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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Main Authors: Masahiko Isaka, Somporn Palasarn, Sanisa Lapanun, Rungtiwa Chanthaket, Nattawut Boonyuen, Saisamorn Lumyong
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/59342
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Institution: Chiang Mai University
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spelling 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
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
Pharmacology, Toxicology and Pharmaceutics
spellingShingle 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
description 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.
format 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
author_sort 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
publishDate 2018
url 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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