CAS: 18956-15-5; (E)-1-(2,6-Dihydroxy-4-Methoxyphenyl)-3-Phenylprop-2-En-1-One

该化合物是一种食草类化合物,具有显著的生物和药理特性.在结构上,它具有一种与甲基稀释法原酮蛋白质相联系的铬骨架,增强了它的活性和互动潜力.该化合物展示了有希望的抗氧化剂,抗炎和抗微生物活动,使其对医学化学和药物开发的研究具有价值.它的独特结构允许有选择地调节酶路径,特别是涉及氧化性压力和炎症的路径.还研究了蛋白铬在合成衍生物方面的潜力,从而改善了生物利用率和目标特性.其稳定性和合成可及性进一步支持其在实验和工业应用中的实用性.

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上下游产品

CAS号1036-72-2 5,7-二甲氧基黄烷酮 | CAS号75291-74-6 (±)- 乔松酮 | CAS号75291-74-6 (±)- 乔松酮

合成工艺路线路线简述

    📜Pinostrobin置于氢氧化钾体系中,用 甲醇 用作溶剂,化学反应生成2',3'-二羟基-4'-甲氧基查耳酮
    参考文献:类黄酮:对乳腺癌细胞抗增殖活性的结构要求.
    标题:类黄酮:对乳腺癌细胞抗增殖活性的结构要求.
    摘要:研究了在a环上具有各种取代基的几类类黄酮(类黄酮,黄烷酮,2'-羟基查耳酮和黄烷-4-醇)对mcf-7人乳腺癌细胞的抗增殖活性.讨论了这些化合物的构效关系.发现2'-羟基查耳酮和甲氧基黄酮是mcf-7细胞生长的有效抑制剂,而黄酮和flavan-4-Ols除7,8-二羟基黄酮外似乎是弱抑制剂.
    Doi:10.1016/s0960-894X(01)00617-5

    海关参考信息

    专利信息


    专利号:US-7851654-B2
    优先权日:2006-04-03
    标题 :Chalcone derivatives, pharmaceutically acceptable salt, method for preparation and uses thereof
    发明人:PARK KI HUN; KIM JIN HYO; SEO WOO DUCK; RYU YOUNG BAE; RYU HYUNG WON; LEE WOO SONG; GAL SANG WAN
    权利人:IND ACADEMIC COOP
    摘要:Disclosed relates to a novel chalcone derivative, pharmaceutically acceptable salt thereof, a method for preparing the same and uses thereof, the chalcone derivative being readily obtained through the steps of: reacting aminoacetophenone with sulfonylchloride under the presence of an appropriate salt; and reacting the compound prepared in the above step with hydroxybenzaldehide under the presence of an appropriate catalyst. The chalcone derivative of formula 1 in accordance with the present invention having strong enzyme inhibitory activities for glycosidase can be effectively used in preventing and treating various diseases induced by glycosidase, and the chalcone derivative of the invention having tyrosinase and melanin synthesis inhibitory activities can be effectively used as a skin-whitening compound.

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.4103/0971-4065.82131
    摘要:Boutabet K, Kebsa W, Alyane M, Lahouel M. Polyphenolic fraction of Algerian propolis protects rat kidney against acute oxidative stress induced by doxorubicin. Indian J Nephrol. 2011 Apr;21(2):101–6.
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