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5-Dibenzofuran-2-yl-2-(oxalyl-amino)-thiophene-3-carboxylic acid | 243985-33-3

中文名称
——
中文别名
——
英文名称
5-Dibenzofuran-2-yl-2-(oxalyl-amino)-thiophene-3-carboxylic acid
英文别名
5-Dibenzofuran-2-yl-2-(oxaloamino)thiophene-3-carboxylic acid
5-Dibenzofuran-2-yl-2-(oxalyl-amino)-thiophene-3-carboxylic acid化学式
CAS
243985-33-3
化学式
C19H11NO6S
mdl
——
分子量
381.365
InChiKey
WZYOJPJKQZTLGI-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):
    4.6
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    145
  • 氢给体数:
    3
  • 氢受体数:
    7

文献信息

  • MODULATORS OF PROTEIN TYROSINE PHOSPHATASES (PTPASES)
    申请人:——
    公开号:US20020002199A1
    公开(公告)日:2002-01-03
    The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTP&agr;, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.
    本发明提供了新型化合物、新型组合物、它们的使用方法以及制备方法,其中这些化合物是药理学上有用的蛋白酪氨酸磷酸酶(PTPase's)抑制剂,例如PTP1B、CD45、SHP-1、SHP-2、PTP&agr;、LAR和HePTP等。这些化合物在治疗I型糖尿病、II型糖尿病、糖耐量受损、胰岛素抵抗、肥胖症、免疫功能障碍(包括凝血系统功能失调的自身免疫性疾病)、过敏性疾病(包括哮喘)、骨质疏松症、增生性疾病(包括癌症和牛皮癣)、合成或效应减少或增加的生长激素相关疾病、合成或反应减少或增加的调节生长激素释放或反应的激素或细胞因子相关疾病、包括阿尔茨海默病和精神分裂症在内的脑部疾病以及传染病治疗中有用。
  • Substituted thiophene compounds as modulators of protein tyrosine phosphatases (PTPases)
    申请人:Jeppesen Lone
    公开号:US20050119332A1
    公开(公告)日:2005-06-02
    The present invention provides novel compounds of formula 1a, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.
    本发明提供了1a式新化合物、新组合物、其使用方法和制备方法,其中这些化合物是药理学上有用的蛋白酪氨酸磷酸酶(PTPase's)抑制剂,如PTP1B、CD45、SHP-1、SHP-2、PTPα、LAR和HePTP等。这些化合物在治疗I型糖尿病、II型糖尿病、受损的葡萄糖耐受性、胰岛素抵抗、肥胖症、免疫功能障碍,包括凝血系统功能障碍的自身免疫性疾病、过敏性疾病,包括哮喘、骨质疏松症,增生性疾病,包括癌症和屑病,合成或效果降低或增加的生长激素的疾病,合成调节释放或响应生长激素的激素或细胞因子的疾病,包括阿尔茨海默病和精神分裂症的大脑疾病,以及传染病方面具有用处。
  • Modulators of protein tyrosine phosphatases (PTPases)
    申请人:——
    公开号:US20020165398A1
    公开(公告)日:2002-11-07
    The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTP&agr;, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimers disease and schizophrenia, and infectious diseases.
    本发明提供了新型化合物、新型组合物、它们的使用方法和制造方法,其中这些化合物是药理学上有用的蛋白酪氨酸磷酸酶(PTPase's)抑制剂,如PTP1B、CD45、SHP-1、SHP-2、PTPα、LAR和HePTP等。这些化合物在治疗I型糖尿病、II型糖尿病、糖耐量受损、胰岛素抵抗、肥胖、免疫功能障碍(包括凝血系统功能障碍的自身免疫疾病)、过敏性疾病(包括哮喘)、骨质疏松症、增生性疾病(包括癌症和屑病)、合成生长激素的减少或增加、调节生长激素释放或响应的激素或细胞因子合成减少或增加的疾病以及包括阿尔茨海默病和精神分裂症在内的脑部疾病和传染性疾病的治疗中是有用的。
  • [EN] MODULATORS OF PROTEIN TYROSINE PHOSPHATASES (PTPASES)<br/>[FR] MODULATEURS DE PROTEINE TYROSINE PHOSPHATASES (PTPASES)
    申请人:NOVO NORDISK A/S
    公开号:WO1999046244A1
    公开(公告)日:1999-09-16
    (EN) The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTP$g(a), LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.(FR) L'invention concerne de nouveaux composés, de nouvelles compositions, des méthodes d'utilisation et des méthodes de fabrication associées. Lesdits composés sont des inhibiteurs de protéine tyrosine phosphatases (PTPases) pharmacologiquement utiles, tels que PTP1B, CD45, SHP-1, SHP-2, PTP$g(a), LAR et HePTP ou analogues. Ces composés sont utiles dans le traitement du diabète du type I, du diabète du type II, de l'intolérance au glucose, de la résistance insulinique, de l'obésité, des dysfonctionnements immunitaires parmi lesquels les maladies auto-immunes entraînant un dysfonctionnement du système de coagulation, des maladies allergiques parmi lesquelles l'asthme, de l'ostéoporose, des troubles proliférants parmi lesquels le cancer et le psoriasis, des maladies entraînant une baisse ou une augmentation de la synthèse ou des effets des hormones de croissance, des maladies entraînant une baisse ou une augmentation de la synthèse des hormones ou cytokines qui régulent la libération d'hormones de croissance ou la réaction à ces hormones, des maladies cérébrales parmi lesquelles la maladie d'Alzheimer et la schizophrénie, et des maladies infectieuses.
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