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Anti‐barnacle Activity of Isocyanides Derived from Amino Acids
Authors:Takuya Fukuda  Hideki Wagatsuma  Yoshifumi Kominami  Yasuyuki Nogata  Erina Yoshimura  Kazuhiro Chiba  Yoshikazu Kitano
Affiliation:1. Laboratory of Bio‐organic Chemistry, Tokyo University of Agriculture and Technology, Fuchu‐shi, Tokyo, Japan;2. Environmental Science Research Laboratory, Central Research Institute of Electric Power Industry, Abiko‐shi, Chiba, Japan;3. CERES Inc., Abiko‐shi, Chiba, Japan
Abstract:Creation of new potent antifouling active compounds is important for the development of environmentally friendly antifouling agents. Fifteen isocyanide congeners derived from proteinogenic amino acids were synthesized, and the antifouling activity and toxicity of these compounds against cypris larvae of the barnacle Balanus amphitrite were investigated. All synthesized amino acid‐isocyanides exhibited potent anti‐barnacle activity with EC50 values of 0.07 – 10.34 μg/ml after 120 h exposure without significant toxicity. In addition, seven compounds showed more than 95% settlement inhibition of the cypris larvae at 10 μg/ml after 120 h exposure without any mortality observed. Considering their structure, these amino acid‐isocyanides would eventually be biodegraded to their original nontoxic amino acids. These should be useful for further research focused on the development of environmentally friendly antifoulants.
Keywords:Antifouling activity  Barnacle  Isocyanide  Amino acids  Structure–  activity relationships
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