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3-Methoxy-6-methyl-xanthon | 92496-81-6

中文名称
——
中文别名
——
英文名称
3-Methoxy-6-methyl-xanthon
英文别名
3-methoxy-6-methylxanthone;3-methoxy-6-methyl-xanthen-9-one;3-Methoxy-6-methylxanthen-9-one
3-Methoxy-6-methyl-xanthon化学式
CAS
92496-81-6
化学式
C15H12O3
mdl
——
分子量
240.258
InChiKey
LJHUSWTYTDDVOG-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):
    3.3
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    3-Methoxy-6-methyl-xanthonN-溴代丁二酰亚胺(NBS)过氧化苯甲酰 作用下, 以 四氯化碳 为溶剂, 反应 6.0h, 生成
    参考文献:
    名称:
    Drifting of heme-coordinating group in imidazolylmethylxanthones leading to improved selective inhibition of CYP11B1
    摘要:
    An abnormal increase in glucocorticoid levels is responsible for pathological disorders affecting different organs and systems, and the selective inhibition of appropriate steroidogenic enzymes represents a validated strategy to restore their physiological levels. In continuing, our studies on CYP11B inhibitors, in this paper a small series of 6-substituted 3-imidazolylmethylxanthones was designed and synthesized, according to the data acquired from previously reported series of derivatives and from a purposely-performed docking study. The new compounds proved to be potent inhibitors of CYP11B isoforms, being effective on CYP1161 in the low nanomolar range and improving selectivity with respect to CYP11B2, compared to previously reported related compounds. These data further confirmed that a suitable mutual arrangement of the imidazolylmethyl pharmacophore and a properly selected substituent on the xanthone core allows a fine tuning of the activity towards the different CYPs and further corroborate the role of the xanthone scaffold as a privileged structure in this field. (C) 2017 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2017.07.078
  • 作为产物:
    描述:
    2-羟基-4-甲氧基苯甲醛3,4-二溴甲苯 在 bis-triphenylphosphine-palladium(II) chloride 、 potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 12.0h, 生成 3-Methoxy-6-methyl-xanthon6-methoxy-2-methylxanthone
    参考文献:
    名称:
    One-step preparation of xanthones via Pd-catalyzed annulation of 1,2-dibromoarenes and salicylaldehydes
    摘要:
    开发了一种通过钯催化 1,2-二溴烯烃和水杨醛环化一步法制备氧杂蒽酮的方法。
    DOI:
    10.1039/b913951f
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文献信息

  • US3949076A
    申请人:——
    公开号:US3949076A
    公开(公告)日:1976-04-06
  • US3961069A
    申请人:——
    公开号:US3961069A
    公开(公告)日:1976-06-01
  • US3980788A
    申请人:——
    公开号:US3980788A
    公开(公告)日:1976-09-14
  • US4005208A
    申请人:——
    公开号:US4005208A
    公开(公告)日:1977-01-25
  • US5516794A
    申请人:——
    公开号:US5516794A
    公开(公告)日:1996-05-14
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