3-(4-fluorophenyl)-1-(naphthalen-1-yl)-2-propen-1-one | 329209-63-4

• 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: 3-(4-fluorophenyl)-1-(naphthalen-1-yl)-2-propen-1-one
• 英文别名: 3-(4-Fluorophenyl)-1-naphthalen-1-ylprop-2-en-1-one
• CAS: 329209-63-4
• 化学式: C₁₉H₁₃FO
• 分子量: 276.31
• InChiKey: ZINDBJFCWYAQOB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  21
• 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：
  17.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-(4-fluorophenyl)-1-(naphthalen-1-yl)-2-propen-1-one 在 吡啶 、 盐酸羟胺 作用下， 反应 0.07h， 以68%的产率得到5-(4-fluorophenyl)-3-(naphthalen-1-yl)-4,5-dihydroisoxazole
  参考文献：
  名称：

  Sharma, Sharda; Pathak, Late V. N.; Madan, Harsha, Indian Journal of Heterocyclic Chemistry, 2010, vol. 19, # 4, p. 337 - 340

  摘要：

  DOI：
• 作为产物：
  描述：

  萘 在 sodium hydroxide 、 三氯化铝 作用下， 以 四氯化碳 、 乙醇 为溶剂， 反应 2.5h， 生成 3-(4-fluorophenyl)-1-(naphthalen-1-yl)-2-propen-1-one
  参考文献：
  名称：

  Synthesis, in vitro antibacterial and antifungal evaluations of 2-amino-4-(1-naphthyl)-6-arylpyrimidines

  摘要：

  A series of 2-amino-4-(1 -naphthyl)-6-arylpyrimidines have been synthesized and characterized by IR, NMR, MS, elemental analyses and evaluated for in vitro antibacterial and antifungal activities. Some of the compounds were found to be active against a limited panel of bacteria and fungi. In particular, compounds 4b and 4e were found to be the most effective analogs against the tested bacterial and fungal strains. (c) 2006 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2006.09.012

文献信息

• Naphthalene-triazolopyrimidine hybrid compounds as potential multifunctional anti-Alzheimer’s agents
  作者：Tarana Umar、Siddharth Gusain、Md Kausar Raza、Shruti Shalini、Jitendra Kumar、Manisha Tiwari、Nasimul Hoda

  DOI：10.1016/j.bmc.2019.06.004

  日期：2019.7

  anti-Alzheimer's agents Naphthalene-triazolopyrimidine hybrids were synthesized and screened in vitro against the two cholinesterases (ChE)s, amyloid β aggregation and for antioxidation activity. Single-crystal X-ray crystallography was utilized for crystal structure determination of one of the compounds. In vitro study of compounds revealed that most of the compounds are capable of inhibiting acetylcholinesterase

  为了构建潜在的抗阿尔茨海默氏病药物，合成了萘-三唑并嘧啶杂合物，并针对两种胆碱酯酶（ChE），淀粉样β聚集和抗氧化活性进行了体外筛选。单晶X射线晶体学用于确定一种化合物的晶体结构。化合物的体外研究表明，大多数化合物都能抑制乙酰胆碱酯酶和丁酰胆碱酯酶的活性。尤其是，化合物4e和4d对AChE的IC50值比标准药物多奈哌齐（IC50 49 nM）低，为8.6至14 nM。化合物4e的最佳结果为IC50为8.6 nM（对于AChE）和150 nM（对于BuChE）。在4a，4c和4h观察到高达多奈哌齐的选择性，甚至更高。通过电子显微镜检查 透射电子显微镜和ThT荧光测定揭示了这样的事实，即合成的杂种表现出淀粉样β自聚集抑制作用。化合物4i和4j在50μM时显示出最高的抑制潜力，分别为85.46％和72.77％。高于标准Aβ崩解剂姜黄素。还分析了它们的抗氧化特性。DPPH自由基清除测定法和ORAC
• Room-Temperature Synthesis of Tetrasubstituted 1,3-Dithioles by Dimerizing Sulfuration of Chalcones with Elemental Sulfur
  作者：Thanh Binh Nguyen、Dinh Hung Mac、Pascal Retailleau

  DOI：10.1021/acs.joc.0c01618

  日期：2020.11.6

  Chalcones were found to undergo sulfurative dimerization with elemental sulfur to tetrasubstituted 1,3-dithioles. The reaction was found to proceed at room temperature in the presence of a nitrogen-base catalyst in DMSO.

  发现查尔酮与元素硫发生硫化二聚反应，生成四取代的1,3-二硫醇。发现反应在室温下在DMSO中在氮基催化剂存在下进行。
• Sharma, Sharda; Pathak, Late V. N.; Madan, Harsha, Indian Journal of Heterocyclic Chemistry, 2010, vol. 19, # 4, p. 337 - 340
  作者：Sharma, Sharda、Pathak, Late V. N.、Madan, Harsha、Sharma, Arvind

  DOI：——

  日期：——
• Synthesis, in vitro antibacterial and antifungal evaluations of 2-amino-4-(1-naphthyl)-6-arylpyrimidines
  作者：N. Ingarsal、G. Saravanan、P. Amutha、S. Nagarajan

  DOI：10.1016/j.ejmech.2006.09.012

  日期：2007.4

  A series of 2-amino-4-(1 -naphthyl)-6-arylpyrimidines have been synthesized and characterized by IR, NMR, MS, elemental analyses and evaluated for in vitro antibacterial and antifungal activities. Some of the compounds were found to be active against a limited panel of bacteria and fungi. In particular, compounds 4b and 4e were found to be the most effective analogs against the tested bacterial and fungal strains. (c) 2006 Elsevier Masson SAS. All rights reserved.