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Marine-Derived Lead Fascaplysin: Pharmacological Activity, Total Synthesis, and Structural Modification

Fascaplysin is a planar structure pentacyclic alkaloid isolated from sponges, which can effectively induce the apoptosis of cancer cells. In addition, fascaplysin has diverse biological activities, such as antibacterial, anti-tumor, anti-plasmodium, etc. Unfortunately, the planar structure of fascap...

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Autores principales: Wang, Chao, Wang, Siyuan, Li, Haonan, Hou, Yonglian, Cao, Hao, Hua, Huiming, Li, Dahong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142289/
https://www.ncbi.nlm.nih.gov/pubmed/37103365
http://dx.doi.org/10.3390/md21040226
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author Wang, Chao
Wang, Siyuan
Li, Haonan
Hou, Yonglian
Cao, Hao
Hua, Huiming
Li, Dahong
author_facet Wang, Chao
Wang, Siyuan
Li, Haonan
Hou, Yonglian
Cao, Hao
Hua, Huiming
Li, Dahong
author_sort Wang, Chao
collection PubMed
description Fascaplysin is a planar structure pentacyclic alkaloid isolated from sponges, which can effectively induce the apoptosis of cancer cells. In addition, fascaplysin has diverse biological activities, such as antibacterial, anti-tumor, anti-plasmodium, etc. Unfortunately, the planar structure of fascaplysin can be inserted into DNA and such interaction also limits the further application of fascaplysin, necessitating its structural modification. In this review, the biological activity, total synthesis and structural modification of fascaplysin will be summarized, which will provide useful information for pharmaceutical researchers interested in the exploration of marine alkaloids and for the betterment of fascaplysin in particular.
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spelling pubmed-101422892023-04-29 Marine-Derived Lead Fascaplysin: Pharmacological Activity, Total Synthesis, and Structural Modification Wang, Chao Wang, Siyuan Li, Haonan Hou, Yonglian Cao, Hao Hua, Huiming Li, Dahong Mar Drugs Review Fascaplysin is a planar structure pentacyclic alkaloid isolated from sponges, which can effectively induce the apoptosis of cancer cells. In addition, fascaplysin has diverse biological activities, such as antibacterial, anti-tumor, anti-plasmodium, etc. Unfortunately, the planar structure of fascaplysin can be inserted into DNA and such interaction also limits the further application of fascaplysin, necessitating its structural modification. In this review, the biological activity, total synthesis and structural modification of fascaplysin will be summarized, which will provide useful information for pharmaceutical researchers interested in the exploration of marine alkaloids and for the betterment of fascaplysin in particular. MDPI 2023-03-31 /pmc/articles/PMC10142289/ /pubmed/37103365 http://dx.doi.org/10.3390/md21040226 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Chao
Wang, Siyuan
Li, Haonan
Hou, Yonglian
Cao, Hao
Hua, Huiming
Li, Dahong
Marine-Derived Lead Fascaplysin: Pharmacological Activity, Total Synthesis, and Structural Modification
title Marine-Derived Lead Fascaplysin: Pharmacological Activity, Total Synthesis, and Structural Modification
title_full Marine-Derived Lead Fascaplysin: Pharmacological Activity, Total Synthesis, and Structural Modification
title_fullStr Marine-Derived Lead Fascaplysin: Pharmacological Activity, Total Synthesis, and Structural Modification
title_full_unstemmed Marine-Derived Lead Fascaplysin: Pharmacological Activity, Total Synthesis, and Structural Modification
title_short Marine-Derived Lead Fascaplysin: Pharmacological Activity, Total Synthesis, and Structural Modification
title_sort marine-derived lead fascaplysin: pharmacological activity, total synthesis, and structural modification
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142289/
https://www.ncbi.nlm.nih.gov/pubmed/37103365
http://dx.doi.org/10.3390/md21040226
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