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5-cyano-N-[2-(2'-methanesulfonyl-3-methoxymethoxybiphenyl-4-yl)ethyl]-2-methoxybenzenesulfonamide | 409359-35-9

中文名称
——
中文别名
——
英文名称
5-cyano-N-[2-(2'-methanesulfonyl-3-methoxymethoxybiphenyl-4-yl)ethyl]-2-methoxybenzenesulfonamide
英文别名
5-cyano-2-methoxy-N-[2-[2-(methoxymethoxy)-4-(2-methylsulfonylphenyl)phenyl]ethyl]benzenesulfonamide
5-cyano-N-[2-(2'-methanesulfonyl-3-methoxymethoxybiphenyl-4-yl)ethyl]-2-methoxybenzenesulfonamide化学式
CAS
409359-35-9
化学式
C25H26N2O7S2
mdl
——
分子量
530.623
InChiKey
FTOOYRVVKBXWOP-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):
    3.3
  • 重原子数:
    36
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    149
  • 氢给体数:
    1
  • 氢受体数:
    9

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

点击查看最新优质反应信息

文献信息

  • 5-Amidino-2-hydroxybenzenesulfonamide derivatives, pharmaceutical compositions containing the same and intermediates for their preparation
    申请人:Okazaki Kosuke
    公开号:US20060116361A1
    公开(公告)日:2006-06-01
    The present invention relates to a 5-amidino-2-hydroxybenzenesulfonamide derivative represented by the general formula: wherein R 1 is a hydrogen atom or an optionally substituted lower alkyl group; R 2 is a di(lower alkyl)amino group, a lower alkyl group, a cycloalkyl group, an optionally substituted aryl group, an optionally substituted heterocycloalkyl group, or an optionally substituted aromatic heterocyclic group; T is an oxygen atom, a sulfur atom, a sulfonyl group etc.; Q is a hydrogen atom or an optionally substituted lower alkyl group; and Z is a hydrogen atom, a hydroxy group etc., or a pharmaceutically acceptable salt thereof, which exert a potent and selective activated blood coagulation factor X inhibitory activity and is useful as an agent for the prevention or treatment of a disease occurred associating an activated blood coagulation factor X, a pharmaceutical composition comprising the same, a pharmaceutical use thereof and an intermediate thereof.
    本发明涉及一种由通式表示的5-酰胺基-2-羟基苯磺酰胺衍生物:其中,R1是氢原子或可选择取代的较低烷基基团;R2是二(较低烷基)氨基基团、较低烷基基团、环烷基团、可选择取代的芳基基团、可选择取代的杂环烷基基团或可选择取代的芳香族杂环基团;T是氧原子、硫原子、磺酰基等;Q是氢原子或可选择取代的较低烷基基团;Z是氢原子、羟基等,或其药学上可接受的盐,具有强效和选择性的活化血凝因子X抑制活性,可用作预防或治疗与活化血凝因子X相关的疾病的药物,包括该药物的制剂、药物用途和中间体。
  • Preventive or therapeutic agent for kidney disease
    申请人:Koizumi Takashi
    公开号:US20050107354A1
    公开(公告)日:2005-05-19
    The present invention relates to an agent for the prevention or treatment of a renal disease comprising as an active ingredient a 5-amidino-2-hydroxybenzenesulfonamide derivative represented by the general formula: wherein R 1 is a hydrogen atom or an optionally substituted alkyl group; R 2 is a dialkylamino group, an alkyl group, a cycloalkyl group, an optionally substituted aryl group etc.; T is an oxygen atom, a sulfur atom etc.; Q is a hydrogen atom or an optionally substituted alkyl group; and Z is a hydrogen atom, a hydroxy group etc., or a pharmaceutically acceptable salt thereof which has an inhibitory effect on mesangial cell proliferation and a decreasing effect on protein excretion in urine, and are useful for preventing or treating of various renal diseases such as IgA nephropathy, diabetic nephropathy, nephritic syndrome and the like.
    本发明涉及一种用于预防或治疗肾脏疾病的药剂,其包含作为活性成分的5-酰胺基-2-羟基苯磺酰胺衍生物,其表示为通式: 其中,R1是氢原子或可选取代的烷基基团;R2是二烷基氨基基团、烷基基团、环烷基团、可选取代的芳基基团等;T是氧原子、硫原子等;Q是氢原子或可选取代的烷基基团;Z是氢原子、羟基等,或其药学上可接受的盐,具有对系膜细胞增殖的抑制作用和对尿蛋白排泄的降低作用,适用于预防或治疗各种肾脏疾病,如IgA肾病、糖尿病肾病、肾炎综合症等。
  • Novel crystals of 5-hydroxycarbamimidoyl-2-hydroxybenzenesulfonamide derivative
    申请人:Mukaiyama Harunobu
    公开号:US20050143457A1
    公开(公告)日:2005-06-30
    The present invention provides a novel crystalline form of n-butyl[4-[2-[2-hydroxy-5-(N-hydroxycarbamimidoyl) benzenesulfonylamino]ethyl]-2′-methanesulfonyl-3-yloxy] acetate hydrochloride, pharmaceutical compositions containing the same and their uses, which exhibits excellent inhibitory activities against activated blood coagulation factor X, and is useful for the treatment or prevention of a tromboembolic disease.
    本发明提供了一种新的结晶形式的n-丁基[4-[2-[2-羟基-5-(N-羟基甲酰基)苯磺酰胺乙基]-2'-甲磺酰基-3-氧基]乙酸盐酸盐,以及包含该物质的制药组合物及其用途,该物质对活化的血凝血因子X具有出色的抑制活性,可用于治疗或预防血栓栓塞性疾病。
  • Crystals of 5-hydroxycarbamimidoyl-2-hydroxybenzenesulfonamide derivative
    申请人:Kissei Pharmaceutical Co., Ltd.
    公开号:US07256215B2
    公开(公告)日:2007-08-14
    The present invention provides a novel crystalline form of n-butyl[4-[2-[2-hydroxy-5-(N-hydroxycarbamimidoyl) benzenesulfonylamino]ethyl]-2′-methanesulfonyl-3-yloxy] acetate hydrochloride, pharmaceutical compositions containing the same and their uses, which exhibits excellent inhibitory activities against activated blood coagulation factor X, and is useful for the treatment or prevention of a tromboembolic disease.
    本发明提供了一种新的n-丁基[4-[2-[2-羟基-5-(N-羟基氨基甲酰基)苯磺酰胺]乙基]-2'-甲磺酰基-3-氧基]乙酸盐酸盐的晶型、含有该晶型的制药组合物及其用途,该晶型对活化的血凝血因子X具有优异的抑制活性,可用于治疗或预防血栓栓塞性疾病。
  • 5-amidino-2-hydroxybenzenesulfonamide derivatives, pharmaceutical compositions containing the same and intermediates for their preparation
    申请人:Kissei Pharmaceutical Co., Ltd.
    公开号:US07208524B2
    公开(公告)日:2007-04-24
    The present invention relates to a 5-amidino-2-hydroxybenzenesulfonamide derivative represented by the general formula: wherein R1 is a hydrogen atom or an optionally substituted lower alkyl group; R2 is a di(lower alkyl)amino group, a lower alkyl group, a cycloalkyl group, an optionally substituted aryl group, an optionally substituted heterocycloalkyl group, or an optionally substituted aromatic heterocyclic group; T is an oxygen atom, a sulfur atom, a sulfonyl group etc.; Q is a hydrogen atom or an optionally substituted lower alkyl group; and Z is a hydrogen atom, a hydroxy group etc., or a pharmaceutically acceptable salt thereof, which exert a potent and selective activated blood coagulation factor X inhibitory activity and is useful as an agent for the prevention or treatment of a disease occurred associating an activated blood coagulation factor X, a pharmaceutical composition comprising the same, a pharmaceutical use thereof and an intermediate thereof.
    本发明涉及一种5-酰胺基-2-羟基苯磺酰胺衍生物,其通式表示为:其中,R1是氢原子或者可选取代的低碳基团;R2是二(低碳基)氨基团、低碳基团、环烷基团、可选取代的芳基团、可选取代的杂环烷基团或者可选取代的芳香族杂环基团;T是氧原子、硫原子、磺酰基等;Q是氢原子或者可选取代的低碳基团;Z是氢原子、羟基等,或其药学上可接受的盐。该化合物具有强效和选择性的激活血凝因子X抑制活性,可用作防治与激活血凝因子X相关的疾病的药物,以及其制剂、药用和中间体。
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