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N-Methansulfonyl-cis-2,6-dimethyl-piperidin | 20722-54-7

中文名称
——
中文别名
——
英文名称
N-Methansulfonyl-cis-2,6-dimethyl-piperidin
英文别名
cis-2,6-dimethyl-1-methylsulfonylpiperidine;cis-2,6-Dimethyl-1-methyl sulfonyl piperidine;(2S,6R)-2,6-dimethyl-1-methylsulfonylpiperidine
N-Methansulfonyl-cis-2,6-dimethyl-piperidin化学式
CAS
20722-54-7
化学式
C8H17NO2S
mdl
——
分子量
191.294
InChiKey
NDRNIFSBRLCSCZ-OCAPTIKFSA-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):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    45.8
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    甲基磺酰氯(2R,6S)-2,6-dimethylpiperidine三乙胺 作用下, 以 二氯甲烷 为溶剂, 以82%的产率得到N-Methansulfonyl-cis-2,6-dimethyl-piperidin
    参考文献:
    名称:
    Active site directed docking studies: Synthesis and pharmacological evaluation of cis-2,6-dimethyl piperidine sulfonamides as inhibitors of acetylcholinesterase
    摘要:
    Hypocholinergic function associated with Alzheimer's disease (AD) is well-accepted hypothesis, in this regard, many research attempts have been made to elevate the reduced cholinergic neurotransmission, among them two main treatment strategies were widely explored, namely stimulation of muscarinic receptor 1 and/or reversible inhibition of acetylcholinesterase (AChE) enzyme. In an attempt to improve the efficacy and to minimize general side effects of these ACNE inhibitors, many lead molecules are developed in research; one among them is piperidine derivative. Donazepil is a widely prescribed ACNE inhibitor which displays a piperidine ring in its structure. In the present study, we have docked cis-2,6-dimethyl piperidine sulfonamides (3a-i) on ACNE enzyme and synthesized by nucleophilic substitution reaction between cis-2,6-dimethyl piperidine and alkyl/aryl sulfonyl chlorides in the presence of triethylamine. These piperidine sulfonamides were subjected to in vitro AChE enzyme inhibition studies and in vivo antiamnesic study to reverse scopolamine induced memory loss in rats. Two derivatives (3a and f) in this class of piperidines (3a-i) showed considerable inhibition against different sources of ACNE in vitro and reduced average number of mistakes done by wistar rats as compared to scopolamine treated group in vivo (rodent memory evaluation). (C) 2009 Published by Elsevier Masson SAS.
    DOI:
    10.1016/j.ejmech.2009.04.042
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