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2-(azetidine-1-sulfonyl)-2-methyl-N-(4-thiophen-2-yl-thiazol-2-yl)-propionamide | 1151712-62-7

中文名称
——
中文别名
——
英文名称
2-(azetidine-1-sulfonyl)-2-methyl-N-(4-thiophen-2-yl-thiazol-2-yl)-propionamide
英文别名
2-(azetidin-1-ylsulfonyl)-2-methyl-N-(4-thiophen-2-yl-1,3-thiazol-2-yl)propanamide
2-(azetidine-1-sulfonyl)-2-methyl-N-(4-thiophen-2-yl-thiazol-2-yl)-propionamide化学式
CAS
1151712-62-7
化学式
C14H17N3O3S3
mdl
——
分子量
371.505
InChiKey
MUTITCUYDLWMHR-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):
    2.4
  • 重原子数:
    23
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    144
  • 氢给体数:
    1
  • 氢受体数:
    7

文献信息

  • Compounds Which Modulate The CB2 Receptor
    申请人:Berry Angela
    公开号:US20100331304A1
    公开(公告)日:2010-12-30
    Compounds of formula (I) are disclosed. Compounds according to the invention bind to and are agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
    公式(I)的化合物被披露。本发明的化合物与CB2受体结合并具有激动剂作用,可用于治疗炎症。那些具有激动剂作用的化合物还可用于治疗疼痛。
  • AROMATIC HETEROCYCLIC FIVE-MEMBERED RING DERIVATIVE HAVING TRPV4 INHIBITORY ACTIVITY
    申请人:Shionogi & Co., Ltd.
    公开号:EP2832731A1
    公开(公告)日:2015-02-04
    The present invention is related to a compound represented by formula (I) wherein R1 is a hydrogen atom, substituted or unsubstituted alkyl, substituted or unsubstituted aromatic carbocyclyl, or the like; X is -N(R3)-, -O-, or -S-; Y is =C(R4)-, or =N-; Z is -N(R7)-, -O-, or -S-; R2 is substituted or unsubstituted alkyloxy, or the like, or a group represented by the following formula: -(CR2aR2b)n-R2c, wherein R2a is each independently a hydrogen atom, halogen, or the like; R2b is each independently a hydrogen atom, halogen, or the like; R2a and R2b which are attached to the same carbon atom may be taken together to form oxo, a substituted or unsubstituted non-aromatic carbocycle, or the like; two of R2a which are attached to the adjacent carbon atoms and/or two of R2b which are attached to the adjacent carbon atoms may be taken together to form a bond; R2c is substituted or unsubstituted aromatic carbocyclyl, or the like; n is an integer from 1 to 3; R3 and R7 are each independently a hydrogen atom, substituted or unsubstituted alkyl, or the like; R4 and R5 are each independently a hydrogen atom, halogen, substituted or unsubstituted alkyl, or the like; R6 is a hydrogen atom, halogen, substituted or unsubstituted alkyl, or the like, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising thereof.
    本发明涉及一种由式(I)表示的化合物 其中 R1 是氢原子、取代或未取代的烷基、取代或未取代的芳香族羰基或类似物;X 是-N(R3)-、-O-或-S-;Y 是=C(R4)-、或=N-;Z 是-N(R7)-、-O-或-S-; R2 是取代或未取代的烷氧基,或类似物,或下式所代表的基团:-(CR2aR2b)n-R2c,其中 R2a 各自独立地为氢原子、卤素或类似物;R2b 各自独立地为氢原子、卤素或类似物;连接到相同碳原子上的 R2a 和 R2b 可一起形成氧代、取代或未取代的非芳香族碳环或类似物;与相邻碳原子相连的两个 R2a 和/或与相邻碳原子相连的两个 R2b 可结合在一起形成键; R2c 是取代或未取代的芳香族碳环或类似物; n 是 1 到 3 的整数; R3 和 R7 各自独立地为氢原子、取代或未取代的烷基或类似物; R4 和 R5 各自独立地为氢原子、卤素、取代或未取代的烷基或类似物; R6 是氢原子、卤素、取代或未取代的烷基或类似物、 或其药学上可接受的盐,或由其组成的药物组合物。
  • COMPOUNDS WHICH MODULATE THE CB2 RECEPTOR
    申请人:Boehringer Ingelheim International GmbH
    公开号:EP2217565A1
    公开(公告)日:2010-08-18
  • AROMATIC 5-MEMBERED HETEROCYCLIC DERIVATIVE HAVING TRPV4-INHIBITING ACTIVITY
    申请人:Shionogi & Co., Ltd.
    公开号:US20170066759A1
    公开(公告)日:2017-03-09
    The present invention is related to a compound represented by formula (I) wherein R 1 is a hydrogen atom, substituted or unsubstituted alkyl, substituted or unsubstituted aromatic carbocyclyl, or the like; X is —N(R 3 )—, —O—, or —S—; Y is ═C(R 4 )—, or ═N—; Z is —N(R 7 )—, —O—, or —S—; R 2 is substituted or unsubstituted alkyloxy, or the like, or a group represented by the following formula: —(CR 2a R 2b ) n —R 2c , wherein R 2a is each independently a hydrogen atom, halogen, or the like; R 2b is each independently a hydrogen atom, halogen, or the like; R 2a and R 2b which are attached to the same carbon atom may be taken together to form oxo, a substituted or unsubstituted non-aromatic carbocycle, or the like; two of R 2a which are attached to the adjacent carbon atoms and/or two of R 2b which are attached to the adjacent carbon atoms may be taken together to form a bond; R 2c is substituted or unsubstituted aromatic carbocyclyl, or the like; n is an integer from 1 to 3; R 3 and R 7 are each independently a hydrogen atom, substituted or unsubstituted alkyl, or the like; R 4 and R 5 are each independently a hydrogen atom, halogen, substituted or unsubstituted alkyl, or the like; R 6 is a hydrogen atom, halogen, substituted or unsubstituted alkyl, or the like, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising thereof.
  • US8546563B2
    申请人:——
    公开号:US8546563B2
    公开(公告)日:2013-10-01
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