苯酚,4,4'-(四氢-3,4-二甲基-2,5-呋喃二基)二[2-甲氧基-,(2R,3R,4S,5R)-rel-(-)-(9CI) | 114422-21-8

• 分子结构分类: 有机化合物 - 木脂素、新木脂素和相关化合物 - 呋喃类木脂素
• 中文名称: 苯酚,4,4'-(四氢-3,4-二甲基-2,5-呋喃二基)二[2-甲氧基-,(2R,3R,4S,5R)-rel-(-)-(9CI)
• 英文名称: machilin-I
• 英文别名: (-)-(7R,7'R,8S,8'R)-4,4'-dihydroxy-3,3'-dimethoxy-7,7'-epoxylignan；3′,3″-dimethoxylarreatricin；Machilin I；4-[(2R,3R,4S,5R)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol
• CAS: 114422-21-8
• 化学式: C₂₀H₂₄O₅
• 分子量: 344.408
• InChiKey: GMXMKSFJQLFOSO-BINDOVRGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  68.2
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  (7R,7′R,8S,8′S)-4,4′-dibenzyloxy-3,3′-dimethoxy-7,7′-epoxylignane-9,9′-diol 在 dimethyl sulfide borane 、 三乙基硼氢化锂 、 甲基磺酰氯 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三乙胺 、 sodium iodide 作用下， 以 四氢呋喃 、 二氯甲烷 、 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， 反应 9.0h， 生成 苯酚,4,4'-(四氢-3,4-二甲基-2,5-呋喃二基)二[2-甲氧基-,(2R,3R,4S,5R)-rel-(-)-(9CI)
  参考文献：
  名称：

  Synthesis of All Stereoisomers of 3,3′-Dimethoxy-7,7′-epoxylignane-4,4′-diol and Their Plant Growth Inhibitory Activity

  摘要：

  All stereoisomers of 3,3'-dimethoxy-7,7'-epoxylignane-4,4'-diol were synthesized to examine the effect of stereochemistry on their plant growth inhibitory activity using lettuce and Italian ryegrass. The effect of structural modifications such as dehydroxylation, methoxylation and hydroxylation at the 9- and 9'-positions of the lignans on the activity was also studied. Most of the epoxylignanes showed higher plant growth inhibitory potency against ryegrass than against lettuce, and the inhibitory activity varied depending on the configurations of each position of the tetrahydrofuran ring (7-, 7'-, 8-, and 8'-positions of the epoxylignanes). Among the 9,9'-position-modified derivatives, the dehydroxy derivatives showed the highest potency. These results suggested that the plant growth inhibitory activity should be influenced by the structure of the epoxylignanes.

  DOI：

  10.1021/jf4046396

文献信息

• Glycosides from the bark of<i>Machilus robusta</i>
  作者：Peng-Bin Bu、Yan-Ru Li、Ming Jiang、Fang Wang、Xiao-Liang Wang、Sheng Lin、Cheng-Gen Zhu、Jian-Gong Shi

  DOI：10.1080/10286020.2013.785530

  日期：2013.5

  Six new glycosidic constituents (1–6), together with 10 known analogs, have been isolated from the bark of Machilus robusta. Structures of the new compounds, including the absolute configurations, were determined by spectroscopic and chemical methods as ( − )-nectandrin B-β-d-glucopyranoside (1), ( − )-(7R,7′R,8S,8′R)-4,4′-dihydroxy-3,3′-dimethoxy-7,7′-epoxylignan-4-O-β-d-glucopyranoside (2), ( − )-(7R

  六个新的糖苷组分（1 - 6），用10个已知类似物一起，已经从树皮中分离润罗布斯塔。（ - ）的新化合物的结构，包括绝对构型，通过光谱和化学方法作为确定-nectandrin B-β- d吡喃葡萄糖苷（1），（ - ） - （7 - [R，7' - [R，8小号， 8' - [R）-4,4'-二羟基-3,3'-二甲氧基- 7,7'- epoxylignan -4- ö -β- d吡喃葡萄糖苷（2），（ - ） - （7 - [R，7' - [R，8 S，8′R）-4,4'-二羟基-3,3'-二甲氧基- 7,7'- epoxylignan -4'- ö -β- d吡喃葡萄糖苷（3），（ - ） - （8小号，8' - [R ） - 4,4'-二羟基-3,3'，5'- trimethoxylignan -4'- ö -β- d吡喃葡萄糖苷（4），（ - ） - （7 - [R，8 - [R）-syringylglycerol
• Synthesis of All Stereoisomers of 3,3′-Dimethoxy-7,7′-epoxylignane-4,4′-diol and Their Plant Growth Inhibitory Activity
  作者：Hisashi Nishiwaki、Kumiko Nakayama、Yoshihiro Shuto、Satoshi Yamauchi

  DOI：10.1021/jf4046396

  日期：2014.1.22

  All stereoisomers of 3,3'-dimethoxy-7,7'-epoxylignane-4,4'-diol were synthesized to examine the effect of stereochemistry on their plant growth inhibitory activity using lettuce and Italian ryegrass. The effect of structural modifications such as dehydroxylation, methoxylation and hydroxylation at the 9- and 9'-positions of the lignans on the activity was also studied. Most of the epoxylignanes showed higher plant growth inhibitory potency against ryegrass than against lettuce, and the inhibitory activity varied depending on the configurations of each position of the tetrahydrofuran ring (7-, 7'-, 8-, and 8'-positions of the epoxylignanes). Among the 9,9'-position-modified derivatives, the dehydroxy derivatives showed the highest potency. These results suggested that the plant growth inhibitory activity should be influenced by the structure of the epoxylignanes.