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4-[3-Cyano-4-[2-(4-methoxyphenyl)ethyl]pyrrol-1-yl]-2-hydroxybenzoic acid | 1072201-72-9

中文名称
——
中文别名
——
英文名称
4-[3-Cyano-4-[2-(4-methoxyphenyl)ethyl]pyrrol-1-yl]-2-hydroxybenzoic acid
英文别名
——
4-[3-Cyano-4-[2-(4-methoxyphenyl)ethyl]pyrrol-1-yl]-2-hydroxybenzoic acid化学式
CAS
1072201-72-9
化学式
C21H18N2O4
mdl
——
分子量
362.385
InChiKey
YEYWKCZXGBBFGE-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):
    3.9
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    95.5
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • 5-MEMBERED HETEROCYCLIC DERIVATIVE AND USE THEREOF FOR MEDICAL PURPOSES
    申请人:Shimizu Kazuo
    公开号:US20100227864A1
    公开(公告)日:2010-09-09
    The present invention provides compounds useful as agents for the prevention or treatment of a disease associated with abnormal serum uric acid level which has a uricosuric activity or the like. The present invention relates to 5-membered heterocyclic derivatives represented by the following general formula (I) having xanthine oxidase inhibitory activities and useful as agents for the prevention or treatment of a disease associated with abnormality of serum uric acid level, prodrugs thereof, or salts thereof. In the formula (I), T represents nitro, cyano and the like; ring J represents aryl or heteroaryl; Q represents carboxy, 5-tetazolyl and the like; Y represents H, OH, NH 2 , halogen, haloalkyl and the like; X 1 and X 2 independently represent CR 2 or N; R 2 represents H, alkyl and the like; R 1 represents halogen, cyano, haloalkyl, A-D-E-G-L-M, -N(-D-L-M) 2 and the like, in the formula, A represents a single bond, O, S and the like; D, G and M independently represent optionally substituted alkylene, cycloalkylene, heterocycloalkylene, arylene, heteroarylene and the like; E and L independently represent a single bond, O, S, COO, SO 2 and the like.
    本发明提供了一种化合物,其具有尿酸排泄活性或类似活性,可用作预防或治疗与异常血清尿酸平相关的疾病的药剂。本发明涉及以下通式(I)表示的具有黄嘌呤化酶抑制活性的5-成员杂环衍生物,其可用作预防或治疗与血清尿酸平异常相关的疾病的药剂、其前药或其盐。在公式(I)中,T表示硝基、基等;环J表示芳基或杂芳基;Q表示羧基、5-四唑基等;Y表示H、OH、NH2、卤素、卤代烷基等;X1和X2独立地表示CR2或N;R2表示H、烷基等;R1表示卤素、基、卤代烷基、A-D-E-G-L-M、-N(-D-L-M)2等,在公式中,A表示单键、O、S等;D、G和M独立地表示可选取代的烷基、环烷基、杂环烷基、芳基、杂芳基等;E和L独立地表示单键、O、S、COO、SO2等。
  • 5-MEMBERED NITROGEN CONTAINING HETEROCYCLIC DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME
    申请人:Shimizu Kazuo
    公开号:US20120289506A1
    公开(公告)日:2012-11-15
    5-membered heterocyclic derivatives represented by general formula (I) having xanthine oxidase inhibitory activities and useful as agents for the prevention or treatment of a disease associated with abnormality of serum uric acid level, prodrugs thereof, or salts thereof. In the formula (I), T represents nitro, cyano and the like; ring J represents aryl or heteroaryl; Q represents carboxy, 5-tetazolyl and the like; Y represents H, OH, NH 2 , halogen, haloalkyl and the like; X 1 and X 2 independently represent CR 2 or N; R 2 represents H, alkyl and the like; R 1 represents halogen, cyano, haloalkyl, A-D-E-G-L-M, —N(-D-L-M) 2 and the like, A represents a single bond, O, S and the like; D, G and M independently represent optionally substituted alkylene, cycloalkylene, heterocycloalkylene, arylene, heteroarylene and the like; E and L independently represent a single bond, O, S, COO, SO 2 and the like.
    通式(I)所表示的5元杂环衍生物具有黄嘌呤化酶抑制活性,并且可作为预防或治疗与血清尿酸平异常相关的疾病的药剂,其前药或盐。在公式(I)中,T表示硝基,基等;环J表示芳基或杂芳基;Q表示羧基,5-四唑基等;Y表示H,OH,NH2,卤素,卤代烷基等;X1和X2独立地表示CR2或N;R2表示H,烷基等;R1表示卤素,基,卤代烷基,A-D-E-G-L-M,-N(-D-L-M)2等,其中A表示单键,O,S等;D,G和M分别表示可选取代的烷基,环烷基,杂环烷基,芳基,杂芳基等;E和L独立地表示单键,O,S,COO,SO2等。
  • US8227500B2
    申请人:——
    公开号:US8227500B2
    公开(公告)日:2012-07-24
  • US9023882B2
    申请人:——
    公开号:US9023882B2
    公开(公告)日:2015-05-05
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