摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-((benzoyl)methylamino)-4,6-dichloro-1H-indole-2-carboxylic acid | 1348512-58-2

中文名称
——
中文别名
——
英文名称
3-((benzoyl)methylamino)-4,6-dichloro-1H-indole-2-carboxylic acid
英文别名
3-[(phenacyl)amino]-2-carboxy-4,6-dichloroindole;4,6-Dichloro-3-[(2-oxo-2-phenylethyl)amino]-1H-indole-2-carboxylic acid;4,6-dichloro-3-(phenacylamino)-1H-indole-2-carboxylic acid
3-((benzoyl)methylamino)-4,6-dichloro-1H-indole-2-carboxylic acid化学式
CAS
1348512-58-2
化学式
C17H12Cl2N2O3
mdl
——
分子量
363.2
InChiKey
MJJKPIVXKSZOBF-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):
    5.1
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    82.2
  • 氢给体数:
    3
  • 氢受体数:
    4

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:
    3-[(phenacyl)amino]-2-carbethoxy-4,6-dichloroindole 在 lithium hydroxide monohydrate 作用下, 以 四氢呋喃 为溶剂, 以64%的产率得到3-((benzoyl)methylamino)-4,6-dichloro-1H-indole-2-carboxylic acid
    参考文献:
    名称:
    3-amidoindolyl derivatives and pharmaceutical compositions thereof
    摘要:
    本发明涉及一类新的3-酰胺和3-磺胺酰胺基的NMDA拮抗剂,以及它们在治疗多种疾病状态中的应用。
    公开号:
    US05189054A1
点击查看最新优质反应信息

文献信息

  • Interleukin-4 gene expression inhibitors
    申请人:——
    公开号:US20040006123A1
    公开(公告)日:2004-01-08
    This invention discloses and claims a class of indole and benzo(b)thiophene derivatives for use in treating allergy, asthma, rhinitis, dermatitis, B-cell lymphomas, tumors and diseases associated with bacterial, rhinovirus or respiratory syncytial virus (RSV) infections. The compounds of this invention are defined by the Formula (I): 1 wherein X, Y, Z, R 1 , R 2 and R 3 are as defined in the specification; or a pharmaceutically acceptable salt thereof. In preferred embodiments of this invention it is also disclosed and claimed that the compounds of this invention are capable of modulating T helper (Th) cells, Th1/Th2, and thereby capable of inhibiting the transcription of interleukin-4 (IL-4) message, IL-4 release or IL-4 production.
    这项发明揭示并声明了一类吲哚和苯并(b)噻吩衍生物,用于治疗过敏、哮喘、鼻炎、皮炎、B细胞淋巴瘤、肿瘤以及与细菌、鼻病毒或呼吸道合胞病毒(RSV)感染相关的疾病。本发明的化合物由下式(I)定义: 1 其中X、Y、Z、R 1 、R 2 和R 3 如规范中所定义;或其药学上可接受的盐。在本发明的优选实施例中,还揭示并声明了本发明的化合物能够调节T辅助(Th)细胞、Th1/Th2,从而能够抑制白细胞介素-4(IL-4)信息的转录、IL-4的释放或IL-4的产生。
  • 3-amidoindolyl derivative
    申请人:Merrell Dow Pharmaceuticals Inc.
    公开号:US05491153A1
    公开(公告)日:1996-02-13
    The present invention is directed to a new class of 3-amido and 3-sulfamido-indolyl NMDA antagonists and their use in the treatment of a number of disease states.
    本发明涉及一种新的3-酰胺和3-磺酰胺基-吲哚基NMDA受体拮抗剂及其在治疗多种疾病状态中的应用。
  • Indole derivatives as interleukin -4 gene expression inhibitors
    申请人:——
    公开号:US20040010029A1
    公开(公告)日:2004-01-15
    This invention discloses and claims a new class of indole derivatives for use in treating allergy, asthma, rhinitis, dermatitis, B-cell lymphomas, tumors and diseases associated with bacterial, rhinovirus or respiratory syncytial virus (RSV) infections. It has now been found that the compounds of this invention are capable of modulating T helper (Th) cells, Th1/Th2, and thereby capable of inhibiting the transcription of interleukin-4 (IL-4) message, IL-4 release or IL-4 production.
    这项发明揭示并声明了一类新的吲哚衍生物,用于治疗过敏、哮喘、鼻炎、皮炎、B细胞淋巴瘤、肿瘤以及与细菌、鼻病毒或呼吸道合胞病毒(RSV)感染相关的疾病。现在已经发现,该发明的化合物能够调节T辅助细胞(Th)细胞、Th1 / Th2,从而能够抑制白细胞介素-4(IL-4)信息的转录、IL-4释放或IL-4的产生。
  • INTERLEUKIN-4 GENE EXPRESSION INHIBITORS
    申请人:ALKAN Sefik S.
    公开号:US20080132481A1
    公开(公告)日:2008-06-05
    This invention discloses and claims a class of indole and benzo(b)thiophene derivatives for use in treating allergy, asthma, rhinitis, dermatitis, B-cell lymphomas, tumors and diseases associated with bacterial, rhinovirus or respiratory syncytial virus (RSV) infections. The compounds of this invention are defined by the Formula (I): wherein X, Y, Z, R 1 , R 2 and R 3 are as defined in the specification; or a pharmaceutically acceptable salt thereof. In preferred embodiments of this invention it is also disclosed and claimed that the compounds of this invention are capable of modulating T helper (Th) cells, Th1/Th2, and thereby capable of inhibiting the transcription of interleukin-4 (IL-4) message, IL-4 release or IL-4 production.
    本发明揭示和声明了一类用于治疗过敏、哮喘、鼻炎、皮炎、B细胞淋巴瘤、肿瘤以及与细菌、鼻病毒或呼吸道合胞病毒(RSV)感染相关的疾病的吲哚和苯并(b)噻吩衍生物。本发明的化合物由公式(I)定义:其中X、Y、Z、R1、R2和R3如规范中所定义;或其药学上可接受的盐。在本发明的优选实施例中,还揭示和声明本发明的化合物能够调节T辅助(Th)细胞,Th1 / Th2,并能够抑制白细胞介素-4(IL-4)信息的转录、IL-4的释放或IL-4的产生。
  • 3-Amidoindolyl derivatives
    申请人:MERRELL PHARMACEUTICALS INC.
    公开号:EP0483881A1
    公开(公告)日:1992-05-06
    The present invention is directed to a new class of 3-amido and 3-sulfamido-indolyl NMDA antagonists and their use in the treatment of a number of disease states.
    本发明涉及一类新的 3-氨基和 3-磺酰胺-吲哚基 NMDA 拮抗剂及其在治疗多种疾病中的应用。
查看更多