Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220

Berkleasmins A-E, five new eremophilane sesquiterpenoids were isolated from the saprobic fungus Berkleasmium nigroapicale BCC 8220. The structures of the new compounds were elucidated by analyses of NMR spectroscopic and mass spectrometry data in combination with chemical means. Berkleasmins A and C...

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Main Authors: Isaka M., Srisanoh U., Veeranondha S., Choowong W., Lumyong S.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-70349220966&partnerID=40&md5=909a8d370317b11990f1215c9a8eeecf
http://cmuir.cmu.ac.th/handle/6653943832/5790
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-57902014-08-30T03:23:28Z Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220 Isaka M. Srisanoh U. Veeranondha S. Choowong W. Lumyong S. Berkleasmins A-E, five new eremophilane sesquiterpenoids were isolated from the saprobic fungus Berkleasmium nigroapicale BCC 8220. The structures of the new compounds were elucidated by analyses of NMR spectroscopic and mass spectrometry data in combination with chemical means. Berkleasmins A and C exhibited cytotoxic activity against cancer cell-lines (NCI-H187, MCF-7, and KB) as well as nonmalignant Vero cells with IC50 values of 1.1-7.5 μg/mL, and these compounds also showed antimalarial activity with respective IC50 of 3.1 and 2.8 μg/mL. © 2009 Elsevier Ltd. All rights reserved. 2014-08-30T03:23:28Z 2014-08-30T03:23:28Z 2009 Article 00404020 10.1016/j.tet.2009.08.077 TETRA http://www.scopus.com/inward/record.url?eid=2-s2.0-70349220966&partnerID=40&md5=909a8d370317b11990f1215c9a8eeecf http://cmuir.cmu.ac.th/handle/6653943832/5790 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Berkleasmins A-E, five new eremophilane sesquiterpenoids were isolated from the saprobic fungus Berkleasmium nigroapicale BCC 8220. The structures of the new compounds were elucidated by analyses of NMR spectroscopic and mass spectrometry data in combination with chemical means. Berkleasmins A and C exhibited cytotoxic activity against cancer cell-lines (NCI-H187, MCF-7, and KB) as well as nonmalignant Vero cells with IC50 values of 1.1-7.5 μg/mL, and these compounds also showed antimalarial activity with respective IC50 of 3.1 and 2.8 μg/mL. © 2009 Elsevier Ltd. All rights reserved.
format Article
author Isaka M.
Srisanoh U.
Veeranondha S.
Choowong W.
Lumyong S.
spellingShingle Isaka M.
Srisanoh U.
Veeranondha S.
Choowong W.
Lumyong S.
Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220
author_facet Isaka M.
Srisanoh U.
Veeranondha S.
Choowong W.
Lumyong S.
author_sort Isaka M.
title Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220
title_short Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220
title_full Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220
title_fullStr Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220
title_full_unstemmed Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220
title_sort cytotoxic eremophilane sesquiterpenoids from the saprobic fungus berkleasmium nigroapicale bcc 8220
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-70349220966&partnerID=40&md5=909a8d370317b11990f1215c9a8eeecf
http://cmuir.cmu.ac.th/handle/6653943832/5790
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