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tert-butyl 2-(4-aminophenyl)ethyl(2-hydroxy-4,6-dimethoxybenzyl)carbamate | 299189-16-5

中文名称
——
中文别名
——
英文名称
tert-butyl 2-(4-aminophenyl)ethyl(2-hydroxy-4,6-dimethoxybenzyl)carbamate
英文别名
tert-butyl N-[2-(4-aminophenyl)ethyl]-N-[(2-hydroxy-4,6-dimethoxyphenyl)methyl]carbamate
tert-butyl 2-(4-aminophenyl)ethyl(2-hydroxy-4,6-dimethoxybenzyl)carbamate化学式
CAS
299189-16-5
化学式
C22H30N2O5
mdl
——
分子量
402.491
InChiKey
TUFXZDQECDQGMP-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):
    3.5
  • 重原子数:
    29
  • 可旋转键数:
    9
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    94.2
  • 氢给体数:
    2
  • 氢受体数:
    6

文献信息

  • Novel lipoic acid heterocyclic or benzene derivatives, preparation and use thereof as medicines
    申请人:——
    公开号:US20030105107A1
    公开(公告)日:2003-06-05
    A subject of the invention is new heterocyclic or benzenic derivatives comprising a lateral chain derived from lipoic acid, which have an inhibitory activity on NO-synthase enzymes producing nitrogen monoxide NO and/or are agents allowing the regeneration of antioxidants or entities trapping the reactive oxygen species (ROS) and which intervene in a more general manner in the redox status of thiol groups. A subject of the invention is also their preparation methods, the pharmaceutical preparations containing them and their use for therapeutic purposes, in particular their use as inhibitors of NO-synthases and/or as agents which intervene in a more general manner in the redox status of thiol groups.
    本发明的一个主题是新的含有来自辛酸的侧链的杂环或苯基衍生物,具有对产生一氧化氮NO的NO合酶酶的抑制活性和/或是允许再生抗氧化剂或捕获活性氧种(ROS)的实体的药剂,这些实体更一般地干预巯基的氧化还原状态。本发明的一个主题还包括它们的制备方法、含有它们的制药制剂以及它们用于治疗目的的用途,特别是它们作为NO合酶的抑制剂和/或作为更一般地干预巯基氧化还原状态的实体的用途。
  • New derivatives of lipoic acid, their preparation, their use as medicaments and the pharmaceutical compositions containing them
    申请人:SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATION SCIENTIFIQUES (S.C.R.A.S)
    公开号:US20040019084A1
    公开(公告)日:2004-01-29
    The invention concerns novel lipoic acid derivatives, which have an inhibiting action with respect to NO-synthase enzymes producing nitrogen monoxide NO and/or are agents enabling the regeneration of antioxidants or entities trapping reactive oxygen species (ROS) and intervening in a more general manner in the redox status of thiol groups. The invention also concerns methods for preparing them, pharmaceutical compositions containing them and their use for therapeutic purposes, particularly their use as NO-synthase inhibitors and/or as agents acting more generally in the redox status of thiol groups.
    本发明涉及新型辛酸生物,其对产生氮氧化物NO的NO合酶酶具有抑制作用和/或是能够再生抗氧化剂或俘获反应性氧化物种(ROS)的实体,并以更一般的方式干预巯基的氧化还原状态。本发明还涉及制备它们的方法,含有它们的制药组合物以及它们作为治疗用途的应用,特别是它们作为NO合酶抑制剂和/或作为更一般地干预巯基氧化还原状态的试剂的应用。
  • New heterocyclic or benzenic derivatives of lipoic acid, their preparation and their use as medicaments
    申请人:Harnett Jeremiah
    公开号:US20050227991A1
    公开(公告)日:2005-10-13
    A subject of the invention is new heterocyclic or benzenic derivatives comprising a lateral chain derived from lipoic acid, which have an inhibitory activity on NO-synthase enzymes producing nitrogen monoxide NO and/or are agents allowing the regeneration of antioxidants or entities trapping the reactive oxygen species (ROS) and which intervene in a more general manner in the redox status of thiol groups. A subject of the invention is also their preparation methods, the pharmaceutical preparations containing them and their use for therapeutic purposes, in particular their use as inhibitors of NO-synthases and/or as agents which intervene in a more general manner in the redox status of thiol groups.
    本发明的主题是新的杂环或苯环衍生物,包括一个来自辛酸的侧链,具有对生成一氧化氮(NO)的NO合酶酶有抑制作用和/或是允许抗氧化剂或捕获反应性氧化物种(ROS)的实体再生的作用,并且以更一般的方式干预基团的氧化还原状态。本发明的主题还包括它们的制备方法、包含它们的药物制剂以及它们作为治疗用途的使用,特别是作为NO合酶酶抑制剂和/或以更一般的方式干预基团的氧化还原状态的药剂的使用。
  • US6887891B2
    申请人:——
    公开号:US6887891B2
    公开(公告)日:2005-05-03
  • US6936715B2
    申请人:——
    公开号:US6936715B2
    公开(公告)日:2005-08-30
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