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| 909029-64-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
909029-64-7
化学式
C18H18N2O4
mdl
——
分子量
326.352
InChiKey
ARESMPNCCXFZOZ-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):
    2.25
  • 重原子数:
    24.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    95.5
  • 氢给体数:
    3.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    四(三苯基膦)钯 1,3-二甲基巴比妥酸1-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺三氟乙酸 作用下, 以 二氯甲烷N,N-二甲基甲酰胺乙腈 为溶剂, 反应 2.0h, 生成 N-[(3S)-2-hydroxy-5-oxooxolan-3-yl]-1-[(naphthalene-1-carbonylamino)carbamoyl]cyclopentane-1-carboxamide
    参考文献:
    名称:
    Synthesis and evaluation of novel 1-(2-acylhydrazinocarbonyl)-cycloalkyl carboxamides as interleukin-1β converting enzyme (ICE) inhibitors
    摘要:
    Novel 1-(2-acylhydrazinocarbonyl)cycloalkyl carboxamides were designed as peptidomimetic inhibitors of interleukin-1 beta converting enzyme (ICE). A short synthesis was developed and moderately potent ICE inhibitors were identified (IC50 values < 100 nM). Most of the synthesized examples were selective for ICE versus the related cysteine proteases caspase-3 and caspase-8, although several dual-acting inhibitors of ICE and caspase-8 were identified. Several of the more potent ICE inhibitors were also shown to inhibit IL-1 beta production in a whole cell assay (IC50 < 500 nM). (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.05.076
  • 作为产物:
    描述:
    naphthalene-1-carboxylic acid hydrazide hydrochloride 、 1,1-环戊基二羧酸盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 168000.0h, 以20%的产率得到
    参考文献:
    名称:
    Synthesis and evaluation of novel 1-(2-acylhydrazinocarbonyl)-cycloalkyl carboxamides as interleukin-1β converting enzyme (ICE) inhibitors
    摘要:
    Novel 1-(2-acylhydrazinocarbonyl)cycloalkyl carboxamides were designed as peptidomimetic inhibitors of interleukin-1 beta converting enzyme (ICE). A short synthesis was developed and moderately potent ICE inhibitors were identified (IC50 values < 100 nM). Most of the synthesized examples were selective for ICE versus the related cysteine proteases caspase-3 and caspase-8, although several dual-acting inhibitors of ICE and caspase-8 were identified. Several of the more potent ICE inhibitors were also shown to inhibit IL-1 beta production in a whole cell assay (IC50 < 500 nM). (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.05.076
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