Department of Life Science and Research Institute for Natural Sciences, Hanyang University, Seoul 133-791, South Korea.
Appl Biochem Biotechnol. 2010 Dec;162(8):2273-83. doi: 10.1007/s12010-010-9001-5. Epub 2010 Jun 11.
This paper reports the synthesis of 28 thiazolidinedione derivatives along with their algicidal activity against microalgae causing harmful algal blooming. Among the 28 compounds tested, most showed effective algicidal activity against Heterosigma akashiwo, Chattonella marina, and Cochlodinium polykrikoides, while non-harmful algae were relatively tolerant to these thiazolidinedione derivatives. Compounds 6, 13, and 22 were the most potent against C. polykrikoides with IC₅₀ values <0.5 µM. Among the thiazolidinedione derivatives tested, compounds 7, 13, 27, and 28 were extremely competent and selective to C. polykrikoides with IC₅₀ values ranging from 0.1 to 2 µM, while C. marina and H. akashiwo showed an IC₅₀ value ranging from 30 to 130 µM. These results show that some thiazolidinedione derivatives can act as potent algicides against harmful algal blooms.
本文报道了 28 种噻唑烷二酮衍生物的合成及其对引发有害藻华的微藻的杀藻活性。在所测试的 28 种化合物中,大多数对赤潮异弯藻、海洋卡盾藻和多甲藻表现出有效的杀藻活性,而无害藻类对这些噻唑烷二酮衍生物相对耐受。化合物 6、13 和 22 对多甲藻的活性最强,IC₅₀ 值<0.5 µM。在所测试的噻唑烷二酮衍生物中,化合物 7、13、27 和 28 对多甲藻具有极高的活性和选择性,IC₅₀ 值在 0.1 到 2 µM 之间,而海洋卡盾藻和赤潮异弯藻的 IC₅₀ 值在 30 到 130 µM 之间。这些结果表明,一些噻唑烷二酮衍生物可以作为有效的杀藻剂来控制有害藻华。