An Unusual Diterpene—Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp.
Three new compounds, enhygromic acid (1) and deoxyenhygrolides A (2) and B (3), were isolated from a marine myxobacterium, Enhygromyxa sp. Compound 1 was found to be an acrylic acid derivative with a rare polycyclic carbon skeleton, decahydroacenaphthylene, by spectroscopic analyses. Compounds 2 and...
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doaj-1b32e6b1917c4e3ca3f7da861850302c2020-11-24T20:41:23ZengMDPI AGMarine Drugs1660-33972017-04-0115410910.3390/md15040109md15040109An Unusual Diterpene—Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp.Tomohiko Tomura0Shiori Nagashima1Satoshi Yamazaki2Takashi Iizuka3Ryosuke Fudou4Makoto Ojika5Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa-ku, Nagoya 464-8601, JapanGraduate School of Bioagricultural Sciences, Nagoya University, Chikusa-ku, Nagoya 464-8601, JapanGraduate School of Bioagricultural Sciences, Nagoya University, Chikusa-ku, Nagoya 464-8601, JapanInstitute for Innovation, Ajinomoto Co., Inc., Kawasaki, Kanagawa 210-8681, JapanR & D Planning Department, Ajinomoto Co., Inc., Chuo-ku, Tokyo 104-8315, JapanGraduate School of Bioagricultural Sciences, Nagoya University, Chikusa-ku, Nagoya 464-8601, JapanThree new compounds, enhygromic acid (1) and deoxyenhygrolides A (2) and B (3), were isolated from a marine myxobacterium, Enhygromyxa sp. Compound 1 was found to be an acrylic acid derivative with a rare polycyclic carbon skeleton, decahydroacenaphthylene, by spectroscopic analyses. Compounds 2 and 3 were deoxy analogs of the known γ-alkylidenebutenolides, enhygrolides. Compound 1 exhibited cytotoxicity against B16 melanoma cells and anti-bacterial activity against Bacillus subtilis, and enhanced the NGF-induced neurite outgrowth of PC12 cells.http://www.mdpi.com/1660-3397/15/4/109marine myxobacteriumditerpeneNGF-enhancing activitycytotoxicityantibacterial activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tomohiko Tomura Shiori Nagashima Satoshi Yamazaki Takashi Iizuka Ryosuke Fudou Makoto Ojika |
spellingShingle |
Tomohiko Tomura Shiori Nagashima Satoshi Yamazaki Takashi Iizuka Ryosuke Fudou Makoto Ojika An Unusual Diterpene—Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp. Marine Drugs marine myxobacterium diterpene NGF-enhancing activity cytotoxicity antibacterial activity |
author_facet |
Tomohiko Tomura Shiori Nagashima Satoshi Yamazaki Takashi Iizuka Ryosuke Fudou Makoto Ojika |
author_sort |
Tomohiko Tomura |
title |
An Unusual Diterpene—Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp. |
title_short |
An Unusual Diterpene—Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp. |
title_full |
An Unusual Diterpene—Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp. |
title_fullStr |
An Unusual Diterpene—Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp. |
title_full_unstemmed |
An Unusual Diterpene—Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp. |
title_sort |
unusual diterpene—enhygromic acid and deoxyenhygrolides from a marine myxobacterium, enhygromyxa sp. |
publisher |
MDPI AG |
series |
Marine Drugs |
issn |
1660-3397 |
publishDate |
2017-04-01 |
description |
Three new compounds, enhygromic acid (1) and deoxyenhygrolides A (2) and B (3), were isolated from a marine myxobacterium, Enhygromyxa sp. Compound 1 was found to be an acrylic acid derivative with a rare polycyclic carbon skeleton, decahydroacenaphthylene, by spectroscopic analyses. Compounds 2 and 3 were deoxy analogs of the known γ-alkylidenebutenolides, enhygrolides. Compound 1 exhibited cytotoxicity against B16 melanoma cells and anti-bacterial activity against Bacillus subtilis, and enhanced the NGF-induced neurite outgrowth of PC12 cells. |
topic |
marine myxobacterium diterpene NGF-enhancing activity cytotoxicity antibacterial activity |
url |
http://www.mdpi.com/1660-3397/15/4/109 |
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