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6-epi-notoamide R | 1429428-87-4

中文名称
——
中文别名
——
英文名称
6-epi-notoamide R
英文别名
(1R,2S,17R,19S)-2-hydroxy-9,9,16,16-tetramethyl-8-oxa-14,23,25-triazaheptacyclo[17.5.2.01,17.03,15.04,13.07,12.019,23]hexacosa-3(15),4(13),5,7(12),10-pentaene-24,26-dione
6-epi-notoamide R化学式
CAS
1429428-87-4
化学式
C26H29N3O4
mdl
——
分子量
447.534
InChiKey
BKNDRWLBSMZASB-GNXRHVIQSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    33
  • 可旋转键数:
    0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    94.7
  • 氢给体数:
    3
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    甲醇N-hydroxy-6-epi-stephacidin A二甲基亚砜 为溶剂, 反应 72.0h, 以7.1%的产率得到6-epi-avrainvillamide
    参考文献:
    名称:
    Isolation and Photoinduced Conversion of 6-epi-Stephacidins from Aspergillus taichungensis
    摘要:
    Three prenylated indole alkaloids with a rare anti bicyclo-[2.2.2]diazaoctane core ring (5-7) were isolated from Aspergillus taichungensis. The structures including absolute configurations were elucidated based on NMR, X-ray, and CD methods. (+)-Versicolamides B and C (8-9) which contain a spiro-center, together with seven analogues (7, 10-15), were isolated as photoinduced conversion products of 6. Biological evaluation indicated that 6 and 7 exhibited significant cytotoxicities with IC50 values in the low micromolar range.
    DOI:
    10.1021/ol400694h
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文献信息

  • Isolation and Photoinduced Conversion of 6-<i>epi</i>-Stephacidins from <i>Aspergillus taichungensis</i>
    作者:Shengxin Cai、Yepeng Luan、Xianglan Kong、Tianjiao Zhu、Qianqun Gu、Dehai Li
    DOI:10.1021/ol400694h
    日期:2013.5.3
    Three prenylated indole alkaloids with a rare anti bicyclo-[2.2.2]diazaoctane core ring (5-7) were isolated from Aspergillus taichungensis. The structures including absolute configurations were elucidated based on NMR, X-ray, and CD methods. (+)-Versicolamides B and C (8-9) which contain a spiro-center, together with seven analogues (7, 10-15), were isolated as photoinduced conversion products of 6. Biological evaluation indicated that 6 and 7 exhibited significant cytotoxicities with IC50 values in the low micromolar range.
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