(5R)-反式-1,7-二苯基-5-羟基庚-6-烯-3-酮 | 93712-74-4

• 物质功能分类: 天然产物 - 酚类
• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二芳基庚烷
• 中文名称: (5R)-反式-1,7-二苯基-5-羟基庚-6-烯-3-酮
• 英文名称: (5R)-1,7-diphenyl-5-hydroxy-(6E)-3-hept-6-enone
• 英文别名: (5R,6E)-1,7-diphenyl-5-hydroxyhept-6-en-3-one；(5R)-trans-1,7-diphenyl-5-hydroxyhept-6-en-3-one；5-Hydroxy-1,7-diphenyl-6-hepten-3-one；(E,5R)-5-hydroxy-1,7-diphenylhept-6-en-3-one
• CAS: 93712-74-4；87095-74-7
• 化学式: C₁₉H₂₀O₂
• 分子量: 280.367
• InChiKey: NEQGOKAKPXXESR-YLZCUGDYSA-N

物化性质

• 溶解度：
  溶于DMSO和甲醇；

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  21
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

制备方法与用途

(5R,6E)-5-羟基-1,7-二苯-6-庚烯-3-酮是胡桃的二氯甲烷提取物，具有显著的抗氧化活性。

反应信息

• 作为反应物：
  描述：

  (5R)-反式-1,7-二苯基-5-羟基庚-6-烯-3-酮 在 palladium on activated charcoal 氢气 作用下， 以 甲醇 为溶剂， 反应 4.0h， 以50 mg的产率得到(S)-1,7-diphenyl-5-hydroxy-3-heptanone
  参考文献：
  名称：

  Kuroyanagi, Masanori; Noro, Tadataka; Fukushima, Seigo, Chemical and pharmaceutical bulletin, 1983, vol. 31, # 5, p. 1544 - 1550

  摘要：

  DOI：

文献信息

• Diarylheptanoids, new phytoestrogens from the rhizomes of Curcuma comosa: Isolation, chemical modification and estrogenic activity evaluation
  作者：Apichart Suksamrarn、Mathurose Ponglikitmongkol、Kanjana Wongkrajang、Anon Chindaduang、Suthadta Kittidanairak、Aroon Jankam、Boon-ek Yingyongnarongkul、Narin Kittipanumat、Ratchanaporn Chokchaisiri、Pichit Khetkam、Pawinee Piyachaturawat

  DOI：10.1016/j.bmc.2008.05.051

  日期：2008.7

  Three new diarylheptanoids, a 1: 2 mixture of (3S)- and (3R)-1-(4-methoxyphenyl)-7-phenyl-(6E)-6-hepten-3-ol (13a and 13b) and 1-(4-hydroxyphenyl)-7-phenyl-( 6E)-6-hepten-3- one ( 15), together with two synthetically known diarylheptanoids 1,7-diphenyl-(1E,3E,5E)-1,3,5-triene(9) and 1-(4-hydroxyphenyl)7-phenyl-(4E,6E)-4,6-heptadien-3- one ( 16), and nine known diarylheptanoids, 2, 8, 10 - 12, 14, a 3: 1 mixture of 17a and 17b, and 18, were isolated from the rhizomes of Curcuma comosa Roxb. The absolute stereochemistry of the isolated compounds has also been determined using the modified Mosher's method. The isolated compounds and the chemically modified analogues were evaluated for their estrogenic-like transcriptional activity using RT-PCR in HeLa cell line. Some of the isolated diarylheptanoids and their modified analogues exhibited estrogenic activity comparable to or higher than that of the phytoestrogen genistein. Based on the transcriptional activation of both estrogenic targets, Bcl-xL and ER beta gene expression, the structural features for a diarylheptanoid to exhibit high estrogenic activity are the presence of an phenolic function conjugated with the aromatic ring at the 7-position, a keto group at the 3-position, and a phenolic hydroxyl group at the p-position of the aromatic ring attached to the 1- position of the heptyl chain. (c) 2008 Elsevier Ltd. All rights reserved.
• Kuroyanagi, Masanori; Noro, Tadataka; Fukushima, Seigo, Chemical and pharmaceutical bulletin, 1983, vol. 31, # 5, p. 1544 - 1550
  作者：Kuroyanagi, Masanori、Noro, Tadataka、Fukushima, Seigo、Aiyama, Ritsuo、Ikuta, Akira、et al.

  DOI：——

  日期：——