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2,6-dimethyl-3-methylthiopyridine | 116651-87-7

中文名称
——
中文别名
——
英文名称
2,6-dimethyl-3-methylthiopyridine
英文别名
2,6-Dimethyl-3-methylsulfanylpyridine
2,6-dimethyl-3-methylthiopyridine化学式
CAS
116651-87-7
化学式
C8H11NS
mdl
——
分子量
153.248
InChiKey
TWNQVKMOLBKVRJ-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:
    209.1±28.0 °C(Predicted)
  • 密度:
    1.05±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    38.2
  • 氢给体数:
    0
  • 氢受体数:
    2

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
  • 下游产品
    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

  • Combination therapy using a chemokine receptor 2 (CCR2) antagonist and a PD-1/PD-L1 inhibitor
    申请人:CHEMOCENTRYX, INC.
    公开号:US11304952B2
    公开(公告)日:2022-04-19
    The present disclosure is drawn to the combination therapy of a Chemokine Receptor 2 (CCR2) antagonist and a PD-1 and/or PD-L1 inhibitor in the treatment of cancer.
    本公开涉及化合因子受体 2 (CCR2) 拮抗剂与 PD-1 和/或 PD-L1 抑制剂在治疗癌症方面的联合疗法。
  • SUBSTITUTED BRIDGED UREA ANALOGS AS SIRTUIN MODULATORS
    申请人:GlaxoSmithKline Intellectual Property(No.2)Limited
    公开号:US20190048016A1
    公开(公告)日:2019-02-14
    The present invention relates to novel substituted bridged urea analog compounds of Formula (I) or pharmaceutically acceptable salts thereof, corresponding pharmaceutical compositions, processes for making and use of such compounds, alone or in combination with other therapeutic agents, as Sirtuin Modulators useful for increasing lifespan of a cell, and in treating and/or preventing a wide variety of diseases and disorders, which include, but are not limited to, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing as well as diseases or disorders that would benefit from increased mitochondrial activity.
  • COMBINATION THERAPY USING A CHEMOKINE RECEPTOR 2 (CCR2) ANTAGONIST AND A PD-1/PD-L1 INHIBITOR
    申请人:CHEMOCENTRYX, INC.
    公开号:US20190134049A1
    公开(公告)日:2019-05-09
    The present disclosure is drawn to the combination therapy of a Chemokine Receptor 2 (CCR2) antagonist and a PD-1 and/or PD-L1 inhibitor in the treatment of cancer.
  • COMPOSITION OF MATTER FOR USE IN ORGANIC LIGHT-EMITTING DIODES
    申请人:KYULUX, INC.
    公开号:US20200203622A1
    公开(公告)日:2020-06-25
    The present disclosure relates to compounds of Formula (I)-(V) as compounds capable of emitting delayed fluorescence and uses of these compounds in organic light-emitting diodes.
  • [EN] IMIDAZOPYRIMIDINES AS EED INHIBITORS AND THE USE THEREOF<br/>[FR] IMIDAZOPYRIMIDINES UTILISÉES EN TANT QU'INHIBITEURS DE EED ET LEUR UTILISATION
    申请人:UNIV MICHIGAN REGENTS
    公开号:WO2021011713A1
    公开(公告)日:2021-01-21
    The present disclosure provides compounds represented by Formula (I) wherein R1, R2, R3, and R4 are as defined in the specification, and the salts and solvates thereof. Compounds of Formula (I) are FED inhibitors. FED inhibitors are useful for the treatment of cancer and other diseases.
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