(2E)-1-naphthalen-2-yl-3-(4-nitrophenyl)prop-2-en-1-one | 62918-37-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: (2E)-1-naphthalen-2-yl-3-(4-nitrophenyl)prop-2-en-1-one
• 英文别名: (E)-1-(naphthalen-2-yl)-3-(p-nitrophenyl)prop-2-en-1-one；(2E)-1-(2-naphthyl)-3-(4-nitrophenyl)-2-propen-1-one；2-Propen-1-one, 1-(2-naphthalenyl)-3-(4-nitrophenyl)-, (E)-；(E)-1-naphthalen-2-yl-3-(4-nitrophenyl)prop-2-en-1-one
• CAS: 62918-37-0
• 化学式: C₁₉H₁₃NO₃
• 分子量: 303.317
• InChiKey: XQOCAPRPFHAHGS-KPKJPENVSA-N

物化性质

• 熔点：
  175 °C(Solv: ethyl ether (60-29-7))
• 沸点：
  488.1±37.0 °C(Predicted)
• 密度：
  1.286±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  23
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  62.9
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (2E)-1-naphthalen-2-yl-3-(4-nitrophenyl)prop-2-en-1-one 在 trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane 、 水 、 双氧水 、 potassium hydroxide 作用下， 以 乙二醇二甲醚 为溶剂， 反应 2.5h， 以92%的产率得到2,3-epoxy-1-(naphthalen-2-yl)-3-(4-nitrophenyl)-propan-1-one
  参考文献：
  名称：

  Facile Epoxidation of α,β-Unsaturated Ketones with trans-3,5-Dihydroperoxy-3,5-dimethyl-1,2-dioxolane as an Efficient Oxidant

  摘要：

  探索了以反式-3,5-二氢过氧-3,5-二甲基-1,2-二噁烷作为高效氧源在反式查尔酮环氧化反应中的应用。反应在室温下温和条件下于碱性溶液中进行，以优异的收率得到相应的环氧化物。

  DOI：

  10.1055/s-0030-1258996
• 作为产物：
  描述：

  对硝基苯甲醛 、 2-萘乙酮 生成 (2E)-1-naphthalen-2-yl-3-(4-nitrophenyl)prop-2-en-1-one
  参考文献：
  名称：

  尿素-2,2-二氢过氧丙烷作为新型氧化剂，可轻松进行α，β-不饱和酮的环氧化

  摘要：

  摘要首次使用脲-2,2-二氢过氧丙烷作为氧源，成功地将各种芳香族α，β-不饱和酮转化为相应的环氧化物。反应在室温下在弱碱性条件下以高产率和短反应时间进行。 图形概要

  DOI：

  10.1007/s13738-016-0980-1

文献信息

• Effects of Structural and Electronic Characteristics of Chalcones on the Activation of Peroxisome Proliferator-Activated Receptor Gamma
  作者：Jason Taylor Schott、Charles Edward Mordaunt、Anthony Joseph Vargas、Martin Antonio Leon、Kevin Hsinwen Chen、Mandeep Singh、Mikiko Satoh、Emilio Leal Cardenas、Santanu Maitra、Nilay Vinod Patel、Hubrecht Johan Peter de Lijser

  DOI：10.1248/cpb.c12-00749

  日期：——

  chalcones with an electron rich group or sterically large groups such as naphthyl on the carbonyl side tend to activate PPARγ. The absence of any strict structural or electronic requirements suggests that the flexibility of the PPARγ ligand binding pocket may allow binding of diverse chalcones with some preference for a slightly larger electron-rich group on the carbonyl side. We predict that further structure-activity

  Chalcones与GW-1929具有一些结构相似性，GW-1929是一种过氧化物酶体增殖物激活的受体-γ（PPARγ）的高选择性强效激动剂。在这项研究中，我们测试了53种结构多样的查耳酮，以鉴定基于GAL4的反式激活分析中PPARγ激活所必需的特征。该屏幕鉴定了几种新颖的PPARγ查尔酮激动剂。我们的结果表明，在羰基侧具有富电子基团或空间较大基团（例如萘基）的查耳酮倾向于激活PPARγ。缺乏任何严格的结构或电子要求表明，PPARγ配体结合口袋的柔韧性可能允许各种查耳酮的结合，并且偏向于羰基侧稍大的富电子基团。
• Metal-Free and Efficient Epoxidation of α,β-Unsaturated Ketones with 1,1,2,2-Tetrahydroperoxy-1,2-Diphenylethane as a Powerful Solid Oxidant
  作者：Kaveh Khosravi、Shirin Naserifar、Boshra Mahmoudi

  DOI：10.1002/jccs.201700026

  日期：2017.6

  1,1,2,2‐Tetrahydroperoxy‐1,2‐diphenylethane was used for the efficient and metal‐free epoxidation of various α,β‐unsaturated ketones, carried out under mild alkaline conditions at room temperature.

  1,1,2,2-四氢过氧1,2-二苯乙烷用于各种α，β-不饱和酮的高效无金属环氧化，在室温下于弱碱性条件下进行。
• Facile epoxidation of α, β-unsaturated ketones with urea-2,2-dihydroperoxypropane as a new oxidant
  作者：Kaveh Khosravi、Shirin Naserifar

  DOI：10.1007/s13738-016-0980-1

  日期：2017.2

  AbstractVarious aromatic α, β-unsaturated ketones were successfully transformed into their corresponding epoxides using urea-2,2-dihydroperoxypropane as the oxygen source for the first time. The reactions were carried out under mild alkaline conditions at room temperature in high yields and short reaction times. Graphical Abstract

  摘要首次使用脲-2,2-二氢过氧丙烷作为氧源，成功地将各种芳香族α，β-不饱和酮转化为相应的环氧化物。反应在室温下在弱碱性条件下以高产率和短反应时间进行。 图形概要
• Synthesis, in vitro and in silico Studies of Naphthalene Pyrazoline Prop-2-en-1-one Derivatives
  作者：B. Prabha、C. Raja、S. Nathiya、M.R. Ezhilarasi

  DOI：10.14233/ajchem.2020.22654

  日期：——

  The synthesized new naphthalene pyrazoline prop-2-en-1-one derivatives (NDPP 1-8) were obtained by the Michael addition reaction of ethyl propanoate, hydrazine hydrate with NPD as a multicomponent scaffold. (E)-1-(naphthalen-3-yl)-3-phenylprop-2-en-1-one (NPD) was formed from 2-acetyl naphthalene and substituted aldehyde via Claisen-Schmidt condensation reaction. The NDPP skeleton structures were confirmed by infrared, 1H & 13C NMR spectral data and elemental analysis. The structure of NDPP compounds was subjected to molecular docking and ADME studies. The result of ADME prediction, compound NDPP 2, which contains electron withdrawing -Cl group has high drug-likeness value 4.21 than the compounds NDPP 4 and 7 which had electron donating CH3 and OCH3 group shows the drug-likeness value 2.62. The NDPP 2 also has high drug score 0.63 than NDPP 4 and NDPP 7 have drug score 0.60 and 0.69, respectively. Docking studies shows that compound NDPP 5 which also contain electron withdrawing NO2 group has good binding affinity value -8.8 Kcal/mol were docked with 1UAG protein. These compounds showed good drug-likeness value 2.25 and drug score 0.65. in vitro Studies have a high inhibition value for the same NO2 substituted derivative. All the compounds have higher binding affinity value than standards binding affinity value.

  合成的新萘吡唑丙烯酮衍生物（NDPP 1-8）是通过乙酸乙酯、水合肼与NPD的Michael加成反应得到的，NPD作为多组分支架。 （E）-1-（萘-3-基）-3-苯基丙烯酮（NPD）是通过2-乙酰基萘和取代醛经过Claisen-Schmidt缩合反应形成的。 通过红外、1H和13C NMR光谱数据以及元素分析确认了NDPP骨架结构。 NDPP化合物的结构经过了分子对接和ADME研究。 ADME预测结果显示，含有电子吸引性-Cl基团的化合物NDPP 2具有较高的药物相似性值4.21，而含有电子供体CH3和OCH3基团的化合物NDPP 4和7显示的药物相似性值为2.62。 NDPP 2的药物评分也较高，为0.63，而NDPP 4和NDPP 7的药物评分分别为0.60和0.69。 对接研究表明，含有电子吸引性NO2基团的化合物NDPP 5与1UAG蛋白对接具有良好的结合亲和力值-8.8Kcal/mol。 这些化合物显示出良好的药物相似性值2.25和药物评分0.65。 体外研究显示具有相同NO2取代衍生物的高抑制值。 所有化合物的结合亲和力值均高于标准结合亲和力值。
• Naphthylchalcones induce apoptosis and caspase activation in a leukemia cell line: The relationship between mitochondrial damage, oxidative stress, and cell death
  作者：Evelyn Winter、Louise Domeneghini Chiaradia、Clarissa A.S. de Cordova、Ricardo José Nunes、Rosendo Augusto Yunes、Tânia Beatriz Creczynski-Pasa

  DOI：10.1016/j.bmc.2010.09.025

  日期：2010.11

  In this study, we investigated the effects of 24 chalcone derivatives from 2-naphthylacetophenone toward a lymphoblastic leukemia cell line (L1210). Three compounds, called R7, R13, and R15, presented concentration- and time-dependent cytotoxicity and induced cellular death by apoptosis via mitochondrial injury and oxidative stress. The effects of these compounds appear to occur through different mechanisms because R13 and R7 induced a greater disturbance of mitochondrial potential, and all compounds induced disturbances of cellular ATP content and increased caspase-3 activity before cellular death. These compounds also interfered with antioxidant enzymes activities and GSH content through different mechanisms. (C) 2010 Elsevier Ltd. All rights reserved.