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3,6-Dihydroxychalcone

中文名称
——
中文别名
——
英文名称
3,6-Dihydroxychalcone
英文别名
(E)-3-(2,5-dihydroxyphenyl)-1-phenylprop-2-en-1-one
3,6-Dihydroxychalcone化学式
CAS
——
化学式
C15H12O3
mdl
——
分子量
240.25
InChiKey
APPPFSLINJPIJH-SOFGYWHQSA-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
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • Biologically active 1,3-bis-aromatic-prop-2-en-1-ones, 1,3-bis-aromatic-propan-1-ones, and 1,3-bis-aromatic-prop-2-yn-1-ones
    申请人:Statens Serum Institute
    公开号:US20030065039A1
    公开(公告)日:2003-04-03
    The invention relates to the use of 1,3-bis-aromatic-prop-2-en-1-ones (chalcones), 1,3-bis-aromatic-propan-1-ones (dihydrochalcones), and 1,3-bis-aromatic-prop-2-yn-1-ones for the preparation of pharmaceutical compositions for the treatment or prophylaxis of a number of serious diseases including i) conditions relating to harmful effects of inflammatory cytokines, ii) conditions involving infection by Helicobacter species, iii) conditions involving infection by viruses, iv) neoplastic disorders, and v) conditions caused by microorganisms or parasites. The invention also relates to novel chalcones and dihydrochalcones (especially alkoxy substituted variants) having advantageous substitution patterns with respect to their effect as drug substances, and to methods of preparing them, as well as to pharmaceutical compositions comprising the novel chalcones. Moreover, the present invention relates to a method for the isolation of Leishmania fumarate reductase, QSAR methodologies for selecting potent compounds for the above-mentioned purposes.
    该发明涉及使用1,3-双芳基-丙-2-烯-1-酮(香豆素)、1,3-双芳基-丙酮-1-酮(二氢香豆素)和1,3-双芳基-丙-2-炔-1-酮制备用于治疗或预防多种严重疾病的药物组合物,包括i)与炎症细胞因子有害作用相关的疾病,ii)涉及幽门螺旋杆菌感染的疾病,iii)涉及病毒感染的疾病,iv)肿瘤性疾病,v)由微生物或寄生虫引起的疾病。该发明还涉及新型香豆素和二氢香豆素(特别是烷氧基取代变体),其具有有利的取代模式,对其作为药物物质的效果,以及制备它们的方法,以及包含新型香豆素的药物组合物。此外,本发明涉及一种用于分离利什曼氏弓形虫富马酸还原酶的方法,以及用于选择上述目的的有效化合物的QSAR方法。
  • NEW DRUG FOR INHIBITING AGGREGATION OF PROTEINS INVOLVED IN DISEASES LINKED TO PROTEIN AGGREGATION AND/OR NEURODEGENERATIVE DISEASES
    申请人:Giese Armin
    公开号:US20110293520A1
    公开(公告)日:2011-12-01
    The present invention relates to a compound represented by formula (E). The present invention also relates to a compound represented by the formula (E) for use in the treatment or prevention of diseases linked to protein aggregation and/or neurodegenerative diseases. Moreover, the present invention relates to pharmaceutical and diagnostic compositions comprising the compound of the invention as well as to a kit. Furthermore, the present invention relates to a method of imaging deposits of aggregated protein. A kit for preparing a detectably labelled compound of the present invention is also disclosed. Formula (E) wherein X, Y and L are independently nondirectionally selected from —C(R 1 )(R 2 )—, —C(R 3 )═, —N(R 4 )—, —N═, —N + (R 5 )═, —O— and —S—; M and Z are independently nondirectionally selected from formula (I) and formula (II).
    本发明涉及一种由公式(E)表示的化合物。本发明还涉及一种由公式(E)表示的化合物,用于治疗或预防与蛋白质聚集和/或神经退行性疾病相关的疾病。此外,本发明涉及包含本发明化合物的制药和诊断组合物,以及一种试剂盒。此外,本发明还涉及一种成像聚集蛋白沉积物的方法。还公开了一种用于制备可检测标记的本发明化合物的试剂盒。公式(E)中,X、Y和L分别独立地从—C(R1)(R2)—、—C(R3)═、—N(R4)—、—N═、—N+(R5)═、—O—和—S—中非定向选择;M和Z分别独立地从公式(I)和公式(II)中非定向选择。
  • DRUG FOR INHIBITING AGGREGATION OF PROTEINS INVOLVED IN DISEASES LINKED TO PROTEIN AGGREGATION AND/OR NEURODEGENERATIVE DISEASES
    申请人:Ludwig-Maximilians-Universität München
    公开号:US20160185730A1
    公开(公告)日:2016-06-30
    The present invention relates to a compound represented by formula (E). The present invention also relates to a compound represented by the formula (E) for use in the treatment or prevention of diseases linked to protein aggregation and/or neurodegenerative diseases. Moreover, the present invention relates to pharmaceutical and diagnostic compositions comprising the compound of the invention as well as to a kit. Furthermore, the present invention relates to a method of imaging deposits of aggregated protein. A kit for preparing a detectably labelled compound of the present invention is also disclosed.
    本发明涉及一种由式(E)所表示的化合物。本发明还涉及一种由式(E)所表示的化合物,用于治疗或预防与蛋白质聚集和/或神经退行性疾病有关的疾病。此外,本发明还涉及包含本发明化合物的制药和诊断组合物,以及一种试剂盒。此外,本发明还涉及一种成像聚集蛋白沉积物的方法。还公开了一种用于制备本发明化合物的可检测标记试剂盒。
  • Drugs for inhibiting aggregation of proteins invoved in diseases linked to protein aggregation and/or neurodegenerative diseases
    申请人:Ludwig-Maximilians-Universität München
    公开号:EP2687513A1
    公开(公告)日:2014-01-22
    The present invention relates to a compound represented by formula (E). The present invention also relates to a compound represented by the formula (E) for use in the treatment or prevention of diseases linked to protein aggregation and/or neurodegenerative diseases. Moreover, the present invention relates to pharmaceutical and diagnostic compositions comprising the compound of the invention as well as to a kit. Furthermore, the present invention relates to a method of imaging deposits of aggregated protein. A kit for preparing a detectably labelled compound of the present invention is also disclosed.
    本发明涉及一种由式(E)代表的化合物。本发明还涉及一种由式(E)代表的化合物,用于治疗或预防与蛋白质聚集相关的疾病和/或神经退行性疾病。此外,本发明还涉及包含本发明化合物的药物和诊断组合物以及试剂盒。此外,本发明还涉及一种对聚集蛋白沉积物成像的方法。本发明还公开了一种用于制备可检测标记的本发明化合物的试剂盒。
  • DRUGS FOR INHIBITING AGGREGATION OF PROTEINS INVOLVED IN DISEASES LINKED TO PROTEIN AGGREGATION AND/OR NEURODEGENERATIVE DISEASES
    申请人:Ludwig-Maximilians-Universität München
    公开号:EP2684873A1
    公开(公告)日:2014-01-15
    The present invention relates to a compound represented by formula (E). The present invention also relates to a compound represented by the formula (E) for use in the treatment or prevention of diseases linked to protein aggregation and/or neurodegenerative diseases. Moreover, the present invention relates to pharmaceutical and diagnostic compositions comprising the compound of the invention as well as to a kit. Furthermore, the present invention relates to a method of imaging deposits of aggregated protein. A kit for preparing a detectably labelled compound of the present invention is also disclosed.
    本发明涉及一种由式(E)代表的化合物。本发明还涉及一种由式(E)代表的化合物,用于治疗或预防与蛋白质聚集相关的疾病和/或神经退行性疾病。此外,本发明还涉及包含本发明化合物的药物和诊断组合物以及试剂盒。此外,本发明还涉及一种对聚集蛋白沉积物成像的方法。本发明还公开了一种用于制备可检测标记的本发明化合物的试剂盒。
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