3-苯磺酰基-1-丙-2-基脲 | 3149-01-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-苯磺酰基-1-丙-2-基脲
• 英文名称: N-benzenesulfonyl-N'-isopropyl-urea
• 英文别名: N-Benzolsulfonyl-N'-isopropyl-harnstoff；1-Isopropyl-3-(phenylsulfonyl)urea；1-(benzenesulfonyl)-3-propan-2-ylurea
• CAS: 3149-01-7
• 化学式: C₁₀H₁₄N₂O₃S
• 分子量: 242.299
• InChiKey: BSCZJJVDWSSENV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  83.6
• 氢给体数：
  2
• 氢受体数：
  3

安全信息

• 海关编码：
  2935009090

反应信息

• 作为产物：
  描述：

  苯磺酰胺 、 alkaline earth salt of/the/ methylsulfuric acid 生成 3-苯磺酰基-1-丙-2-基脲
  参考文献：
  名称：

  Cardani et al., Farmaco, Edizione Scientifica, 1957, vol. 12, p. 375,376,378

  摘要：

  DOI：

文献信息

• [EN] BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS<br/>[FR] COMPOSÉS DE BENZÈNESULFONAMIDE ET LEUR UTILISATION EN TANT QU'AGENTS THÉRAPEUTIQUES
  申请人：XENON PHARMACEUTICALS INC

  公开号：WO2013064983A1

  公开（公告）日：2013-05-10

  This invention is directed to benzensulfonamide compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment of sodium channel-mediated diseases or conditions, such as pain.

  这项发明涉及苯磺酰胺化合物，作为其立体异构体、对映异构体、互变异构体或它们的混合物；或者它们的药用可接受盐、溶剂合物或前药，用于治疗钠通道介导的疾病或症状，如疼痛。
• Dihydroxypyrimidine carboxamide inhibitors of HIV integrase
  申请人：Di Francesco E. Maria

  公开号：US20070083045A1

  公开（公告）日：2007-04-12

  4,5-Dihydroxypyrimidine-6-carboxamides of formula: are described as inhibitors of HIV integrase and inhibitors of HIV replication, wherein R 1 , R 2 , R 3 and R 4 are defined herein. These compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of preventing, treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are also described.

  本文描述了式子中R1，R2，R3和R4被定义的4,5-二羟基嘧啶-6-羧酰胺化合物，其作为HIV整合酶抑制剂和HIV复制抑制剂。这些化合物对于预防和治疗HIV感染以及预防、延迟AIDS发病和治疗AIDS非常有用。这些化合物可以作为化合物本身或药物可接受的盐形式用于对抗HIV感染和AIDS。这些化合物及其盐可以与其他抗病毒药物、免疫调节剂、抗生素或疫苗组合使用，作为制药组合物的成分。本文还描述了预防、治疗或延迟AIDS发病以及预防或治疗HIV感染的方法。
• BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS
  申请人：XENON PHARMACEUTICALS INC.

  公开号：US20140296245A1

  公开（公告）日：2014-10-02

  This invention is directed to benzensulfonamide compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment of sodium channel-mediated diseases or conditions, such as pain.

  本发明涉及苯磺酰胺化合物，包括其立体异构体、对映异构体、互变异构体或其混合物；或其药学上可接受的盐、溶剂化合物或前药，用于治疗钠通道介导的疾病或病况，例如疼痛。
• External regulation of gene expression
  申请人：E.I. DU PONT DE NEMOURS AND COMPANY

  公开号：EP0388186A1

  公开（公告）日：1990-09-19

  The preparation and use of nucleic acid promoter fragments derived from several genes from corn, petunia and tobacco which are highly responsive to a number of substituted benzenesulfonamides and related compounds are described. These promoter fragments are useful in creating recombinant DNA constructions comprising nucleic acid sequences encoding any desired gene product operably linked to such promoter fragments which can be utilized to transform plants and bring the expression of the gene product under external chemical control in various tissues of monocotyledonous and dicotyledonous plant.

  本文描述了从玉米、矮牵牛和烟草的几个基因中提取的核酸启动子片段的制备和使用方法，这些基因对一些取代的苯磺酰胺类化合物和相关化合物有很强的反应性。这些启动子片段可用于创建重组 DNA 结构，该结构包含编码任何所需基因产物的核酸序列，可与这些启动子片段操作性连接，从而可用于转化植物，并在单子叶和双子叶植物的各种组织中使基因产物的表达受到外部化学控制。
• EXTERNAL REGULATION OF GENE EXPRESSION
  申请人：E.I. DU PONT DE NEMOURS AND COMPANY

  公开号：EP0463056A1

  公开（公告）日：1992-01-02