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

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...

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Autores principales: Harmalkar, Dipesh S., Mali, Jyotirling R., Sivaraman, Aneesh, Choi, Yongseok, Lee, Kyeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080957/
https://www.ncbi.nlm.nih.gov/pubmed/35539907
http://dx.doi.org/10.1039/c8ra02872a
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author Harmalkar, Dipesh S.
Mali, Jyotirling R.
Sivaraman, Aneesh
Choi, Yongseok
Lee, Kyeong
author_facet Harmalkar, Dipesh S.
Mali, Jyotirling R.
Sivaraman, Aneesh
Choi, Yongseok
Lee, Kyeong
author_sort Harmalkar, Dipesh S.
collection PubMed
description 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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spelling pubmed-90809572022-05-09 Schweinfurthins A–Q: isolation, synthesis, and biochemical properties Harmalkar, Dipesh S. Mali, Jyotirling R. Sivaraman, Aneesh Choi, Yongseok Lee, Kyeong RSC Adv Chemistry 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. The Royal Society of Chemistry 2018-06-08 /pmc/articles/PMC9080957/ /pubmed/35539907 http://dx.doi.org/10.1039/c8ra02872a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Harmalkar, Dipesh S.
Mali, Jyotirling R.
Sivaraman, Aneesh
Choi, Yongseok
Lee, Kyeong
Schweinfurthins A–Q: isolation, synthesis, and biochemical properties
title Schweinfurthins A–Q: isolation, synthesis, and biochemical properties
title_full Schweinfurthins A–Q: isolation, synthesis, and biochemical properties
title_fullStr Schweinfurthins A–Q: isolation, synthesis, and biochemical properties
title_full_unstemmed Schweinfurthins A–Q: isolation, synthesis, and biochemical properties
title_short Schweinfurthins A–Q: isolation, synthesis, and biochemical properties
title_sort schweinfurthins a–q: isolation, synthesis, and biochemical properties
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080957/
https://www.ncbi.nlm.nih.gov/pubmed/35539907
http://dx.doi.org/10.1039/c8ra02872a
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