1-(3-fluorobenzylidene)semicarbazide | 120445-37-6

• 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: 1-(3-fluorobenzylidene)semicarbazide
• 英文别名: m-fluorobenzaldehyde semicarbazone；3-fluoro-benzaldehyde-semicarbazone；3-Fluor-benzaldehyd-semicarbazon；3-Fluorobenzaldehyde semicarbazone；[(E)-(3-fluorophenyl)methylideneamino]urea
• CAS: 120445-37-6
• 化学式: C₈H₈FN₃O
• 分子量: 181.169
• InChiKey: YRCLJTJKKFDSMU-VZUCSPMQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  13
• 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：
  67.5
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  间氟氯苄 在 乙醇 、 二氧化碳 、 乌洛托品 作用下， 生成 1-(3-fluorobenzylidene)semicarbazide
  参考文献：
  名称：

  232.芳香族侧链反应的机理，特别涉及取代基的极性效应。第十四部分。醛-氰醇与卤代苯甲醛的反应：卤素取代基的极性作用

  摘要：

  DOI：

  10.1039/jr9490001089

文献信息

• Semicarbazone derivatives as urease inhibitors: Synthesis, biological evaluation, molecular docking studies and in-silico ADME evaluation
  作者：Syeda Uroos Qazi、Shafiq Ur Rahman、Asia Naz Awan、Mariya al-Rashida、Rima D. Alharthy、Asnuzilawati Asari、Abdul Hameed、Jamshed Iqbal

  DOI：10.1016/j.bioorg.2018.03.029

  日期：2018.9

  A series of hydrazinecarboxamide derivatives were synthesized and examined against urease for their inhibitory activity. Among the series, the 1-(3-fluorobenzylidene)semicarbazide (4a) (IC50 = 0.52 ± 0.45 µM), 4u (IC50 = 1.23 ± 0.32 µM) and 4h (IC50 = 2.22 ± 0.32 µM) were found most potent. Furthermore, the molecular docking study was also performed to demonstrate the binding mode of the active hydrazinecarboxamide

  合成了一系列肼甲酰胺衍生物，并检查了其对脲酶的抑制活性。在该系列中， 发现最多的是1-（3-氟亚苄基）氨基脲（4a）（IC 50  = 0.52±0.45 µM），4u（IC 50  = 1.23±0.32 µM）和4h（IC 50 = 2.22±0.32 µM）。有力的。此外，还进行了分子对接研究，以证明活性肼甲酰胺与脲酶的结合方式。为了估计化合物的药物相似性，进行了计算机模拟ADME评估。所有化合物均表现出良好的ADME分布以及良好的预测口服生物利用度。
• Some aryl semicarbazones possessing anticonvulsant activitie
  作者：JR Dimmock、KK Sidhu、SD Tumber、SK Basran、M Chen、JW Quail、J Yang、I Rozas、DF Weaver

  DOI：10.1016/0223-5234(96)88237-7

  日期：——

  A number of aryl semicarbazones displayed anticonvulsant activity in the maximal electroshock (MES) and subcutaneous pentylenetetrazole (scPTZ) screens when administered intraperitoneally to mice. When given by the oral route to rats, protection was afforded in the MES but not scPTZ tests. Correlations were noted between the sigma and sigma* values of the aryl substituents, the interplanar angles made by the aryl rings with the adjacent carbimino groups and the shapes of certain semicarbazones determined by X-ray crystallography, and the activities in the rat oral MES screen. Molecular modeling studies revealed a number of statistically significant descriptors which contributed to anticonvulsant activity.
• COMPOUNDS AND METHODS OF TREATING INFECTIONS
  申请人：Neoculi Pty Ltd

  公开号：EP2991968B1

  公开（公告）日：2021-11-10
• METHODS FOR TREATING PROTOZOAN INFECTIONS
  申请人：Neoculi Pty Ltd

  公开号：EP3188722A1

  公开（公告）日：2017-07-12
• COMPOSITIONS FOR ENHANCING NITROGEN STABILIZERS AND METHODS AND USES THEREOF
  申请人：Verdesian Life Sciences U.S., LLC

  公开号：EP4103534A1

  公开（公告）日：2022-12-21