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2-(3-pyridylthio)pyrimidine

中文名称
——
中文别名
——
英文名称
2-(3-pyridylthio)pyrimidine
英文别名
2-Pyridin-3-ylsulfanylpyrimidine;2-pyridin-3-ylsulfanylpyrimidine
2-(3-pyridylthio)pyrimidine化学式
CAS
——
化学式
C9H7N3S
mdl
——
分子量
189.241
InChiKey
AFAXJJPAGZEUGD-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):
    1.5
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    64
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-吡啶溴化镁 、 2-thiocyanatopyrimidine四氢呋喃 为溶剂, 反应 1.0h, 以76%的产率得到2-(3-pyridylthio)pyrimidine
    参考文献:
    名称:
    Nagasaki, Izuru; Matsumoto, Miyuki; Yamashita, Masanori, Heterocycles, 1999, vol. 51, # 5, p. 1015 - 1024
    摘要:
    DOI:
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文献信息

  • RE-TRAFFICKING OF HERG REVERSES LONG QT SYNDROME 2 PHENOTYPE IN HUMAN IPS-DERIVED CARDIOMYOCYTES
    申请人:Singapore Health Services Pte Ltd
    公开号:EP2972323A2
    公开(公告)日:2016-01-20
  • RATIONAL COMBINATION THERAPY FOR THE TREATMENT OF CANCER
    申请人:Memorial Sloan Kettering Cancer Center
    公开号:EP3359196B1
    公开(公告)日:2022-03-16
  • METHODS AND COMPOSITIONS FOR TREATING INFLAMMATORY AND FIBROTIC PULMONARY DISORDERS
    申请人:University of Houston System
    公开号:US20210401987A1
    公开(公告)日:2021-12-30
    The present disclosure addresses inflammatory lung diseases, such as COPD, and fibrotic lung diseases such as idiopathic pulmonary fibrosis, from the standpoint of inhibiting or ablating pathogenic epithelial stem cells found in the pulmonary tract.
  • US9797883B2
    申请人:——
    公开号:US9797883B2
    公开(公告)日:2017-10-24
  • [EN] RE-TRAFFICKING OF HERG REVERSES LONG QT SYNDROME 2 PHENOTYPE IN HUMAN IPS-DERIVED CARDIOMYOCYTES<br/>[FR] RE-TRAFIC DU PHÉNOTYPE DU SYNDROME 2 DU QT LONG INVERSE DE HERG DANS DES CARDIOMYOCYTES DÉRIVÉS DE CELLULES PLURIPOTENTES INDUITES (IPS) HUMAINES
    申请人:SINGAPORE HEALTH SERV PTE LTD
    公开号:WO2014142760A2
    公开(公告)日:2014-09-18
    The present invention relates to generating hiPSC-derived cardiomyocytes and embryoid bodies that recapitulate the disease phenotype of Long QT Syndrome and their use in developing pharmacological treatments thereof. The present invention also includes the use of a compound which inhibits the ubiquitin-proteasome pathway for the preparation of a medicament for the prophylaxis or treatment of a disease associated with prolonged ventricular repolarization (cardiac arrhythmia) caused by one or more mutations in the amino acid sequence of the hERG potassium channel.
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