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2-(4-chloro-phenoxy)-6-methyl-nicotinic acid | 65239-36-3

中文名称
——
中文别名
——
英文名称
2-(4-chloro-phenoxy)-6-methyl-nicotinic acid
英文别名
2-(4-Chlorophenoxy)-6-methylpyridine-3-carboxylic acid
2-(4-chloro-phenoxy)-6-methyl-nicotinic acid化学式
CAS
65239-36-3
化学式
C13H10ClNO3
mdl
——
分子量
263.68
InChiKey
HXAZUGQXFCLTTQ-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

物化性质

  • 熔点:
    144-145 °C(Solv: ethanol (64-17-5); water (7732-18-5))
  • 沸点:
    401.8±45.0 °C(Predicted)
  • 密度:
    1.359±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    59.4
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-(4-chloro-phenoxy)-6-methyl-nicotinic acid 生成 7-chloro-2-methyl-chromeno[2,3-b]pyridin-5-one
    参考文献:
    名称:
    NANTKA-NAMIRSKI P.; PIECHACZEK J.; WROTEK J., ACTA POL. PHARM., 1977, 34, NO 1, 1-7
    摘要:
    DOI:
  • 作为产物:
    描述:
    2-氯-6-甲基烟酸乙酯caesium carbonate 、 lithium hydroxide 作用下, 以 四氢呋喃N,N-二甲基乙酰胺 为溶剂, 反应 52.0h, 生成 2-(4-chloro-phenoxy)-6-methyl-nicotinic acid
    参考文献:
    名称:
    Discovery of a new class of glucosylceramide synthase inhibitors
    摘要:
    A novel series of potent inhibitors of glucosylceramide synthase are described. The optimization of biochemical and cellular potency as well as ADME properties led to compound 23c. Broad tissue distribution was obtained following oral administration to mice. Thus 23c could be another useful tool compound for studying the effects of GCS inhibition in vitro and in vivo. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.09.037
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文献信息

  • [EN] GLUCOSYLCERAMIDE SYNTHASE INHIBITORS<br/>[FR] INHIBITEURS DE LA GLUCOSYLCÉRAMIDE SYNTHASE
    申请人:EXELIXIS INC
    公开号:WO2010091104A1
    公开(公告)日:2010-08-12
    The present invention comprises glucosylceramide synthase (GCS) inhibitors of structural formula (I), and pharmaceutically acceptable salts thereof, wherein R1, E, A, L, X1, Q, R4, R5, m and n, are as defined herein, as well as N-oxides of them and pharmaceutically acceptable salts thereof. The invention further comprises composition comprising the compounds, N-oxides, and/or pharmaceutically acceptable salts thereof. The invention also comprises use of the compounds and compositions for treating diseases in which GCS is a mediator or is implicated. The invention also comprises use of the compounds in and for the manufacture of medicaments, particularly for treating diseases in which GCS is a mediator or is implicated.
  • Discovery of a new class of glucosylceramide synthase inhibitors
    作者:Elena Koltun、Steven Richards、Vicky Chan、Jason Nachtigall、Hongwang Du、Kevin Noson、Adam Galan、Naing Aay、Art Hanel、Amanda Harrison、Jeff Zhang、Kwang-Ai Won、Danny Tam、Fawn Qian、Tao Wang、Patricia Finn、Kathleen Ogilvie、Jon Rosen、Raju Mohan、Christopher Larson、Peter Lamb、John Nuss、Patrick Kearney
    DOI:10.1016/j.bmcl.2011.09.037
    日期:2011.11
    A novel series of potent inhibitors of glucosylceramide synthase are described. The optimization of biochemical and cellular potency as well as ADME properties led to compound 23c. Broad tissue distribution was obtained following oral administration to mice. Thus 23c could be another useful tool compound for studying the effects of GCS inhibition in vitro and in vivo. (C) 2011 Elsevier Ltd. All rights reserved.
  • NANTKA-NAMIRSKI P.; PIECHACZEK J.; WROTEK J., ACTA POL. PHARM., 1977, 34, NO 1, 1-7
    作者:NANTKA-NAMIRSKI P.、 PIECHACZEK J.、 WROTEK J.
    DOI:——
    日期:——
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