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N-benzylnorcodeine methanesulfonate | 130727-25-2

中文名称
——
中文别名
——
英文名称
N-benzylnorcodeine methanesulfonate
英文别名
——
N-benzylnorcodeine methanesulfonate化学式
CAS
130727-25-2
化学式
CH4O3S*C24H25NO3
mdl
——
分子量
471.574
InChiKey
GRSGJQWTAPYVMC-ZKGMEJJTSA-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

  • 作为反应物:
    描述:
    N-benzylnorcodeine methanesulfonate甲烷磺酸 作用下, 反应 1.0h, 生成 (R)-N-benzylnorapocodeine
    参考文献:
    名称:
    (R)- and (S)-enantiomers of 11-hydroxy- and 10,11-dihydroxy-N-allylnoraporphine: synthesis and affinity for dopamine receptors in rat brain tissue
    摘要:
    The R-(-)- and S-(+)-enantiomers of 11-hydroxy-N-allyl (4), and 10,11-dihydroxy-N-allyl (3) congeners of 11-hydroxy-N-n-propylnoraporphine (11-OH-NPa, 2) or N-n-propylnorapomorphine (NPA, 1) were synthesized. Binding affinity of these compounds at dopamine (DA) receptor sites was evaluated with a membrane preparation of corpus striatum from rat brain. The R/S enantiomeric receptor affinity ratio was enhanced by allylic substitution of 3 and 4 and their R isomers had high DA receptor affinity similar to that of the N-n-propyl congeners. These N-allylaporphines are proposed as useful precursors to the preparation of their tritiated N-n-propyl enantiomers.
    DOI:
    10.1021/jm00105a005
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