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Structure-activity relationships of trichothecenes against COLO201 cells and Cochliobolus miyabeanus: The role of 12-epoxide and macrocyclic moieties
Authors:Manami Matsumoto  Mami Nishiyama  Hayato Maeda  Akio Tonouchi  Katsuhiro Konno  Masaru Hashimoto
Institution:1. Faculty of Agriculture and Life Science, Hirosaki University, 3-Bunkyo-cho, Hirosaki 036-8561, Japan;2. Institute of Natural Medicine, University of Toyama, Toyama 930-0194, Japan
Abstract:The novel trichothecene 12-deoxytrichodermin (3) was isolated from the fungus Trichoderma sp. 1212-03, and included with other known natural trichothecenes in a structure-activity relationship investigation against a human colon cancer cell line (COLO201) and filamentous fungus Cochliobolus miyabeanus. This revealed that the 12-epoxide functionality is critical for the cytotoxicity of simple trichothecenes trichodermin (4) and deoxynivalenol (2), while not critical for the cytotoxicity of roridin J (6) and epiisororidin E (8). In contrast, 12-epoxide is essential for the antifungal activity.
Keywords:ZACLXWTWERGCLX-MDUHGFIHSA-N  LINOMUASTDIRTM-LZTLOYDTSA-N  BRWCYDPJMOLPNV-VWOPQJGGSA-N  UMWRLMZMQORKQX-YNHJSRRZSA-N  MCGWYAODOJPYQT-BZRMNHKCSA-N  KEEQQEKLEZRLDS-ZJYSOYOTSA-N  IWFOIUWPNYEUAI-SKDXVWSPSA-N  GQZHWXPIODBFNT-NXWORCLISA-N  VSOQGZVTMDLALA-KEXFJWRRSA-N  FSBDKDZPVYYVHZ-DIDGDQROSA-N  QRZOAFBSHUOELI-XQPBFMIJSA-N  Trichothecenes  12-Deoxytrichothecenes  Cytotoxicity  Structure-activity relationship
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