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: Masahiko Isaka, Urarat Srisanoh, Sukitaya Veeranondha, Wilunda Choowong, Saisamorn Lumyong
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/59339
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-593392018-09-10T03:23:49Z Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220 Masahiko Isaka Urarat Srisanoh Sukitaya Veeranondha Wilunda Choowong Saisamorn Lumyong Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics 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 IC50values of 1.1-7.5 μg/mL, and these compounds also showed antimalarial activity with respective IC50of 3.1 and 2.8 μg/mL. © 2009 Elsevier Ltd. All rights reserved. 2018-09-10T03:14:02Z 2018-09-10T03:14:02Z 2009-10-24 Journal 00404020 2-s2.0-70349220966 10.1016/j.tet.2009.08.077 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70349220966&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59339
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Masahiko Isaka
Urarat Srisanoh
Sukitaya Veeranondha
Wilunda Choowong
Saisamorn Lumyong
Cytotoxic eremophilane sesquiterpenoids from the saprobic fungus Berkleasmium nigroapicale BCC 8220
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 IC50values of 1.1-7.5 μg/mL, and these compounds also showed antimalarial activity with respective IC50of 3.1 and 2.8 μg/mL. © 2009 Elsevier Ltd. All rights reserved.
format Journal
author Masahiko Isaka
Urarat Srisanoh
Sukitaya Veeranondha
Wilunda Choowong
Saisamorn Lumyong
author_facet Masahiko Isaka
Urarat Srisanoh
Sukitaya Veeranondha
Wilunda Choowong
Saisamorn Lumyong
author_sort Masahiko Isaka
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 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70349220966&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/59339
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