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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th-cmuir.6653943832-512942018-09-04T06:01:33Z Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11 Ubonta Sommart Vatcharin Rukachaisirikul Kongkiat Trisuwan Kwanruthai Tadpetch Souwalak Phongpaichit Sita Preedanon Jariya Sakayaroj Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology 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. 2018-09-04T05:59:57Z 2018-09-04T05:59:57Z 2012-03-01 Journal 18767486 18743900 2-s2.0-84856713796 10.1016/j.phytol.2011.11.010 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84856713796&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51294 |
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Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology Ubonta Sommart Vatcharin Rukachaisirikul Kongkiat Trisuwan Kwanruthai Tadpetch Souwalak Phongpaichit Sita Preedanon Jariya Sakayaroj Tricycloalternarene derivatives from the endophytic fungus Guignardia bidwellii PSU-G11 |
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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. |
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author |
Ubonta Sommart Vatcharin Rukachaisirikul Kongkiat Trisuwan Kwanruthai Tadpetch Souwalak Phongpaichit Sita Preedanon Jariya Sakayaroj |
author_facet |
Ubonta Sommart Vatcharin Rukachaisirikul Kongkiat Trisuwan Kwanruthai Tadpetch Souwalak Phongpaichit Sita Preedanon Jariya Sakayaroj |
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Ubonta Sommart |
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 |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84856713796&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51294 |
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