6-Methoxy-2-phenyl-1,2-benzothiazol-3-one | 167544-98-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻唑类
• 英文名称: 6-Methoxy-2-phenyl-1,2-benzothiazol-3-one
• CAS: 167544-98-1
• 化学式: C₁₄H₁₁NO₂S
• 分子量: 257.313
• InChiKey: QFVBGNFSFIRRBX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  54.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  6-Methoxy-2-phenyl-1,2-benzothiazol-3-one 在 三溴化硼 作用下， 以 二氯甲烷 为溶剂， 以20%的产率得到MIF164
  参考文献：
  名称：

  Benzisothiazolones as modulators of macrophage migration inhibitory factor

  摘要：

  Substituted N-phenylbenzisothiazolones have been investigated as inhibitors of the tautomerase activity of the proinflammatory cytokine MIF (macrophage migration inhibitory factor). Numerous compounds were found to possess antagonist activity in the low micromolar range with the most potent being the 6-hydroxy analog 1w. Compound 1w and the p-cyano analog 1c were also shown to exhibit significant inhibition of the binding of MIF to its transmembrane receptor CD74. Consistently, both compounds were also found to retard the MIF-dependent phosphorylation of ERK1/2 in human synovial fibroblasts. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.05.127
• 作为产物：
  描述：

  N-苯基-4-甲氧基苯甲酰胺 在 sodium periodate 、 氯化亚砜 、 四甲基乙二胺 、 仲丁基锂 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 为溶剂， 反应 17.0h， 生成 6-Methoxy-2-phenyl-1,2-benzothiazol-3-one
  参考文献：
  名称：

  Benzisothiazolones as modulators of macrophage migration inhibitory factor

  摘要：

  Substituted N-phenylbenzisothiazolones have been investigated as inhibitors of the tautomerase activity of the proinflammatory cytokine MIF (macrophage migration inhibitory factor). Numerous compounds were found to possess antagonist activity in the low micromolar range with the most potent being the 6-hydroxy analog 1w. Compound 1w and the p-cyano analog 1c were also shown to exhibit significant inhibition of the binding of MIF to its transmembrane receptor CD74. Consistently, both compounds were also found to retard the MIF-dependent phosphorylation of ERK1/2 in human synovial fibroblasts. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.05.127

文献信息

• [EN] METHODS AND COMPOUNDS TO TREAT SARS INFECTIONS<br/>[FR] PROCÉDÉS ET COMPOSÉS POUR TRAITER LES INFECTIONS À SARS-COV-2
  申请人：UNIV CALIFORNIA

  公开号：WO2022081984A1

  公开（公告）日：2022-04-21

  This disclosure features chemical entities (e.g., a compound (e.g., a compound of Formula (I), (II), (III), or (IV)), or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that inhibit the main protease (MPro) of a coronavirus (e.g., SARS-CoV-2). Said chemical entities are useful, e.g., for treating a coronavirus infection (e.g., SARS-CoV-2 infection (e.g., COVID-19)) in a subject (e.g., a human). This disclosure also features compositions containing the same as well as methods of using and making the same.

  本文披露了一些化合物（例如，化合物（例如，公式（I），（II），（III）或（IV）的化合物），或药物的可接受盐，和/或水合物，和/或共晶体，和/或化合物的药物组合），它们能够抑制冠状病毒（例如，SARS-CoV-2）的主要蛋白酶（MPro）。这些化合物可用于治疗受体（例如，人类）的冠状病毒感染（例如，SARS-CoV-2感染（例如，COVID-19））。本文还涉及含有相同化合物的组合物，以及使用和制备这些化合物的方法。
• Anti-fouling compositions or fouling control of harmful aquatic oranisms
  申请人：SUMITOMO CHEMICAL COMPANY LIMITED

  公开号：EP0644243B1

  公开（公告）日：1999-01-27
• Benzisothiazolones as modulators of macrophage migration inhibitory factor
  作者：William L. Jorgensen、Alexander Trofimov、Xin Du、Alissa A. Hare、Lin Leng、Richard Bucala

  DOI：10.1016/j.bmcl.2011.05.127

  日期：2011.8

  Substituted N-phenylbenzisothiazolones have been investigated as inhibitors of the tautomerase activity of the proinflammatory cytokine MIF (macrophage migration inhibitory factor). Numerous compounds were found to possess antagonist activity in the low micromolar range with the most potent being the 6-hydroxy analog 1w. Compound 1w and the p-cyano analog 1c were also shown to exhibit significant inhibition of the binding of MIF to its transmembrane receptor CD74. Consistently, both compounds were also found to retard the MIF-dependent phosphorylation of ERK1/2 in human synovial fibroblasts. (C) 2011 Elsevier Ltd. All rights reserved.