1-苯并呋喃-5-硫醇 | 90590-07-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并呋喃
• 中文名称: 1-苯并呋喃-5-硫醇
• 中文别名: 戊基糖,6-脱氧(9CI)
• 英文名称: 5-Mercaptobenzofuran
• 英文别名: 5-Benzofuranthiol；1-benzofuran-5-thiol
• CAS: 90590-07-1
• 化学式: C₈H₆OS
• 分子量: 150.201
• InChiKey: PPFDCKWSHHGOQP-UHFFFAOYSA-N

物化性质

• 沸点：
  241.3±13.0 °C(Predicted)
• 密度：
  1.262±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  14.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  5-(N,N-dimethylcarbamoyl)thiobenzofuran 在 氢氧化钾 作用下， 以 甲醇 为溶剂， 以97%的产率得到1-苯并呋喃-5-硫醇
  参考文献：
  名称：

  Sulfone derivatives, process for their production and use thereof

  摘要：

  一个由以下式表示的化合物： 其中R是一个环烃基团，或类似物；W是一个键，或类似物；X是一个二价碳氢基团，或类似物；Y和Z分别独立地为—N(R6)—或类似物；环A是一个含氮杂环环，或类似物；R5和R6独立地为氢原子、一个碳氢基团，或类似物；Z′是亚胺基团，或类似物；a为0、1或2；b为0或1，或其盐。

  公开号：

  US20030187023A1

文献信息

• [EN] INHIBITION OF OLIG2 ACTIVITY<br/>[FR] INHIBITION DE L'ACTIVITÉ D'OLIG2
  申请人：CURTANA PHARMACEUTICALS INC

  公开号：WO2018039621A1

  公开（公告）日：2018-03-01

  Described herein are compounds and pharmaceutical compositions containing such compounds, which inhibit the activity of Olig2. Also described herein are methods of using such Olig2 inhibitors, alone and in combination with other compounds, for treating cancer and other diseases. In particular the Olig2 inhibitors may be used to treat glioblastoma.

  本文描述了含有这些化合物的化合物和药物组合物，这些化合物抑制Olig2的活性。本文还描述了使用这种Olig2抑制剂的方法，单独或与其他化合物结合，用于治疗癌症和其他疾病。特别是Olig2抑制剂可用于治疗胶质母细胞瘤。
• [EN] INHIBITING OTUB1<br/>[FR] INHIBITION DE L'OTUB1
  申请人：INTEGRAL EARLY DISCOVERY INC

  公开号：WO2020223551A1

  公开（公告）日：2020-11-05

  The present disclosure is directed to compounds of formulas (I) - (VII), which are useful as modulators of OTUB1. The compounds are further useful in the inhibition of OTUB1 and the treatment of diseases or disorders associated with the inhibition of OTUB1. For instance, the disclosure is concerned with compounds and compositions for inhibition of OTUB1, methods of treating diseases associated with the inhibition of OTUB1 (e.g., inflammatory diseases like irritable bowel disease and Lupus), and methods of synthesis of these compounds.

  本公开涉及的是公式(I)-(VII)的化合物，它们可用作OTUB1的调节剂。这些化合物还可用于抑制OTUB1和治疗与抑制OTUB1相关的疾病或疾病。例如，本公开涉及用于抑制OTUB1的化合物和组合物，治疗与抑制OTUB1相关的疾病的方法（例如，炎症性疾病，如肠易激综合征和红斑狼疮），以及这些化合物的合成方法。
• AMINO ACID INHIBITORS OF CYTOCHROME P450
  申请人：Eissenstat Michael

  公开号：US20110124578A1

  公开（公告）日：2011-05-26

  Methods of inhibiting cytochrome P450 enzymes are provided that can be used for improving the treatment of diseases by preventing degradation of drugs or other molecules by cytochrome P450. Pharmaceutical compositions are provided that eases can act as boosters to improve the pharmacokinetics, enhance the bioavailability, and enhance the therapeutic effect of drugs that undergo in vivo degradation by cytochrome P450 enzymes.

  提供了抑制细胞色素P450酶的方法，可用于通过防止细胞色素P450对药物或其他分子的降解来改善疾病的治疗。提供了药物组合物，可作为增强剂，改善药物的药代动力学，增强生物利用度，并增强在体内通过细胞色素P450酶降解的药物的治疗效果。
• SULFONE DERIVATIVES, PROCESS FOR THEIR PRODUCTION AND USE THEREOF
  申请人：Takeda Chemical Industries, Ltd.

  公开号：EP1302462A1

  公开（公告）日：2003-04-16

  A compound represented by the formula: wherein R is a cyclic hydrocarbon group, or the like; W is a bond, or the like; X is a divalent hydrocarbon group, or the like; Y and Z are each independently -N(R6)- or the like; ring A is a nitrogen-containing heterocyclic ring, or the like; R5 and R6 are independently hydrogen atom, a hydrocarbon group, or the like; Z' is imidoyl group, or the like; a is 0, 1 or 2; and b is 0 or 1, or a salt thereof.

  一种由式表示的化合物： 其中 R 是环状烃基，或类似物；W 是键，或类似物；X 是二价烃基，或类似物；Y 和 Z 各自独立地是 -N(R6)- 或类似物；环 A 是含氮杂环，或类似物；R5 和 R6 独立地是氢原子、烃基，或类似物；Z'是咪唑酰基，或类似物；a 是 0、1 或 2；b 是 0 或 1，或其盐。
• SUBSTITUTED INDOLE COMPOUNDS
  申请人：BRISTOL-MYERS SQUIBB COMPANY

  公开号：US20210253593A1

  公开（公告）日：2021-08-19

  Disclosed are compounds of Formula (I) or salts thereof, wherein Ring Het, R 1 , R 2 , R 3 , R 4 , R 5 , m, n, and p are defined herein. Also disclosed are methods of using such compounds as inhibitors of signaling through Toll-like receptor 7, or 8, or 9, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating inflammatory and autoimmune diseases.