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Aaptamine Derivatives with Antifungal and Anti-HIV-1 Activities from the South China Sea Sponge Aaptos aaptos

Five new alkaloids of aaptamine family, compounds (1–5) and three known derivatives (6–8), have been isolated from the South China Sea sponge Aaptos aaptos. The structures of all compounds were unambiguously elucidated by spectroscopic analyses, as well as by comparison with the literature data. Com...

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Autores principales: Yu, Hao-Bing, Yang, Fan, Sun, Fan, Li, Jing, Jiao, Wei-Hua, Gan, Jian-Hong, Hu, Wen-Zhen, Lin, Hou-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278215/
https://www.ncbi.nlm.nih.gov/pubmed/25532563
http://dx.doi.org/10.3390/md12126003
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author Yu, Hao-Bing
Yang, Fan
Sun, Fan
Li, Jing
Jiao, Wei-Hua
Gan, Jian-Hong
Hu, Wen-Zhen
Lin, Hou-Wen
author_facet Yu, Hao-Bing
Yang, Fan
Sun, Fan
Li, Jing
Jiao, Wei-Hua
Gan, Jian-Hong
Hu, Wen-Zhen
Lin, Hou-Wen
author_sort Yu, Hao-Bing
collection PubMed
description Five new alkaloids of aaptamine family, compounds (1–5) and three known derivatives (6–8), have been isolated from the South China Sea sponge Aaptos aaptos. The structures of all compounds were unambiguously elucidated by spectroscopic analyses, as well as by comparison with the literature data. Compounds 1–2 are characterized with triazapyrene lactam skeleton, whereas compounds 4–5 share an imidazole-fused aaptamine moiety. These compounds were evaluated in antifungal and anti-HIV-1 assays. Compounds 3, 7, and 8 showed antifungal activity against six fungi, with MIC values in the range of 4 to 64 μg/mL. Compounds 7–8 exhibited anti-HIV-1 activity, with inhibitory rates of 88.0% and 72.3%, respectively, at a concentration of 10 μM.
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spelling pubmed-42782152015-01-08 Aaptamine Derivatives with Antifungal and Anti-HIV-1 Activities from the South China Sea Sponge Aaptos aaptos Yu, Hao-Bing Yang, Fan Sun, Fan Li, Jing Jiao, Wei-Hua Gan, Jian-Hong Hu, Wen-Zhen Lin, Hou-Wen Mar Drugs Article Five new alkaloids of aaptamine family, compounds (1–5) and three known derivatives (6–8), have been isolated from the South China Sea sponge Aaptos aaptos. The structures of all compounds were unambiguously elucidated by spectroscopic analyses, as well as by comparison with the literature data. Compounds 1–2 are characterized with triazapyrene lactam skeleton, whereas compounds 4–5 share an imidazole-fused aaptamine moiety. These compounds were evaluated in antifungal and anti-HIV-1 assays. Compounds 3, 7, and 8 showed antifungal activity against six fungi, with MIC values in the range of 4 to 64 μg/mL. Compounds 7–8 exhibited anti-HIV-1 activity, with inhibitory rates of 88.0% and 72.3%, respectively, at a concentration of 10 μM. MDPI 2014-12-16 /pmc/articles/PMC4278215/ /pubmed/25532563 http://dx.doi.org/10.3390/md12126003 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yu, Hao-Bing
Yang, Fan
Sun, Fan
Li, Jing
Jiao, Wei-Hua
Gan, Jian-Hong
Hu, Wen-Zhen
Lin, Hou-Wen
Aaptamine Derivatives with Antifungal and Anti-HIV-1 Activities from the South China Sea Sponge Aaptos aaptos
title Aaptamine Derivatives with Antifungal and Anti-HIV-1 Activities from the South China Sea Sponge Aaptos aaptos
title_full Aaptamine Derivatives with Antifungal and Anti-HIV-1 Activities from the South China Sea Sponge Aaptos aaptos
title_fullStr Aaptamine Derivatives with Antifungal and Anti-HIV-1 Activities from the South China Sea Sponge Aaptos aaptos
title_full_unstemmed Aaptamine Derivatives with Antifungal and Anti-HIV-1 Activities from the South China Sea Sponge Aaptos aaptos
title_short Aaptamine Derivatives with Antifungal and Anti-HIV-1 Activities from the South China Sea Sponge Aaptos aaptos
title_sort aaptamine derivatives with antifungal and anti-hiv-1 activities from the south china sea sponge aaptos aaptos
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278215/
https://www.ncbi.nlm.nih.gov/pubmed/25532563
http://dx.doi.org/10.3390/md12126003
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