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2-hydroxypyrrole-3-acetic acid ethyl ester | 740839-23-0

中文名称
——
中文别名
——
英文名称
2-hydroxypyrrole-3-acetic acid ethyl ester
英文别名
ethyl 2-(2-hydroxy-1H-pyrrol-3-yl)acetate
2-hydroxypyrrole-3-acetic acid ethyl ester化学式
CAS
740839-23-0
化学式
C8H11NO3
mdl
——
分子量
169.18
InChiKey
JZASETZSNMHSJE-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):
    0.8
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    62.3
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

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文献信息

  • 2-Aryl-acetic acids, their derivatives and pharmaceutical compositions containing them
    申请人:Moriconi Alessio
    公开号:US20060223842A1
    公开(公告)日:2006-10-05
    Selected 2-arylacetic acids, their derivatives and pharmaceutical compositions that contain these compounds are useful in inhibiting chemotactic activation of neutrophils (PMN leukocytes) induced by the interaction of Interleukin-8 (IL-8) with CXCR1 and CXCR2-membrane receptors. The compounds are used for the prevention and treatment of pathologies deriving from said activation. In particular, 2(ortho)-substituted arylacetic acids or their derivatives, such as amides and sulfonamides, lack cyclo-oxygenase inhibition activity and are particularly useful in the treatment of neutrophil-dependent pathologies such as psoriasis, ulcerative colitis, melanoma, chronic obstructive pulmonary disease (COPD), bullous pemphigoid, rheumatoid arthritis, idiopathic fibrosis, glomerulonephritis and in the prevention and treatment of damages caused by ischemia and reperfusion.
    选择的2-芳基乙酸及其衍生物和包含这些化合物的药物组合物对于抑制由白细胞介素-8(IL-8)与CXCR1和CXCR2膜受体相互作用引起的嗜中性粒细胞(PMN白细胞)趋化活化非常有用。这些化合物用于预防和治疗由该活化引起的病理。特别是2(邻)-取代芳基乙酸或其衍生物,例如酰胺和磺酰胺,缺乏环氧合酶抑制活性,特别适用于治疗嗜中性粒细胞依赖性病理,如银屑病、溃疡性结肠炎、黑色素瘤、慢性阻塞性肺疾病(COPD)、大疱性类天疱疮、类风湿性关节炎、特发性纤维化、肾小球肾炎以及缺血再灌注引起的损伤的预防和治疗。
  • 2-ARYL-ACETIC ACIDS, THEIR DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    申请人:MORICONI Alessio
    公开号:US20110195967A1
    公开(公告)日:2011-08-11
    Selected 2-arylacetic acids, their derivatives and pharmaceutical compositions that contain these compounds are useful in inhibiting chemotactic activation of neutrophils (PMN leukocytes) induced by the interaction of Interleukin-8 (IL-8) with CXCR1 and CXCR2 membrane receptors. The compounds are used for the prevention and treatment of pathologies deriving from their activation. In particular, 2(ortho)-substituted arylacetic acids or their derivatives, such as amides and sulfonamides, lack cyclo-oxygenase inhibition activity and are particularly useful in the treatment of neutrophil-dependent pathologies such as psoriasis, ulcerative colitis, melanoma, chronic obstructive pulmonary disease (COPD), bullous pemphigoid, rheumatoid arthritis, idiopathic fibrosis, glomerulonephritis and in the prevention and treatment of damages caused by ischemia and reperfusion.
    选定的2-芳基乙酸及其衍生物和包含这些化合物的制药组合物可用于抑制由白细胞介素8(IL-8)与CXCR1和CXCR2膜受体相互作用引起的中性粒细胞(PMN白细胞)的趋化激活。这些化合物用于预防和治疗由其激活引起的病理状况。特别是2-(邻)取代芳基乙酸或其衍生物,如酰胺和磺酰胺,缺乏环氧化酶抑制活性,特别适用于治疗中性粒细胞依赖性病理状况,如银屑病,溃疡性结肠炎,黑色素瘤,慢性阻塞性肺疾病(COPD),大疱性天疱病,类风湿性关节炎,特发性纤维化,肾小球肾炎以及预防和治疗缺血再灌注引起的损伤。
  • US7776909B2
    申请人:——
    公开号:US7776909B2
    公开(公告)日:2010-08-17
  • US8648110B2
    申请人:——
    公开号:US8648110B2
    公开(公告)日:2014-02-11
  • US8871784B2
    申请人:——
    公开号:US8871784B2
    公开(公告)日:2014-10-28
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