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4-{2-[3-(3-Fluoro-4-methoxy-phenyl)-prop-1-ynyl]-8-methyl-5,7-dioxo-7H-thiazolo[3,2-c]pyrimidin-6-ylmethyl}-cyclohexanecarboxylic acid | 449800-84-4

中文名称
——
中文别名
——
英文名称
4-{2-[3-(3-Fluoro-4-methoxy-phenyl)-prop-1-ynyl]-8-methyl-5,7-dioxo-7H-thiazolo[3,2-c]pyrimidin-6-ylmethyl}-cyclohexanecarboxylic acid
英文别名
4-[[2-[3-(3-Fluoro-4-methoxyphenyl)prop-1-ynyl]-8-methyl-5,7-dioxo-[1,3]thiazolo[3,2-c]pyrimidin-6-yl]methyl]cyclohexane-1-carboxylic acid
4-{2-[3-(3-Fluoro-4-methoxy-phenyl)-prop-1-ynyl]-8-methyl-5,7-dioxo-7H-thiazolo[3,2-c]pyrimidin-6-ylmethyl}-cyclohexanecarboxylic acid化学式
CAS
449800-84-4
化学式
C25H25FN2O5S
mdl
——
分子量
484.548
InChiKey
LFENGYVTNRGCAP-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):
    3.7
  • 重原子数:
    34
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    112
  • 氢给体数:
    1
  • 氢受体数:
    7

文献信息

  • Combination of an allosteric carboxylic inhibitor of matrix metalloproteinase-13 with celecoxib or valdecoxib
    申请人:——
    公开号:US20040019053A1
    公开(公告)日:2004-01-29
    This invention provides a combination, comprising an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof, with celecoxib, or a pharmaceutically acceptable salt thereof, or valdecoxib, or a pharmaceutically acceptable salt thereof. This invention also provides a method of treating a disease that is responsive to inhibition of MMP-13 and cyclooxygenase-2, comprising administering to a patient suffering from such a disease the invention combination comprising an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof, with celecoxib, or a pharmaceutically acceptable salt thereof, or valdecoxib, or a pharmaceutically acceptable salt thereof. This invention also provides a pharmaceutical composition, comprising the invention combination comprising an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof, with celecoxib, or a pharmaceutically acceptable salt thereof, or valdecoxib, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent, or excipient. The invention combination may also be further combined with other pharmaceutical agents depending on the disease being treated.
    该发明提供了一种组合物,包括MMP-13的变构羧酸抑制剂或其药用盐,与Celecoxib或其药用盐,或Valdecoxib或其药用盐。该发明还提供了一种治疗对MMP-13和环氧合酶-2抑制敏感的疾病的方法,包括向患有这种疾病的患者施用包括MMP-13的变构羧酸抑制剂或其药用盐,与Celecoxib或其药用盐,或Valdecoxib或其药用盐的组合物。该发明还提供了一种药物组合物,包括包括MMP-13的变构羧酸抑制剂或其药用盐,与Celecoxib或其药用盐,或Valdecoxib或其药用盐的组合物,以及药用载体、稀释剂或赋形剂。该发明组合物还可以根据所治疗的疾病进一步与其他药物代理结合。
  • Combination of an allosteric carboxylic inhibitor of matrix metalloproteinase-13 with a selective inhibitor of cyclooxygenase-2 that is not celecoxib or valdecoxib
    申请人:——
    公开号:US20040019054A1
    公开(公告)日:2004-01-29
    This invention provides a combination, comprising an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof, with a selective inhibitor of COX-2, or a pharmaceutically acceptable salt thereof, that is not celecoxib or valdecoxib. This invention also provides a method of treating a disease that is responsive to inhibition of MMP-13 and cyclooxygenase-2, comprising administering to a patient suffering from such a disease the invention combination comprising an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof, with a selective inhibitor of COX-2, or a pharmaceutically acceptable salt thereof, that is not celecoxib or valdecoxib. This invention also provides a pharmaceutical composition, comprising the invention combination comprising an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof, with a selective inhibitor of COX-2, or a pharmaceutically acceptable salt thereof, that is not celecoxib or valdecoxib, and a pharmaceutically acceptable carrier, diluent, or excipient. This invention also provides a combination comprising an NSAID, or a pharmaceutically acceptable salt thereof, and an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof. This invention also provides a pharmaceutical composition, comprising the invention combination comprising an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof, with an NSAID, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent, or excipient. This invention also provides a method of treating a disease that is responsive to inhibition of MMP-13 and cyclooxygenase-1 or cyclooxygenase-2, comprising administering to a patient suffering from such a disease the invention combination comprising an allosteric carboxylic inhibitor of MMP-13, or a pharmaceutically acceptable salt thereof, with an NSAID, or a pharmaceutically acceptable salt thereof. The invention combinations may also be further combined with other pharmaceutical agents depending on the disease being treated.
    本发明提供一种组合物,包括MMP-13的变构羧酸抑制剂或其药用盐,以及COX-2的选择性抑制剂或其药用盐,但不包括司来昔布或瓦来昔布。本发明还提供一种治疗对MMP-13和环氧合酶-2抑制响应的疾病的方法,包括向患有该疾病的患者施用包括MMP-13的变构羧酸抑制剂或其药用盐,以及COX-2的选择性抑制剂或其药用盐的本发明组合物,但不包括司来昔布或瓦来昔布。本发明还提供一种药物组合物,包括MMP-13的变构羧酸抑制剂或其药用盐,以及COX-2的选择性抑制剂或其药用盐的本发明组合物,但不包括司来昔布或瓦来昔布,以及药用载体、稀释剂或赋形剂。本发明还提供一种组合物,包括NSAID或其药用盐,以及MMP-13的变构羧酸抑制剂或其药用盐。本发明还提供一种药物组合物,包括MMP-13的变构羧酸抑制剂或其药用盐,以及NSAID或其药用盐的本发明组合物,以及药用载体、稀释剂或赋形剂。本发明还提供一种治疗对MMP-13和环氧合酶-1或环氧合酶-2抑制响应的疾病的方法,包括向患有该疾病的患者施用包括MMP-13的变构羧酸抑制剂或其药用盐,以及NSAID或其药用盐的本发明组合物。根据所治疾病的不同,本发明组合物也可以与其他药物组合。
  • BICYCLIC PYRIMIDINE MATRIX METALLOPROTEINASE INHIBITORS
    申请人:Dyer Dennis Richard
    公开号:US20060040957A1
    公开(公告)日:2006-02-23
    Selective MMP-13 inhibitors are bicyclic pyrimidines of the Formula I or a pharmaceutically acceptable salt thereof, wherein R 1 is hydrogen or alkyl; R 2 , R 3 , and R 4 include hydrogen, halo, alkyl, C≡C(CH 2 ) m aryl, CO 2 alkyl, CO 2 (CH 2 ) m aryl, COHN alkyl, and CONH(CH 2 ) m aryl; and X is O, S, SO, SO 2 , CH 2 , C═O, CHOH, NH, or NR 5 . A compound of Formula I, or a pharmaceutically acceptable salt thereof, is useful for treating cancer or arthritis.
    选择性MMP-13抑制剂是公式I的双环嘧啶或其药学上可接受的盐,其中R1为氢或烷基;R2,R3和R4包括氢,卤素,烷基,C≡C(CH2)芳基,CO2烷基, ( )芳基,COHN烷基和CONH( )芳基;X为O,S,SO,SO2, ,C═O,CHOH,NH或NR5。公式I的化合物或其药学上可接受的盐,可用于治疗癌症或关节炎。
  • COMBINATION OF AN ALLOSTERIC CARBOXYLIC INHIBITOR OF MATRIX METALLOPROTEINASE-13 WITH CELECOXIB OR VALDECOXIB
    申请人:Warner-Lambert Company LLC
    公开号:EP1530467A2
    公开(公告)日:2005-05-18
  • PHARMACEUTICAL COMPOSITIONS COMPRISING AN ALLOSTERIC CARBOXYLIC INHIBITOR OF MATRIX METALLOPROTEINASE-13 AND A SELECTIVE INHIBITOR OF CYCLOOXYGENASE-2
    申请人:Warner-Lambert Company LLC
    公开号:EP1530475A2
    公开(公告)日:2005-05-18
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