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二正戊基亚砜 | 4253-99-0

中文名称
二正戊基亚砜
中文别名
——
英文名称
dipentyl sulfone
英文别名
1,1'-sulfonylbispentane;Pentyl sulfone;1-pentylsulfonylpentane
二正戊基亚砜化学式
CAS
4253-99-0
化学式
C10H22O2S
mdl
——
分子量
206.349
InChiKey
NLUGCAKOZAODBF-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):
    3.2
  • 重原子数:
    13
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    42.5
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2904100000

SDS

SDS:d9e8d151fb0fe39afb32997b5e462d54
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    1,1’-亚硫酰基二戊烷硫酸 作用下, 以 溶剂黄146 为溶剂, 生成 二正戊基亚砜
    参考文献:
    名称:
    Bhatta, D.; Behera, S. M.; Mohanty, S. R., Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical, 1987, vol. 26, # 9, p. 778 - 780
    摘要:
    DOI:
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文献信息

  • Compositions for Treatment of Cystic Fibrosis and Other Chronic Diseases
    申请人:Vertex Pharmaceuticals Incorporated
    公开号:US20150231142A1
    公开(公告)日:2015-08-20
    The present invention relates to pharmaceutical compositions comprising an inhibitor of epithelial sodium channel activity in combination with at least one ABC Transporter modulator compound of Formula A, Formula B, Formula C, or Formula D. The invention also relates to pharmaceutical formulations thereof, and to methods of using such compositions in the treatment of CFTR mediated diseases, particularly cystic fibrosis using the pharmaceutical combination compositions.
    本发明涉及含有上皮钠通道活性抑制剂与至少一种ABC转运蛋白调节剂化合物(A式、B式、C式或D式)的药物组合物。该发明还涉及这些药物配方,以及使用这些组合物治疗CFTR介导的疾病,特别是囊性纤维化的方法。
  • [EN] FARNESOID X RECEPTOR AGONISTS AND USES THEREOF<br/>[FR] AGONISTES DU RÉCEPTEUR FARNÉSOÏDE X ET LEURS UTILISATIONS
    申请人:METACRINE INC
    公开号:WO2018170166A1
    公开(公告)日:2018-09-20
    Described herein are compounds that are farnesoid X receptor agonists, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders associated with farnesoid X receptor activity.
    本文描述了一些是法尼索酸X受体激动剂的化合物,制备这类化合物的方法,包含这类化合物的药物组合物和药物,以及使用这类化合物治疗与法尼索酸X受体活性相关的疾病、疾病或紊乱的方法。
  • 5-arylsulfonyl indoles useful for treating disease
    申请人:——
    公开号:US20030060498A1
    公开(公告)日:2003-03-27
    The invention provides derivatives of 5-arylsulfonyl indole and 5-arylsulfonyl indoline compounds which may be in the form of pharmaceutical acceptable salts or compositions that are useful in treating central nervous system diseases such as anxiety and depression. The invention also includes intermediates and processes to make the compounds, isotopically-labeled forms of the compounds and the use of the isotopically labeled forms of the compounds to perform nuclear magnetic resonance imaging and positron emission tomography.
    这项发明提供了5-芳基磺酰基吲哚和5-芳基磺酰基吲哚啉化合物的衍生物,这些衍生物可以是药用可接受的盐或组合物的形式,对于治疗中枢神经系统疾病如焦虑和抑郁具有用处。该发明还包括制备这些化合物的中间体和过程,这些化合物的同位素标记形式以及利用这些化合物的同位素标记形式进行核磁共振成像和正电子发射断层扫描的用途。
  • COMPOSITIONS FOR TREATMENT OF CYSTIC FIBROSIS AND OTHER CHRONIC DISEASES
    申请人:Van Goor Fredrick F.
    公开号:US20110098311A1
    公开(公告)日:2011-04-28
    The present invention relates to pharmaceutical compositions comprising an inhibitor of epithelial sodium channel activity in combination with at least one ABC Transporter modulator compound of Formula A, Formula B, Formula C, or Formula D. The invention also relates to pharmaceutical formulations thereof, and to methods of using such compositions in the treatment of CFTR mediated diseases, particularly cystic fibrosis using the pharmaceutical combination compositions.
    本发明涉及包含上皮钠通道活性抑制剂与至少一种ABC转运蛋白调节剂化合物(A式、B式、C式或D式)的药物组合物。该发明还涉及这些药物配方,以及使用这些组合物治疗CFTR介导的疾病,特别是囊性纤维化的方法。
  • COMPOUNDS THAT MODULATE INTRACELLULAR CALCIUM
    申请人:Whitten Jeffrey P.
    公开号:US20110263612A1
    公开(公告)日:2011-10-27
    Described herein are compounds and pharmaceutical compositions containing such compounds, which modulate the activity of store-operated calcium (SOC) channels. Also described herein are methods of using such SOC channel modulators, alone and in combination with other compounds, for treating diseases or conditions that would benefit from inhibition of SOC channel activity.
    本文描述了含有这些化合物的化合物和药物组合物,这些化合物调节储存操作钙(SOC)通道的活性。本文还描述了使用这种SOC通道调节剂的方法,单独或与其他化合物结合,用于治疗需要抑制SOC通道活性的疾病或症状。
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