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Densazalin, a New Cytotoxic Diazatricyclic Alkaloid from the Marine Sponge Haliclona densaspicula

Densazalin, a polycyclic alkaloid, was isolated from the marine sponge Haliclona densaspicula collected in Korea. The complete structure of the compound was determined by spectroscopic methods, including 1D and 2D nuclear magnetic resonance techniques, high-resolution mass spectrometry, and comparis...

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Autores principales: Hwang, Buyng Su, Jeong, Yong Tae, Lee, Sangbum, Jeong, Eun Ju, Rho, Jung-Rae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198397/
https://www.ncbi.nlm.nih.gov/pubmed/34070629
http://dx.doi.org/10.3390/molecules26113164
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author Hwang, Buyng Su
Jeong, Yong Tae
Lee, Sangbum
Jeong, Eun Ju
Rho, Jung-Rae
author_facet Hwang, Buyng Su
Jeong, Yong Tae
Lee, Sangbum
Jeong, Eun Ju
Rho, Jung-Rae
author_sort Hwang, Buyng Su
collection PubMed
description Densazalin, a polycyclic alkaloid, was isolated from the marine sponge Haliclona densaspicula collected in Korea. The complete structure of the compound was determined by spectroscopic methods, including 1D and 2D nuclear magnetic resonance techniques, high-resolution mass spectrometry, and comparison of the calculated and measured electronic circular dichroism spectra. Densazalin possesses a unique 5,11-diazatricyclo[7.3.1.0(2,7)]tridecan-2,4,6-triene moiety, which is connected by two linear carbon chains. This compound was derived from the biogenetic precursor bis-1,3-dialkylpyridnium. Densazalin exhibited cytotoxic activity on two human tumor cell lines (AGS and HepG2) in the Cell Counting Kit-8 (CCK-8) bioassay, with IC(50) values ranging from 15.5 to 18.4 μM.
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spelling pubmed-81983972021-06-14 Densazalin, a New Cytotoxic Diazatricyclic Alkaloid from the Marine Sponge Haliclona densaspicula Hwang, Buyng Su Jeong, Yong Tae Lee, Sangbum Jeong, Eun Ju Rho, Jung-Rae Molecules Article Densazalin, a polycyclic alkaloid, was isolated from the marine sponge Haliclona densaspicula collected in Korea. The complete structure of the compound was determined by spectroscopic methods, including 1D and 2D nuclear magnetic resonance techniques, high-resolution mass spectrometry, and comparison of the calculated and measured electronic circular dichroism spectra. Densazalin possesses a unique 5,11-diazatricyclo[7.3.1.0(2,7)]tridecan-2,4,6-triene moiety, which is connected by two linear carbon chains. This compound was derived from the biogenetic precursor bis-1,3-dialkylpyridnium. Densazalin exhibited cytotoxic activity on two human tumor cell lines (AGS and HepG2) in the Cell Counting Kit-8 (CCK-8) bioassay, with IC(50) values ranging from 15.5 to 18.4 μM. MDPI 2021-05-25 /pmc/articles/PMC8198397/ /pubmed/34070629 http://dx.doi.org/10.3390/molecules26113164 Text en © 2021 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 Article
Hwang, Buyng Su
Jeong, Yong Tae
Lee, Sangbum
Jeong, Eun Ju
Rho, Jung-Rae
Densazalin, a New Cytotoxic Diazatricyclic Alkaloid from the Marine Sponge Haliclona densaspicula
title Densazalin, a New Cytotoxic Diazatricyclic Alkaloid from the Marine Sponge Haliclona densaspicula
title_full Densazalin, a New Cytotoxic Diazatricyclic Alkaloid from the Marine Sponge Haliclona densaspicula
title_fullStr Densazalin, a New Cytotoxic Diazatricyclic Alkaloid from the Marine Sponge Haliclona densaspicula
title_full_unstemmed Densazalin, a New Cytotoxic Diazatricyclic Alkaloid from the Marine Sponge Haliclona densaspicula
title_short Densazalin, a New Cytotoxic Diazatricyclic Alkaloid from the Marine Sponge Haliclona densaspicula
title_sort densazalin, a new cytotoxic diazatricyclic alkaloid from the marine sponge haliclona densaspicula
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198397/
https://www.ncbi.nlm.nih.gov/pubmed/34070629
http://dx.doi.org/10.3390/molecules26113164
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