2-氯-4-硝基苯磺酰胺 | 31150-99-9

• 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: 2-氯-4-硝基苯磺酰胺
• 英文名称: 2-Chlor-4-nitro-benzolsulfonsaeure-amid
• 英文别名: 2-Sulfamoyl-5-nitro-chlorbenzol；2-Chlor-4-nitro-benzol-sulfonamid；2-chloro-4-nitro-benzenesulfonic acid amide；2-chloro-4-nitro-benzenesulfonamide；2-Chloro-4-nitrobenzenesulfonamide
• CAS: 31150-99-9
• 化学式: C₆H₅ClN₂O₄S
• 分子量: 236.636
• InChiKey: QHVQQUVAILWCLB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  114
• 氢给体数：
  1
• 氢受体数：
  5

安全信息

• 海关编码：
  2935009090

反应信息

• 作为产物：
  描述：

  benzyl(2-chloro-4-nitrophenyl)sulfane 在 氯 、 溶剂黄146 作用下， 生成 2-氯-4-硝基苯磺酰胺
  参考文献：
  名称：

  The Cleavage of Organic Sulfides with Chlorine¹

  摘要：

  DOI：

  10.1021/ja01216a063

文献信息

• [EN] ANTIPROLIFERATIVE 2-(SULFO-PHENYL)-AMINOTHIAZOLE DERIVATIVES<br/>[FR] DERIVES DE 2-(SULFO-PHENYL)-AMINOTHIAZOLE ANTIPROLIFERATIFS
  申请人：PFIZER

  公开号：WO2004072070A1

  公开（公告）日：2004-08-26

  Aminothiazole compounds substituted with sulfur-containing groups are represented by the Formula (I), and their pharmaceutically acceptable salts, prodrugs, active metabolites, and pharmaceutically acceptable salts of said metabolites are described. These agents modulate and/or inhibit the cell proliferation and activity of protein kinases and are useful as pharmaceuticals for treating malignancies and other disorders.

  含有硫基取代基团的氨基噻唑化合物由化学式(I)表示，并描述了它们的药用可接受盐、前药、活性代谢物以及所述代谢物的药用可接受盐。这些药物调节和/或抑制细胞增殖和蛋白激酶活性，可用作治疗恶性肿瘤和其他疾病的药物。
• Pyrrole Derivatives As Pharmaceutical Agents
  申请人：Canne Bannen Lynne

  公开号：US20080234270A1

  公开（公告）日：2008-09-25

  Compounds, compositions and methods for modulating the activity of receptors are provided. In particular compounds and compositions are provided for modulating the activity of receptors and for the treatment, prevention, or amelioration of one or more symptoms of disease or disorder directly or indirectly related to the activity of the receptors.

  提供了用于调节受体活性的化合物、组合物和方法。特别提供了用于调节受体活性的化合物和组合物，以及用于治疗、预防或改善与受体活性直接或间接相关的一种或多种疾病或紊乱的症状的方法。
• Antiproliferative 2-(sulfo-phenyl)-aminothiazole derivatives and pharmaceutical compositions, and methods for their use
  申请人：Pfizer, Inc.

  公开号：US20040176431A1

  公开（公告）日：2004-09-09

  Aminothiazole compounds substituted with sulfur-containing groups are represented by the Formula (I), and their pharmaceutically acceptable salts, prodrugs, active metabolites, and pharmaceutically acceptable salts of said metabolites are described. 1 These agents modulate and/or inhibit the cell proliferation and activity of protein kinases and are useful as pharmaceuticals for treating malignancies and other disorders.

  含有硫基取代的氨基噻唑化合物的化学式为(I)，其药物可接受的盐、前药、活性代谢物和药物可接受的代谢物的描述如下。这些药物可以调节和/或抑制细胞增殖和蛋白激酶活性，是治疗恶性肿瘤和其他疾病的药物。
• Heterocyclic Carboxamide Compounds as Steroid Nuclear Receptors Ligands
  申请人：Flatt Brenton T.

  公开号：US20110144128A1

  公开（公告）日：2011-06-16

  Heterocyclic carboxamide compounds are described herein as being useful in modulating the activity of steroid nuclear receptors. Pharmaceutical compositions containing the compounds, methods of using the compounds and processes for making the compounds are also described.

  本文介绍了杂环羧酰胺化合物作为调节类固醇核受体活性的有用物质。还描述了含有这些化合物的制药组合物，使用这些化合物的方法以及制造这些化合物的过程。
• Sulfonamide analogues of galiellalactone
  申请人：GLACTONE PHARMA DEVELOPMENT AB

  公开号：US10781197B2

  公开（公告）日：2020-09-22

  Disclosed are sulfonamide analogues of galiellactone of formula (I) as STAT3-inhibitors for use in the treatment of a STAT3 signaling related disorder, e.g. solid cancers, hematological cancers, benign tumors, hyperproliferative diseases, inflammations, autoimmune diseases, graft or transplant rejections, delayed physiological function of grafts or transplants, neurodegenerative diseases and viral infections. The sulfonamide comprises a cyclic substituent.

  本发明公开了作为 STAT3 抑制剂的式(I)的镓内酯磺酰胺类似物，用于治疗 STAT3 信号转导相关疾病，如实体癌、血液肿瘤、良性肿瘤、过度增殖性疾病、炎症、自身免疫性疾病、移植物或移植排斥、移植物或移植的生理功能延迟、神经退行性疾病和病毒感染。磺酰胺包括一个环状取代基。