Reference - Detail
| RRC ID | 6998 |
|---|---|
| Author | Ogura K, Sugahara T, Maruyama M, Akiyama K, Yamauchi S. |
| Title | Improved syntheses of morinol C and D by employing Mizoroki-Heck reaction and their cytotoxic and antimicrobial activities. |
| Journal | Biosci Biotechnol Biochem |
| Abstract |
Improved syntheses of optically pure (-)- and (+)-morinol C, and (-)- and (+)-morinol D were achieved by employing the Mizoroki-Heck reaction to construct the cinnamyl moiety. The protective group of the alkene substrate affected the yield of this key reaction. The reaction with a combination of the acetate-protected olefin and 4-methoxyphenylboronic acid gave the best result producing morinol C and D. All stereoisomers of morinol C and D showed cytotoxic activity, with (R,R)-morinol C showing the highest antibacterial activity. |
| Volume | 74(8) |
| Pages | 1641-4 |
| Published | 2010-1-1 |
| DOI | 10.1271/bbb.100255 |
| PII | JST.JSTAGE/bbb/100255 |
| PMID | 20699576 |
| MeSH | Anti-Infective Agents / chemical synthesis* Anti-Infective Agents / chemistry Anti-Infective Agents / pharmacology* Anti-Infective Agents / toxicity Bacteria / drug effects Cell Line, Tumor Humans Microbial Sensitivity Tests Pyrans / chemical synthesis* Pyrans / chemistry Pyrans / pharmacology* Pyrans / toxicity |
| IF | 1.516 |
| Times Cited | 3 |
| WOS Category | FOOD SCIENCE & TECHNOLOGY CHEMISTRY, APPLIED BIOTECHNOLOGY & APPLIED MICROBIOLOGY BIOCHEMISTRY & MOLECULAR BIOLOGY |
| Resource | |
| General Microbes | JCM 1649 JCM 11481 JCM 6977 JCM 7579 |