N-ethyl-N'-(3-{[3-(morpholin-4-ylcarbonyl)-1,4'-bipiperidin-1'-yl]carbonyl}-1-benzothiophen-2-yl)urea | 953821-75-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: N-ethyl-N'-(3-{[3-(morpholin-4-ylcarbonyl)-1,4'-bipiperidin-1'-yl]carbonyl}-1-benzothiophen-2-yl)urea
• 英文别名: 1-Ethyl-3-[3-[4-[3-(morpholine-4-carbonyl)piperidin-1-yl]piperidine-1-carbonyl]-1-benzothiophen-2-yl]urea
• CAS: 953821-75-5
• 化学式: C₂₇H₃₇N₅O₄S
• 分子量: 527.688
• InChiKey: ORTWPLVAVOBEEB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  37
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  123
• 氢给体数：
  2
• 氢受体数：
  6

文献信息

• NITROGEN-CONTAINING HETEROCYCLIC COMPOUND
  申请人：Fukatsu Kohji

  公开号：US20090281097A1

  公开（公告）日：2009-11-12

  The object of the present invention is to provide a compound having an ACC inhibitory action, which is useful for the prophylaxis or treatment of obesity, diabetes, hypertension, hyperlipidemia, cardiac failure, diabetic complications, metabolic syndrome, sarcopenia and the like, and has superior properties such as efficacy, duration of activity, specificity, low toxicity and the like. The present invention provides a compound represented by the following formula wherein ring M is a 5- or 6-membered aromatic ring; W is C or N; K is an optionally substituted methylene group or an optionally substituted imino group; R is a hydrogen atom, an optionally substituted hydrocarbon group, an optionally substituted hydroxy group or an optionally substituted heterocyclic group; T and U are independently a hydrogen atom or a substituent or, T and U form, together with ring M, an optionally substituted bicyclic ring; D and G are independently a carbonyl group or a sulfonyl group; ring P is an optionally substituted piperidine or an optionally substituted piperazine; B is CH or N; ring Q is an optionally substituted monocyclic ring; A is C, CH or N; and J is an optionally substituted hydrocarbon group, an optionally substituted heterocyclic group or an optionally substituted amino group, provided that when the W moiety of ring M is ═N— or —N═, then U should be absent, or a salt thereof.

  本发明的目的是提供一种具有ACC抑制作用的化合物，该化合物可用于预防或治疗肥胖症、糖尿病、高血压、高脂血症、心力衰竭、糖尿病并发症、代谢综合征、肌肉萎缩等疾病，并具有优异的功效、持续时间、特异性、低毒性等优良性质。本发明提供一种由下式表示的化合物： 其中，环M是5-或6-成员芳香环；W是C或N；K是可选地取代的亚甲基基团或可选地取代的亚氨基基团；R是氢原子、可选地取代的烃基、可选地取代的羟基或可选地取代的杂环基；T和U分别是氢原子或取代基，或者T和U与环M一起形成可选地取代的双环环；D和G分别是羰基基团或磺酰基团；环P是可选地取代的哌啶基或可选地取代的哌嗪基；B是CH或N；环Q是可选地取代的单环环；A是C、CH或N；J是可选地取代的烃基、可选地取代的杂环基或可选地取代的氨基基团，前提是当环M的W基团为═N—或—N═时，U应该不存在，或其盐。