(E)-1-(4-Hydroxyphenyl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one

• 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: (E)-1-(4-Hydroxyphenyl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one
• 英文别名: 1-(4-hydroxyxyphenyl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one
• 化学式: C₁₈H₁₈O₅
• 分子量: 314.338
• InChiKey: RPLSXUHFLZEMSS-RMKNXTFCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  23
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  65
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  顺式-2,4,5-三甲氧基-1-丙烯基苯 在 potassium permanganate 、 碳酸氢钠 、 potassium hydroxide 作用下， 以 乙醇 、 水 为溶剂， 生成 (E)-1-(4-Hydroxyphenyl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one
  参考文献：
  名称：

  Synthesis, anticancer and antioxidant activities of 2,4,5-trimethoxy chalcones and analogues from asaronaldehyde: Structure–activity relationship

  摘要：

  2,4,5-Trimethoxy chalcones and analogues were synthesized from asaronaldehyde derived from beta-asarone. These novel compounds when tested against three human tumour cell lines (MCF-7, SW-982 and HeLa) using MTT assay, revealed that chalcones possessing electron donor groups in para position to carbonyl moiety of phenyl ring A, showed better inhibitory activity (2, 3, 4, 6, 7, 10, 17). When evaluated for antioxidant activities, compound 15 exhibited better free radical scavenging property in DPPH assay while compounds 2, 3, 5, 7, 9, 10, 11, 16, and 18 showed significant NO scavenging activity. All compounds exhibited very good phenyl hydrazine induced haemolysis of erythrocytes in phenylhydrazine assay. Structure activity relationship (SAR) study using in-silico analysis matched well with in-vitro tumour cell inhibitory activity. (C) 2013 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2013.01.018

文献信息

• Antileishmanial Chalcones:  Statistical Design, Synthesis, and Three-Dimensional Quantitative Structure−Activity Relationship Analysis
  作者：Simon Feldbæk Nielsen、Søren Brøgger Christensen、Gabriele Cruciani、Arsalan Kharazmi、Tommy Liljefors

  DOI：10.1021/jm980410m

  日期：1998.11.1

  coefficient plots indicate that steric interactions between the chalcones and the target are of major importance for the potencies of the compounds. A comparison of the coefficient plots for the antileishmanial effect and the lymphocyte-suppressing activity discloses significant differences which should make it possible to design chalcones having a high antileishmanial activity without suppressing the

  已经合成了大量取代的查耳酮，并测试了其对抗盲肠和淋巴细胞的抑制活性。使用统计方法设计了查耳酮的一个子集。通过使用GRID / GOLPE方法，使用67种化合物（抗肠蠕动活性）和63种化合物（抑制淋巴细胞的活性）对训练组和9种化合物作为外部验证组进行了3D-QSAR分析。在GOLPE中实施的具有区域选择功能的智能区域定义程序将变量数量减少到大约1300个，从而产生了高质量的3D-QSAR模型（​​淋巴细胞抑制模型，R2 =0。90，Q2 = 0.80；反兽皮模型，R2 = 0.73，Q2 = 0.63）。系数图表明，查耳酮与靶标之间的空间相互作用对于化合物的效能至关重要。抗菌剂作用和淋巴细胞抑制活性的系数图的比较揭示了显着的差异，这应该使设计具有高抗菌剂活性的查耳酮成为可能，而又不抑制淋巴细胞的增殖。
• Synthesis and spectroscopic characterizations of hexakis[(1-(4′-oxyphenyl)-3-(substituted-phenyl)prop-2-en-1-one)]cyclotriphosphazenes: their <i>in vitro</i> cytotoxic activity, theoretical analysis and molecular docking studies
  作者：Hacer Doğan、Mehmet Refik Bahar、Eray Çalışkan、Suat Tekin、Harun Uslu、Feride Akman、Kenan Koran、Süleyman Sandal、Ahmet Orhan Görgülü

  DOI：10.1080/07391102.2020.1846621

  日期：2022.5.3

  Abstract The hexachlorocyclotriphosphaze compound (N3P3Cl6, HCCP) was reacted with excess (E)-(1-(4′-oxyphenyl)-3-(substituted-phenyl)prop-2-en-1-ones (2-11) to produce hexakis[(1-(4-oxyphenyl)-3-(substituted-phenyl)prop-2-en-1-one)]cyclotriphosphazenes (CP 2-11). The structures of products (CP 2-11) were confirmed using elemental analysis, FT-IR, MS spectral analysis as well as 31P, 1H and 13C-APT

  摘要 六氯环三磷化合物（N 3 P 3 Cl 6，HCCP）与过量的（E）-（1-（4'-氧基苯基）-3-（取代的苯基）prop-2-en-1-ones （2- 11)生产hexakis[(1-(4-oxyphenyl)-3-(取代-phenyl)prop-2-en-1-one)]cyclotriphosphazenes (CP 2-11) . 产品结构(CP 2-11 ) )使用元素分析、FT-IR、MS 光谱分析以及31 P、1 H 和13C-APT NMR 技术及其通过 TGA 和 DSC 技术测定的热性能。计算了 HOMO-LUMO 能隙和化学反应性标识符，并查看了 HOMO 和 LUMO 图像。根据计算，CP 2-11的化学势均为负值，表明分子是稳定的。CP 2-11的体外细胞毒性研究及其活性潜力通过Autodock Vina 软件的分子对接研究进行评估。发现CP 2-11化合物对人类癌细胞系（A2780、LNCaP
• Stilbene–Chalcone Hybrids: Design, Synthesis, and Evaluation as a New Class of Antimalarial Scaffolds That Trigger Cell Death through Stage Specific Apoptosis
  作者：Naina Sharma、Dinesh Mohanakrishnan、Amit Shard、Abhishek Sharma、Saima、Arun K. Sinha、Dinkar Sahal

  DOI：10.1021/jm201216y

  日期：2012.1.12

  Novel stilbene-chalcone (S-C) hybrids were synthesized via a sequential Claisen-Schmidt-Knoevenagel-Heck approach and evaluated for antiplasmodial activity in in vitro red cell culture using SYBR Green I assay. The most potent hybrid (11) showed IC50 of 2.2, 1.4, and 6.4 mu M against 3D7 (chloroquine sensitive), Indo, and Dd2 (chloroquine resistant) strains of Plasmodium falciparum, respectively. Interestingly, the respective individual stilbene (IC50 > 100 mu M), chalcone (IC50 = 11.5 mu M), or an equimolar mixture of stilbene and chalcone (IC50 = 32.5 mu M) were less potent than 11. Studies done using specific stage enriched cultures and parasite in continuous culture indicate that 11 and 18 spare the schizont but block the progression of the parasite life cycle at the ring or the trophozoite stages. Further, 11 and 18 caused chromatin condensation, DNA fragmentation, and loss of mitochondrial membrane potential in Plasmodium falciparum, thereby suggesting their ability to cause apoptosis in malaria parasite.
• 10.17344/acsi.2022.7080
  作者：Sirka, Lütfiye、Doğan, Hacer、Bahar, Mehmet Refik、Çalışkan, Eray、Tekin, Suat、Uslu, Harun、Koran, Kenan、Sandal, Süleyman、Görgülü, Ahmet Orhan

  DOI：10.17344/acsi.2022.7080

  日期：——
• Synthesis, anticancer and antioxidant activities of 2,4,5-trimethoxy chalcones and analogues from asaronaldehyde: Structure–activity relationship
  作者：Suvarna Shenvi、Krishna Kumar、Kaushik S. Hatti、K. Rijesh、Latha Diwakar、G. Chandrasekara Reddy

  DOI：10.1016/j.ejmech.2013.01.018

  日期：2013.4

  2,4,5-Trimethoxy chalcones and analogues were synthesized from asaronaldehyde derived from beta-asarone. These novel compounds when tested against three human tumour cell lines (MCF-7, SW-982 and HeLa) using MTT assay, revealed that chalcones possessing electron donor groups in para position to carbonyl moiety of phenyl ring A, showed better inhibitory activity (2, 3, 4, 6, 7, 10, 17). When evaluated for antioxidant activities, compound 15 exhibited better free radical scavenging property in DPPH assay while compounds 2, 3, 5, 7, 9, 10, 11, 16, and 18 showed significant NO scavenging activity. All compounds exhibited very good phenyl hydrazine induced haemolysis of erythrocytes in phenylhydrazine assay. Structure activity relationship (SAR) study using in-silico analysis matched well with in-vitro tumour cell inhibitory activity. (C) 2013 Elsevier Masson SAS. All rights reserved.