phenyl-ethanediyl diisocyanate | 5868-32-6

• 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: phenyl-ethanediyl diisocyanate
• 英文别名: 1.2-Diisocyanato-1-phenyl-aethan；Phenyl-aethandiyldiisocyanat；Phenylaethylendiisocyanat；1,2-Diisocyanatoethylbenzene
• CAS: 5868-32-6
• 化学式: C₁₀H₈N₂O₂
• 分子量: 188.186
• InChiKey: VDDIDKWDKHSMKA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  58.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  phenyl-ethanediyl diisocyanate 、 水 生成 alkaline earth salt of/the/ methylsulfuric acid
  参考文献：
  名称：

  Curtius, Journal fur praktische Chemie (Leipzig 1954), 1930, vol. <2> 125, p. 63,80

  摘要：

  DOI：
• 作为产物：
  描述：

  phenyl-succinyl azide 在 苯 作用下， 生成 phenyl-ethanediyl diisocyanate
  参考文献：
  名称：

  Curtius, Journal fur praktische Chemie (Leipzig 1954), 1930, vol. <2> 125, p. 63,80

  摘要：

  DOI：

文献信息

• Imidazole and benzimidazole derivatives useful as histamine H3 antagonists
  申请人：Aslanian G. Robert

  公开号：US20060166960A1

  公开（公告）日：2006-07-27

  Disclosed are compounds of the formula or a pharmaceutically acceptable salt or solvate thereof, wherein: n is 2-5; R is R 3 -aryl, R 3 -heteroaryl, R 3 -cycloalkyl, R 3 -heterocycloalkyl, alkyl, haloalkyl, —OR 4 , —SR 4 or —S(O) 1-2 R 5 ; R 1 and R 2 are H or optionally substituted phenyl or optionally substituted and X is —O— or —S—; or R 1 and R 2 , together with the carbon atoms to which they are attached form optionally substituted and X is —O—, —S— or —NR 7 —; Z is and the remaining variables are as defined in the specification; also disclosed are pharmaceutical compositions comprising the compounds of formula I; also disclosed are methods of treating allergy, allergy-induced airway responses, congestion, obesity and metabolic syndrome using the compounds of Formula I, as well as combinations with other drugs useful for treating those diseases.

  揭示了以下公式化合物或其药学上可接受的盐或溶剂，其中：n为2-5；R为R3-芳基，R3-杂环芳基，R3-环烷基，R3-杂环烷基，烷基，卤代烷基，—OR4，—SR4或—S(O)1-2R5；R1和R2为H或可选择地取代的苯基或可选择地取代的，X为—O—或—S—；或R1和R2，连同它们连接的碳原子形成可选择地取代的，X为—O—，—S—或—NR7—；Z为，其余变量如规范中所定义；还揭示了包括公式I化合物的药物组合物；还揭示了使用公式I化合物治疗过敏、过敏引起的气道反应、充血、肥胖和代谢综合征的方法，以及与其他用于治疗这些疾病的药物的组合。
• Quinazoline derivatives
  申请人：——

  公开号：US20040034046A1

  公开（公告）日：2004-02-19

  The invention concerns quinazoline derivatives of Formula (I) wherein each of m, R 1 , n, R 2 and R 3 have any of the meanings defined in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an anti-invasive agent in the containment and/or treatment of solid tumour disease.

  这项发明涉及式（I）的喹唑啉衍生物，其中m、R1、n、R2和R3中的每一个具有描述中定义的任意含义；它们的制备方法；含有它们的药物组合物；以及它们在制造用作抗侵袭剂的药物中用于抑制和/或治疗实体肿瘤疾病的用途。
• Quinazoline derivatives with anti-tumour activity
  申请人：AstraZeneca AB

  公开号：US20040048881A1

  公开（公告）日：2004-03-11

  The invention concerns quinazoline derivatives of Formula I 1 wherein each of m, R 1 , n, R 2 and R 3 have any of the meanings defined in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an anti-invasive agent in the containment and/or treatment of solid tumour disease.

  这项发明涉及式I的喹唑啉衍生物，其中m、R1、n、R2和R3中的每一个具有描述中定义的任意含义；它们的制备方法，含有它们的药物组合物以及它们在制造用作抗侵袭剂的药物的过程中在固体肿瘤疾病的控制和/或治疗中的使用。
• TREATING PAIN, DIABETES, AND DISORDERS OF LIPID METABOLISM
  申请人：Harris M. Joel

  公开号：US20080070892A1

  公开（公告）日：2008-03-20

  Disclosed is a method of treating a disease or condition (e.g., pain, diabetes or disorders of lipid metabolism) comprising administering an azetidine derivative of the formula I selected from the group consisting of the compounds defined by Tables 1, 2, 3a, 3b, 3c, 3d and 4a.

  揭示了一种治疗疾病或病症（例如疼痛、糖尿病或脂质代谢紊乱）的方法，包括给予从表1、2、3a、3b、3c、3d和4a定义的化合物组中选择的式I的吖啶衍生物。
• Azetidinone Derivatives and Methods of Use Thereof
  申请人：Aslanian G. Robert

  公开号：US20080076750A1

  公开（公告）日：2008-03-27

  The present invention relates to methods for treating or preventing a disorder of lipid metabolism, pain, diabetes, a vascular condition, demyelination or nonalcoholic fatty liver disease, comprising administering a compound having the formula or a pharmaceutically acceptable salt, solvate, ester, prodrug or stereoisomer thereof, wherein: R 1 and R 2 are defined in Tables 1-6 herein, and R 3 is -phenyl, -4-chlorophenyl, -2-pyridyl, or -3-pyridyl.

  本发明涉及治疗或预防脂质代谢紊乱、疼痛、糖尿病、血管疾病、脱髓鞘或非酒精性脂肪肝病的方法，包括给予具有以下结构式的化合物或其药学上可接受的盐、溶剂化合物、酯、前药或立体异构体： R 1 和 R 2 在本文的表1-6中定义，并且 R 3 为-苯基、-4-氯苯基、-2-吡啶基或-3-吡啶基。