(4-Fluorophenyl)carbamodithioic acid

• 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: (4-Fluorophenyl)carbamodithioic acid
• 化学式: C₇H₆FNS₂
• 分子量: 187.262
• InChiKey: NESJBMWMWJLKGI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  45.1
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (4-Fluorophenyl)carbamodithioic acid 在 aluminum oxide 、 sodium monochloroacetic acid 、 一水合肼 、 溶剂黄146 作用下， 反应 4.09h， 生成 methyl (R)-4-((5S,8R,9S,10S,13R,14S,17R)-3-(2-((4-fluorophenyl)carbamothioyl)hydrazineylidene)-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
  参考文献：
  名称：

  Microwave-Assisted Synthesis and Antibacterial Activity of Novel Chenodeoxycholic Acid Thiosemicarbazone Derivatives

  摘要：

  报告了一种在无溶剂条件下利用微波辐照合成新型酚去氧胆酸硫代氨基甲酸脲衍生物的快速高效方法。十种新型化合物的合成收率良好。通过 1H NMR、IR、ESI-MS 光谱和元素分析阐明了它们的结构。初步结果表明，其中一些化合物对鼠伤寒杆菌和大肠杆菌具有抑制作用。

  DOI：

  10.3184/174751911x13129090186347
• 作为产物：
  描述：

  二硫化碳 、 4-氟苯胺 在 三乙胺 作用下， 以 乙醇 为溶剂， 生成 (4-Fluorophenyl)carbamodithioic acid
  参考文献：
  名称：

  异硫氰酸酯衍生物的合成，体外原虫活性和分子对接研究。

  摘要：

  从Noscapine，胆汁酸，氨基酸和一些芳香族化合物开始合成了新型异硫氰酸酯衍生物。测试了合成衍生物对四种单细胞原生动物即布鲁氏锥虫，克鲁氏梭菌，杜氏利什曼原虫和恶性疟原虫的抗寄生虫活性。有趣的是，七个异硫氰酸酯类似物表现出对多形利什曼原虫的抗寄生虫活性，其IC50值为0.4至1.0 µM，选择性指数（SI）为7.8至18.4，与标准药物miltefosine相当（IC50 = 0.7μM）。化合物7h表现出最佳的抗菌活性，IC50值为0.4 µM。七种产品表现出对杜氏布鲁氏菌的抑制活性，IC50值低于2.0μM，SI值在2.7至29.3之间。Noscapine的4种伯胺衍生物和5种异硫氰酸酯衍生物表现出抗血浆活性，IC50在1.1-2.7 µM的范围内，SI值在1.1至14.5之间。异硫氰酸酯衍生物7c表现出抗克氏锥虫的IC50值为1.9 µM和SI4。进行了分子对接和ADMET研究，

  DOI：

  10.1016/j.bmc.2019.115185

文献信息

• Design, Synthesis and Antiproliferative Activities of Diaryl Thiourea Derivatives as Anticancer Agents
  作者：Jianwen Yao、Zuopeng He、Jing Chen、Daquan Chen、Wei Sun、Wenfang Xu

  DOI：10.1002/cjoc.201200708

  日期：2012.10

  Two new series of diaryl thiourea containing sorafenib derivatives 9a–9t were designed and synthesized, and their antiproliferative activities against PC‐3, HCT116 and MDA‐MB‐231 cell lines were evaluated. All compounds generally showed antiproliferative activity to PC‐3 cells, most of the analogs exhibited potent antiproliferative activity to HCT116 cells, and compounds 9e, 9f, 9o and 9p demonstrated

  设计并合成了两个新的含索拉非尼衍生物9a - 9t的二芳基硫脲系列产品，并评估了它们对PC-3，HCT116和MDA-MB-231细胞系的抗增殖活性。所有化合物通常对PC-3细胞均具有抗增殖活性，大多数类似物均对HCT116细胞具有有效的抗增殖活性，化合物9e，9f，9o和9p对所有这三种细胞系均具有抑制活性。所有新合成的化合物的结构均通过1 H NMR，13 C NMR和HRMS确定。
• Design, synthesis and biological evaluation of thiourea and nicotinamide-containing sorafenib analogs as antitumor agents
  作者：Xiangkai Kong、Zeyu Yao、Zuopeng He、Wenfang Xu、Jianwen Yao

  DOI：10.1039/c4md00536h

  日期：——

  Thiourea and nicotinamide-containing sorafenib analogs with better antiproliferative and anti-angiogenic activities than sorafenib were well designed and synthesized.

  硫脲和烟酰胺含量比索拉非尼更好的抗增殖和抗血管生成活性的类索拉非尼类似物已经被设计和合成。
• Cobalt mediated by desulfurization toward the synthesis of isothiocyanates
  作者：Mohan Seelam、Bajivali Shaik、Prasada Rao Kammela

  DOI：10.1080/00397911.2016.1224351

  日期：2016.11.1

  ABSTRACT A highly efficient and simple protocol for the construction of aromatic and aliphatic isothiocyanates from their respective amines in the presence of cheap, readily available, and air-stable cobalt catalyst is described. All reactions were carried out under optimized reaction conditions and gave target products in good to excellent yields within shorter reaction time. GRAPHICAL ABSTRACT

  摘要描述了在廉价、易得且空气稳定的钴催化剂存在下，从各自的胺中构建芳香族和脂肪族异硫氰酸酯的高效且简单的方案。所有反应均在优化的反应条件下进行，并在较短的反应时间内以良好至极好的收率得到目标产物。图形概要
• Design, synthesis and biological evaluation of novel thiosemicarbazide analogues as potent anticonvulsant agents
  作者：Reshma J. Nevagi、Avinash S. Dhake、Harsha I. Narkhede、Prabhjeet Kaur

  DOI：10.1016/j.bioorg.2014.04.002

  日期：2014.6

  Novel thiosemicarbazide derivatives were synthesised and evaluated for their anticonvulsant activity and neurotoxicity. Anticonvulsant activity was done for grand mal and petit mal types of epilepsies by maximal electroshock (MES) and pentylenetetrazol (PTZ) induced convulsions methods respectively. Rotarod test was done to determine neurotoxicity. Amongst synthesised compounds, N-(4-bromophenyl) 2-[(2-phenylhydrazinyl) carbonothioyl] hydrazinecarbothioamide (5e) is a broad-spectrum anticonvulsant agent since it was active in both (MES) and (PTZ) induced seizure models with no neurotoxicity and N, N-(bis(chlorophenyl) hydrazine-1,2-dicarbothoamide (5g) acts as a selective agent for grand mal epilepsy. (C) 2014 Elsevier Inc. All rights reserved.
• Thiourea and thioether derivatives of sorafenib: synthesis, crystal structure, and antiproliferative activity
  作者：Jianwen Yao、Jing Chen、Zuopeng He、Wei Sun、Hao Fang、Wenfang Xu

  DOI：10.1007/s00044-012-0400-8

  日期：2013.8

  A series of novel sorafenib derivatives containing diaryl thiourea and thioether, 9a-u, was designed and synthesized, and their antiproliferative activities against HCT116 and MDA-MB-231 cell lines were also evaluated and described. Most compounds exhibited potent antiproliferative activity against HCT116 cells with IC50 = 1.8-80.4 mu M. Compounds 9p, 9r, and 9s demonstrated competitive antiproliferative activities to sorafenib, against all two cancer cell lines. The structures of all the newly synthesized compounds were determined by H-1 NMR, C-13 NMR, and HRMS, and compound 9n was characterized by single-crystal X-ray diffraction. Primary structure-activity relationships (SAR) have also been established.