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(3-氯-2,4-二氟苯基)甲醇 | 886501-09-3

中文名称
(3-氯-2,4-二氟苯基)甲醇
中文别名
——
英文名称
(3-chloro-2,4-difluorophenyl)methanol
英文别名
3-Chloro-2,4-difluorobenzyl alcohol
(3-氯-2,4-二氟苯基)甲醇化学式
CAS
886501-09-3
化学式
C7H5ClF2O
mdl
——
分子量
178.566
InChiKey
OTKPKQYYPKSFPG-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):
    1.9
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 海关编码:
    2906299090

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Beta-secretase modulators and methods of use
    申请人:Zhong Wenge
    公开号:US20070185144A1
    公开(公告)日:2007-08-09
    The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula I wherein A, B, W, R 3 , R 4 , R 5 , i and j are defined herein. The invention also comprises pharmaceutical compositions including one or more compounds of Formula I, methods of use for these compounds, including treatment of AD and related diseases, by administering the compound(s) of Formula I, or compositions including them, to a subject. The invention also comprises further embodiments of Formulas II and III, intermediates and processes useful for the preparation of compounds of the invention.
    本发明涉及一类新型化合物,可用于调节β-分泌酶酶活性和治疗β-分泌酶介导的疾病,包括阿尔茨海默病(AD)和相关疾病。在一种实施方式中,化合物具有通式I,其中A、B、W、R3、R4、R5、i和j在此定义。本发明还包括包含一个或多个通式I化合物的药物组合物,以及使用这些化合物的方法,包括通过将通式I化合物或包含它们的组合物给予受试者治疗AD和相关疾病。本发明还包括通式II和III的进一步实施方式,以及用于制备本发明化合物的中间体和过程。
  • Beta-Secretase modulators and methods of use
    申请人:Amgen Inc.
    公开号:US07973047B2
    公开(公告)日:2011-07-05
    The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula I wherein A, B, W, R3, R4, R5, i and j are defined herein. The invention also comprises pharmaceutical compositions including one or more compounds of Formula I, methods of use for these compounds, including treatment of AD and related diseases, by administering the compound(s) of Formula I, or compositions including them, to a subject. The invention also comprises further embodiments of Formulas II and III, intermediates and processes useful for the preparation of compounds of the invention.
    本发明涉及一类新的化合物,用于调节Beta-分泌酶酶活性和治疗Beta-分泌酶介导的疾病,包括阿尔茨海默氏病(AD)和相关疾病。在一种实施例中,所述化合物具有一般式I,其中A、B、W、R3、R4、R5、i和j在此定义。本发明还涉及包括一种或多种I式化合物的制药组合物,以及使用这些化合物的方法,包括通过将I式化合物或包含它们的组合物用于治疗AD和相关疾病来给予受试者。本发明还涉及进一步的II式和III式的实施例,以及制备本发明化合物的中间体和过程。
  • BETA-SECRETASE MODULATORS AND METHODS OF USE
    申请人:Zhong Wenge
    公开号:US20100222338A1
    公开(公告)日:2010-09-02
    The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula I wherein A, B, W, R 3 , R 4 , R 5 , i and j are defined herein. The invention also comprises pharmaceutical compositions including one or more compounds of Formula I, methods of use for these compounds, including treatment of AD and related diseases, by administering the compound(s) of Formula I, or compositions including them, to a subject. The invention also comprises further embodiments of Formulas II and III, intermediates and processes useful for the preparation of compounds of the invention.
    本发明涉及一类新型化合物,可用于调节β-分泌酶酶活性和治疗β-分泌酶介导的疾病,包括阿尔茨海默病(AD)和相关疾病。在一种实施例中,该化合物具有一般式I,其中A、B、W、R3、R4、R5、i和j在此被定义。本发明还包括包含一种或多种I式化合物的制药组合物,以及使用这些化合物的方法,包括通过将I式化合物或包含它们的组合物用于治疗AD和相关疾病来给受试者施用。本发明还包括进一步的II式和III式的实施例,以及用于制备本发明化合物的中间体和方法。
  • Zaindole derivatives and their use as ERK kinase inhibitors
    申请人:AGV Discovery ENSCM
    公开号:US10995089B2
    公开(公告)日:2021-05-04
    The present invention concerns a compound of formula (I): H or one of its pharmaceutically acceptable salts, especially for use as inhibitors of the ERK kinase activity in particular ERK2 activity, it also concerns prodrugs of these compounds.
    本发明涉及式 (I):H或其药学上可接受的盐之一,特别是用作ERK激酶活性,尤其是ERK2活性的抑制剂,它还涉及这些化合物的原药。
  • AZAINDOLE DERIVATIVES AND THEIR USE AS ERK KINASE INHIBITORS
    申请人:AGV Discovery
    公开号:EP3377491A1
    公开(公告)日:2018-09-26
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