2-naphthaldehyde-[4-(2-hydroxy-5-methoxyphenyl)-1,3-thiazol-2-yl]hydrazone | 1427161-65-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2-naphthaldehyde-[4-(2-hydroxy-5-methoxyphenyl)-1,3-thiazol-2-yl]hydrazone
• 英文别名: 4-Methoxy-2-[2-[2-(2-naphthylmethylene)hydrazino]thiazol-4-yl]phenol；4-methoxy-2-[2-[2-(naphthalen-2-ylmethylidene)hydrazinyl]-1,3-thiazol-4-yl]phenol
• CAS: 1427161-65-6
• 化学式: C₂₁H₁₇N₃O₂S
• 分子量: 375.451
• InChiKey: LWUVMZHUZYASMO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.4
• 重原子数：
  27
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  95
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  2-萘甲醛 在 吡啶 作用下， 以 乙醇 为溶剂， 反应 8.0h， 生成 2-naphthaldehyde-[4-(2-hydroxy-5-methoxyphenyl)-1,3-thiazol-2-yl]hydrazone
  参考文献：
  名称：

  Synthesis and anti-Candida activity of novel 2-hydrazino-1,3-thiazole derivatives

  摘要：

  Eighteen new hydrazino-1,3-thiazole derivatives were evaluated against 8 strains of multi-resistant Candida spp. Introduction of an indolyl moiety linked to the hydrazone function enhanced the in vitro anti-Candida activity, with an activity spectrum towards Candida albicans strains. Introduction of a (S)-2-aminoethyl chain on the thiazole nucleus largely enhanced the in vitro antifungal activity, with a selectivity oriented towards non-C. albicans species. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.01.039

文献信息

• Synthesis and anti-Candida activity of novel 2-hydrazino-1,3-thiazole derivatives
  作者：Ludovic T. Maillard、Sébastien Bertout、Ophélie Quinonéro、Gülşen Akalin、Gülhan Turan-Zitouni、Pierre Fulcrand、Fatih Demirci、Jean Martinez、Nicolas Masurier

  DOI：10.1016/j.bmcl.2013.01.039

  日期：2013.3

  Eighteen new hydrazino-1,3-thiazole derivatives were evaluated against 8 strains of multi-resistant Candida spp. Introduction of an indolyl moiety linked to the hydrazone function enhanced the in vitro anti-Candida activity, with an activity spectrum towards Candida albicans strains. Introduction of a (S)-2-aminoethyl chain on the thiazole nucleus largely enhanced the in vitro antifungal activity, with a selectivity oriented towards non-C. albicans species. (C) 2013 Elsevier Ltd. All rights reserved.