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The ecdysteroid agonist/antagonist and brassinosteroid-like activities of synthetic brassinosteroid/ecdysteroid hybrid molecules

机译:合成油菜素甾体/蜕皮甾类杂合分子的蜕皮甾体激动剂/拮抗剂和类油菜甾体活性

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摘要

A series of synthetic hybrid brassinosteroid/ecdysteroid structures has been assessed for their ecdysteroid agonist/antagonist activities in the Drosophila melanogaster B_(II) cell bioassay and for brassinosteroid-like activity in the rice lamina inclination test. Most of the compounds proved inactive for ecdysteroid agonist activity, demonstrating the specificity of the ecdysteroid receptor for compounds closely structurally related to 20-hydroxyecdysone. However, compound 18, with 14α-hydroxy-7-en-6-one and 22S-hydroxy functionalities (as in most active ecdysteroids), possessed distinct agonist activity (median effective concentration = 1.4 * 10~(-5) M), although this is still almost 2000-fold less active than 20-hydroxyecdysone (25). Compounds 13 and 15 possessed weak agonist activity. Compounds 5, 11 and 14 weakly antagonised the action of 20-hydroxyecdysone (at 5 * 10~(-8) M) on B_(II) cells. In the brassinosteroid bioassay, most of the tested compounds showed activity. This may reflect the metabolic capability of plant tissue to convert test compounds to more active analogues. However, it is clear that biological activity declines as the structure of the test compound deviates further from that of castasterone (16). Three ecdysteroids (25, 26 and 27) are completely inactive in the rice lamina inclination test. These studies demonstrate the high specificities of the insect ecdysteroid receptor and the plant brassinosteroid receptor and indicate that phytoecdysteroids, even in high concentrations, would not interfere with brassinosteroid signalling pathways in plants where the two classes of compounds co-occur. Equally, brassinosteroids would not interfere with ecdysteroid signalling in insects, especially if one takes into account the low concentrations of brassinosteroids in the diet of phytophagous insects.
机译:已经评估了一系列合成的油菜素甾体/蜕皮甾体混合结构在果蝇B_(II)细胞生物测定中的蜕皮甾体激动剂/拮抗剂活性,以及​​在水稻​​薄层倾斜试验中评估了油菜素甾体样活性。多数化合物被证明对蜕皮甾类激动剂活性无活性,这表明蜕皮甾类受体对于与20-羟基蜕皮激素结构密切相关的化合物的特异性。但是,具有14α-羟基-7-en-6-one和22S-羟基官能团的化合物18(与大多数活性蜕皮甾类化合物一样)具有独特的激动剂活性(中位有效浓度= 1.4 * 10〜(-5)M),尽管它的活性仍然比20-羟基蜕皮激素低2000倍(25)。化合物13和15具有弱的激动剂活性。化合物5、11和14弱拮抗20-羟基蜕皮酮(5 * 10〜(-8)M时)对B_(II)细胞的作用。在油菜素类固醇生物测定中,大多数被测化合物均具有活性。这可能反映了植物组织将测试化合物转化为更具活性的类似物的代谢能力。然而,很明显,随着受试化合物的结构进一步偏离蓖麻甾酮的生物活性,生物活性会下降(16)。在水稻叶片倾斜试验中,三种蜕皮甾类(25、26和27)完全没有活性。这些研究证明了昆虫蜕皮类固醇受体和植物类油菜素类固醇受体的高度特异性,并表明即使在高浓度下,植物蜕皮类固醇也不会干扰植物中类油菜素类固醇信号传导途径的共同存在。同样,油菜素固醇不会干扰昆虫中蜕皮激素的信号传导,尤其是如果考虑到植物吞噬性昆虫饮食中油菜素固醇的浓度较低。

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