| Marine Drugs | |
| SAR of Sponge-Inspired Hemibastadin Congeners Inhibiting Blue Mussel PhenolOxidase | |
| Hendrik Niemann2  Jens Hagenow2  Mi-Young Chung2  Claire Hellio1  Horst Weber2  Peter Proksch2  | |
| [1] LEMAR UMR 6539 UBO CNRS Ifremer IRD, European Institute of Marine Studies (IUEM), Université de Bretagne Occidentale (UBO), European University of Brittany (UEB), Technopole Brest-Iroise, 29280 Plouzané, France; E-Mail:;Institute of Pharmaceutical Biology and Biotechnology, Heinrich-Heine-University Düsseldorf, Universitätsstrasse 1, Geb. 26.23, 40225 Düsseldorf, Germany; E-Mails: | |
| 关键词:
antifouling;
hemibastadin;
phenoloxidase;
sponges;
copper;
|
|
| DOI : 10.3390/md13053061 | |
| 来源: mdpi | |
PDF
|
|
【 摘 要 】
Hemibastadin derivatives, including the synthetically-derived 5,5′-dibromohemibastadin-1 (DBHB), are potent inhibitors of blue mussel phenoloxidase (PO), which is a key enzyme involved in the firm attachment of this invertebrate to substrates and, thus, a promising molecular target for anti-fouling research. For a systematic investigation of the enzyme inhibitory activity of hemibastadin derivatives, we have synthesized nine new congeners, which feature structural variations of the DBHB core structure. These structural modifications include, e.g., different halogen substituents present at the aromatic rings, different amine moieties linked to the (
【 授权许可】
CC BY
© 2015 by the authors; licensee MDPI, Basel, Switzerland.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202003190012554ZK.pdf | 336KB |
PDF