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1,2,3,4-四氢喹啉-8-羧酸乙酯 | 118128-79-3

中文名称
1,2,3,4-四氢喹啉-8-羧酸乙酯
中文别名
——
英文名称
ethyl ester of 1,2,3,4-tetrahydroquinoline-8-carboxylic acid
英文别名
Ethyl 1,2,3,4-tetrahydroquinoline-8-carboxylate
1,2,3,4-四氢喹啉-8-羧酸乙酯化学式
CAS
118128-79-3
化学式
C12H15NO2
mdl
——
分子量
205.257
InChiKey
ARCBMLYSIMSYFQ-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):
    2.5
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    38.3
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:ace26c37b6be1d063ccd60748212faac
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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
  • 下游产品
    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

  • AMIDE COMPOUND
    申请人:Nozawa Eisuke
    公开号:US20110144153A1
    公开(公告)日:2011-06-16
    [Problems] A compound, which is useful as an active ingredient of a pharmaceutical composition, for example, a pharmaceutical composition for treating chronic renal failure and/or diabetic nephropathy, is provided. [Solving Means] The present inventors have conducted extensive studies on a compound having an EP4 receptor antagonistic activity, and confirmed that the amide compound of the present invention has an EP4 receptor antagonistic activity, thereby completing the present invention. The amide compound of the present invention has an EP4 receptor antagonistic activity, and can be used as an active ingredient of a pharmaceutical composition for preventing and/or treating various EP4-related diseases, for example, chronic renal failure and/or diabetic nephropathy, and the like.
    【问题】提供一种化合物,该化合物可用作药物组合物的活性成分,例如用于治疗慢性肾衰竭和/或糖尿病肾病的药物组合物。 【解决方法】本发明人对具有EP4受体拮抗活性的化合物进行了广泛的研究,并确认本发明的酰胺化合物具有EP4受体拮抗活性,从而完成了本发明。本发明的酰胺化合物具有EP4受体拮抗活性,可用作预防和/或治疗各种EP4相关疾病的药物组合物的活性成分,例如慢性肾衰竭和/或糖尿病肾病等。
  • Amide compound
    申请人:Nozawa Eisuke
    公开号:US08598355B2
    公开(公告)日:2013-12-03
    [Problems] A compound, which is useful as an active ingredient of a pharmaceutical composition, for example, a pharmaceutical composition for treating chronic renal failure and/or diabetic nephropathy, is provided. [Solving Means] The present inventors have conducted extensive studies on a compound having an EP4 receptor antagonistic activity, and confirmed that the amide compound of the present invention has an EP4 receptor antagonistic activity, thereby completing the present invention. The amide compound of the present invention has an EP4 receptor antagonistic activity, and can be used as an active ingredient of a pharmaceutical composition for preventing and/or treating various EP4-related diseases, for example, chronic renal failure and/or diabetic nephropathy, and the like.
    【问题】提供一种化合物,该化合物可用作药物组合物的活性成分,例如用于治疗慢性肾功能衰竭和/或糖尿病肾病的药物组合物。 【解决方法】本发明人对具有EP4受体拮抗活性的化合物进行了广泛的研究,并确认本发明的酰胺化合物具有EP4受体拮抗活性,从而完成了本发明。本发明的酰胺化合物具有EP4受体拮抗活性,可用作预防和/或治疗各种与EP4相关的疾病的药物组合物的活性成分,例如慢性肾功能衰竭和/或糖尿病肾病等。
  • 4-(Indol-7-ylcarbonylaminomethyl)cyclohexanecarboxylic acid derivatives as EP4 receptor antagonists useful for the treatment of chronic renal failure or diabetic nephropathy
    申请人:Astellas Pharma Inc.
    公开号:EP2565191A1
    公开(公告)日:2013-03-06
    The present invention relates to amide compounds of formula I which are EP4 receptor antagonists and useful for treating chronic renal failure and/or diabetic nephropathy. Ring D is a group of formula II; V and W are CH; R45 is -CH2-B5; B5 represents a bicyclic hetero ring which may be substituted with one or more groups selected from the group consisting of halogen and C1-6 alkyl; R46 is H, halogen, C1-6 alkyl which may be substituted with one or more halogens, or -O-C1-6 alkyl; -NR1-YR2 - is -NH-CH2-; Ring E is cyclohexane-1,4-diyl; and -Z-R3 is -CO2H.
    本发明涉及式 I 的酰胺化合物,它们是 EP4 受体拮抗剂,可用于治疗慢性肾衰竭和/或糖尿病肾病。 环 D 是式 II 的基团; V 和 W 是 CH; R45 是-CH2-B5; B5 代表可被一个或多个选自卤素和 C1-6 烷基的基团取代的双环杂环; R46 是 H、卤素、可被一个或多个卤素取代的 C1-6 烷基或 -O-C1-6 烷基; -NR1-YR2-是-NH-CH2-; 环 E 是环己烷-1,4-二基;以及 -Z-R3为-CO2H。
  • Palladium-Catalyzed Oxidative Carbonylation of Aromatic C–H Bonds of <i>N</i>-Alkylanilines with CO and Alcohols for the Synthesis of <i>o</i>-Aminobenzoates
    作者:Ming Chen、Zhi-Hui Ren、Yao-Yu Wang、Zheng-Hui Guan
    DOI:10.1021/jo502581p
    日期:2015.1.16
    A Pd(II)-catalyzed CH monocarbonylation of N-alkylanilines for the synthesis of o-aminobenzoates has been developed. Various aliphatic alcohols and phenol were tolerated in the reaction to afford the corresponding o-aminobenzoates in good yields under mild balloon pressure of CO.
  • EP2277858
    申请人:——
    公开号:——
    公开(公告)日:——
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