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Field grown day-neutral, June-bearing and everbearing strawberry cultivars responded similarly to GA3 in most cases. GA3 stimulated daughter-plant production in ‘Hecker’ (DN) and suppressed it in ‘Guardian’ (June). Fifty mg l?1 GA3 increased initial runner production of all cultivars, while both 50 and 100 mg l?1 GA3 increased fruit yield the year following treatment. In greenhouse studies, GA3 initially increased leaf number, petiole length and runner production, but the effects diminished with time. Phthalimide at 1000 mg l?1 was most effective in increasing leaf number.  相似文献   
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A series of N-substituted phthalimide derivatives were synthesized based on a pharmacophore study of paecilocin A (a natural PPAR-γ agonist) and synthetic leads. The introduction of hydrophilic and hydrophobic groups to the phthalimide skeleton yielded compounds 3–14. Compound 7 showed significant PPAR-γ activation in a luciferase assay using rat liver Ac2F cells. Docking simulations showed that a free hydroxyl group on the phthalimide head and a suitable hydrophilic tail, including a phenyl linker, were beneficial for PPAR-γ activation. Compound 7 and rosiglitazone concentration-dependently activated PPAR-γ with EC50 values of 0.67 μM and 0.028 μM, respectively. These phthalimide derivatives could be further investigated as a new class of PPAR-γ ligands.  相似文献   
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Thermodormancy of celery seeds incubated in the dark at 22°C was alleviated by two N-substituted phthalimides to the same extent as that normally achieved with a mixture of the gibberellins A4 and A7. As previously demonstrated with GA4+7, the highly dormant cultivar ‘Lathom Blanching’ responded more to phthalimides in the presence of cytokinin, whereas ‘Florida 683’ required no cytokinin to elicit the maximum response to phthalimide treatment. Seed-soak treatments with either N-substituted phthalimide improved both the rate of germination and the percentage seedling emergence of both cultivars sown in compost under glasshouse conditions.  相似文献   
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N(N-叔丁基芳酰氨基)邻苯二甲酰亚胺的合成及其杀虫活性   总被引:1,自引:0,他引:1  
通过叔丁基肼与邻苯二甲酸酐反应,进一步N-苯甲酰化,合成了11个N-(N-叔丁基芳酰氨基)邻苯二甲酰亚胺类化合物,结构经元素分析、MS和1H NMR确证。初步生物活性测试表明,部分化合物具有较好的杀虫活性。  相似文献   
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邻苯二甲酰亚胺(PI)和灭菌丹总量作为灭菌丹残留限量标准,造成茶叶中灭菌丹检测的假阳性误判,成为阻碍我国茶叶出口主要因素之一。本文优化了QuEChERS前处理条件,建立了气相色谱串联质谱法检测茶叶中PI残留的方法。样品经乙腈提取,多壁碳纳米管、十八烷基硅烷和苯磺基强阳离子交换剂组成的混合分散吸附剂净化。在10、20、50、100βμg∙kg-1添加水平下,回收率为73%~104%,相对标准偏差低于20%。方法定量限为10.0βμg∙kg-1。该方法简便、可靠、准确,灵敏度高,适用于茶叶中PI残留检测。  相似文献   
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