CAS: 6554-98-9; (E)-4-Styrylphenol

该化合物是一种有机化合物,其特点是由两枚双环连接的两枚苯环组成,是二苯的衍生物,具体以一个苯环的副位置的氢氧基组(OH)为特征,该化合物因其潜在的生物活动而闻名,包括抗氧化特性和癌症研究中可能的应用;跨四-环氧二氧二苯乙烯在室温中通常是固体,在乙醇和二甲基硫氧化物等有机溶剂中可溶解,但在水中溶解性有限;其分子式为C14H12O,其结构相对简单,允许各种化学修改;该化合物在医药化学和材料科学领域具有兴趣,特别是其在其他化合物合成中的作用及其潜在治疗效果方面.应当参考安全数据,以便处理和使用,如任何化学物质一样.

结构式图片

上下游产品

ethylmagnesium iodide E-1-(phenyl)-2-(4'-methoxyphenyl)ethene benzyltriphenylphosphonium chloride 4-hydroxy-benzaldehydetrans-stilbenyl-(4)-oxy)-ethyl]-aminediethyl-[2-(trans-stilbenyl-(4)-oxy)-ethyl]-amine trans-stilben-4-yloxy-acetonitriletrans-stilben-4-yloxy-acetonitrile trans-stilben-4-yloxy-propyl)-aminedibutyl-(3-trans-stilben-4-yloxy-propyl)-amine (Z)-1-(4-hydroxyphenyl)-2-phenylethene

合成工艺路线路线简述

    📜4-碘乙酰基苯酚置于palladium Diacetate,三苯基膦,Lithium Hydroxide体系中,用 四氢呋喃,N,N-二甲基甲酰胺 作为反应溶剂,化学反应 22.0H,反应生成 反式-4-羟基芪
    参考文献:Galloyl Esters Of Trans-Stilbenes Are Inhibitors Of Fasn With Anticancer Activity On Non-Small Cell Lung Cancer Cells
    标题:Galloyl Esters Of Trans-Stilbenes Are Inhibitors Of Fasn With Anticancer Activity On Non-Small Cell Lung Cancer Cells
    摘要:Fatty Acid Synthase (Fasn) Is A Lipogenic Enzyme That Is Selectively Upregulated In Malignant Cells. There Is Growing Consensus On The Oncogenicity Of Fasn-Driven Lipogenesis And The Potential Of Fasn As A Druggable Target In Cancer. Here,We Report The Synthesis And Fasn Inhibitory Activities Of Two Novel Galloyl Esters Of Trans-Stilbene Ec1 And Ec5. Inhibition Of Fasn Was Accompanied By A Loss In Akt Activation And Profound Apoptosis In Several Non-Small Cell Lung Cancer (Nsclc) Cells At The Growth Inhibitory Concentrations Of Ec1 And Ec5. Both Fasn And Phospho-Akt Levels Were Concurrently Downregulated. However,Addition Of A Lipid Concentrate To The Treated Cells Reinstated Cell Viability And Reversed The Loss Of Fasn And Akt Protein Levels,Thus Recapitulating The Causal Relationship Between Fasn Inhibition And The Loss In Cell Viability. (C) 2019 Elsevier Masson Sas. All Rights Reserved.
    DOI:10.1016/j.Ejmech.2019.111597

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Non-Peptidic Inhibitors Of Human Neutrophil Elastase: The Design And Synthesis Of Sulfonanilide-Containing Inhibitors
    作者:Katsuhiro Imaki,Takanori Okada,Yoshisuke Nakayama,Yuuki Nagao,Kaoru Kobayashi,Yasuhiro Sakai,Tetsuya Mohri,Takaaki Amino,Hisao Nakai,Masanori Kawamura |发布日期:1996.12
    摘要:A Novel Series Of Pivaloyloxy Benzene Derivatives Has Been Identified As Potent And Selective Human Neutrophil Elastase (Hne) Inhibitors. Convergent Syntheses Were Developed In Order To Identify The Inhibitors Which Are Intravenously Effective In An Animal Model. A Compound Of Particular Interest Is The Sulfonanilide-Containing Analogues. Structure-Activity Relationships Are Discussed. Structural Requirements

    合成参考文献

    合成方法参考DOI号:10.1021/acs.j°C.5b01047
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