3-<4-Aethyl-phenyl>-4H-<1.2.4>oxadiazol-5-on | 59812-01-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3-<4-Aethyl-phenyl>-4H-<1.2.4>oxadiazol-5-on
• 英文别名: 3-(4-ethyl-phenyl)-4H-[1,2,4]oxadiazol-5-one；3-(4-ethylphenyl)-4H-1,2,4-oxadiazol-5-one
• CAS: 59812-01-0
• 化学式: C₁₀H₁₀N₂O₂
• 分子量: 190.202
• InChiKey: NEDQTDBQXBUDGL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  50.7
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  N-Ethoxycarbonyl-4-ethyl-benzylthioamid 、 羟胺 以85%的产率得到
  参考文献：
  名称：

  GEORGE B.; PAPADOPOULOS E. P., J. ORG. CHEM., 1976, 41, NO 20, 3233-3237

  摘要：

  DOI：

文献信息

• 4-ALKYNYL IMIDAZOLE DERIVATIVE AND MEDICINE COMPRISING SAME AS ACTIVE INGREDIENT
  申请人：KAKEN PHARMACEUTICAL CO., LTD.

  公开号：US20160130232A1

  公开（公告）日：2016-05-12

  There are provided 4-alkynylimidazole derivatives represented by the following general formula (I) or phamaceutically acceptable salts thereof; the derivatives have a superior EP4 receptor antagonistic action and are useful as pharmaceuticals for the treatment of diseases associated with the EP4 receptor, for example, as anti-inflammatory and/or analgesic drugs for inflammatory diseases and diseases that involve various kinds of pains, and further as pharmaceuticals for the treatment of immune diseases that result from inflammations as evoked by tissue destruction due to the activation of Th1 cells and/or Th17 cells:

  提供了以下一般式(I)所代表的4-炔基咪唑衍生物或其药用盐；这些衍生物具有优越的EP4受体拮抗作用，可用作治疗与EP4受体相关的疾病的药物，例如，作为抗炎和/或镇痛药物，用于治疗炎症性疾病和涉及各种疼痛的疾病，进一步作为治疗由于Th1细胞和/或Th17细胞激活引起的组织破坏所致的炎症导致的免疫性疾病的药物：
• Fused Heterocyclic Compounds and Use Thereof
  申请人：Barbosa Joseph

  公开号：US20080293650A1

  公开（公告）日：2008-11-27

  Fused heterocylic compounds of the following Formula wherein R 1 , R 2 , R 5 , Z, J 1 and J 2 are described herein, and analogs thereof are provided which are useful in treating leukocyte activation-associated disorders.

  以下式子描述的融合杂环化合物，其中R1、R2、R5、Z、J1和J2在此处描述，并提供了其类似物，可用于治疗白细胞激活相关疾病。
• Cyclic Amine Compound and Use Thereof for the Prophylaxis or Treatment of Hypertension
  申请人：Kuroita Takanobu

  公开号：US20100121048A1

  公开（公告）日：2010-05-13

  The present invention relates to a compound represented by the formula: (I) wherein ring A is a 5- or 6-membered aromatic heterocycle optionally having substituent (s); U, V and W are each independently C or N, provided that when any one of U, V and W is N, then the others should be C; Ra and Rb are each independently a cyclic group optionally having substituent(s), a C 1-10 alkyl group optionally having substituent(s), a C 2-10 alkenyl group optionally having substituent(s), or a C 2-10 alkynyl group optionally having substituent(s); X is a bond, or a spacer having 1 to 6 atoms in the main chain; Y is a spacer having 1 to 6 atoms in the main chain; Rc is a hydrocarbon group optionally containing heteroatom(s) as the constituting atom(s), which optionally has substituent(s); m and n are each independently 1 or 2; and ring B optionally further has substituent(s), or a salt thereof. The compound of the present invention has excellent renin inhibitory activity, and thus is useful as an agent for the prophylaxis or treatment of hypertension, various organ damages attributable to hypertension, and the like.

  本发明涉及一种由式(I)表示的化合物：其中，环A是一种5或6成员的芳香杂环，可选地具有取代基；U、V和W分别独立地为C或N，但当U、V和W中的任何一个为N时，其他的应为C；Ra和Rb分别独立地为一个环状基团，可选地具有取代基；一个C1-10烷基，可选地具有取代基；一个C2-10烯基，可选地具有取代基；或一个C2-10炔基，可选地具有取代基；X是一条键或具有1到6个原子的主链间隔；Y是具有1到6个原子的主链间隔；Rc是一个含有杂原子作为构成原子的碳氢基团，可选地具有取代基；m和n分别独立地为1或2；环B可选地具有取代基，或其盐。本发明的化合物具有优异的肾素抑制活性，因此可用作预防或治疗高血压、高血压引起的各种器官损伤等的药物。
• TRPM8 ANTAGONISTS AND THEIR USE IN TREATMENTS
  申请人：AMGEN INC.

  公开号：US20140171639A1

  公开（公告）日：2014-06-19

  Compounds of Formula I are useful as antagonists of TRPM8. Such compounds are useful in treating a number of TRPM8 mediated disorders and conditions and may be used to prepare medicaments and pharmaceutical compositions useful for treating such disorders and conditions. Examples of such disorders include, but are not limited to, migraines and neuropathic pain. Compounds of Formula I have the following structure: where the definitions of the variables are provided herein.

  式I的化合物可作为TRPM8的拮抗剂。这些化合物可用于治疗许多TRPM8介导的疾病和病况，并可用于制备用于治疗这些疾病和病况的药物和制剂。这些疾病的例子包括但不限于偏头痛和神经病性疼痛。式I的化合物具有以下结构：其中变量的定义在此提供。
• STABLE PEPTIDE-BASED FURIN INHIBITORS
  申请人：Day Robert

  公开号：US20150141324A1

  公开（公告）日：2015-05-21

  It is provided furin inhibitors and their uses for treating pathogen infection. Particularly, it is provided a method or use for the treatment of a pathogen infection, in a subject, comprising administering to the subject a therapeutically effective amount of the furin inhibitors or the composition disclosed, thereby preventing or treating pathogen infection, in the subject.

  本发明提供了抑制酶furin及其用于治疗病原体感染的方法。特别地，本发明提供了一种治疗主体的病原体感染的方法或用途，包括向该主体投予治疗有效量的furin抑制剂或所披露的组合物，从而预防或治疗该主体的病原体感染。