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7N,12N-dimethyldehydroaspidostomide D | 1609960-21-5

中文名称
——
中文别名
——
英文名称
7N,12N-dimethyldehydroaspidostomide D
英文别名
——
7N,12N-dimethyldehydroaspidostomide D化学式
CAS
1609960-21-5
化学式
C17H10Br5N3O
mdl
——
分子量
671.806
InChiKey
PUQKHQHDORHGNU-UHFFFAOYSA-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

反应信息

  • 作为产物:
    描述:
    aspidostomide D碘甲烷 在 sodium hydride 作用下, 以 二甲基亚砜 为溶剂, 反应 1.33h, 以60%的产率得到7N,12N-dimethyldehydroaspidostomide D
    参考文献:
    名称:
    Bromopyrrole Alkaloids Isolated from the Patagonian Bryozoan Aspidostoma giganteum
    摘要:
    Nine new bromopyrrole alkaloids, aspidostomides A-H and aspidazide A (1-9), were isolated from the Patagonian bryozoan Aspidostoma giganteum. Aspidostomides A-H have dibromotyrosine- or bromotryptophan-derived moieties forming either linear amides or pyrroloketopiperazine-type lactams with a bromopyrrole carboxylic acid as a common structural motif. On the other hand, aspidazide A is a rare asymmetric acyl azide formed by an N-N link of two different pyrroloketopiperazine lactams and is the first isolated compound of this class from marine invertebrates. This work is the first report of secondary metabolites isolated from a bryozoan from the Patagonian region. The structures of compounds 1-9 were elucidated by spectroscopic methods and chemical transformations. One of these compounds, aspidostomide E (5), was moderately active against the 786-O renal carcinoma cell line.
    DOI:
    10.1021/np500012y
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