1-methoxybenzothieno[3,2-b]quinolin-11(5H)-one | 1265087-58-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 硫色烯
• 英文名称: 1-methoxybenzothieno[3,2-b]quinolin-11(5H)-one
• CAS: 1265087-58-8
• 化学式: C₁₆H₁₁NO₂S
• 分子量: 281.335
• InChiKey: JHYWMDOYIPBOQW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  20.0
• 可旋转键数：
  1.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  42.09
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  1-methoxybenzothieno[3,2-b]quinolin-11(5H)-one 在 三氯氧磷 、 水 、 sodium hydroxide 作用下， 反应 3.0h， 生成 1-methoxy-11-chlorobenzothieno[3,2-b]quinoline
  参考文献：
  名称：

  Benzothieno[3,2-b]quinolinium and 3-(phenylthio)quinolinium compounds: Synthesis and evaluation against opportunistic fungal pathogens

  摘要：

  Substitution around 5-methyl benzothieno[3,2-b] quinolinium (2) ring system was explored in order to identify positions of substitution that could improve its antifungal profile. The 3-methoxy (10b) was active against C. albicans, C. neoformans, and A. fumigatus and the 4-chloro (10f) analog showed moderate increases in anti-cryptococcal and anti-aspergillus activities. The effectiveness of 10b and 10f were validated in murine models of candidiasis and cryptococcosis, respectively. The efficacy of 10f in reducing brain cryptococcal infection and its observation in the brain of mice injected with this quaternary compound confirm the capacity of these compounds to cross the blood-brain barrier of mice. Overall, several of the chloro and methoxy substituted compounds showed significant improvements in activity against A. fumigatus, the fungal pathogen prevalent in patients receiving organ transplant. Opening the benzothiophene ring of 2 to form 1-(5-cyclohexylpentyl)-3-(phenylthio) quinolinium compound (3) resulted in the identification of several novel compounds with over 50-fold increases in potency (cf. 2) while retaining low cytotoxicities. Thus, compound 3 constitutes a new scaffold for development of drugs against opportunistic infections. Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmc.2010.11.008
• 作为产物：
  描述：

  2-methoxy-6-(2-phenylsulfanyl-acetylamino)-benzoic acid 在 磷酸 、 sodium hydroxide 作用下， 以 水 为溶剂， 反应 3.0h， 生成 1-methoxybenzothieno[3,2-b]quinolin-11(5H)-one
  参考文献：
  名称：

  Benzothieno[3,2-b]quinolinium and 3-(phenylthio)quinolinium compounds: Synthesis and evaluation against opportunistic fungal pathogens

  摘要：

  Substitution around 5-methyl benzothieno[3,2-b] quinolinium (2) ring system was explored in order to identify positions of substitution that could improve its antifungal profile. The 3-methoxy (10b) was active against C. albicans, C. neoformans, and A. fumigatus and the 4-chloro (10f) analog showed moderate increases in anti-cryptococcal and anti-aspergillus activities. The effectiveness of 10b and 10f were validated in murine models of candidiasis and cryptococcosis, respectively. The efficacy of 10f in reducing brain cryptococcal infection and its observation in the brain of mice injected with this quaternary compound confirm the capacity of these compounds to cross the blood-brain barrier of mice. Overall, several of the chloro and methoxy substituted compounds showed significant improvements in activity against A. fumigatus, the fungal pathogen prevalent in patients receiving organ transplant. Opening the benzothiophene ring of 2 to form 1-(5-cyclohexylpentyl)-3-(phenylthio) quinolinium compound (3) resulted in the identification of several novel compounds with over 50-fold increases in potency (cf. 2) while retaining low cytotoxicities. Thus, compound 3 constitutes a new scaffold for development of drugs against opportunistic infections. Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmc.2010.11.008