290821-39-5

• 常用中文名：Cimiracemoside D
• 常用英文名：CiMiraceMoside D
• CAS号：290821-39-5
• 分子式：C₃₇H₅₈O₁₁
• 分子量：678.850
• 相关类别： 研究领域 其他
• 发布时间：2019-01-30 10:31:19
• 更新时间：2026-07-16 17:13:00
• Cimiracemoside D是黑升麻植物提取的天然化合物，活性背景未知。

名称

• 中文名: 乙酰升麻新醇-3-O-α-L-阿拉伯糖苷
• 英文名: cimiracemoside D
• 中文别名: 12Β-O-乙酰升麻醇-3-O-Α-L-吡喃阿拉伯糖苷; (2,4S,6,7,9R,9,9bR,10R,12R,13S,15R,15aS,15bR)-15-羟基-13-(2-羟基丙-2-基)-3,3,9a,10,15a-五甲基-4-(((2S,3R,4S,5S)-3,4,5-三羟基四氢-2H-吡喃-2-基)氧基)十八氢-7H-12,14a-环氧环丙并[1',8a']萘并[2',1':4,5]茚并[2,1-b]氧杂环庚-9-基 乙酸酯; CIMIRACEMOSIDE D 游离态; 乙酰升麻新醇-3-阿拉伯糖苷
• 英文别名: (2,4S,6,7,9R,9,9bR,10R,12R,13S,15R,15aS,15bR)-15-Hydroxy-13-(2-hydroxypropan-2-yl)-3,3,9a,10,15a-pentamethyl-4-(((2S,3R,4S,5S)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)octadecahydro-7H-12,14a-oxycyclopropa[1',8a']naphtho[2',1':4,5]indeno[2,1-b]oxin-9-yl acetate; α-L-Arabinopyranoside, (2S,4aR,5aR,7R,7aR,7bR,8R,10R,11S,13R,13aS,13bR,15aR)-7-(acetyloxy)heptadecahydro-13-hydroxy-11-(1-hydroxy-1-methylethyl)-1,1,7a,8,13a-pentamethyl-10,12a-epoxy-2H,5H-cyclopr opa[1',8'a]naphth[2',1':4,5]indeno[2,1-b]oxepin-2-yl; inhibit,Cimiracemoside D,Inhibitor; (3beta,12beta,15alpha,16alpha,23R,24S)-12-(Acetyloxy)-16,23:16,24-dioxy-15,25-dihydroxy-9,19-cyclolanostan-3-yl alpha-L-abinopyranoside; α-L-abinopyranoside, (3β,12β,15α,16α,23R,24S)-12-(acetyloxy)-16,23:16,24-dioxy-15,25-dihydroxy-9,19-cyclolanostan-3-yl; 12Β-ACETOXYCIMIGENOL-3-O-Α-L-ABINOPYRANSIDE; Cimiracemoside D, 10 mM in DMSO; CIMIRACEMOSIDE; (2R,3S,4R,7R,9S,12R,14R,16R,17R,18R,19R,21R,22S)-9-(α-L-Arabinopyranosyloxy)-2-hydroxy-22-(2-hydroxy-2-propanyl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0.0.0.0.0]tetracos-16-yl acetate; Cimiracemoside D, BR

物化性质

• 密度: 1.3±0.1 g/cm3
• 沸点: 773.3±60.0 °C at 760 mmHg
• 分子式: C₃₇H₅₈O₁₁
• 分子量: 678.850
• 闪点: 234.7±26.4 °C
• 精确质量: 678.397888
• PSA: 164.37000
• LogP: 5.18
• 蒸汽压: 0.0±6.0 mmHg at 25°C
• 折射率: 1.603
• 储存条件: -20°C

生物活性

• 描述: Cimiracemoside D是黑升麻植物提取的天然化合物,活性背景未知。
• 相关类别:
  信号通路 >> 其他 >> 其他
  研究领域 >> 其他
  天然产物 >> 类固醇
• 参考文献:

  [1]. Cicek SS, et al. Development of a fast and convenient method for the isolation of triterpene saponins from Actaea racemosa by high-speed countercurrent chromatography coupled with evaporative light scattering detection. Planta Med. 2010 Mar;76(5):467-73.

  [2]. Sun L, et al. New triterpene diglycosides from the rhizome of Cimifuga foetida. Molecules. 2008 Aug 13;13(8):1712-21.