583037-95-0Relevant articles and documents
Anti-AGEs and antiparasitic activity of an original prenylated isoflavonoid and flavanones isolated from Derris ferruginea
Morel, Sylvie,Helesbeux, Jean-Jacques,Séraphin, Denis,Derbré, Séverine,Gatto, Julia,Aumond, Marie-Christine,Abatuci, Yannick,Grellier, Philippe,Beniddir, Mehdi A.,Le Pape, Patrice,Pagniez, Fabrice,Litaudon, Marc,Landreau, Anne,Richomme, Pascal
, p. 498 - 503 (2013)
A new isoflavonoid, 5-hydroxy-3-(4-hydroxyphenyl)-8-isopropenyl-8,9- dihydro-4H-furo-[2,3-h]-chromen-4-one named derrisisoflavone G (1), four known prenylated flavanones (2-5), four known isoflavonoids (6-9) and two phenolic derivatives (10, 11) have been
GLYOXALASE I INHIBITOR AND USE THEREOF
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Paragraph 0061; 0064; 0065, (2018/10/24)
PROBLEM TO BE SOLVED: To provide a glyoxalase I inhibitor that is a compound showing antitumor activity. SOLUTION: The present invention provides a glyoxalase I inhibitor comprising a compound represented by the following formula, and an antitumor agent. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT
Synthesis of lupiwighteone via a para-Claisen-Cope rearrangement
Al-Maharik, Nawaf,Botting, Nigel P.
, p. 4177 - 4181 (2007/10/03)
The lanthanide catalysed para-Claisen-Cope rearrangement has been used as the key step in a short synthesis of the prenylated isoflavone, lupiwighteone. The Mitsunobu reaction was employed for the 5-O-prenylation of the acid/base sensitive acetylated isof
