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2-[(2-chloro-4-nitro)phenyl]-5-benzoxazoleacetic acid methyl ester | 695186-48-2

中文名称
——
中文别名
——
英文名称
2-[(2-chloro-4-nitro)phenyl]-5-benzoxazoleacetic acid methyl ester
英文别名
Methyl 2-[2-(2-chloro-4-nitrophenyl)-1,3-benzoxazol-5-yl]acetate
2-[(2-chloro-4-nitro)phenyl]-5-benzoxazoleacetic acid methyl ester化学式
CAS
695186-48-2
化学式
C16H11ClN2O5
mdl
——
分子量
346.727
InChiKey
FPZLXDWBUKGCBZ-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):
    3.7
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    98.2
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-[(2-chloro-4-nitro)phenyl]-5-benzoxazoleacetic acid methyl ester 在 lithium hydroxide 、 溶剂黄146三乙胺 作用下, 以 四氢呋喃乙醇 为溶剂, 生成 2-(2-(2-Chloro-4-(3-(3-methoxyphenyl)acrylamido)phenyl)benzo[d]oxazol-5-yl)acetic acid
    参考文献:
    名称:
    Furanyl-1,3-thiazol-2-yl and benzoxazol-5-yl acetic acid derivatives: novel classes of heparanase inhibitor
    摘要:
    Using a furanylthiazole acetic acid as a starting point, a novel series of benzoxazol-5-yl acetic acid derivatives have been identified as heparanase inhibitors. Several compounds possess an IC50 of similar to 200 nM against heparanase, for example, trans 2-[4-[3-(3,4-dichlorophenylamino)-3-oxo-1-propenyl]-2-fluorophenyl]benzoxazol-5-yl acetic acid (16e). Several of the compounds show anti-angiogenic properties. Improvement to the DMPK profile of compounds has provided compounds of potential use in in vivo models. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.03.014
  • 作为产物:
    描述:
    参考文献:
    名称:
    Furanyl-1,3-thiazol-2-yl and benzoxazol-5-yl acetic acid derivatives: novel classes of heparanase inhibitor
    摘要:
    Using a furanylthiazole acetic acid as a starting point, a novel series of benzoxazol-5-yl acetic acid derivatives have been identified as heparanase inhibitors. Several compounds possess an IC50 of similar to 200 nM against heparanase, for example, trans 2-[4-[3-(3,4-dichlorophenylamino)-3-oxo-1-propenyl]-2-fluorophenyl]benzoxazol-5-yl acetic acid (16e). Several of the compounds show anti-angiogenic properties. Improvement to the DMPK profile of compounds has provided compounds of potential use in in vivo models. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.03.014
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文献信息

  • [EN] BENZOXAZOLE, BENZTHIAZOLE AND BENZIMIDAZOLE ACID DERIVATIVES AND THEIR USE AS HEPARANASE INHIBITORS<br/>[FR] DERIVES D'ACIDES DE BENZOXAZOLE, DE BENZOTHIAZOLE, ET DE BENZIMIDAZOLE PHARMACEUTIQUEMENT ACTIFS
    申请人:OXFORD GLYCOSCIENCES UK LTD
    公开号:WO2004046122A3
    公开(公告)日:2004-07-15
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