(3E)-3-[hydroxy-(pyridin-2-ylamino)methylidene]-2-methyl-1,1-dioxo-1λ6,2-benzothiazin-4-one

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻嗪类
• 英文名称: (3E)-3-[hydroxy-(pyridin-2-ylamino)methylidene]-2-methyl-1,1-dioxo-1λ6,2-benzothiazin-4-one
• 化学式: C₁₅H₁₃N₃O₄S
• 分子量: 331.3
• InChiKey: LDJVNWFKNMYYNT-FYWRMAATSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  23
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  108
• 氢给体数：
  2
• 氢受体数：
  7

文献信息

• [EN] MICROSOMAL PROSTAGLANDIN E SYNTHASE-1 (MPGES1) INHIBITORS<br/>[FR] INHIBITEURS DE PROSTAGLANDINE E SYNTHASE-1 (MPGES1) MICROSOMALE
  申请人：NOVASAID AB

  公开号：WO2011023812A1

  公开（公告）日：2011-03-03

  A compound of formula (I): as well as pharmaceutically acceptable salts thereof, and a pharmaceutical composition comprising the compound. The compound is useful for the treatment of disorder selected from inflammatory diseases, nociceptive pain, auto-immune disease, breathing disorders, fever, cancer, inflammation related anorexia, Alzheimer's disease and cardiovascular diseases.

  公式（I）的化合物，以及其药用盐，以及包括该化合物的药物组合物。该化合物用于治疗选择自炎性疾病、伤害性疼痛、自身免疫疾病、呼吸系统疾病、发热、癌症、与炎症相关的厌食症、阿尔茨海默病和心血管疾病的紊乱。
• [EN] PIPERIDINYL BENZOIMIDAZOLE DERIVATIVES AS MPGES-1 INIHIBITORS<br/>[FR] DÉRIVÉS DE PIPÉRIDINYL BENZOIMIDAZOLE COMME INHIBITEURS DE MPGES-1
  申请人：NOVASAID AB

  公开号：WO2012117062A1

  公开（公告）日：2012-09-07

  A compound of formula (I) as well as pharmaceutically acceptable salts thereof, and a pharmaceutical composition comprising the compound. The compound is useful for the treatment of disorder selected from inflammatory diseases, pain, auto-immune disease, breathing disorders, fever, cancer, inflammation related anorexia, overactive bladder, familial adenomatous polyposis (FAP) condition, neurodegenerative diseases, bone diseases and cardiovascular diseases.

  式（I）的化合物及其药用盐，以及包含该化合物的药物组合物。该化合物可用于治疗选择自炎症性疾病、疼痛、自身免疫疾病、呼吸系统疾病、发热、癌症、与炎症相关的厌食症、膀胱过度活跃、家族性腺瘤性息肉病（FAP）病情、神经退行性疾病、骨病和心血管疾病的混合物。
• [EN] NOVEL PIPERIDINYL BENZOIMIDAZOLE DERIVATIVES AS MPGES-1 INHIBITORS<br/>[FR] NOUVEAUX DÉRIVÉS PIPÉRIDINYLE BENZOIMIDAZOLE UTILISÉS COMME INHIBITEURS DE LA MPGES-1
  申请人：CADILA PHARMACEUTICALS LTD

  公开号：WO2014204370A1

  公开（公告）日：2014-12-24

  The compounds 1-(5-chloro-6-methyl-1-(6-(trifluoromethyl)pyridin-2-yl)-1H-benzo[d]imidazol- 2-yl)-N-((3S,4R)-4-hydroxytetrahydrofuran-3-yl)piperidine-4-carboxamide and l-(6-chloro-5- methy1-1-(6-(trifluoromethyl)pyridin-2-yl)-1H-benzo[d]imidazol-2-yl)-N-((3S,4R)-4- hydroxytetrahydrofuran-3-yl)piperidine-4-carboxamide, as well as pharmaceutically acceptable salts thereof, and a pharmaceutical composition comprising any one of these compounds. The compound are useful for the treatment and/or prevention of a disorder selected from an inflammatory disease; an autoimmune disease; pain; a breathing disorder; cancer; a cardiovascular disease; a neurodegenerative disease; a bone disease; a disorder due to familial adenomatous polyposis (FAP) condition; overactive bladder; fever; and inflammation-related anorexia.

  化合物1-(5-氯-6-甲基-1-(6-(三氟甲基)吡啶-2-基)-1H-苯并[d]咪唑-2-基)-N-((3S,4R)-4-羟基四氢呋喃-3-基)哌啶-4-甲酰胺和1-(6-氯-5-甲基-1-(6-(三氟甲基)吡啶-2-基)-1H-苯并[d]咪唑-2-基)-N-((3S,4R)-4-羟基四氢呋喃-3-基)哌啶-4-甲酰胺，以及其药学上可接受的盐，以及包含这些化合物中任何一种的药物组合物。这些化合物可用于治疗和/或预防选择自炎症性疾病；自身免疫疾病；疼痛；呼吸障碍；癌症；心血管疾病；神经退行性疾病；骨疾病；由家族性腺瘤性息肉症（FAP）病情导致的障碍；膀胱过度活跃；发热；以及与炎症相关的厌食症的障碍。
• [EN] PIPERIDINYL BENZOIMIDAZOLE DERIVATIVES AS MPGE-1 INHIBITORS<br/>[FR] DÉRIVÉS DE PIPÉRIDINYLBENZOIMIDAZOLE UTILISÉS COMME INHIBITEURS DE MPGE-1
  申请人：CADILA PHARMACEUTICALS LTD

  公开号：WO2014204371A1

  公开（公告）日：2014-12-24

  The compounds (R)-1-(5-chloro-6-methyl-1-(6-(trifluoromethyl)pyridin-2-yl)-1H- benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide and (R)-1-(6-chloro- -methyl-1-(6-(trifluoromethyl)pyridin-2-yl)-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3- yl)piperidine-4-carboxamide, as well as pharmaceutically acceptable salts thereof, and a pharmaceutical composition comprising any one of thesecompounds. The compoundsareuseful for the treatmentand/or preventionof a disorder selected from an inflammatory disease; an autoimmune disease; pain; a breathing disorder; cancer; a cardiovascular disease; a neurodegenerative disease; a bone disease; a disorder due to familial adenomatous polyposis (FAP) condition; overactive bladder; fever; and inflammation-related anorexia.

  化合物(R)-1-(5-氯-6-甲基-1-(6-(三氟甲基)吡啶-2-基)-1H-苯并[d]咪唑-2-基)-N-(四氢呋喃-3-基)哌啶-4-羧酰胺和(R)-1-(6-氯-6-甲基-1-(6-(三氟甲基)吡啶-2-基)-1H-苯并[d]咪唑-2-基)-N-(四氢呋喃-3-基)哌啶-4-羧酰胺，以及其药学上可接受的盐，以及包含这些化合物中的任何一种的药物组合物。这些化合物可用于治疗和/或预防炎症性疾病；自身免疫疾病；疼痛；呼吸障碍；癌症；心血管疾病；神经退行性疾病；骨疾病；由家族性腺瘤性息肉症（FAP）引起的疾病；膀胱过度活跃；发热；以及与炎症相关的厌食症。
• [EN] PHOSPHATE DERIVATIVES<br/>[FR] DERIVES PHOSPHATES
  申请人：VITAL HEALTH SCIENCES PTY LTD

  公开号：WO2004092187A1

  公开（公告）日：2004-10-28

  According to the invention, there is provided a phosphate derivative of a phenolic hydroxy compound comprising the reaction product of the following steps: (d) reacting the phenolic hydroxy compound with an alkyl α:ω dialdehyde or a sugar-like polyhydroxy dialdehyde to form a hemiacetal; (e) reducing the terminal aldehyde group on the product from step (a) to a hydroxyl group; and (f) phosphorylating the hydroxyl group formed in step (b) to produce a phosphate derivative of the phenolic hydroxy compound.

  根据发明，提供了一种酚羟基化合物的磷酸酯衍生物，其包括以下步骤的反应产物：(d)将酚羟基化合物与烷基α:ω双醛或类似糖的多羟基双醛反应形成半缩醛；(e)将步骤(a)产物上的末端醛基还原为羟基；(f)磷酸化在步骤(b)中形成的羟基，以产生酚羟基化合物的磷酸酯衍生物。