Reference - Detail
RRC ID | 15719 |
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Author | Nakato T, Yamauchi S, Tago R, Akiyama K, Maruyama M, Sugahara T, Kishida T, Koba Y. |
Title | Syntheses and antimicrobial activity of tetrasubstituted tetrahydrofuran lignan stereoisomers. |
Journal | Biosci Biotechnol Biochem |
Abstract |
The syntheses of all stereoisomers of tetrasubstituted tetrahydrofuran lignan were accomplished, and the antimicrobial activity was examined. The 9,9'-diol compound bearing (7R,7'R,8R,8'R) and (7R,7'S,8R,8'R) stereochemistry showed the strongest antibacterial activity against Listeria denitrificans and Bacillus subtilis, respectively. It was also found that (-)-virgatusin bearing (7S,7'R,8S,8'S) stereochemistry had strongest antifungal activity. |
Volume | 73(7) |
Pages | 1608-17 |
Published | 2009-7-1 |
DOI | 10.1271/bbb.90107 |
PII | JST.JSTAGE/bbb/90107 |
PMID | 19584535 |
MeSH | Anti-Infective Agents / chemical synthesis Anti-Infective Agents / chemistry* Anti-Infective Agents / pharmacology* Bacteria / drug effects Furans / chemistry* Lignans / chemical synthesis Lignans / chemistry* Lignans / pharmacology* Microbial Sensitivity Tests Stereoisomerism Structure-Activity Relationship |
IF | 1.516 |
Times Cited | 10 |
WOS Category | FOOD SCIENCE & TECHNOLOGY CHEMISTRY, APPLIED BIOTECHNOLOGY & APPLIED MICROBIOLOGY BIOCHEMISTRY & MOLECULAR BIOLOGY |
Resource | |
General Microbes | JCM 1649 JCM 6977 JCM 7579 JCM 11481 |