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1,4,5-trimethyl-1H-pyrrole-2-carboxylic acid | 1071432-30-8

中文名称
——
中文别名
——
英文名称
1,4,5-trimethyl-1H-pyrrole-2-carboxylic acid
英文别名
1,4,5-trimethylpyrrole-2-carboxylic acid
1,4,5-trimethyl-1H-pyrrole-2-carboxylic acid化学式
CAS
1071432-30-8
化学式
C8H11NO2
mdl
——
分子量
153.181
InChiKey
VNBZZIUAYRGKGP-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):
    1.3
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    42.2
  • 氢给体数:
    1
  • 氢受体数:
    2

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

  • 作为产物:
    描述:
    ethyl 5-hydroxymethyl-1,4-dimethyl-1H-pyrrole-2-carboxylate 在 palladium-carbon 氢气四氢呋喃sodium hydroxide乙醚盐酸 、 ice 、 作用下, 以 乙醇 为溶剂, 反应 314.0h, 以to obtain 1,4,5-trimethyl-1H-pyrrole-2-carboxylic acid (0.79 g)的产率得到1,4,5-trimethyl-1H-pyrrole-2-carboxylic acid
    参考文献:
    名称:
    Ornithine derivative
    摘要:
    提供的是一种化合物,可用作慢性肾功能不全的治疗剂和糖尿病肾病的治疗剂。本发明人对具有对抗EP4受体作用的鸟氨酸衍生物进行了广泛的研究,结果发现通过在化合物的鸟氨酸部分的C末端引入环状烷基,可以改善其物理化学性质,例如溶解度等,从而赋予其更优越的药物特性。因此,他们完成了本发明。本发明的化合物显示出良好的对抗EP4受体的作用,因此可用作慢性肾功能不全和糖尿病肾病的治疗剂。
    公开号:
    US08030489B2
点击查看最新优质反应信息

文献信息

  • ORNITHINE DERIVATIVE
    申请人:Astellas Pharma Inc.
    公开号:EP2141147A1
    公开(公告)日:2010-01-06
    Provided is a compound which is useful as a therapeutic agent for chronic renal insufficiency and a therapeutic agent for diabetic nephropathy. The present inventors have made extensive studies on an ornithine derivative having an antagonistic action against an EP4 receptor, and as a result, they have found that by introducing cycloalkanediyl at a C terminal of the ornithine part of the compound of the present invention, the physicochemical properties such as solubility, and the like can be improved, thereby giving further preferred properties as a pharmaceutical. Therefore, they have completed the present invention. The compound of the present invention exhibits a good antagonistic action against an EP4 receptor, and thus, it is useful as a therapeutic agent for chronic renal insufficiency and diabetic nephropathy.
    提供了一种化合物,可用作慢性肾功能不全的治疗剂和糖尿病肾病的治疗剂。目前的发明人对具有对EP4受体拮抗作用的鸟氨酸衍生物进行了广泛研究,结果发现通过在目前发明的化合物的鸟氨酸部分的C末端引入环烷基,可以改善物理化学性质,如溶解性等,从而赋予其作为药物的更优越性质。因此,他们完成了这项发明。目前发明的化合物对EP4受体表现出良好的拮抗作用,因此,它可用作慢性肾功能不全和糖尿病肾病的治疗剂。
  • MONOMER AND MULTIMERIC ANTI-HBV AGENTS
    申请人:Emory University
    公开号:EP3860991A1
    公开(公告)日:2021-08-11
  • US8030489B2
    申请人:——
    公开号:US8030489B2
    公开(公告)日:2011-10-04
  • [EN] MONOMER AND MULTIMERIC ANTI-HBV AGENTS<br/>[FR] AGENTS ANTI-VHB MONOMÈRES ET MULTIMÈRES
    申请人:UNIV EMORY
    公开号:WO2020072955A1
    公开(公告)日:2020-04-09
    The present invention is directed to compounds, compositions and methods for preventing, treating or curing hepatitis B (HBV) infection in human subjects or other animal hosts. The compounds are as also pharmaceutically acceptable, salts, prodrugs, and other derivatives thereof as pharmaceutical compositions and methods for treatment, prevention or eradication of HBV infection.
  • Ornithine derivative
    申请人:Astellas Pharma Inc.
    公开号:US08030489B2
    公开(公告)日:2011-10-04
    Provided is a compound which is useful as a therapeutic agent for chronic renal insufficiency and a therapeutic agent for diabetic nephropathy. The present inventors have made extensive studies on an ornithine derivative having an antagonistic action against an EP4 receptor, and as a result, they have found that by introducing cycloalkanediyl at a C terminal of the ornithine part of the compound of the present invention, the physicochemical properties such as solubility, and the like can be improved, thereby giving further preferred properties as a pharmaceutical. Therefore, they have completed the present invention. The compound of the present invention exhibits a good antagonistic action against an EP4 receptor, and thus, it is useful as a therapeutic agent for chronic renal insufficiency and diabetic nephropathy.
    提供的是一种化合物,可用作慢性肾功能不全的治疗剂和糖尿病肾病的治疗剂。本发明人对具有对抗EP4受体作用的鸟氨酸衍生物进行了广泛的研究,结果发现通过在化合物的鸟氨酸部分的C末端引入环状烷基,可以改善其物理化学性质,例如溶解度等,从而赋予其更优越的药物特性。因此,他们完成了本发明。本发明的化合物显示出良好的对抗EP4受体的作用,因此可用作慢性肾功能不全和糖尿病肾病的治疗剂。
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