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3-(2-((3-methyl-1-(3,5-dimethylphenyl)butyl)carbamoyl)-4-(fluoren-2-ylmethyloxy)phenyl)propanoic acid | 499156-48-8

中文名称
——
中文别名
——
英文名称
3-(2-((3-methyl-1-(3,5-dimethylphenyl)butyl)carbamoyl)-4-(fluoren-2-ylmethyloxy)phenyl)propanoic acid
英文别名
3-[2-[[1-(3,5-dimethylphenyl)-3-methylbutyl]carbamoyl]-4-(9H-fluoren-2-ylmethoxy)phenyl]propanoic acid
3-(2-((3-methyl-1-(3,5-dimethylphenyl)butyl)carbamoyl)-4-(fluoren-2-ylmethyloxy)phenyl)propanoic acid化学式
CAS
499156-48-8
化学式
C37H39NO4
mdl
——
分子量
561.721
InChiKey
RLWGJDCNOLWVIG-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):
    8
  • 重原子数:
    42
  • 可旋转键数:
    11
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    75.6
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • CARBOXYLIC ACID DERIVATIVES AND PHARMACEUTICAL AGENT COMPRISING THE SAME AS ACTIVE INGREDIENT
    申请人:Tani Kousuke
    公开号:US20090318703A1
    公开(公告)日:2009-12-24
    A carboxylic acid derivative of formula (I): wherein R 1 is —COOH, —COOR 6 , etc.; A is a single bond, alkylene, etc.; R 2 is alkyl, alkoxy, etc.; B is a carbocyclic ring or a heterocyclic ring; Q is alkylnene-Cyc2, etc.; D is a linking chain; and R 3 is alkyl, a carbocyclic ring or a heterocyclic ring, or a non-toxic salt thereof. The compound of formula (I) binds to PGE 2 receptor, especially subtypes EP 3 and/or EP 4 and show the antagonizing activity, are useful for the prevention and/or treatment of diseases induced pain, itch, urticaria, allergy, urinary frequency, urinary disturbance, Alzheimer's disease, cancer, dysmenorrhea, endometriosis, etc.
    化学式为(I)的羧酸生物:其中R1为—COOH,—COOR6等;A为单键,烷基等;R2为烷基,烷氧基等;B为碳环或杂环;Q为烷基烯-Cyc2等;D为连接链;R3为烷基,碳环或杂环,或其无毒盐。化合物(I)与PGE2受体结合,特别是亚型EP3和/或EP4,并显示拮抗活性,对于预防和/或治疗由疼痛、瘙痒、荨麻疹、过敏、尿频、尿液障碍、阿尔茨海默病、癌症、痛经、子宫内膜异位症等引起的疾病有用。
  • Carboxylic acid derivative compounds and drugs comprising these compounds as the active ingredient
    申请人:Tani Kousuke
    公开号:US20060258728A1
    公开(公告)日:2006-11-16
    A carboxylic acid derivative of formula (I): wherein R 1 is —COOH, —COOR 6 , etc.; A is a single bond, alkylene, etc.; R 2 is alkyl, alkoxy, etc.; B is a carbocyclic ring or a heterocyclic ring; Q is alkylnene-Cyc2, etc.; D is a linking chain; and R 3 is alkyl, a carbocyclic ring or a heterocyclic ring, or a non-toxic salt thereof. The compound of formula (I) binds to PGE 2 receptor, especially subtypes EP 3 and/or EP 4 and show the antagonizing activity, are useful for the prevention and/or treatment of diseases induced pain, itch, urticaria, allergy, urinary frequency, urinary disturbance, Alzheimer's disease, cancer, dysmenorrhea, endometriosis, etc.
    化学式为(I)的羧酸生物:其中R1为—COOH,—COOR6等;A为单键,烷基等;R2为烷基,烷氧基等;B为碳环或杂环;Q为烷基烯-Cyc2等;D为连接链;R3为烷基,碳环或杂环,或其无毒盐。化合物(I)与PGE2受体结合,特别是亚型EP3和/或EP4,并显示拮抗活性,可用于预防和/或治疗因疼痛、瘙痒、荨麻疹、过敏、尿频、尿障碍、阿尔茨海默病、癌症、痛经、子宫内膜异位症等引起的疾病。
  • CARBOXYLIC ACID DERIVATIVE COMPOUNDS AND DRUGS COMPRISING THESE COMPOUNDS AS THE ACTIVE INGREDIENT
    申请人:ONO PHARMACEUTICAL CO., LTD.
    公开号:EP1431267A1
    公开(公告)日:2004-06-23
    A carboxylic acid derivative of formula (I): wherein R1 is -COOH, -COOR6, etc.; A is a single bond, alkylene, etc.; R2 is alkyl, alkoxy, etc.; B is a carbocyclic ring or a heterocyclic ring; Q is alkylnene-Cyc2, etc.; D is a linking chain; and R3 is alkyl, a carbocyclic ring or a heterocyclic ring, or a non-toxic salt thereof. The compound of formula (I) binds to PGE2 receptor, especially subtypes EP3 and/or EP4 and show the antagonizing activity, are useful for the prevention and/or treatment of diseases induced pain, itch, urticaria, allergy, urinary frequency, urinary disturbance, Alzheimer's disease, cancer, dysmenorrhea, endometriosis, etc.
    式(I)的羧酸生物: 其中 R1 为-COOH、-COOR6 等;A 为单键、亚烷基等;R2 为烷基、烷氧基等;B 为碳环或杂环;Q 为烷基烯-Cyc2 等;D 为连接链;R3 为烷基、碳环或杂环,或其无毒盐。式(I)化合物能与 PGE2 受体,特别是 EP3 和/或 EP4 亚型结合并显示出拮抗活性,可用于预防和/或治疗诱发疼痛、瘙痒、荨麻疹、过敏、尿频、排尿障碍、老年痴呆症、癌症、痛经、子宫内膜异位症等疾病。
  • US7491748B2
    申请人:——
    公开号:US7491748B2
    公开(公告)日:2009-02-17
  • US7786161B2
    申请人:——
    公开号:US7786161B2
    公开(公告)日:2010-08-31
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