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Schweinfurthins A-Q: isolation, synthesis, and biochemical properties.
Harmalkar, Dipesh S; Mali, Jyotirling R; Sivaraman, Aneesh; Choi, Yongseok; Lee, Kyeong.
Afiliação
  • Harmalkar DS; College of Pharmacy, Dongguk University-Seoul Goyang 10326 Republic of Korea kaylee@dongguk.edu.
  • Mali JR; College of Pharmacy, Dongguk University-Seoul Goyang 10326 Republic of Korea kaylee@dongguk.edu.
  • Sivaraman A; College of Pharmacy, Dongguk University-Seoul Goyang 10326 Republic of Korea kaylee@dongguk.edu.
  • Choi Y; Department of Biotechnology, Korea University Seoul 02841 Republic of Korea.
  • Lee K; College of Pharmacy, Dongguk University-Seoul Goyang 10326 Republic of Korea kaylee@dongguk.edu.
RSC Adv ; 8(38): 21191-21209, 2018 Jun 08.
Article em En | MEDLINE | ID: mdl-35539907
ABSTRACT
Stilbene analogues have shown remarkable structural diversity constituting simple or tangled structures, which have attracted the synthetic as well as the medicinal chemistry communities. Schweinfurthins are a family of prenylated/geranylated/farnesylated stilbenes that are isolated from an African plant belonging to the Macaranga species. These compounds have displayed potency towards central nervous system, renal and breast cancer cell lines. Specifically, these compounds have been found to be potent and selective inhibitors of cell growth in the National Cancer Institute's 60 cell-line screen. In this review article, we described the isolation, synthesis, and biochemical properties of schweinfurthins.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article