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N-(4-methylpentyl)methanesulfonamide

中文名称
——
中文别名
——
英文名称
N-(4-methylpentyl)methanesulfonamide
英文别名
——
N-(4-methylpentyl)methanesulfonamide化学式
CAS
——
化学式
C7H17NO2S
mdl
——
分子量
179.28
InChiKey
RXHYOLUFHIGPDN-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):
    1.4
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    54.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • BENZIMIDAZOLE AND IMADAZOPYRIDINE CARBOXIMIDAMIDE COMPOUNDS
    申请人:Gilead Sciences, Inc.
    公开号:US20160333009A1
    公开(公告)日:2016-11-17
    The present disclosure provides indoleamine 2,3-dioxygenase 1 (IDOL) inhibitors of Formula I: or pharmaceutically acceptable salts thereof, in which X, L, n, m, R 1 , R 2a , R 2b , R n , R m , and R t are as defined herein, as well as pharmaceutical compositions that include a compound of Formula I, or pharmaceutically acceptable salts thereof, and methods of using the same to treat conditions mediated by IDO1.
    本公开提供了式I的吲哌酮2,3-二氧化酶1(IDOL)抑制剂: 或其药学上可接受的盐,其中X、L、n、m、R 1 、R 2a 、R 2b 、R n 、R m 和R t 如本文所定义,以及包括式I化合物的药物组合物,或其药学上可接受的盐,并使用这些方法来治疗由IDO1介导的疾病。
  • AZA-benzothiophenyl compounds and methods of use
    申请人:Savy Pierre Pascal
    公开号:US20080081821A1
    公开(公告)日:2008-04-03
    The invention relates to azabenzothiophenyl compounds of Formula I with anti-cancer and/or anti-inflammatory activity and more specifically to azabenzothiophenyl compounds which inhibit MEK kinase activity. The invention provides compositions and methods useful for inhibiting abnormal cell growth or treating a hyperproliferative disorder, or treating an inflammatory disease in a mammal. The invention also relates to methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
    本发明涉及一种具有抗癌和/或抗炎活性的Formula I的氮杂苯并噻吩化合物,更具体地,涉及一种抑制MEK激酶活性的氮杂苯并噻吩化合物。本发明提供了用于抑制异常细胞生长或治疗哺乳动物的增殖性疾病或治疗炎症性疾病的组合物和方法。本发明还涉及使用该化合物进行哺乳动物细胞的体外、原位和体内诊断或治疗,或相关病理条件的方法。
  • Aza-benzofuranyl compounds and methods of use
    申请人:Savy Pierre Pascal
    公开号:US20080085886A1
    公开(公告)日:2008-04-10
    The invention relates to azabenzofuranyl compounds of Formula I with anti-cancer and/or anti-inflammatory activity and more specifically to azabenzofuranyl compounds which inhibit MEK kinase activity. The invention provides compositions and methods useful for inhibiting abnormal cell growth or treating a hyperproliferative disorder, or treating an inflammatory disease in a mammal. The invention also relates to methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
    本发明涉及具有抗癌和/或抗炎活性的Formula I的氮杂苯并呋喃化合物,更具体地涉及抑制MEK激酶活性的氮杂苯并呋喃化合物。本发明提供了用于抑制异常细胞生长或治疗哺乳动物的增生性疾病或治疗炎症性疾病的组合物和方法。本发明还涉及使用该化合物进行哺乳动物细胞的体外、原位和体内诊断或治疗,或相关病理条件的方法。
  • AZA-INDOLYL COMPOUNDS AND METHODS OF USE
    申请人:Goodacre Simon Charles
    公开号:US20080242655A1
    公开(公告)日:2008-10-02
    The invention relates to azaindolyl compounds of Formula I with anti-cancer and/or anti-inflammatory activity and more specifically to azaindolyl compounds which inhibit MEK kinase activity. The invention provides compositions and methods useful for inhibiting abnormal cell growth or treating a hyperproliferative disorder, or treating an inflammatory disease in a mammal. The invention also relates to methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
    本发明涉及具有抗癌和/或抗炎活性的Formula I的吡唑吲哚类化合物,更具体地涉及抑制MEK激酶活性的吡唑吲哚类化合物。本发明提供了用于抑制异常细胞生长或治疗哺乳动物的增生性疾病或治疗炎症性疾病的组合物和方法。本发明还涉及使用该化合物进行哺乳动物细胞的体外、原位和体内诊断或治疗,或相关病理条件的方法。
  • BENZIMIDAZOLE RESPIRATORY SYNCYTIAL VIRUS INHIBITORS
    申请人:Cooymans Ludwig Paul
    公开号:US20130267508A1
    公开(公告)日:2013-10-10
    Benzimidazoles having inhibitory activity on RSV replication and having the formula the prodrugs, N-oxides, addition salts, quaternary amines, metal complexes and stereochemically isomeric forms thereof, compositions containing these compounds as active ingredient and processes for preparing these compounds and compositions.
    若干苯并咪唑化合物具有抑制RSV复制的活性,其化学式为,其前药、N-氧化物、加合盐、季盐、属配合物及其立体化学异构体形式,含有这些化合物作为活性成分的组合物以及制备这些化合物和组合物的方法。
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