5-(aminosulfonyl)-2,3-difluorobenzoic acid | 716361-75-0

• 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: 5-(aminosulfonyl)-2,3-difluorobenzoic acid
• 英文别名: 2,3-Difluoro-5-sulfamoylbenzoic acid
• CAS: 716361-75-0
• 化学式: C₇H₅F₂NO₄S
• 分子量: 237.184
• InChiKey: DUTXUYKNDRNTKB-UHFFFAOYSA-N

物化性质

• 沸点：
  457.1±55.0 °C(Predicted)
• 密度：
  1.702±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  106
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  甲醇 、 5-(aminosulfonyl)-2,3-difluorobenzoic acid 在 氯化亚砜 作用下， 生成 5-(aminosulfonyl)-2,3-difluorobenzoic acid methyl ester
  参考文献：
  名称：

  Thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV: Structure-based drug design, synthesis, and biological evaluation

  摘要：

  A novel series of potent thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV was discovered using structure-based drug design. Synthesis, structure-activity relationship, and optimization of physicochemical properties are described. Low nanomolar potency was achieved, and selected compounds with improved thermodynamic solubility showed promising in vitro inhibition of carbonic anhydrase activity in rabbit iris ciliary body homogenate.

  DOI：

  10.1016/j.bmc.2010.03.014
• 作为产物：
  描述：

  5-(chlorosulfonyl)-2,3-difluorobenzoic acid 在 氨 作用下， 以 二氯甲烷 为溶剂， 生成 5-(aminosulfonyl)-2,3-difluorobenzoic acid
  参考文献：
  名称：

  Thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV: Structure-based drug design, synthesis, and biological evaluation

  摘要：

  A novel series of potent thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV was discovered using structure-based drug design. Synthesis, structure-activity relationship, and optimization of physicochemical properties are described. Low nanomolar potency was achieved, and selected compounds with improved thermodynamic solubility showed promising in vitro inhibition of carbonic anhydrase activity in rabbit iris ciliary body homogenate.

  DOI：

  10.1016/j.bmc.2010.03.014

文献信息

• [EN] FLUORINATED BENZENESULFONAMIDES AS INHIBITORS OF CARBONIC ANHYDRASE<br/>[FR] BENZÈNESULFONAMIDES FLUORÉS À UTILISER EN TANT QU'INHIBITEURS D'ANHYDRASE CARBONIQUE
  申请人：UNIV VILNIUS

  公开号：WO2014062044A1

  公开（公告）日：2014-04-24

  Invention is related to novel compounds - fluorinated benzenesulfonamides of general formula (I). The compounds can be used in biomedicine as active ingredients in pharmaceutical formulations, because they inhibit enzymes which participate in disease progression. ˙

  本发明涉及一种新型化合物 - 一般式(I)的氟化苯磺酰胺。这些化合物可用于生物医学中作为药物配方的活性成分，因为它们抑制参与疾病进展的酶。
• Ccr5 antagonists as therapeutic agents
  申请人：Kazmierski Mieczyslaw Wieslaw

  公开号：US20060229336A1

  公开（公告）日：2006-10-12

  The present invention relates to compounds of formula (I) or a pharmaceutically acceptable derivatives thereof, useful in the treatment of prophylazis of CCR5-related diseases and disorders, for example, in the inhibition of HIV replication, the prevention or treatment of HIV infection, and in the treatment of the resulting acquired immune deficiency syndrome (AIDS).

  本发明涉及式(I)化合物或其药学上可接受的衍生物，用于预防CCR5相关疾病和障碍的治疗，例如，抑制HIV复制，预防或治疗HIV感染，以及治疗由此产生的获得性免疫缺陷综合症（AIDS）。
• FLUORINATED BENZENESULFONAMIDES AS INHIBITORS OF CARBONIC ANHYDRASE
  申请人：VILNIUS UNIVERSITY

  公开号：US20150266900A1

  公开（公告）日：2015-09-24

  Novel fluorinated benzenesulfonamides compounds of general formula (I) can be used in biomedicine as active ingredients in pharmaceutical formulations, because they inhibit enzymes which participate in disease progression.

  通式（I）的新型氟代苯磺酰胺化合物可以作为药物制剂中的活性成分在生物医学中使用，因为它们可以抑制参与疾病进展的酶。
• PIPERIDINE DERIVATIVES AS CCR5 ANTAGONISTS
  申请人：SMITHKLINE BEECHAM CORPORATION

  公开号：EP1569646A2

  公开（公告）日：2005-09-07
• US7645771B2
  申请人：——

  公开号：US7645771B2

  公开（公告）日：2010-01-12