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Schweinfurthins A-Q: isolation, synthesis, and biochemical properties

Authors
Harmalkar, Dipesh S.Mali, Jyotirling R.Sivaraman, AneeshChoi, YongseokLee, Kyeong
Issue Date
2018
Publisher
ROYAL SOC CHEMISTRY
Citation
RSC ADVANCES, v.8, no.38, pp.21191 - 21209
Indexed
SCIE
SCOPUS
Journal Title
RSC ADVANCES
Volume
8
Number
38
Start Page
21191
End Page
21209
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/80937
DOI
10.1039/c8ra02872a
ISSN
2046-2069
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.
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생명과학대학 (생명공학부)
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