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6-hydroxy-7-methoxychroman-2-carboxylic acid phenyl amide

中文名称
——
中文别名
——
英文名称
6-hydroxy-7-methoxychroman-2-carboxylic acid phenyl amide
英文别名
6-hydroxy-7-methoxychroman-2-carboxylic acid phenylamide;KL-1156;6-hydroxy-7-methoxy-N-phenyl-3,4-dihydro-2H-chromene-2-carboxamide
6-hydroxy-7-methoxychroman-2-carboxylic acid phenyl amide化学式
CAS
——
化学式
C17H17NO4
mdl
——
分子量
299.326
InChiKey
JXCMRGWJFGLXJJ-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):
    2.8
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    67.8
  • 氢给体数:
    2
  • 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:
    参考文献:
    名称:
    Synthesis and evaluation of 6-hydroxy-7-methoxy-4-chromanone- and chroman-2-carboxamides as antioxidants
    摘要:
    A series of 6-hydroxy-7-methoxy-4-chromanone- (2a-e) and chroman-2-carboxamides (3a-e) were synthesized and their antioxidant activities were evaluated. While compounds 2a-e were less active, compounds 3a-e exhibited more potent inhibition of lipid peroxidation initiated by Fe2+ and ascorbic acid in rat brain homogenates. Among them, N-arylsubstituted-chroman-2-carboxamides (3d and 3e) exhibited 25-40 times more potent inhibition than trolox (1). The DPPH radical scavenging activity of compound 3d was comparable to that of trolox. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.03.118
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文献信息

  • Clonidine to treat pain locally
    申请人:Medtronic, Inc.
    公开号:EP2363122A1
    公开(公告)日:2011-09-07
    The present invention is directed to systems and methods for contributing to the local treatment of pain. More specifically, the present invention is directed to the use of one or more NFKB inhibiting compounds, particularly clonidine, in the manufacture of a medicament for the treatment of pain wherein said medicament is for local administration to a patient in need thereof.
    本发明涉及有助于局部治疗疼痛的系统和方法。更具体地说,本发明涉及将一种或多种 NFKB 抑制化合物,特别是氯硝柳胺,用于制造治疗疼痛的药物,其中所述药物用于对有需要的患者进行局部给药。
  • Systems and Methods to Treat Pain Locally
    申请人:Burright N. Eric
    公开号:US20060253100A1
    公开(公告)日:2006-11-09
    Disclosed herein are systems and methods for contributing to the local treatment of pain. More specifically, the disclosed systems and methods contribute to the local treatment pain by inhibiting the NFκB family of transcription factors.
    本文公开了有助于局部治疗疼痛的系统和方法。更具体地说,所公开的系统和方法通过抑制转录因子 NFκB 家族来促进疼痛的局部治疗。
  • NFKAPPAB INHIBITORS TO TREAT PAIN LOCALLY
    申请人:MEDTRONIC, INC.
    公开号:EP2043625A1
    公开(公告)日:2009-04-08
  • COMPOSITIONS AND METHODS FOR MODULATING IMMUNE RESPONSES
    申请人:THE UNIVERSITY OF QUEENSLAND
    公开号:EP2077821B1
    公开(公告)日:2019-08-14
  • Implant pellet comprising clonidine to treat pain locally
    申请人:Medtronic, Inc.
    公开号:EP2363122B1
    公开(公告)日:2014-06-11
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