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3-chloromethyl-6,6-dimethyl-5, 6-dihydro-imidazo [2,1-b] thiazole | 864677-78-1

中文名称
——
中文别名
——
英文名称
3-chloromethyl-6,6-dimethyl-5, 6-dihydro-imidazo [2,1-b] thiazole
英文别名
3-(Chloromethyl)-6,6-dimethyl-5,6-dihydroimidazo[2,1-b]thiazole;3-(chloromethyl)-6,6-dimethyl-5H-imidazo[2,1-b][1,3]thiazole
3-chloromethyl-6,6-dimethyl-5, 6-dihydro-imidazo [2,1-b] thiazole化学式
CAS
864677-78-1
化学式
C8H11ClN2S
mdl
——
分子量
202.708
InChiKey
QCZJKWKRYIDOIX-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):
    1.1
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    40.9
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    3-chloromethyl-6,6-dimethyl-5, 6-dihydro-imidazo [2,1-b] thiazole4-二甲氨基吡啶 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下, 以 N,N-二甲基甲酰胺乙腈 为溶剂, 反应 5.66h, 生成
    参考文献:
    名称:
    [EN] GLYCOMIMETIC-PEPTIDOMIMETIC INHIBITORS OF E-SELECTINS AND CXCR4 CHEMOKINE RECEPTORS
    [FR] INHIBITEURS GLYCOMIMÉTIQUES-PEPTIDOMIMÉTIQUES DE SÉLECTINES E ET DE RÉCEPTEURS DE CHIMIOKINE CXCR4
    摘要:
    公开号:
    WO2012061662A9
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文献信息

  • [EN] IMIDAZOLINE DERIVATIVES AS CXCR4 MODULATORS<br/>[FR] DÉRIVÉS D'IMIDAZOLINE UTILISÉS EN TANT QUE MODULATEURS DE CXCR4
    申请人:UNIV PARIS
    公开号:WO2020201096A1
    公开(公告)日:2020-10-08
    The present invention provides novel compounds of formula (I) and pharmaceutical compositions containing these compounds. The compounds of formula (I) can act as CXCR4 modulators that specifically target the CXCR4 minor pocket, and they have further been found to inhibit the production of inflammatory cytokines in immune cells, which renders these compounds highly advantageous for use in therapy, particularly in the treatment or prevention of an inflammatory disorder, an autoimmune disorder, an autoinflammatory disorder, or an interferonopathy, such as, e.g., lupus erythematosus, dermatomyositis or rheumatoid arthritis.
    本发明提供了化合物的新结构(I)及含有这些化合物的药物组合物。式(I)化合物可以作为CXCR4调节剂,特异性靶向CXCR4小口袋,并且进一步发现能够抑制免疫细胞中炎症细胞因子的产生,使得这些化合物在治疗中具有极大的优势,特别适用于治疗或预防炎症性疾病、自身免疫性疾病、自身炎症性疾病或干扰素病,例如红斑狼疮、皮肌炎或类风湿性关节炎。
  • [EN] ISOTHIOUREA DERIVATIVES<br/>[FR] DERIVES D'ISOTHIO-UREE
    申请人:NOVARTIS AG
    公开号:WO2005085219A1
    公开(公告)日:2005-09-15
    The present invention relates to isothiourea derivatives, processes for their production, their uses, in particular in transplantation, autoimmune or infectious diseases, and pharmaceutical compositions containing them.
    本发明涉及异硫脲衍生物,其生产过程,它们的用途,特别是在移植,自身免疫或感染性疾病中的应用,以及包含它们的制药组合物。
  • ISOTHIOUREA DERIVATIVES
    申请人:Novartis AG
    公开号:EP1720845A1
    公开(公告)日:2006-11-15
  • Isothiourea derivatives
    申请人:Glickman Fraser
    公开号:US20070161618A1
    公开(公告)日:2007-07-12
    The present invention relates to isothiourea derivatives, processes for their production, their uses, in particular in transplantation, autoimmune or infectious diseases, and pharmaceutical compositions containing them.
  • IMIDAZOLINE DERIVATIVES AS CXCR4 MODULATORS
    申请人:Université de Paris
    公开号:US20220144853A1
    公开(公告)日:2022-05-12
    The present invention provides novel compounds of formula (I) and pharmaceutical compositions containing these compounds. The compounds of formula (I) can act as CXCR4 modulators that specifically target the CXCR4 minor pocket, and they have further been found to inhibit the production of inflammatory cytokines in immune cells, which renders these compounds highly advantageous for use in therapy, particularly in the treatment or prevention of an inflammatory disorder, an autoimmune disorder, an autoinflammatory disorder, or an interferonopathy, such as, e.g., lupus erythematosus, dermatomyositis or rheumatoid arthritis.
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