摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-methyl-N-trimethylsilyl-ethanesulfonamide | 163163-45-9

中文名称
——
中文别名
——
英文名称
N-methyl-N-trimethylsilyl-ethanesulfonamide
英文别名
N-methyl-N-trimethylsilylethanesulfonamide
N-methyl-N-trimethylsilyl-ethanesulfonamide化学式
CAS
163163-45-9
化学式
C6H17NO2SSi
mdl
——
分子量
195.358
InChiKey
YPNUCOGOQRPGOQ-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    0.0
  • 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

点击查看最新优质反应信息

文献信息

  • Sulfonamide-substituted benzopyran derivatives, processes for their
    申请人:Hoechst Marion Roussel Deutschland GmbH
    公开号:US06008245A1
    公开(公告)日:1999-12-28
    Sulfonamide-substituted benzopyran derivatives, processes for their preparation, their use as a medicament, and pharmaceutical preparations comprising them Compounds of the formula I ##STR1## having the meanings of the substituents indicated in the claims are outstandingly active substances for the production of medicaments for the prophylaxis and for the therapy of cardiovascular disorders, in particular arrhythmias, for the treatment of ulcers of the gastrointestinal region or for the treatment of diarrheal diseases.
    磺胺基取代的苯并吡喃衍生物,其制备方法,其作为药物的用途,以及包含它们的药物制剂。具有如下式I的化合物 ##STR1## 其中在索赔中指示的取代基的含义,是用于预防和治疗心血管疾病,特别是心律失常,用于治疗胃肠道溃疡或腹泻疾病的药物的杰出活性物质。
  • Sulfonamide-substituted fused 7-membered ring compounds, their use as a medicament, and pharmaceutical preparations comprising them
    申请人:Aventis Pharma Deutschland GmbH
    公开号:US06333349B1
    公开(公告)日:2001-12-25
    The present invention relates to compounds of formula I, in which X1, X2, X3, X4, Y1, Y2, Y3, Y4, R(3), R(4) and R(5) have the meanings mentioned in the specification, their preparation and their use, in particular in pharmaceuticals. The compounds effect the potassium channel or the IKs channel opened by cyclic adenosine monophosphate (cAMP) and are outstandingly suitable as pharmaceutical active compounds, for example for the prophylaxis and therapy of cardiovascular disorders, in particular arrhythmias, for the treatment of ulcers of the gastrointestinal region or for the treatment of diarrheal disorders.
    本发明涉及式I的化合物,其中X1、X2、X3、X4、Y1、Y2、Y3、Y4、R(3)、R(4)和R(5)具有规范中提到的含义,它们的制备和使用,尤其是在制药方面的应用。这些化合物影响由环磷酸腺苷(cAMP)打开的钾通道或IKs通道,并且非常适合作为药物活性化合物,例如用于心血管疾病的预防和治疗,尤其是心律失常,用于胃肠道溃疡的治疗或用于腹泻疾病的治疗。
  • Yang; Scherz; Bahinski, Journal of Pharmacology and Experimental Therapeutics, 2000, vol. 294, # 3, p. 955 - 962
    作者:Yang、Scherz、Bahinski、Bennett、Murray
    DOI:——
    日期:——
查看更多