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4-ethoxy-N-(2-{(2Z)-2-[1-(2-hydroxy-1-naphthyl)ethylidene]hydrazino}-2-oxoethyl)-N-(4-methylphenyl)benzenesulfonamide | 415964-15-7

中文名称
——
中文别名
——
英文名称
4-ethoxy-N-(2-{(2Z)-2-[1-(2-hydroxy-1-naphthyl)ethylidene]hydrazino}-2-oxoethyl)-N-(4-methylphenyl)benzenesulfonamide
英文别名
2-(N-(4-ethoxyphenyl)sulfonyl-4-methylanilino)-N-[(Z)-1-(2-hydroxynaphthalen-1-yl)ethylideneamino]acetamide
4-ethoxy-N-(2-{(2Z)-2-[1-(2-hydroxy-1-naphthyl)ethylidene]hydrazino}-2-oxoethyl)-N-(4-methylphenyl)benzenesulfonamide化学式
CAS
415964-15-7
化学式
C29H29N3O5S
mdl
——
分子量
531.632
InChiKey
FDSZMQJDKINTMD-OFWBYEQRSA-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):
    5.4
  • 重原子数:
    38
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    117
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • Pharmaceutically active sulfanilide derivatives
    申请人:——
    公开号:US20040072816A1
    公开(公告)日:2004-04-15
    The present invention relates to sulfanilide derivatives of formula (I), in which R 1 and R 2 are optionally substituted aryl and heteroaryl groups and the other variables are as defined in the claims, for use as pharmaceutically active compounds, as well as pharmaceutical formulations containing such sulfanilide derivatives. Said derivatives are useful in the treatment and/or prevention of preterm labor, premature birth, dysmenorrhea, inappropriate secretion of vasopressin, congestive heart failure, arterial hypertension, liver cirrhosis, nephrotic syndrome and ocular hypertension. In particular, the present invention is related to sulfanilide derivatives displaying a substantial modulatory, in particular antagonistic activity, of the oxytocin and/or vasopressin receptor. More preferably, said compounds are useful in the treatment and/or prevention of disease states mediated by oxytocin and/or vasopressin, including preterm labor, premature birth, dysmenorrhea, inappropriate secretion of vasopressin, congestive heart failure, arterial hypertension, liver cirrhosis, nephrotic syndrome and ocular hypertension. The present invention is furthermore related to novel sulfanilide derivatives as well as to methods of their preparation.
    本发明涉及式(I)的磺胺基苯酰胺衍生物,其中R1和R2是可选择取代的芳基和杂环芳基基团,其他变量如权利要求中所定义,用作药用活性化合物,以及含有这种磺胺基苯酰胺衍生物的药物配方。所述衍生物在治疗和/或预防早产、早产、痛经、抗利尿素分泌不当、充血性心力衰竭、动脉高血压、肝硬化、肾病综合征和眼压增高方面具有用途。具体而言,本发明涉及显示对催产素和/或抗利尿素受体具有显著调节作用,特别是拮抗活性的磺胺基苯酰胺衍生物。更具体地说,所述化合物在治疗和/或预防由催产素和/或抗利尿素介导的疾病状态方面具有用途,包括早产、早产、痛经、抗利尿素分泌不当、充血性心力衰竭、动脉高血压、肝硬化、肾病综合征和眼压增高。本发明还涉及新型磺胺基苯酰胺衍生物以及其制备方法。
  • [EN] PHARMACEUTICALLY ACTIVE SULFANILIDE DERIVATIVES<br/>[FR] DERIVES DE SULFANILIDE ACTIFS DU POINT DE VUE PHARMACEUTIQUE
    申请人:APPLIED RESEARCH SYSTEMS
    公开号:WO2002032864A1
    公开(公告)日:2002-04-25
    The present invention relates to sulfanilide derivatives of formula (I), in which R?1 and R2¿ are optionally substituted aryl and heteroaryl groups and the other variables are as defined in the claims, for use as pharmaceutically active compounds, as well as pharmaceutical formulations containing such sulfanilide derivatives. Said derivatives are useful in the treatment and/or prevention of preterm labor, premature birth, dysmenorrhea, inappropriate secretion of vasopressin, congestive heart failure, arterial hypertension, liver cirrhosis, nephrotic syndrome and ocular hypertension. In particular, the present invention is related to sulfanilide derivatives displaying a substantial modulatory, in particular antagonistic activity, of the oxytocin and/or vasopressin receptor. More preferably, said compounds are useful in the treatment and/or prevention of disease states mediated by oxytocin and/or vasopressin, including preterm labor, premature birth, dysmenorrhea, inappropriate secretion of vasopressin, congestive heart failure, arterial hypertension, liver cirrhosis, nephrotic syndrome and ocular hypertension. The present invention is furthermore related to novel sulfanilide derivatives as well as to methods of their preparation.
    本发明涉及公式(I)的磺胺基苯酰亚胺生物,其中R1和R2是可选取代的芳基和杂环芳基基团,其他变量如权利要求所定义,用作药物活性化合物,以及含有这种磺胺基苯酰亚胺生物的药物配方。所述衍生物在治疗和/或预防早产、早产、痛经、抗利尿激素不当分泌、充血性心力衰竭、动脉高血压、肝硬化、肾病综合征和眼压增高方面有用。特别是,本发明涉及显示 oxytocin 和/或 vasopressin 受体的实质性调节活性,特别是拮抗活性的磺胺基苯酰亚胺生物。更好地,这些化合物在治疗和/或预防由 oxytocin 和/或 vasopressin 介导的疾病状态方面有用,包括早产、早产、痛经、抗利尿激素不当分泌、充血性心力衰竭、动脉高血压、肝硬化、肾病综合征和眼压增高。本发明还涉及新的磺胺基苯酰亚胺生物以及它们的制备方法。
  • PHARMACEUTICALLY ACTIVE SULFANILIDE DERIVATIVES
    申请人:Applied Research Systems ARS Holding N.V.
    公开号:EP1335901A1
    公开(公告)日:2003-08-20
  • US7312358B2
    申请人:——
    公开号:US7312358B2
    公开(公告)日:2007-12-25
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