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2-(4-fluoro-2-chlorophenoxy)-2-methyl-propionic acid | 898265-63-9

中文名称
——
中文别名
——
英文名称
2-(4-fluoro-2-chlorophenoxy)-2-methyl-propionic acid
英文别名
2-(2-Chloro-4-fluorophenoxy)-2-methylpropanoic acid
2-(4-fluoro-2-chlorophenoxy)-2-methyl-propionic acid化学式
CAS
898265-63-9
化学式
C10H10ClFO3
mdl
——
分子量
232.639
InChiKey
OJMQZWOHNQSNPF-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

  • 沸点:
    330.0±27.0 °C(Predicted)
  • 密度:
    1.338±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2-(4-fluoro-2-chlorophenoxy)-2-methyl-propionic acid 在 O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate 、 三氟乙酸 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 27.0h, 生成
    参考文献:
    名称:
    Adamantane sulfone and sulfonamide 11-β-HSD1 Inhibitors
    摘要:
    Potent and selective adamantane sulfone and sulfonamide inhibitors of 11-beta-HSD-1 have been discovered. Selected compounds from these series have robust pharmacokinetic profiles and strongly inhibit liver, fat, and brain HSD1 for extended periods after oral dosing.
    DOI:
    10.1016/j.bmcl.2006.10.008
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文献信息

  • Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme
    申请人:Patel R. Jyoti
    公开号:US20060281773A1
    公开(公告)日:2006-12-14
    The present invention relates to compounds which are inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme. The present invention further relates to the use of inhibitors of 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme for the treatment of non-insulin dependent type 2 diabetes, insulin resistance, obesity, lipid disorders, metabolic syndrome and other diseases and conditions that are mediated by excessive glucocorticoid action.
    本发明涉及抑制11-β-羟基类固醇脱氢酶1型酶的化合物。本发明进一步涉及使用11-β-羟基类固醇脱氢酶1型酶抑制剂治疗非胰岛素依赖性2型糖尿病、胰岛素抵抗、肥胖症、脂质代谢紊乱、代谢综合征和其他由过度糖皮质激素作用介导的疾病和状况。
  • TRIAZOLE DERIVATIVE OR SALT THEREOF
    申请人:Yoshimura Seiji
    公开号:US20110105460A1
    公开(公告)日:2011-05-05
    [Problem] A compound, which can be used for preventing or treating diseases, in which 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) is concerned, in particular, diabetes, insulin resistance, dementia, schizophrenia and depression, is provided. [Means for Solution] It was found that a triazole derivative, in which one of the 3- and 5-positions of the triazole ring has (di)alkylmethyl or cycloalkyl, each of which is substituted with —O— (aryl or a heterocyclic group, each of which may be substituted, or lower alkylene-cycloalkyl), and the other thereof has aryl, a heterocyclic group or cycloalkyl, each of which may be substituted, or a pharmaceutically acceptable salt thereof exhibits potent 11β-HSD1 inhibitory action. From the above, the triazole derivative of the present invention can be used for preventing or treating diabetes, insulin resistance, dementia, schizophrenia and depression.
    [问题] 提供一种可用于预防或治疗疾病的化合物,其中涉及11β-羟基类固醇脱氢酶1型(11β-HSD1),特别是糖尿病、胰岛素抵抗、痴呆症、精神分裂症和抑郁症。 [解决方案] 发现一种三唑衍生物,其中三唑环的3-和5-位置之一具有(二)烷基甲基或环烷基,每个基团都被取代为-O-(苯基或杂环基,每个基团都可以被取代,或较低的烷基-环烷基),另一个位置具有苯基、杂环基或环烷基,每个基团都可以被取代,或其药学上可接受的盐,表现出强效的11β-HSD1抑制作用。因此,本发明的三唑衍生物可用于预防或治疗糖尿病、胰岛素抵抗、痴呆症、精神分裂症和抑郁症。
  • Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme
    申请人:Link James T.
    公开号:US20110218214A1
    公开(公告)日:2011-09-08
    The present invention relates to compounds which are inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme. The present invention further relates to the use of inhibitors of 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme for the treatment of non-insulin dependent type 2 diabetes, insulin resistance, obesity, lipid disorders, metabolic syndrome and other diseases and conditions that are mediated by excessive glucocorticoid action.
    本发明涉及一种抑制11-β-羟基类固醇脱氢酶1型酶的化合物。本发明还涉及使用11-β-羟基类固醇脱氢酶1型酶抑制剂治疗非胰岛素依赖型2型糖尿病、胰岛素抵抗、肥胖症、脂质代谢紊乱、代谢综合征和其他由过度糖皮质激素作用介导的疾病和病症。
  • INHIBITORS OF THE 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 1 ENZYME
    申请人:Bitner R. Scott
    公开号:US20130045978A1
    公开(公告)日:2013-02-21
    The present invention relates to inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme and their use in treatment of non-insulin dependent type 2 diabetes, insulin resistance, obesity, lipid disorders, metabolic syndrome, central nervous system disorders, and diseases and conditions that are related to excessive glucocorticoids.
    本发明涉及11-β-羟基类固醇脱氢酶1型酶的抑制剂及其在治疗非胰岛素依赖型2型糖尿病、胰岛素抵抗、肥胖症、脂质代谢紊乱、代谢综合症、中枢神经系统疾病以及与过度糖皮质激素相关的疾病和状况中的应用。
  • WO2006/74244
    申请人:——
    公开号:——
    公开(公告)日:——
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