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2,7,9-trihydroxy-3-(4,5,7-trihydroxy-2-oxo-2H-chromene-3-yl)-2,3-dihydro-4H-furo[3,2-c]chromene-4-one | 835597-62-1

中文名称
——
中文别名
——
英文名称
2,7,9-trihydroxy-3-(4,5,7-trihydroxy-2-oxo-2H-chromene-3-yl)-2,3-dihydro-4H-furo[3,2-c]chromene-4-one
英文别名
2,7,9-trihydroxy-3-(4,5,7-trihydroxy-2-okso-2H-chromen-3-yl)-2,3-dihydro-4H-furo[3,2-c]chromen-4-one;2,7,9-Trihydroxy-3-(4,5,7-trihydroxy-2-oxochromen-3-yl)-2,3-dihydrofuro[3,2-c]chromen-4-one
2,7,9-trihydroxy-3-(4,5,7-trihydroxy-2-oxo-2H-chromene-3-yl)-2,3-dihydro-4H-furo[3,2-c]chromene-4-one化学式
CAS
835597-62-1
化学式
C20H12O11
mdl
——
分子量
428.309
InChiKey
WPTRFZPVDHYQGF-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):
    1.1
  • 重原子数:
    31
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    183
  • 氢给体数:
    6
  • 氢受体数:
    11

反应信息

  • 作为反应物:
    描述:
    2,7,9-trihydroxy-3-(4,5,7-trihydroxy-2-oxo-2H-chromene-3-yl)-2,3-dihydro-4H-furo[3,2-c]chromene-4-onesodium hydroxide 作用下, 以 为溶剂, 生成 2,7,9-trihydroxy-3-(4,5,7-trihydroxy-2-okso-2H-chromen-3-yl)-2,3-dihydro-4H-furo[3,2-c]chromen-4-one monosodium salt
    参考文献:
    名称:
    [EN] FUROCHROMENE DERIVATIVE WITH ANTI-INFLAMMATORY ACTIVITY
    [FR] DERIVE DE FUROCHROMENE A ACTIVITE ANTI-INFLAMMATOIRE
    摘要:
    本发明涉及式(I)的新化合物及其药学上可接受的盐和溶剂化物;制备该化合物的过程和反应中间体;包含该化合物的药物组合物;以及在哮喘以及其他人类免疫系统疾病、疾病或疾病情况的预防和治疗中使用该化合物。
    公开号:
    WO2005095411A1
  • 作为产物:
    描述:
    草酸醛4,5,7-三羟基香豆素 以 phosphate buffer 、 乙腈 为溶剂, 反应 5.0h, 以60%的产率得到2,7,9-trihydroxy-3-(4,5,7-trihydroxy-2-oxo-2H-chromene-3-yl)-2,3-dihydro-4H-furo[3,2-c]chromene-4-one
    参考文献:
    名称:
    [EN] FUROCHROMENE DERIVATIVE WITH ANTI-INFLAMMATORY ACTIVITY
    [FR] DERIVE DE FUROCHROMENE A ACTIVITE ANTI-INFLAMMATOIRE
    摘要:
    本发明涉及式(I)的新化合物及其药学上可接受的盐和溶剂化物;制备该化合物的过程和反应中间体;包含该化合物的药物组合物;以及在哮喘以及其他人类免疫系统疾病、疾病或疾病情况的预防和治疗中使用该化合物。
    公开号:
    WO2005095411A1
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文献信息

  • [EN] SUBSTITUTED FUROCHROMENES, PREPARATION THEREOF AND THEIR ANTIINFLAMMATORY ACTION<br/>[FR] FUROCHROMENES SUBSTITUES, PREPARATION DE CEUX-CI ET LEUR ACTION ANTI-INFLAMMATOIRE
    申请人:PLIVA ISTRAZIVACKI INST D O O
    公开号:WO2005010007A1
    公开(公告)日:2005-02-03
    The invention relates to novel compounds of formula (I) including all their tautomers to pharmaceutically acceptable salts and solvates thereof, to processes and reactive intermediates for the preparation thereof; to processes and reactive intermediates for the preparation of compounds of formula (II) including all their stereoisomers and tautomers to the use of the compounds of the formula (II) as suitable precursors for the preparation of the compounds of the formula (I) as well as to use of the compounds of the formula (I) and of the compounds of the formula (II) as therapeutically active agents in the prophylaxis and treatment of asthma and other inflammatory diesases and conditions in humans.
    该发明涉及公式(I)的新化合物,包括所有其互变异构体,以及其药学上可接受的盐和溶剂化合物;用于其制备的过程和活性中间体;用于制备公式(II)化合物的过程和活性中间体,包括其所有立体异构体和互变异构体;将公式(II)化合物用作公式(I)化合物的适当前体的用途,以及将公式(I)化合物和公式(II)化合物用作在人类预防和治疗哮喘和其他炎症性疾病和症状中的治疗活性剂的用途。
  • Substituted furochromenes, preparation thereof and their antiinflammatory action
    申请人:Mercep Mladen
    公开号:US20060148889A1
    公开(公告)日:2006-07-06
    The invention relates to novel compounds of the formula (I) including all their tautomers, to pharmaceutically acceptable salts and solvates thereof, to processes and reactive intermediates for the preparation thereof, and to processes and reactive intermediates for the preparation of the compounds of the formula (II) including all their stereoisomers and tautomers to the use of the compounds of the formula (II) as suitable precursors for the preparation of the compounds of the formula (I) as well as to use of the compounds of the formula (I) and of the compounds of the formula (II) as therapeutically active agents in the prophylaxis and treatment of asthma and other inflammatory diesases and conditions in humans.
    本发明涉及公式(I)的新化合物及其所有互变异构体,其药学上可接受的盐和溶剂化物,以及其制备的过程和反应中间体,以及公式(II)的化合物及其所有立体异构体和互变异构体的制备过程和反应中间体。本发明还涉及使用公式(II)的化合物作为制备公式(I)的合适前体,以及使用公式(I)和公式(II)的化合物作为治疗哮喘和其他人类炎症疾病和病况的治疗活性剂的用途。
  • Coumarin derivative as antiviral agent, pharmaceutical composition thereof, its preparation and use
    申请人:I-NOVA MEDICINSKA ISTRAZIVANJA D.O.O.
    公开号:US10266545B2
    公开(公告)日:2019-04-23
    The present invention discloses the novel coumarin derivative of formula (1): its synthesis, pharmaceutical composition, preparation and use thereof. The pharmaceutical composition including: (1) the novel coumarin derivative of formula (1) as active pharmaceutical ingredient; and (2) one or more pharmaceutical excipients, required to yield final dosage forms suitable for therapeutic administration. The composition is safe and efficient therapeutic agent for viral diseases including the acquired immunodeficiency syndrome (AIDS).
    本发明公开了式 (1) 的新型香豆素生物: 的合成、药物组合物、制备及其用途。该药物组合物包括:(1) 作为活性药物成分的式 (1) 新型香豆素生物;(2) 一种或多种药用赋形剂,这些赋形剂需要制成适合治疗用药的最终剂型。该组合物是治疗包括获得性免疫缺陷综合征(艾滋病)在内的病毒性疾病的安全有效的治疗剂。
  • SUBSTITUTED FUROCHROMENES, PREPARATION THEREOF AND THEIR ANTIINFLAMMATORY ACTION
    申请人:PLIVA-ISTRAZIVACKI INSTITUT d.o.o.
    公开号:EP1648902A1
    公开(公告)日:2006-04-26
  • COUMARIN DERIVATIVE AS ANTIVIRAL AGENT, PHARMACEUTICAL COMPOSITION THEREOF, ITS PREPARATION AND USE
    申请人:I-NOVA MEDICINSKA ISTRAZIVANJA d.o.o.
    公开号:EP3277692B1
    公开(公告)日:2019-09-11
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