3-(4-dimethylamino-phenyl)-1-furan-2-yl-propenone | 14385-66-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: 3-(4-dimethylamino-phenyl)-1-furan-2-yl-propenone
• 英文别名: 1-(4-Dimethylamino-phenyl)-3-(2-furyl)-prop-1-en-3-on；3-[4-(Dimethylamino)phenyl]-1-(2-furanyl)-2-propen-1-one；3-[4-(dimethylamino)phenyl]-1-(furan-2-yl)prop-2-en-1-one
• CAS: 14385-66-1
• 化学式: C₁₅H₁₅NO₂
• 分子量: 241.29
• InChiKey: HSRLRBJNFBZQDP-UHFFFAOYSA-N

物化性质

• 熔点：
  94-95 °C(Solv: ethanol (64-17-5); water (7732-18-5))
• 沸点：
  395.5±42.0 °C(Predicted)
• 密度：
  1.145±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  33.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-(4-dimethylamino-phenyl)-1-furan-2-yl-propenone 在 potassium carbonate 作用下， 以 乙醇 、 丙酮 为溶剂， 生成 ((4-(5-(4-dimethylaminophenyl)-3-(furyl)-4,5-dihydropyrazol-1-yl)phenyl)sulfonyl)-N'-benzylurea
  参考文献：
  名称：

  Antidiabetic effect of novel benzenesulfonylureas as PPAR-γ agonists and their anticancer effect

  摘要：

  Twenty one pyrazoline containing benzenesulfonylureas were synthesized and docked against PPAR-gamma target. All the compounds were first screened for their antidiabetic potential by oral glucose tolerance test and then six active compounds were assessed on STZ diabetic model. It was found that five compounds showed significantly high antidiabetic activity in comparison to glibenclamide as well as rosiglitazone (standard drugs). The active compounds were evaluated for their effect on body weight since weight management is one of the main concerns associated with sulfonylureas. Finally, the most active compound 6f was shown to elevate PPAR-gamma gene expression. The synthesized compounds were also screened for anticancer activity by National Cancer Institute. Five compounds (5i, 6e, 6g, 6i and 6j) were selected at one dose level and showed potency against cancers. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2015.08.062
• 作为产物：
  描述：

  2-乙酰基呋喃 、 对二甲氨基苯甲醛 在 sodium hydroxide 作用下， 以 甲醇 、 水 为溶剂， 反应 6.0h， 生成 3-(4-dimethylamino-phenyl)-1-furan-2-yl-propenone
  参考文献：
  名称：

  设计和合成1-乙酰-3,5-二芳基-4,5-二氢（1 H）吡唑类化合物作为一种新型的潜在非嘌呤黄嘌呤氧化酶抑制剂的合理方法

  摘要：

  黄嘌呤氧化酶是一种复杂的钼黄素蛋白，可催化黄嘌呤羟化为尿酸。合理设计和合成了1-乙酰基3,5-二芳基-4,5-二氢（1 H）吡唑的53种类似物，并首次评估了其体外黄嘌呤氧化酶抑制活性。提出了有关结构活动关系的一些概念。六种化合物41，42，44，46，55和59被认为是最有效对抗XO带IC 50范围为5.3μM至15.2μM。化合物59成为最有效的XO抑制剂（IC 50 = 5.3μM）。通过分子模拟已经确定了59与XO活性位点氨基酸残基的一些重要相互作用。

  DOI：

  10.1016/j.bmc.2011.01.058

文献信息

• Detection of uronium salts
  申请人：Almog Joseph

  公开号：US20060084176A1

  公开（公告）日：2006-04-20

  Methods and kits for colorimetric identification of uronium salts, such as explosives.

  用比色法鉴别炸药等脲盐的方法和试剂盒。
• Effect of ring A and ring B substitution on the cytotoxic potential of pyrazole tethered chalcones
  作者：Kunal Nepali、Kanika Kadian、Ritu Ojha、Rajni Dhiman、Atul Garg、Gagandip Singh、Abhishek Buddhiraja、Preet Mohinder Singh Bedi、Kanaya Lal Dhar

  DOI：10.1007/s00044-011-9824-9

  日期：2012.10

  Chalcone is an aromatic ketone that forms the central core for a variety of important biological compounds, which are collectively known as chalcones. The cytotoxic potential of chalcones which consists of C-6-C-3-C-6 units gets enhanced by the incorporation of pyrazole ring as proved by our earlier studies. Thus in the present work, pyrazoles of chalcones with ring A substituted by furan, naphthalene and variety of substituted phenyl rings has been prepared and evaluated for in vitro cytotoxic activity against PC-3, OVCAR, IMR-32, HEP-2 human cancer cell lines.All the synthesized compounds were evaluated for in vitro cytotoxicity against PC-3, OVCAR, IMR-32, HEP-2 human cancer cell lines. Compound 68 was found to be the most potent showing broad spectrum of cytotoxicity against all the cell lines .
• A rational approach for the design and synthesis of 1-acetyl-3,5-diaryl-4,5-dihydro(1H)pyrazoles as a new class of potential non-purine xanthine oxidase inhibitors
  作者：Kunal Nepali、Gurinderdeep Singh、Anil Turan、Amit Agarwal、Sameer Sapra、Raj Kumar、Uttam C. Banerjee、Prabhakar K. Verma、Naresh K. Satti、Manish K. Gupta、Om P. Suri、K.L. Dhar

  DOI：10.1016/j.bmc.2011.01.058

  日期：2011.3

  Xanthine oxidase is a complex molybdoflavoprotein that catalyses the hydroxylation of xanthine to uric acid. Fifty three analogues of 1-acetyl-3,5-diaryl-4,5-dihydro(1H)pyrazoles were rationally designed and synthesized and evaluated for in vitro xanthine oxidase inhibitory activity for the first time. Some notions about structure activity relationships are presented. Six compounds 41, 42, 44, 46,

  黄嘌呤氧化酶是一种复杂的钼黄素蛋白，可催化黄嘌呤羟化为尿酸。合理设计和合成了1-乙酰基3,5-二芳基-4,5-二氢（1 H）吡唑的53种类似物，并首次评估了其体外黄嘌呤氧化酶抑制活性。提出了有关结构活动关系的一些概念。六种化合物41，42，44，46，55和59被认为是最有效对抗XO带IC 50范围为5.3μM至15.2μM。化合物59成为最有效的XO抑制剂（IC 50 = 5.3μM）。通过分子模拟已经确定了59与XO活性位点氨基酸残基的一些重要相互作用。
• Antidiabetic effect of novel benzenesulfonylureas as PPAR-γ agonists and their anticancer effect
  作者：Chetna Kharbanda、Mohammad Sarwar Alam、Hinna Hamid、Kalim Javed、Abhijeet Dhulap、Sameena Bano、Yakub Ali

  DOI：10.1016/j.bmcl.2015.08.062

  日期：2015.10

  Twenty one pyrazoline containing benzenesulfonylureas were synthesized and docked against PPAR-gamma target. All the compounds were first screened for their antidiabetic potential by oral glucose tolerance test and then six active compounds were assessed on STZ diabetic model. It was found that five compounds showed significantly high antidiabetic activity in comparison to glibenclamide as well as rosiglitazone (standard drugs). The active compounds were evaluated for their effect on body weight since weight management is one of the main concerns associated with sulfonylureas. Finally, the most active compound 6f was shown to elevate PPAR-gamma gene expression. The synthesized compounds were also screened for anticancer activity by National Cancer Institute. Five compounds (5i, 6e, 6g, 6i and 6j) were selected at one dose level and showed potency against cancers. (C) 2015 Elsevier Ltd. All rights reserved.