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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-9080957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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