1326308-16-0Relevant articles and documents
New silybin scaffold for chemical diversification: Synthesis of novel 23-phosphodiester silybin conjugates
Zarrelli, Armando,Romanucci, Valeria,Greca, Marina Della,De Napoli, Lorenzo,Previtera, Lucio,Di Fabio, Giovanni
, p. 45 - 48 (2013)
Silybin is the major component (ca. 30%) of the silymarin complex extracted from the seeds of Silybum marianum, with multiple biological activities operating at various cell levels. As an ongoing effort toward the exploitation of natural products as scaffolds for chemical diversification at readily accessible positions, we present here an efficient synthetic procedure to obtain new 23-phosphodiester silybin conjugates with different labels. A key point in our approach is the new 3,5,7,20-tetra-O-acetylsilybin-23-phosphoramidite, useful for a variety of derivatizations following a reliable and well-known chemistry. The feasibility of the procedure has been demonstrated by preparing new 23-silybin conjugates, exploiting standard phosphoramidite chemistry. Georg Thieme Verlag Stuttgart · New York.
Regioselective synthesis of 7-O-esters of the flavonolignan silibinin and SARs lead to compounds with overadditive neuroprotective effects
Schramm, Simon,Huang, Guozheng,Gunesch, Sandra,Lang, Florian,Roa, Judit,H?gger, Petra,Sabaté, Raimon,Maher, Pamela,Decker, Michael
supporting information, p. 93 - 107 (2018/02/15)
A series of neuroprotective hybrid compounds was synthesized by conjugation of the flavonolignan silibinin with natural phenolic acids, such as ferulic, cinnamic and syringic acid. Selective 7-O-esterfication without protection groups was achieved by appl
New C-23 modified of silybin and 2,3-dehydrosilybin: Synthesis and preliminary evaluation of antioxidant properties
Zarrelli, Armando,Sgambato, Alessandro,Petito, Valentina,De Napoli, Lorenzo,Previtera, Lucio,Di Fabio, Giovanni
supporting information; experimental part, p. 4389 - 4392 (2011/09/15)
Silybin is the major flavonolignan of silymarin and it displays a plethora of biological effects, generally ascribed to its antioxidant properties. Herein we shall describe an efficient synthetic strategy to obtain a variety of new and more water-soluble