2-amino-5-methylsulfanyl-N-thiazol-2-ylbenzamide | 603107-81-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-amino-5-methylsulfanyl-N-thiazol-2-ylbenzamide
• 英文别名: 2-Amino-5-(methylsulfanyl)-N-(1,3-thiazol-2-yl)benzamide；2-amino-5-methylsulfanyl-N-(1,3-thiazol-2-yl)benzamide
• CAS: 603107-81-9
• 化学式: C₁₁H₁₁N₃OS₂
• 分子量: 265.36
• InChiKey: RVNJXDOKFBSGKR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  122
• 氢给体数：
  2
• 氢受体数：
  5

文献信息

• NOVEL AMINOBENZAMIDE DERIVATIVE
  申请人：BANYU PHARMACEUTICAL CO., LTD.

  公开号：EP1496052A1

  公开（公告）日：2005-01-12

  This invention relates to a novel compound represented by the formula (I): or a pharmaceutically acceptable salt thereof,    wherein    R1 is -S(O)p-A, -S-(O)q-B or -O-D, wherein p and q, which are the same or different, each represent an integer from 0 to 2, A is a straight chain C1-C10 alkyl group which may be substituted by R10, and B and D each independently represent R12 which may be substituted by R10;    R2 is a hydrogen atom, a halogen atom, or a straight chain or branched C1-C6 alkyl group which may be substituted by R10;    X1 and X2 each independently represent N or CH, but cannot both be N;    the formula (II): shows a monocyclic or bicyclic heteroaryl group which has a nitrogen atom adjacent to the carbon atom bonded to the amide group, and the heteroaryl group may be substituted by R10;    R10 is R11, or a hydrocarbon group which may be substituted by R11;    R11 is, for example, a hydrogen atom or amino; and    R12 is, for example, phenyl, thiazolyl, pyridyl or methylene dioxyphenyl. The compound according to this invention has a glucokinase activation effect, and for example, is useful in the treatment and prevention of diabetes mellitus, and in the prevention of its complications such as diabetic nephropathy, diabetic retinopathy, diabetic neuropathy and diabetic arteriosclerosis.

  本发明涉及一种由式(I)代表的新型化合物： 或其药学上可接受的盐、 其中 R1是-S(O)p-A、-S-(O)q-B或-O-D，其中p和q相同或不同，各自代表0至2的整数，A是可被R10取代的直链C1-C10烷基，B和D各自独立地代表可被R10取代的R12； R2 是氢原子、卤素原子或可被 R10 取代的直链或支链 C1-C6 烷基； X1 和 X2 各自独立地代表 N 或 CH，但不能都是 N； 式 (II)： 表示单环或双环杂芳基，该杂芳基具有一个与酰胺基键合的碳原子相邻的氮原子，该杂芳基可被 R10 取代； R10 是 R11，或可被 R11 取代的烃基； R11 例如是氢原子或氨基；以及 R12 例如是苯基、噻唑基、吡啶基或亚甲基二氧苯基。 根据本发明的化合物具有葡萄糖激酶活化作用，例如，可用于治疗和预防糖尿病，以及预防其并发症，如糖尿病肾病、糖尿病视网膜病变、糖尿病神经病变和糖尿病动脉硬化。
• Novel aminobenzamide derivative
  申请人：Nishimura Teruyuki

  公开号：US20050282815A1

  公开（公告）日：2005-12-22

  This invention relates to a novel compound represented by the formula (I): or a pharmaceutically acceptable salt thereof, wherein R 1 is —S(O)p-A, —S—(O)q-B or —O-D, wherein p and q, which are the same or different, each represent an integer from 0 to 2, A is a straight chain C1-C10 alkyl group which may be substituted by R 10 , and B and D each independently represent R 12 which may be substituted by R 10 ; R 2 is a hydrogen atom, a halogen atom, or a straight chain or branched C1-C6 alkyl group which may be substituted by R 10 ; X 1 and X 2 each independently represent N or CH, but cannot both be N; the formula (II): shows a monocyclic or bicyclic heteroaryl group which has a nitrogen atom adjacent to the carbon atom bonded to the amide group, and the heteroaryl group may be substituted by R 10 ; R 10 is R 11 , or a hydrocarbon group which may be substituted by R 11 ; R 11 is, for example, a hydrogen atom or amino; and R 12 is, for example, phenyl, thiazolyl, pyridyl or methylene dioxyphenyl. The compound according to this invention has a glucokinase activation effect, and for example, is useful in the treatment and prevention of diabetes mellitus, and in the prevention of its complications such as diabetic nephropathy, diabetic retinopathy, diabetic neuropathy and diabetic arteriosclerosis.

  本发明涉及一种由式（I）代表的新型化合物： 或其药学上可接受的盐，其中 R 1 是-S(O)p-A、-S-(O)q-B 或-O-D，其中 p 和 q 相同或不同，各代表 0 至 2 的整数，A 是可被 R 取代的直链 C1-C10 烷基 10 B 和 D 各自独立地代表 R 12 可被 R 10 ; R 2 是氢原子、卤素原子或直链或支链 C1-C6 烷基，可被 R 10 ; X 1 和 X 2 各自独立地代表 N 或 CH，但不能都是 N； 式 (II)： 表示一个单环或双环杂芳基，该杂芳基具有一个与酰胺基键合的碳原子相邻的氮原子，该杂芳基可被 R 10 ; R 10 是 R 11 或可被 R 11 取代的烃基 11 ; R 11 例如是氢原子或氨基；以及 R 12 例如是苯基、噻唑基、吡啶基或亚甲基二氧苯基。根据本发明的化合物具有葡萄糖激酶活化作用，例如，可用于治疗和预防糖尿病，以及预防其并发症，如糖尿病肾病、糖尿病视网膜病变、糖尿病神经病变和糖尿病动脉硬化。
• US7253188B2
  申请人：——

  公开号：US7253188B2

  公开（公告）日：2007-08-07