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具有酪氨酸酶抑制活性的Broussonin C全合成及其结构简化
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作者 陈慧娟 张兴平 +1 位作者 李明明 王扣 《天然产物研究与开发》 CAS CSCD 北大核心 2024年第7期1226-1230,1181,共6页
Broussonin C是从构树(Broussonetia papyrifera)中分离得到的一种1,3-二芳基丙烷类化合物,具有较好的酪氨酸酶抑制活性。本文以2,4-二羟基苯甲醛为起始原料,经6步反应得到broussonin C,实现其首次全合成。该法操作简单、收率高。同时,... Broussonin C是从构树(Broussonetia papyrifera)中分离得到的一种1,3-二芳基丙烷类化合物,具有较好的酪氨酸酶抑制活性。本文以2,4-二羟基苯甲醛为起始原料,经6步反应得到broussonin C,实现其首次全合成。该法操作简单、收率高。同时,在类似物研究中发现,broussonin C无异戊烯基片段的结构类似物酪氨酸酶抑制活性更好,实现了对其结构的有效简化。 展开更多
关键词 broussonin C 酪氨酸酶抑制活性 全合成 结构简化
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Broussonin E suppresses LPS-induced inflammatory response in macrophages via inhibiting MAPK pathway and enhancing JAK2-STAT3 pathway 被引量:17
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作者 HUANG Shao-Peng GUAN Xin +6 位作者 KAI Guo-Yin XU Ya-Zhou XU Yuan WANG Hao-Jie PANG Tao ZHANG Lu-Yong LIU Ying 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2019年第5期372-380,共9页
Macrophages play an important role in inflammation, and excessive and chronic activation of macrophages leads to systemic inflammatory diseases, such as atherosclerosis and rheumatoid arthritis. In this paper, we expl... Macrophages play an important role in inflammation, and excessive and chronic activation of macrophages leads to systemic inflammatory diseases, such as atherosclerosis and rheumatoid arthritis. In this paper, we explored the anti-inflammatory effect of broussonin E, a novel phenolic compound isolated from the barks of Broussonetia kanzinoki, and its underlying molecular mechanisms. We discovered that Broussonin E could suppress the LPS-induced pro-inflammatory production in RAW264.7 cells, involving TNF-α, IL-1β, IL-6, COX-2 and iNOS. And broussonin E enhanced the expressions of anti-inflammatory mediators such as IL-10, CD206 and arginase-1(Arg-1) in LPS-stimulated RAW264.7 cells. Further, we demonstrated that broussonin E inhibited the LPS-stimulated phosphorylation of ERK and p38 MAPK. Moreover, we found that broussonin E could activate janus kinase(JAK) 2, signal transducer and activator of transcription(STAT) 3. Downregulated pro-inflammatory cytokines and upregulated anti-inflammatory factors by broussonin E were abolished by using the inhibitor of JAK2-STAT3 pathway, WP1066. Taken together, our results showed that broussonin E could suppress inflammation by modulating macrophages activation state via inhibiting the ERK and p38 MAPK and enhancing JAK2-STAT3 signaling pathway, and can be further developed as a promising drug for the treatment of inflammation-related diseases such as atherosclerosis. 展开更多
关键词 broussonin E MACROPHAGE polarization Inflammation Janus KINASE 2 Signal transducer and ACTIVATOR of transcription 3
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去甲基构树宁B的合成
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作者 樊宏宇 张羽 《合成化学》 CAS CSCD 2017年第11期948-952,共5页
以1,3-二羟基苯和对羟基苯甲醛为起始原料,经赫氏酰化、羟基保护、克莱森-斯密特缩合及催化氢化反应首次合成天然产物去甲基构树宁B,总收率40.9%,其结构经~1H NMR,^(13)C NMR和HR-MS(ESI-TOF)确证。
关键词 构树宁 1 3-二芳基丙烷 催化氢化 药物合成
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