Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11

Four new tricycloalternarene derivatives, guignarenones A-D (1-4), along with known (6S,9R)-vomifoliol were isolated from the endophytic fungus Guignardia bidwellii PSU-G11. Their structures were determined on the basis of spectroscopic data. The absolute configurations in 1 were assigned using a co...

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Main Authors: Sommart U., Rukachaisirikul V., Trisuwan K., Tadpetch K., Phongpaichit S., Preedanon S., Sakayaroj J.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-84856713796&partnerID=40&md5=b73e161f83a39fb5ad775a03303fab18
http://cmuir.cmu.ac.th/handle/6653943832/6831
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spelling th-cmuir.6653943832-68312014-08-30T03:51:17Z Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11 Sommart U. Rukachaisirikul V. Trisuwan K. Tadpetch K. Phongpaichit S. Preedanon S. Sakayaroj J. Four new tricycloalternarene derivatives, guignarenones A-D (1-4), along with known (6S,9R)-vomifoliol were isolated from the endophytic fungus Guignardia bidwellii PSU-G11. Their structures were determined on the basis of spectroscopic data. The absolute configurations in 1 were assigned using a combination of the modified Mosher's method and NOEDIFF data. Compound 1 displayed mild cytotoxic activity against oral cavity cancer and African green monkey kidney fibroblast (Vero) cell lines. © 2011 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved. 2014-08-30T03:51:17Z 2014-08-30T03:51:17Z 2012 Article 18743900 10.1016/j.phytol.2011.11.010 http://www.scopus.com/inward/record.url?eid=2-s2.0-84856713796&partnerID=40&md5=b73e161f83a39fb5ad775a03303fab18 http://cmuir.cmu.ac.th/handle/6653943832/6831 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Four new tricycloalternarene derivatives, guignarenones A-D (1-4), along with known (6S,9R)-vomifoliol were isolated from the endophytic fungus Guignardia bidwellii PSU-G11. Their structures were determined on the basis of spectroscopic data. The absolute configurations in 1 were assigned using a combination of the modified Mosher's method and NOEDIFF data. Compound 1 displayed mild cytotoxic activity against oral cavity cancer and African green monkey kidney fibroblast (Vero) cell lines. © 2011 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved.
format Article
author Sommart U.
Rukachaisirikul V.
Trisuwan K.
Tadpetch K.
Phongpaichit S.
Preedanon S.
Sakayaroj J.
spellingShingle Sommart U.
Rukachaisirikul V.
Trisuwan K.
Tadpetch K.
Phongpaichit S.
Preedanon S.
Sakayaroj J.
Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11
author_facet Sommart U.
Rukachaisirikul V.
Trisuwan K.
Tadpetch K.
Phongpaichit S.
Preedanon S.
Sakayaroj J.
author_sort Sommart U.
title Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11
title_short Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11
title_full Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11
title_fullStr Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11
title_full_unstemmed Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11
title_sort tricycloalternarene derivatives from the endophytic fungus guignardia bidwellii psu-g11
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-84856713796&partnerID=40&md5=b73e161f83a39fb5ad775a03303fab18
http://cmuir.cmu.ac.th/handle/6653943832/6831
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