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5-(acetyloxy)-2,2-dimethyl-3,4-dihydro-2H-benzo[h]chromen-6-yl glycinate hydrochloride | 876062-70-3

中文名称
——
中文别名
——
英文名称
5-(acetyloxy)-2,2-dimethyl-3,4-dihydro-2H-benzo[h]chromen-6-yl glycinate hydrochloride
英文别名
(5-Acetyloxy-2,2-dimethyl-3,4-dihydrobenzo[h]chromen-6-yl) 2-aminoacetate;hydrochloride
5-(acetyloxy)-2,2-dimethyl-3,4-dihydro-2H-benzo[h]chromen-6-yl glycinate hydrochloride化学式
CAS
876062-70-3
化学式
C19H21NO5*ClH
mdl
——
分子量
379.84
InChiKey
RVZTYMSYENCQGQ-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):
    3.15
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    87.8
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

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文献信息

  • Quinone prodrug compositions and methods of use
    申请人:Ashwell A. Mark
    公开号:US20060035963A1
    公开(公告)日:2006-02-16
    The present invention relates to quinone prodrug compositions and therapeutic methods using such prodrug compositions. Preferably, the quinone compounds of the invention are napthoquinone compounds such as β-lapachone or β-lapachone analogs. The quinone prodrug compositions of the invention exhibit improved solubility, stability, bioavailability, and pharmacokinetic properties, as well as improved plasma half-life in vivo.
    本发明涉及醌类前药组合物及使用这种前药组合物的治疗方法。本发明的醌类化合物最好是醌类化合物,例如β-醌或β-醌类似物。本发明的醌类前药组合物表现出改善的溶解度、稳定性、生物利用度和药物动力学特性,以及在体内改善的血浆半衰期。
  • AMINOACID CONJUGATES OF BETA-LAPACHONE FOR TUMOR TARGETING
    申请人:ARQULE, INC.
    公开号:EP1877097A2
    公开(公告)日:2008-01-16
  • US7812051B2
    申请人:——
    公开号:US7812051B2
    公开(公告)日:2010-10-12
  • US8614228B2
    申请人:——
    公开号:US8614228B2
    公开(公告)日:2013-12-24
  • [EN] QUINONE PRODRUG COMPOSITIONS AND METHODS OF USE<br/>[FR] COMPOSITIONS DE PROMEDICAMENTS A BASE DE QUINONE ET METHODES D'UTILISATION
    申请人:ARQULE INC
    公开号:WO2006020719A2
    公开(公告)日:2006-02-23
    The present invention relates to quinone prodrug compositions and therapeutic methods using such prodrug compositions. Preferably, the quinone compounds of the invention are napthoquinone compounds such as β-lapachone or β-lapachone analogs. The quinone prodrug compositions of the invention exhibit improved solubility, stability, bioavailability, and pharmacokinetic properties, as well as improved plasma half-life in vivo.
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