(E,4R)-4-hydroxy-4,5,5-trimethyl-3-(3-oxobut-1-enyl)cyclohex-2-enone | 1416779-56-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (E,4R)-4-hydroxy-4,5,5-trimethyl-3-(3-oxobut-1-enyl)cyclohex-2-enone
• 英文别名: (4R)-4-hydroxy-4,5,5-trimethyl-3-[(E)-3-oxobut-1-enyl]cyclohex-2-en-1-one
• CAS: 1416779-56-0
• 化学式: C₁₃H₁₈O₃
• 分子量: 222.284
• InChiKey: INWVNVRZQKDXQG-GFUIURDCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  54.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (R)-(+)-α-甲氧基-α-(三氟甲基)苯乙酸 、 (E,4R)-4-hydroxy-4,5,5-trimethyl-3-(3-oxobut-1-enyl)cyclohex-2-enone 以 氘代吡啶 为溶剂， 反应 24.0h， 生成
  参考文献：
  名称：

  Two new compounds from Senecio cannabifolius

  摘要：

  Chemical investigation of the water extracts from the Senecio cannabifolius Less. led us to find two new compounds (1 and 2), along with 12 known compounds (3-14). The two new compounds were determined as (E, 4R)-4-hydroxy-4,5,5-trimethyl-3-(3-oxobut-1-enyl)cyclohex-2-enone (1) and (E)-4-((1S, 3R, 4R)-1-hydroxy-4,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)but-1-en-3-o-ne (2), respectively. The structures of other compounds were elucidated by extensive analysis of spectral data and in comparison with the literature values. Compounds 1 and 2 were evaluated for inhibitory activity against lipopolysaccharide-induced NO production in RAW 264.7 macrophages, and compound 1 showed potent inhibitory activity with IC50 value of 30.65 mu M.

  DOI：

  10.1080/10286020.2012.697456