Proteasome inhibitors from Neoboutonia melleri

Journal of Natural Products

Volumn 75, Issue 1, 2012, Pages 34-47

  Long, Christophe ^a   Beck, Joseéphine ^a   Cantagrel, Freédeéric ^a   Marcourt, Laurence ^a   Vendier, Laure ^b   David, Bruno ^a   Plisson, Fabien ^a   Derguini, Fadila ^a   Vandenberghe, Isabelle ^a   Aussagues, Yannick ^a   Ausseil, Freédeéric ^a   Lavaud, Catherine ^c   Sautel, François ^a   Massiot, Georges ^a  

^a INSTITUT DE RECHERCHE PIERRE FABRE   (France)

^b LCC LABORATOIRE DE CHIMIE DE COORDINATION   (France)

^c CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

1,2 DIHYDRO 1ALPHA HYDROXY 22 DE O ACETYLNEOBOUTOMELLERONE; 1,2 DIHYDRO 22 DE O ACETYL 26 DEOXYNEOBOUTOMELLERONE; 1,2 DIHYDRO 22 DE O ACETYLNEOBOUTOMELLERONE; 1,2 DIHYDRONEOBOUTOMELLERONE; 16 ACETYL 3BETA,22BETA DIHYDROXY 24 METHYLCYCLOART 24 (24A)EN 23 ON 29 OIC ACID; 16 ACETYL 3BETA,26 DIHYDROXY 24 METHYL 25XI CYCLOART 24 (24A)EN 23 ON 29 OIC ACID; 18 HYDROXYNEOBOUTOMELLERONE; 22 DE O ACETYL 24A NOR 24,25 DIDEHYDRO 26 DEOXYNEOBOUTOMELLERONE; 22 DE O ACETYL 26 DEOXYNEOBOUTOMELLERONE; 22 DE O ACETYLNEOBOUTOMELLERONE; 22,23,26 TRIHYDROXY 29 NOR 24 METHYL 16,22 EPOXYCYCLOARTA 1,24 (24A)DIENE 3,23 DIONE; 23,24,24A,25,26,27 HEXA NOR NEOBOUTOMELLERON 22 AL; 23,24,24A,25,26,27 HEXA NOR NEOBOUTOMELLERON 22 OIC ACID; 24A NOR 24,25 DIDEHYDRO 26 DEOXYNEOBOUTOMELLERONE; 25 EPI NEOBOUTOMELLERONE; 26 DEOXYNEOBOUTOMELLERONE; 3BETA,16BETA,22BETA TRIHYDROXY 24 METHYL(16,23:23,26)DIEPOXYCYCLOART 24 (24A)EN 29 OIC ACID; 6BETA HYDROXY 22 DE O ACETYLNEOBOUTOMELLERONE; 6BETA HYDROXY 26 DEOXYNEOBOUTOMELLERONE; 6BETA HYDROXYNEOBOUTOMELLERONE; 6BETA,7BETA OXIDONEOBOUTOMELLERONE; 9,10 DI EPI 22 DE O ACETYL 25XI NEOBOUTOMELLERONE; 9,10 DI EPI 24A NOR 24,25 DIDEHYDRO 26 DEOXYNEOBOUTOMELLERONE; 9,10 DI EPI 25XI NEOBOUTOMELLERONE; 9,10 DI EPI 26 DEOXYNEOBOUTOMELLERONE; ANTINEOPLASTIC AGENT; NEOBOUTONIA MELLERI EXTRACT; PLANT EXTRACT; PROTEASOME INHIBITOR; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; DRUG ACTIVITY; DRUG ISOLATION; DRUG STRUCTURE; EUPHORBIACEAE; NEOBOUTONIA MELLERI; PLANT LEAF; SPECTROMETRY; STEREOCHEMISTRY; STRUCTURE ACTIVITY RELATION; SUBSTITUTION REACTION; ULTRAVIOLET IRRADIATION; X RAY CRYSTALLOGRAPHY;

CAMEROON; EUPHORBIACEAE; MOLECULAR STRUCTURE; PLANT LEAVES; PLANT STEMS; PROTEASOME ENDOPEPTIDASE COMPLEX; STRUCTURE-ACTIVITY RELATIONSHIP; TRITERPENES;

NEOBOUTONIA MELLERI;

EID: 84856411945     PISSN: 01633864     EISSN: 15206025     Source Type: Journal    
DOI: 10.1021/np200441h     Document Type: Article

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