(E)-6-(3-(4-(2-methoxyphenyl)-5,6-dihydropyridin-1(2H)-yl)-3-oxoprop-1-en-1-yl)-3,4-dihydro-1,8-naphthyridin-2(1H)-one | 1441343-80-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: (E)-6-(3-(4-(2-methoxyphenyl)-5,6-dihydropyridin-1(2H)-yl)-3-oxoprop-1-en-1-yl)-3,4-dihydro-1,8-naphthyridin-2(1H)-one
• 英文别名: 6-[(E)-3-[4-(2-methoxyphenyl)-3,6-dihydro-2H-pyridin-1-yl]-3-oxoprop-1-enyl]-3,4-dihydro-1H-1,8-naphthyridin-2-one
• CAS: 1441343-80-1
• 化学式: C₂₃H₂₃N₃O₃
• 分子量: 389.454
• InChiKey: RMQXCPZDEODPPK-RMKNXTFCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  29
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  71.5
• 氢给体数：
  1
• 氢受体数：
  4

文献信息

• [EN] ANTIBACTERIAL PIPERIDINYL SUBSTITUTED 3,4-DIHYDRO-1H-[1,8]NAPHTHYRIDINONES<br/>[FR] 3,4-DIHYDRO-1H[1,8]NAPHTYRIDINONES SUBSTITUÉES PAR PIPÉRIDINYLE ANTIBACTÉRIENNES
  申请人：JANSSEN R & D IRELAND

  公开号：WO2013021052A1

  公开（公告）日：2013-02-14

  The present invention is related to novel compounds of formula (I) that inhibit the activity of the Fab1 enzyme which are therefore useful in the treatment of bacterial infections. It further relates to pharmaceutical compositions comprising these compounds, and chemical processes for preparing these compounds.

  本发明涉及一种公式（I）的新化合物，它们抑制Fab1酶的活性，因此在治疗细菌感染方面具有用途。还涉及包括这些化合物的药物组合物，以及制备这些化合物的化学过程。
• Antibacterial piperidinyl substituted 3,4-dihydro-1H-[1,8]naphthyridinones
  申请人：Guillemont Jerôme Emile Georges

  公开号：US20140163038A1

  公开（公告）日：2014-06-12

  The present invention is related to novel compounds of formula (I) that inhibit the activity of the Fab1 enzyme which are therefore useful in the treatment of bacterial infections. It further relates to pharmaceutical compositions comprising these compounds, and chemical processes for preparing these compounds.

  本发明涉及一种公式(I)的新化合物，其抑制Fab1酶的活性，因此在治疗细菌感染方面非常有用。此外，本发明还涉及包含这些化合物的药物组合物以及制备这些化合物的化学过程。
• SUBSTITUTED PYRIDINE DERIVATIVES AS FABI INHIBITORS
  申请人：Aurigene Discovery Technologies Limited

  公开号：US20140336153A1

  公开（公告）日：2014-11-13

  The present invention provides substituted pyridine derivatives of formula (I), which may be therapeutically useful as as anti-bacterial agents, more particularly FabI inhibitors. Formula (I) in which R1 to R5 and L have the meanings given in the specification, and pharmaceutically acceptable salts thereof that are useful in the treatment and prevention in diseases or disorder, in particular their use in diseases or disorder where there is an advantage anti-bacterial agents, more particularly FabI inhibitors. The present invention also provides methods for synthesizing and administering the FabI inhibitor compounds. The present invention also provides pharmaceutical formulations comprising at least one of the FabI inhibitor compounds together with a pharmaceutically acceptable carrier, diluent or excipient therefor.

  本发明提供了式（I）的取代吡啶衍生物，其可作为抗菌剂，更特别地是FabI抑制剂，具有治疗上的用途。式（I）中，R1至R5和L具有规范中所给出的含义，以及其药学上可接受的盐，在特定的疾病或疾病预防治疗中有用，特别是在有优势的抗菌剂，更特别地是FabI抑制剂的疾病或疾病预防治疗中的使用。本发明还提供了合成和给予FabI抑制剂化合物的方法。本发明还提供了包含至少一种FabI抑制剂化合物的药物配方，以及与其药学上可接受的载体、稀释剂或赋形剂一起使用的药物配方。
• ANTIBACTERIAL PIPERIDINYL SUBSTITUTED 3,4-DIHYDRO-1H-[1,8]NAPHTHYRIDINONES
  申请人：Janssen Sciences Ireland Unlimited Company

  公开号：EP2742047B1

  公开（公告）日：2021-05-12
• US9012634B2
  申请人：——

  公开号：US9012634B2

  公开（公告）日：2015-04-21