S-(4-chloro-phenyl)-isothiourea | 51512-95-9

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: S-(4-chloro-phenyl)-isothiourea
• 英文别名: S-(4-Chlor-phenyl)-isothioharnstoff；4-Chlorophenyl carbamimidothioate；(4-chlorophenyl) carbamimidothioate
• CAS: 51512-95-9
• 化学式: C₇H₇ClN₂S
• 分子量: 186.665
• InChiKey: VGEPJOGUSMXIOZ-UHFFFAOYSA-N

物化性质

• 沸点：
  302.4±44.0 °C(predicted)
• 密度：
  1.39±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  11
• 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：
  75.2
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  S-(4-chloro-phenyl)-isothiourea 在 亚硝酸 作用下， 生成 S-(4-chloro-phenyl)-N,N'-dinitroso-isothiourea; S-(4-chloro-phenyl)-isothiourea salt
  参考文献：
  名称：

  Arndt, Justus Liebigs Annalen der Chemie, 1913, vol. 396, p. 20

  摘要：

  DOI：
• 作为产物：
  描述：

  氰胺 、 4-氯苯硫酚 生成 S-(4-chloro-phenyl)-isothiourea
  参考文献：
  名称：

  Arndt, Justus Liebigs Annalen der Chemie, 1913, vol. 396, p. 20

  摘要：

  DOI：

文献信息

• Degradation of MAC13243 and studies of the interaction of resulting thiourea compounds with the lipoprotein targeting chaperone LolA
  作者：Courtney A. Barker、Sarah E. Allison、Soumaya Zlitni、Nick Duc Nguyen、Rahul Das、Giuseppe Melacini、Alfredo A. Capretta、Eric D. Brown

  DOI：10.1016/j.bmcl.2013.02.005

  日期：2013.4

  The discovery of novel small molecules that function as antibacterial agents or cellular probes of biology is hindered by our limited understanding of bacterial physiology and our ability to assign mechanism of action. We previously employed a chemical genomic strategy to identify a novel small molecule, MAC13243, as a likely inhibitor of the bacterial lipoprotein targeting chaperone, LolA. Here, we report on the degradation of MAC13243 into the active species, S-(4-chlorobenzyl)isothiourea. Analogs of this compound (e.g., A22) have previously been characterized as inhibitors of the bacterial actin-like protein, MreB. Herein, we demonstrate that the antibacterial activity of MAC13243 and the thiourea compounds are similar; these activities are suppressed or sensitized in response to increases or decreases of LolA copy number, respectively. We provide STD NMR data which confirms a physical interaction between LolA and the thiourea degradation product of MAC13243, with a K-d of similar to 150 mu M. Taken together, we conclude that the thiourea series of compounds share a similar cellular mechanism that includes interaction with LolA in addition to the well-characterized target MreB. (C) 2013 Elsevier Ltd. All rights reserved.
• Arylation of thiourea by aryldiazonium salts
  作者：B. V. Kopylova、L. V. Yashkina、R. Kh. Freidlina

  DOI：10.1007/bf00926133

  日期：1973.12