γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199
Two new γ-lactones, eutypellins A (1) and B (2), and two ent-eudesmane sesquiterpenes, ent-4(15)-eudesmen-11-ol-1-one (3) and ent-4(15)-eudesmen-1α,11-diol (4), together with three known pimarane diterpenes, diaporthein B, scopararane A, and libertellenone C, were isolated from the endophytic fungus...
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th-cmuir.6653943832-593422018-09-10T03:23:51Z γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199 Masahiko Isaka Somporn Palasarn Sanisa Lapanun Rungtiwa Chanthaket Nattawut Boonyuen Saisamorn Lumyong Biochemistry, Genetics and Molecular Biology Chemistry Medicine Pharmacology, Toxicology and Pharmaceutics Two new γ-lactones, eutypellins A (1) and B (2), and two ent-eudesmane sesquiterpenes, ent-4(15)-eudesmen-11-ol-1-one (3) and ent-4(15)-eudesmen-1α,11-diol (4), together with three known pimarane diterpenes, diaporthein B, scopararane A, and libertellenone C, were isolated from the endophytic fungus Eutypella sp. BCC 13199. The structures of these compounds were elucidated by interpretation of spectroscopic data. The absolute configuration of 4 was confirmed by application of the modified Mosher's method. Eutypellin A (1) and sesquiterpene 3 exhibited weak cytotoxic activities. © 2009 American Chemical Society and American Society of Pharmacognosy. 2018-09-10T03:14:04Z 2018-09-10T03:14:04Z 2009-09-25 Journal 01633864 2-s2.0-70349479408 10.1021/np900316x https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70349479408&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59342 |
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Biochemistry, Genetics and Molecular Biology Chemistry Medicine Pharmacology, Toxicology and Pharmaceutics Masahiko Isaka Somporn Palasarn Sanisa Lapanun Rungtiwa Chanthaket Nattawut Boonyuen Saisamorn Lumyong γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199 |
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Two new γ-lactones, eutypellins A (1) and B (2), and two ent-eudesmane sesquiterpenes, ent-4(15)-eudesmen-11-ol-1-one (3) and ent-4(15)-eudesmen-1α,11-diol (4), together with three known pimarane diterpenes, diaporthein B, scopararane A, and libertellenone C, were isolated from the endophytic fungus Eutypella sp. BCC 13199. The structures of these compounds were elucidated by interpretation of spectroscopic data. The absolute configuration of 4 was confirmed by application of the modified Mosher's method. Eutypellin A (1) and sesquiterpene 3 exhibited weak cytotoxic activities. © 2009 American Chemical Society and American Society of Pharmacognosy. |
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Journal |
author |
Masahiko Isaka Somporn Palasarn Sanisa Lapanun Rungtiwa Chanthaket Nattawut Boonyuen Saisamorn Lumyong |
author_facet |
Masahiko Isaka Somporn Palasarn Sanisa Lapanun Rungtiwa Chanthaket Nattawut Boonyuen Saisamorn Lumyong |
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Masahiko Isaka |
title |
γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199 |
title_short |
γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199 |
title_full |
γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199 |
title_fullStr |
γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199 |
title_full_unstemmed |
γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199 |
title_sort |
γ-lactones and ent-eudesmane sesquiterpenes from the endophytic fungus eutypella sp. bcc 13199 |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70349479408&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59342 |
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