摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4,6-Dimethyloctan-3,5-dione

中文名称
——
中文别名
——
英文名称
4,6-Dimethyloctan-3,5-dione
英文别名
2,4-dimethyloctane-3,5-dione
4,6-Dimethyloctan-3,5-dione化学式
CAS
——
化学式
C10H18O2
mdl
——
分子量
170.25
InChiKey
HMICEBPJFQKUJR-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):
    2.2
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • PYRIDAZINE COMPOUND
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP3118200A1
    公开(公告)日:2017-01-18
    The present provides a pyridazine compound having an inhibiting effect on Stearoyl-CoA desaturase (SCD) (in particular, SCD1). The present provides a compound represented by formula (where each symbol is as defined as in the Specification) or a salt thereof
    本发明提供了一种对硬脂酰辅酶A去饱和酶(SCD)(特别是SCD1)具有抑制作用的吡啶啉化合物。本发明提供了一种由以下公式表示的化合物(其中每个符号如规范中定义)或其盐。
  • HETEROCYCLIC COMPOUND
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US20210363130A1
    公开(公告)日:2021-11-25
    Provided is a compound that may have a superior CDK12 inhibitory action and is expected to be useful as a prophylactic or therapeutic drug for cancer and the like. A compound represented by the following formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof.
    提供了一种可能具有优越的CDK12抑制作用并且预计可用作癌症等疾病的预防或治疗药物的化合物。具有以下化学式(I)所代表的化合物,其中每个符号如描述中所述,或其盐。
  • HETEROCYCLIC COMPOUND AND USE THEREFOR
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US20150126487A1
    公开(公告)日:2015-05-07
    The present invention provides a compound having a cholinergic muscarinic M1 receptor positive allosteric modulator activity, and useful as a prophylactic or therapeutic drug for Alzheimer's disease, schizophrenia, pain, a sleep disorder and the like. The present invention relates to a compound represented by the formula (I): wherein R 1 is an optionally substituted amino group or an optionally substituted cyclic amino group, R 2 and R 3 are each independently a hydrogen atom or a substituent, X is —CH═ or —N═, and ring A is an optionally substituted 5- to 10-membered ring, or a salt thereof.
    本发明提供了一种具有胆碱能肌动蛋白M1受体正变构调节剂活性的化合物,可用作预防或治疗阿尔茨海默病、精神分裂症、疼痛、睡眠障碍等药物。本发明涉及一种由式(I)表示的化合物:其中R1是可选取代的氨基或可选取代的环状氨基,R2和R3各自独立地是氢原子或取代基,X是—CH═或—N═,环A是可选取代的5-至10-成员环,或其盐。
  • Fused heterocyclic compound
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US10577382B2
    公开(公告)日:2020-03-03
    Provided is a compound represented by the following formula, or a salt thereof: [wherein each symbol is as defined herein].
    本文提供了下式所代表的化合物或其盐: [其中各符号与本文定义相同]。
  • NITROGEN-CONTAINING HETEROCYCLIC COMPOUND
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP2921480B1
    公开(公告)日:2017-10-11
查看更多