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3-tert-butoxy-azetidine-1-carboxylic acid (2-methyl-3-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridazin-3-yl}-phenyl)-amide | 1147529-00-7

中文名称
——
中文别名
——
英文名称
3-tert-butoxy-azetidine-1-carboxylic acid (2-methyl-3-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridazin-3-yl}-phenyl)-amide
英文别名
3-(tert-butoxy)-N-(2-methyl-3-(1-methyl-5-((5-(morpholin-4-ylcarbonyl)pyridin-2-yl)amino)-6-oxo-1,6-dihydropyridazin-3-yl)phenyl)azetidine-1-carboxamide;N-[2-methyl-3-[1-methyl-5-[[5-(morpholine-4-carbonyl)pyridin-2-yl]amino]-6-oxopyridazin-3-yl]phenyl]-3-[(2-methylpropan-2-yl)oxy]azetidine-1-carboxamide
3-tert-butoxy-azetidine-1-carboxylic acid (2-methyl-3-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridazin-3-yl}-phenyl)-amide化学式
CAS
1147529-00-7
化学式
C30H37N7O5
mdl
——
分子量
575.668
InChiKey
OYOLTXFPZYWKCV-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):
    1.8
  • 重原子数:
    42
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    129
  • 氢给体数:
    2
  • 氢受体数:
    8

文献信息

  • BTK protein kinase inhibitors
    申请人:Dewdney Nolan James
    公开号:US20090105209A1
    公开(公告)日:2009-04-23
    This application discloses pyridine and pyrimidine compounds according to formula I wherein R 1 , R 2 , R 3 , R 4 , R 5 , X 1 and A are as described herein which inhibit Btk. The compounds disclosed herein are useful to modulate the activity of Btk and treat diseases associated with excessive Btk activity. The compounds are further useful to treat inflammatory and auto immune diseases associated with aberrant B-cell proliferation such as rheumatoid arthritis. Also disclosed are compositions containing compounds of formula I and at least one carrier, diluent or excipient.
    这个申请公开了根据公式I的吡啶嘧啶化合物,其中R1、R2、R3、R4、R5、X1和A如本文所述,可抑制Btk。所公开的化合物有助于调节Btk的活性,并治疗与Btk活性过度相关的疾病。这些化合物进一步用于治疗与异常B细胞增殖相关的炎症和自身免疫疾病,如类风湿性关节炎。还公开了包含公式I化合物和至少一种载体、稀释剂或助剂的组合物。
  • [EN] PYRIDAZINONES AND THEIR USE AS BTK INHIBITORS<br/>[FR] PYRIDAZINONES ET LEUR UTILISATION COMME INHIBITEURS DE LA BTK
    申请人:CGI PHARMACEUTICALS INC
    公开号:WO2010056875A1
    公开(公告)日:2010-05-20
    Compounds of Formula (I) that inhibit Btk are described herein. Pharmaceutical compositions comprising at least one compound of Formula (I), together with at least one pharmaceutically acceptable vehicle chosen from carriers, adjuvants, and excipients, are described. Methods of treating patients suffering from certain diseases responsive to inhibition of Btk activity and/ or B-cell activity are described. Methods for determining the presence of Btk in a sample are described.
    本文描述了抑制Btk的化合物(I)。描述了包含至少一种化合物(I)的药物组合物,以及至少一种从载体、辅料和赋形剂中选择的药用可接受载体。描述了治疗对Btk活性和/或B细胞活性抑制敏感的患者的方法。描述了检测样品中Btk存在的方法。
  • PYRIDAZINONES, METHOD OF MAKING, AND METHOD OF USE THEREOF
    申请人:Barbosa JR. Antonio J.M.
    公开号:US20110301145A1
    公开(公告)日:2011-12-08
    Compounds of Formula I that inhibit Btk are described herein. Pharmaceutical compositions comprising at least one compound of Formula I, together with at least one pharmaceutically acceptable vehicle chosen from carriers, adjuvants, and excipients, are described. Methods of treating patients suffering from certain diseases responsive to inhibition of Btk activity and/or B-cell activity are described. Methods for determining the presence of Btk in a sample are described.
    本文描述了化学式I的化合物,其能够抑制Btk。本文还描述了包含至少一种化学式I化合物的制药组合物,以及至少选择自载体、佐剂和赋形剂中的一种药学可接受载体的制药组合物。本文还描述了治疗对Btk活性和/或B细胞活性抑制有响应的某些疾病的患者的方法。本文还描述了检测样品中Btk存在的方法。
  • NOVEL KINASE INHIBITORS
    申请人:F. Hoffmann-La Roche AG
    公开号:EP2426109A1
    公开(公告)日:2012-03-07
    Pyridine and pyrimidine compounds according to formula I wherein R1, R2, R3, R4, R5, X1 and A are as described herein which inhibit Btk. The compounds disclosed herein are useful to modulate the activity of Btk and treat diseases associated with excessive Btk activity. The compounds are further useful to treat inflammatory and auto immune diseases associated with aberrant B-cell proliferation such as rheumatoid arthritis. Also disclosed are compositions containing compounds of formula I and at least one carrier, diluent or excipient.
    符合式 I 的吡啶嘧啶化合物 其中 R1、R2、R3、R4、R5、X1 和 A 如本文所述,可抑制 Btk。本文公开的化合物可用于调节 Btk 的活性和治疗与 Btk 活性过高有关的疾病。这些化合物还可用于治疗与 B 细胞异常增殖有关的炎症和自身免疫疾病,如类风湿性关节炎。还公开了含有式 I 化合物和至少一种载体、稀释剂或赋形剂的组合物。
  • PYRIDAZINONES AND THEIR USE AS BTK INHIBITORS
    申请人:Gilead Connecticut, Inc.
    公开号:EP2365970B1
    公开(公告)日:2018-03-21
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