6-isobutylpyrimidine-2,4(1H,3H)-dione | 139541-34-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 6-isobutylpyrimidine-2,4(1H,3H)-dione
• 英文别名: 6-(2-methylpropyl)-1H-pyrimidine-2,4-dione
• CAS: 139541-34-7
• 化学式: C₈H₁₂N₂O₂
• 分子量: 168.195
• InChiKey: VYASQHCIMSCHQU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  58.2
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  6-isobutylpyrimidine-2,4(1H,3H)-dione 在 barium dihydroxide 、 硫酸 、 氨 、 水 、 硝酸 、 iron(II) sulfate 、 N,N-二乙基苯胺 、 三氯氧磷 作用下， 以 乙醇 为溶剂， 反应 8.08h， 生成 6-isobutyl-2,4,5-triaminopyrimidine
  参考文献：
  名称：

  Bowden, Keith; Bright, Andrew C., Journal of Chemical Research, Miniprint, 1992, # 2, p. 514 - 539

  摘要：

  DOI：
• 作为产物：
  描述：

  5-甲基-3-羰基己酸乙酯 在 盐酸 、 水 、 sodium ethanolate 、 氯乙酸 作用下， 以 乙醇 为溶剂， 反应 13.0h， 生成 6-isobutylpyrimidine-2,4(1H,3H)-dione
  参考文献：
  名称：

  Bowden, Keith; Bright, Andrew C., Journal of Chemical Research, Miniprint, 1992, # 2, p. 514 - 539

  摘要：

  DOI：

文献信息

• 6, 11-bridged tricyclic macrolides
  申请人：Or Sun Yat

  公开号：US20070082853A1

  公开（公告）日：2007-04-12

  The present invention discloses compounds of formula I, or pharmaceutically acceptable salts, esters, or prodrugs thereof: which exhibit antibacterial properties. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject in need of antibiotic treatment. The invention also relates to methods of treating a bacterial infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The invention further includes process by which to make the compounds of the present invention.

  本发明公开了具有以下结构的化合物I，或其药学上可接受的盐、酯或前药：这些化合物具有抗菌性能。本发明还涉及包括上述化合物的药物组合物，用于治疗需要抗生素治疗的受试者。该发明还涉及通过给受试者施用包含本发明化合物的药物组合物来治疗受试者的细菌感染的方法。该发明还包括制备本发明化合物的方法。
• 3,6-BRIDGED TYLOSIN DERIVATIVES
  申请人：Qiu Yao-Ling

  公开号：US20080039406A1

  公开（公告）日：2008-02-14

  The present invention discloses compounds of formula I, or pharmaceutically acceptable salts, esters, or prodrugs thereof: which exhibit antibacterial properties. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject in need of antibiotic treatment. The invention also relates to methods of treating a bacterial infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The invention further includes process by which to make the compounds of the present invention.

  本发明公开了化合物I的结构，或其药学上可接受的盐、酯或前药：这些化合物具有抗菌性能。本发明还涉及包含上述化合物的药物组合物，用于给需要抗生素治疗的受试者进行治疗。本发明还涉及通过给受试者施用包含本发明化合物的药物组合物来治疗受试者的细菌感染的方法。本发明还包括制备本发明化合物的方法。
• BRIDGED CARBAMATE MACROLIDES
  申请人：Kim Heejin

  公开号：US20080027012A1

  公开（公告）日：2008-01-31

  The present invention discloses compounds of formulae (I) and (II) or pharmaceutically acceptable salts, esters, or prodrugs thereof: which exhibit antibacterial properties. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject in need of antibiotic treatment. The invention also relates to methods of treating a bacterial infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The invention further includes process by which to make the compounds of the present invention.

  本发明公开了式(I)和(II)的化合物或其药学上可接受的盐、酯或前药：这些化合物具有抗菌性能。本发明还涉及含有上述化合物的药物组合物，用于治疗需要抗生素治疗的受试者。该发明还涉及通过给予含有本发明化合物的药物组合物来治疗受试者的细菌感染的方法。该发明还包括制备本发明化合物的方法。
• DIHYDROPTERIDINONES I
  申请人：Boehringer Ingelheim International GmbH

  公开号：US20130225549A1

  公开（公告）日：2013-08-29

  The present invention relates to dihydropteridinones, their use as modulators of γ-secretase and to pharmaceutical compositions containing said compounds. In particular, the present invention relates to compounds which interfere with γ-secretase and/or its substrate and therefore modulate the formation of Aβ peptides.

  本发明涉及二氢喜树碱酮，它们作为γ-分泌酶调节剂的用途以及含有该化合物的药物组合物。具体而言，本发明涉及干扰γ-分泌酶和/或其底物的化合物，因此调节Aβ肽的形成。
• [EN] DIHYDROPTERIDINONES I<br/>[FR] DIHYDROPTÉRIDINONES I
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2014127815A1

  公开（公告）日：2014-08-28

  The present invention relates to dihydropteridinones, their use as modulators of γ-secretase and to pharmaceutical compositions containing said compounds. In particular, the present invention relates to compounds which interfere with γ-secretase and/or its substrate and therefore modulate the formation of Αβ peptides.

  本发明涉及二氢喜树碱酮，其作为γ-分泌酶调节剂的用途，以及含有该化合物的制药组合物。具体而言，本发明涉及干扰γ-分泌酶和/或其底物的化合物，从而调节Αβ肽的形成。