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| 1198398-18-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1198398-18-3
化学式
C33H34ClF2NO4SSi
mdl
——
分子量
642.239
InChiKey
UQLZKPHAIJLLJD-NSJVFKKDSA-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:
    四丁基氟化铵 作用下, 生成 [(3S,5R)-4-(4-chlorophenyl)sulfonyl-5-(3,5-difluorophenyl)morpholin-3-yl]methanol
    参考文献:
    名称:
    Novel orally active morpholine N-arylsulfonamides γ-secretase inhibitors with low CYP 3A4 liability
    摘要:
    A new class of 2,6-disubstituted morpholine N-arylsulfonamide gamma-secretase inhibitors was designed based on the introduction of a morpholine core in lieu or piperidine in our lead series. This resulted in compounds with improved CYP 3A4 profiles. Several analogs that were active at lowering Ab levels in Tg CRND8 mice upon oral administration were identified. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.09.055
  • 作为产物:
    描述:
    三苯基膦偶氮二甲酸二乙酯 作用下, 生成
    参考文献:
    名称:
    Novel orally active morpholine N-arylsulfonamides γ-secretase inhibitors with low CYP 3A4 liability
    摘要:
    A new class of 2,6-disubstituted morpholine N-arylsulfonamide gamma-secretase inhibitors was designed based on the introduction of a morpholine core in lieu or piperidine in our lead series. This resulted in compounds with improved CYP 3A4 profiles. Several analogs that were active at lowering Ab levels in Tg CRND8 mice upon oral administration were identified. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.09.055
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