S,5S)-1,4,5-trihydroxyheptadecyl]oxolan-2-yl]nonyl]-2H-furan-5-one

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(2R)-4-[(Z,11R,12R)-11,12-dihydroxytriacont-15-enyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(2S)-2-hydroxy-7-[(2R,5S)-5-[(1R,4S,5R,6S)-1,4,5,6-tetrahydroxynonadecyl]oxolan-2-yl]heptyl]-2-methyl-2H-furan-5-one

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2,4-cis-Bullatanocinone

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(5R)-3-[12-[(2S,3R)-3-[2-[(2S,3R)-3-Dodecyloxiranyl]ethyl]oxiranyl]dodecyl]-5-methyl-2(5H)-furanone

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(2R)-2-methyl-4-[(2R,8S,15R)-2,8,15-trihydroxy-15-[(2S,5R)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]pentadecyl]-2H-furan-5-one

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(2R)-4-[(2S)-2-hydroxy-9-[(2S,5R)-5-[(1R,4S,5R)-1,4,5-trihydroxyheptadecyl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[12-[(2R,3R)-3-[(E)-octadec-3-enyl]oxiran-2-yl]dodecyl]-2H-furan-5-one

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(2S)-4-[(2R)-9-[(2R,5S)-5-[(1S,4S)-1,4-Dihydroxy-4-[(2S,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]butyl]oxolan-2-yl]-2-hydroxynonyl]-2-methyl-2H-furan-5-one

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(2R)-4-[(13R)-13-[(2R,5S)-5-[(2R,5S)-5-[(1S,5R)-1,5-dihydroxyundecyl]oxolan-2-yl]oxolan-2-yl]-13-hydroxytridecyl]-2-methyl-2H-furan-5-one

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(2R)-4-[14-[(2S,3S)-3-[2-[(2S,3S)-3-dodecyloxiran-2-yl]ethyl]oxiran-2-yl]tetradecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(17S)-17-hydroxy-17-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]heptadecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(13R)-13-Hydroxy-13-[(2R,5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one

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(17R,18R,21R,22S)-reticulation-1

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(3S,4R,5S)-3-[(8S,13S)-8,13-dihydroxy-13-[(2R,5R)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-4-hydroxy-5-methyloxolan-2-one

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(3R,5R)-5-[(9R)-9-hydroxy-9-[(2S,5R)-5-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]nonyl]-3-(2-oxopropyl)oxolan-2-one

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(2S)-4-[(2R)-2-hydroxy-9-[(2R,5S)-5-[(2S,5R)-5-[(1R,4R,5S)-1,4,5-trihydroxypentadecyl]oxolan-2-yl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(2S)-2-hydroxy-7-[(2S,5R)-5-[(Z,1R,8S,9R)-1,8,9-trihydroxyhenicos-4-enyl]oxolan-2-yl]heptyl]-2-methyl-2H-furan-5-one

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(5S)-5-Methyl-3-[(2R,8R,13R)-2,8,13-trihydroxy-13-[(2R,2'R,5R,5'R)-octahydro-5'-[(1S)-1-hydroxyundecyl][2,2'-bifuran]-5-yl]tridecyl]-2(5H)-furanone

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(2S)-4-[(2R)-2-hydroxy-9-[(2S,5S)-5-[(1S,4S,5S)-1,4,5-trihydroxyheptadecyl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(2R)-2-hydroxy-7-[(2S,5S)-5-[(1S,4R,5R)-1,4,5-trihydroxynonadecyl]oxolan-2-yl]heptyl]-2-methyl-2H-furan-5-one

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(3S,5S)-5-[(11S)-11-hydroxy-11-[(2R,5R)-5-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-3-(2-oxopropyl)oxolan-2-one

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(5S)-3-[(2R)-9-[(2R,5S)-5-[(1S,4S)-4-[(2S,5R,6S)-6-Decyltetrahydro-5-hydroxy-2H-pyran-2-yl]-1,4-dihydroxybutyl]tetrahydro-2-furanyl]-2-hydroxynonyl]-5-methyl-2(5H)-furanone

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(2S)-2-methyl-4-[(2R,6S,11R,13S)-2,6,11,13-tetrahydroxy-13-[(2R,5S)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2S)-4-[(2R,11R)-2,11-dihydroxy-11-[(2S,5S)-5-[(2S,5S)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

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(5S)-3-[(2R)-2-Hydroxy-9-[(2R,5S)-tetrahydro-5-[(1S,4R,5S)-1,4,5-trihydroxyheptadecyl]-2-furanyl]nonyl]-5-methyl-2(5H)-furanone

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(2S)-4-[(2R,8R)-2,8-dihydroxy-9-[(2R,5S)-5-[(1S,4R,5R)-1,4,5-trihydroxyheptadecyl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(2R)-4-[(2S,13S)-13-[(2S,5S)-5-[(1R,6S)-1,6-dihydroxypentadecyl]oxolan-2-yl]-2,13-dihydroxy-8-oxotridecyl]-2-methyl-2H-furan-5-one

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(2R)-2-methyl-4-[(2S,5R,11S,13S)-2,5,11,13-tetrahydroxy-13-[(2S,5S)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2R)-2-methyl-4-[(2S,6S,11R,17R)-2,6,11,17-tetrahydroxy-17-[(2S,5S)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]heptadecyl]-2H-furan-5-one

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(2S)-2-methyl-4-[(2R,10R,11R)-2,10,11-trihydroxy-14-[(2S,5R)-5-[(E,1S)-1-hydroxytetradec-9-enyl]oxolan-2-yl]tetradecyl]-2H-furan-5-one

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(2R)-2-methyl-4-[(2S,8R,10R,13R)-2,8,10,13-tetrahydroxy-13-[(2S,5R)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(3S,5S)-5-[(11S)-11-hydroxy-11-[(2R,5R)-5-[(2R,5S)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-3-(2-oxopropyl)oxolan-2-one

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(2R)-4-[(2R)-9-[(2S,5S)-5-[(1S,4R)-1,4-dihydroxy-4-[(2R,5R)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]butyl]oxolan-2-yl]-2-hydroxynonyl]-2-methyl-2H-furan-5-one

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(2S)-4-[14-[(2S,3S)-3-[(E)-hexadec-3-enyl]oxiran-2-yl]tetradecyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[12-[(2R,3R)-3-[2-[(2R,3R)-3-tetradecyloxiran-2-yl]ethyl]oxiran-2-yl]dodecyl]-2H-furan-5-one

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(2S)-4-[(2R,8R)-2,8-dihydroxy-9-[(2R,5S)-5-[(1S,4S,5S)-1,4,5-trihydroxyheptadecyl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[7-[(2S,5R)-5-[(Z,1R,8S,9R)-1,8,9-trihydroxyhenicos-4-enyl]oxolan-2-yl]heptyl]-2H-furan-5-one

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(2S)-4-[(13S)-13-hydroxy-13-[(2R,5S)-5-[(1R)-1-hydroxypentadecyl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[9-[(2R,5R)-5-[(1S,4R)-4-[(2R,5R)-5-[(1S,5S)-1,5-dihydroxyundecyl]oxolan-2-yl]-1,4-dihydroxybutyl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[(2S,8S,9R,13S)-2,8,9,13-tetrahydroxy-13-[(2S,5S)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2S)-2-methyl-4-[7-[(2S,3R)-3-[(2S,3R)-3-nonadecyloxiran-2-yl]oxiran-2-yl]heptyl]-2H-furan-5-one

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(2R)-4-[(2R)-9-[(2S,5S)-5-[(1R,4S)-1,4-dihydroxy-4-[(2S,5S)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]butyl]oxolan-2-yl]-2-hydroxynonyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(2R)-2-hydroxy-7-[(2R,5R)-5-[(1R,2R,4S,5R)-1,2,4,5-tetrahydroxynonadecyl]oxolan-2-yl]heptyl]-2-methyl-2H-furan-5-one

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(2S)-4-[9-[(2R,5R)-5-[(1S,4R)-1,4-dihydroxy-4-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]butyl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(2R)-2-methyl-4-[(2S,8R,10S,13S)-2,8,10,13-tetrahydroxy-13-[(2S,5S)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2R)-2-methyl-4-[(2R,6R,8S,10R,13R)-2,6,8,10,13-pentahydroxy-13-[(2R,5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2S)-4-[(11R)-11-hydroxy-11-[(2R,5S)-5-[(2S,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(2R)-9-[(2S,5R)-5-[(1S,4R)-1,4-dihydroxy-4-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]butyl]oxolan-2-yl]-2-hydroxynonyl]-2-methyl-2H-furan-5-one

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12,15-cis-Bullatalicin

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(2S)-2-methyl-4-[(2S,8R,9S,13S)-2,8,9,13-tetrahydroxy-13-[(2R,5S)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2S)-4-[(2R,8S)-2,8-dihydroxy-9-[(2S,5R)-5-[(2R,5S)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one

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(5S)-5-Methyl-3-(11Z,15Z)-11,15-triacontadien-1-yl-2(5H)-furanone

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(2S)-4-[(E)-16-[(2S,3S)-3-dodecyloxiran-2-yl]hexadec-13-enyl]-2-methyl-2H-furan-5-one

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(2S)-4-[14-[(2S,3S)-3-[(Z)-hexadec-3-enyl]oxiran-2-yl]tetradecyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[(2R,6R,8S,13R)-2,6,8,13-tetrahydroxy-13-[(2R,5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(3R,5R)-5-[(9R)-9-hydroxy-9-[(2R,5R)-5-[(2S,5R)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]nonyl]-3-(2-oxopropyl)oxolan-2-one

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(2R)-4-[(2S,11S)-2,11-dihydroxy-11-[(2R,5R)-5-[(2R,5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[(2R,10S,13R)-2,10,13-trihydroxy-13-[(2S,5S)-5-[(2S,5S)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2R)-4-[(11S)-11-hydroxy-11-[(2S,5R)-5-[(1S)-1-hydroxyheptadecyl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(2R,13R)-2,13-dihydroxy-13-[(2S,5S)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]-9-oxotridecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(2R,13S)-2,13-dihydroxy-13-[(2R,5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]-8-oxotridecyl]-2-methyl-2H-furan-5-one

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(2S)-2-methyl-4-[(2R,8S,13S)-2,8,13-trihydroxy-13-[(2S,5S)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(3S,4R,5S)-4-hydroxy-3-[(13R)-13-hydroxy-13-[(2R,5R)-5-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-5-methyloxolan-2-one

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(5S)-3-(13Z,17Z)-13,17-Dotriacontadien-1-yl-5-methyl-2(5H)-furanone

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(2S)-2-methyl-4-[(2S,8S,9R,13S)-2,8,9,13-tetrahydroxy-13-[(2R,5S)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(S)-3-[(2R,8R,13R)-13-[(2R)-5alpha-[(S)-1-Hydroxytridecyl]tetrahydrofuran-2beta-yl]-2,8,13-trihydroxytridecyl]-5-methylfuran-2(5H)-one

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(3S,4R,5S)-3-[9-[(2R,5R)-5-[(1R,4R)-1,4-dihydroxy-4-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]butyl]oxolan-2-yl]nonyl]-4-hydroxy-5-methyloxolan-2-one

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(2R)-2-methyl-4-[(2S,8S,11E,15E,19S,20R)-2,8,19,20-tetrahydroxydotriaconta-11,15-dienyl]-2H-furan-5-one

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(3S,5S)-5-[(5R,11R)-5,11-dihydroxy-11-[(2S,5S)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]undecyl]-3-(2-oxopropyl)oxolan-2-one

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(2S)-2-methyl-4-[(2S,7S,13R)-2,7,13-trihydroxy-13-[(2S,5S)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one

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(2S)-4-[(11S)-11-hydroxy-11-[(2R,5R)-5-[(2R,5R)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

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(2R)-4-[12-[(2R,3R)-3-[2-[(2R,3S)-3-[2-[(2R,3R)-3-decyloxiran-2-yl]ethyl]oxiran-2-yl]ethyl]oxiran-2-yl]dodecyl]-2-methyl-2H-furan-5-one

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(3R,5R)-5-[(11S)-11-hydroxy-11-[(2R,5S)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]-5-oxoundecyl]-3-(2-oxopropyl)oxolan-2-one

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(3S,5R)-5-[(11S)-11-hydroxy-11-[(2R,5R)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]-6-oxoundecyl]-3-(2-oxopropyl)oxolan-2-one

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(2R)-4-[(13R)-13-hydroxy-13-[(2R,5S)-5-[(2S,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one

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(2R)-4-[(13R)-13-hydroxy-13-[(2R,5S)-5-[(Z,1R)-1-hydroxypentadec-4-enyl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one

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(2S)-4-[(10S,13R)-10,13-dihydroxy-13-[(2S,5S)-5-[(2S,5S)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one

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annonaceae

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M. Carmen Zafra-Polo

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900917-5

Bruno Figadère

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900917-5

Teresa Gallardo

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900917-5

JoséR. Tormo

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900917-5

Diego Cortes

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900917-5

publication date

23 April 2003

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900917-5

published in

Phytochemistry

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volume

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issue

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900917-5

page(s)

1087-1117

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cites work

Acetogenins from Annonaceae, inhibitors of mitochondrial complex I.

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https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Solamin, a cytotoxic mono-tetrahydrofuranic γ-lactone acetogenin from Annona muricata seeds

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Bis-tetrahydrofuran acetogenins from annonaceae

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Absolute Stereochemistries of Giganin and Longanin, Bioactive Non-tetrahydrofuran Ring Annonaceous Acetogenins from Asimina longifolia

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Coriadienin, the first annonaceous acetogenin with two double bonds isolated from Annona coriaceae

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Tonkinelin: a novel annonaceous acetogenin from Uvaria tonkinensis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Isolation of Montecristin, a Key Metabolite in Biogenesis of Acetogenins from Annona muricata and Its Structure Elucidation by Using Tandem Mass Spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Cohibins A and B, acetogenins from roots of Annona muricata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Muridienin-1 and -2: The missing links in the biogenetic precursors of acetogenins of annonaceae

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Acetogenins from Porcelia macrocarpa: Stereochemical determination of 2-alkyl-3-hydroxy-4-methyl γ-lactones by 13C NMR spectroscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Isoacetogenins, Artifacts Issued from Translactonization from Annonaceous Acetogenins

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Epomusenins A and B, two acetogenins from fruits of Rollinia mucosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Recent advances in Annonaceous acetogenins

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Annotemoyin-1 and -2: Two Novel Monotetrahydrofuranic γ-Lactone Acetogenins from the Seeds ofAnnona atemoya

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Asitribin and Asiminenins A and B, Novel Bioactive Annonaceous Acetogenins from the Seeds of Asimina triloba

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

16,19-cis-murisolin and murisolin a, two novel bioactive mono-tetrahydrofuran annonaceous acetogenins from Asimina triloba seeds

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Tonkinecin, a novel bioactive annonaceous acetogenin from Uvaria tonkinesis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Longifolicin, longicoricin, and gigantetroneninone, three novel bioactive mono-tetrahydrofuran annonaceous acetogenins from Asimina longifolia (Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

4-deoxyannomontacin and (2,4-cis and trans)-annomontacinone, new bioactive mono-tetrahydrofuran annonaceous acetogenins from Goniothalamus giganteus.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Longicin and goniothalamicinone: novel bioactive monotetrahydrofuran acetogenins from Asimina longifolia

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Additional bioactive acetogenins, annomutacin and (2,4-trans and cis)-10R-annonacin-A-ones, from the leaves of Annona muricata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Five novel mono-tetrahydrofuran ring acetogenins from the seeds of Annona muricata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Rollinecins A and B: two new bioactive annonaceous acetogenins from Rollinia mucosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

4-Acetyl Annonacin and 4-Acetyl Xylomaticin: Two Novel Bioactive Mono-Tetrahydrofuran Annonaceous Acetogenins fromAsimina Longifolia(Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Disepalin, a New Acetogenin fromDisepalum Anomalum(Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Novel mono-tetrahydrofuran ring acetogenins, from the bark of Annona squamosa, showing cytotoxic selectivities for the human pancreatic carcinoma cell line, PACA-2.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Six acetogenins from Uvaria tonkinesis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Gigantransenins A, B, and C, novel mono-THF acetogenins bearing trans double bonds, from Goniothalamus giganteus (Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Muricatocins A and B, Two New Bioactive Monotetrahydrofuran Annonaceous Acetogenins from the Leaves of Annona muricata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

New Bioactive Monotetrahydrofuran Annonaceous Acetogenins, Annomuricin C and Muricatocin C, from the Leaves of Annona muricata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Annohexocin, a novel mono-THF acetogenin with six hydroxyls, from Annona muricata (Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Coriaheptocins A and B, the First Heptahydroxylated Acetogenins, Isolated from the Roots ofAnnonacoriacea1

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Annonaceous Acetogenins from the Seeds of Annona squamosa. Non-adjacent Bis-tetrahydrofuranic Acetogenins.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Coriacin and 4-Deoxycoriacin, Two New Mono-THF Acetogenins from the Roots OfAnnona coriacea

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Murihexocins A and B, two novel mono-THF acetogenins with six hydroxyls, from Annona muricata (Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Five New Monotetrahydrofuran Ring Acetogenins from the Leaves ofAnnona muricata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

cis-gigantrionenin and 4-acetyl gigantetrocin A, two new bioactive annonaceous acetogenins from Goniothalamus giganteus, and the stereochemistries of acetogenin 1,2,5-triols

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Applying Mosher's method to acetogenins bearing vicinal diols. The absolute configurations of muricatetrocin C and rollidecins A and B, new bioactive acetogenins from Rollinia mucosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Glaucafilin, an acetogenin from Annona glauca

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Acetogenins from Annona glabra seeds

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Biologically active acetogenins from stem bark of Asimina triloba

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Asimilobin and cis- and trans-murisolinones, novel bioactive Annonaceous acetogenins from the seeds of Asimina triloba.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Acetogenins from seeds of Annona reticulata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

New Type of Mono-tetrahydrofuran Ring Acetogenins fromGoniothalamus donnaiensis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Mono-tetrahydrofuran ring acetogenins from Goniothalamus donnaiensis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

The absolute configuration of trilobacin and trilobin, a novel highly potent acetogenin from the stem bark of Asimina triloba (Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Atemoyacin A: A new bis-tetrahydrofuranyl annonaceous acetogenin from Annona atemoya H.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Squamotacin: an annonaceous acetogenin with cytotoxic selectivity for the human prostate tumor cell line (PC-3).

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

New bioactive adjacent bis-THF annonaceous acetogenins from Annona bullata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Araticulin, a bis-tetrahydrofuran polyketide from Annona itcrassiflora seeds

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Annonisin, a bis-tetrahydrofuran acetogenin from Annona atemoya seeds

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Three new adjacent bis-tetrahydrofuran acetogenins with four hydroxyl groups from Asimina triloba

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Longimicins A-D: novel bioactive acetogenins from Asimina longifolia (annonaceae) and structure-activity relationships of asimicin type of annonaceous acetogenins.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Rollimembrin, a novel acetogenin inhibitor of mammalian mitochondrial complex I

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

The absolute configuration of adjacent bis-THF acetogenins and asiminocin, a novel highly potent asimicin isomer from Asimina triloba.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Muconin and Mucoxin: Additional Nonclassical Bioactive Acetogenins from Rollinia mucosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Bioactive annonaceous acetogenins from Rollinia mucosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Acetogenins from the bark of Uvaria pauci-ovulata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Goniodenin, a New Bioactive Annonaceous Acetogenin from Goniothalamus giganteus and Its Conversion to Tri-THF Acetogenins

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Absolute Stereochemistries of Sylvaticin and 12,15-cis-Sylvaticin, Bioactive C-20,23-cis Non-adjacent Bistetrahydrofuran Annonaceous Acetogenins, from Rollinia mucosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Additional bioactive annonaceous acetogenins from Asimina triloba (Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Toward Chemical Libraries of Annonaceous Acetogenins. Total Synthesis of Trilobacin

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Novel Acetogenins from the Leaves of Annona purpurea

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

30-, 31-, and 32-hydroxybullatacinones: bioactive terminally hydroxylated annonaceous acetogenins from Annona bullata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Bioactive acetogenins from seeds of Annona cherimolia

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Mucocin: A New Annonaceous Acetogenin Bearing a Tetrahydropyran Ring

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Aromin and aromicin, two new bioactive annonaceous acetogenins, possessing an unusual bis-THF ring structure, from Xylopia aromatica (Annonaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

First synthesis of a new acetogenin of annonaceae, reticulatamol : Activated tin hydride with enhanced reducing ability

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Annonaceous acetogenins: a review

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Molecular mode of action of annonins

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Mode of action of bullatacin: a potent antitumor and pesticidal annonaceous acetogenin

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Natural substances (acetogenins) from the family Annonaceae are powerful inhibitors of mitochondrial NADH dehydrogenase (Complex I)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Mode of action of bullatacin, a potent antitumor acetogenin: inhibition of NADH oxidase activity of HeLa and HL-60, but not liver, plasma membranes.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

The Annonaceous acetogenin bullatacin is cytotoxic against multidrug-resistant human mammary adenocarcinoma cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

The respiratory-chain NADH dehydrogenase (complex I) of mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Origin and functional consequences of the complex I defect in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Determination of structure-activity relationships of Annonaceous acetogenins by inhibition of oxygen uptake in rat liver mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

The mechanism of proton and electron transport in mitochondrial complex I.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

The Interaction of Q Analogs, Particularly Hydroxydecyl Benzoquinone (Idebenone), with the Respiratory Complexes of Heart Mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

The specificity of mitochondrial complex I for ubiquinones

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Genetic evidence for the existence of two quinone related inhibitor binding sites in NADH-CoQ reductase.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Tumor cell growth inhibition by several Annonaceous acetogenins in an in vitro disk diffusion assay.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Cherimolin-1, new selective inhibitor of the first energy-coupling site of the NADH: ubiquinone oxidoreductase (complex I).

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Antitumor Cytotoxicity and Stereochemistry of Polyketides fromGoniothalamus amuyon

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021

Bistetrahydrofuranoid acetogenins from Rollinia sericea

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900917-5

7 January 2021