2-(4-phenoxyphenoxy)ethanethiol | 87545-50-4

• 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: 2-(4-phenoxyphenoxy)ethanethiol
• CAS: 87545-50-4
• 化学式: C₁₄H₁₄O₂S
• mdl: MFCD16324223
• 分子量: 246.33
• InChiKey: FCFPQSUSBJMVPC-UHFFFAOYSA-N

物化性质

• 熔点：
  45 °C
• 沸点：
  372.5±27.0 °C(Predicted)
• 密度：
  1.147±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  17
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.142
• 拓扑面积：
  19.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(4-phenoxyphenoxy)ethanethiol 在 三甲基溴硅烷 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 77.0h， 生成 1-[(4-phenoxyphenoxyeth-1-ylthio)ethyl] 1,1-bisphosphonic acid
  参考文献：
  名称：

  WC-9 的含氟类似物和结构相关类似物对抗两种细胞内寄生虫：克氏锥虫和弓形虫的活性

  摘要：

  两种专性细胞内寄生虫，克氏锥虫（恰加斯病的病原体）和弓形虫（弓形虫病的病原体），在感染后上调宿主细胞的甲羟戊酸途径，这表明该宿主途径可能是潜在的药物靶点。在这项工作中，设计、合成了许多结构与WC-9 （4-苯氧基苯氧基乙基硫氰酸酯）（一种已知的角鲨烯合酶抑制剂）相关的化合物，并评估了它们对组织培养细胞中克氏弓形虫和刚地弓形虫生长的影响。两种含氟衍生物，3-(3-氟苯氧基)-和3-(4-氟苯氧基)苯氧基乙基硫氰酸盐，针对T的速殖子表现出半最大有效浓度(EC 50 )值分别为1.6和4.9μm 。 .​​​​此外，2-[3-（苯氧基）苯氧基乙硫基]乙基-1,1-二膦酸酯是一种含有 3-苯氧基苯氧基和二膦酸酯基团的混合抑制剂，具有亚微摩尔水平的抗弓形虫增殖活性（EC 50 = 0.7 μ m ），这表明两个官能团的联合抑制作用。

  DOI：

  10.1002/cmdc.201600505
• 作为产物：
  描述：

  2-(4-phenoxyphenoxy)ethyl thiocyanate 在 sodium methylate 、 溶剂黄146 、 锌 作用下， 生成 2-(4-phenoxyphenoxy)ethanethiol
  参考文献：
  名称：

  Structure−Activity Relationship of New Growth Inhibitors of Trypanosoma cruzi

  摘要：

  Several drugs bearing the 4-phenoxyphenoxy skeleton and other closely related structures were designed, synthesized, and evaluated as antiproliferative agents against Trypanosoma cruzi, the etiologic agent of Chagas' disease. The new class of drugs was envisioned by modifying the nonpolar 4-phenoxyphenoxy moiety replacing selected aromatic protons by different groups via electrophilic aromatic substitution reactions as well as introducing a sulfur atom at the polar extreme. Of the designed compounds, sulfur-containing derivatives were shown to be potent antireplicative agents against T. cruzi. Among these drugs, 4-phenoxyphenoxyethyl thiocyanate (compound 56) proved to be an extremely active growth inhibitor of the epimastigote forms of T. cruzi and displayed an IC50 of 2.2 mu M. Under the same assay conditions, this drug was much more active than Nifurtimox, one of the drugs currently in clinical use to control this disease. This thiocyanate derivative was also a very active inhibitor against the intracellular form of the parasite at the nanomolar level. Other sulfur derivatives prepared also exhibited very potent antiproliferative action against T. cruzi. The presence of a sulfur atom at the polar extreme for this family of compounds seems to be very important for biological action because this atom was always associated with high inhibition values. 4-Phenoxyphenoxyethyl thiocyanate presents very good prospective not only as a lead drug but also as a potential chemotherapeutic agent.

  DOI：

  10.1021/jm970860z

文献信息

• Thiolcarbamate compounds, and their production and use
  申请人：SUMITOMO CHEMICAL COMPANY, LIMITED

  公开号：EP0071463A1

  公开（公告）日：1983-02-09

  A thiolcarbamate compound of the formula: wherein X is an oxygen atom, a sulfur atom or a methylene group, R- is a hydrogen atom, a C--C4 alkyl group or a C3-C4 alkenyl group and R2 is a C--C, alkyl group, a C--C, alkenyl group, a C--C, alkynyl group or a cyclopropyl group, which is useful as an insect controlling agent.

  一种硫醇氨基甲酸酯化合物，其式如下 其中 X 是氧原子、硫原子或亚甲基，R- 是氢原子、C-C4 烷基或 C3-C4 烯基，R2 是 C-C烷基、C-C烯基、C-C炔基或环丙基，可用作昆虫防治剂。
• Design, Synthesis, and Biological Evaluation of Aryloxyethyl Thiocyanate Derivatives against <i>Trypanosoma cruzi</i>
  作者：Eleonora Elhalem、Brian N. Bailey、Roberto Docampo、István Ujváry、Sergio H. Szajnman、Juan B. Rodriguez

  DOI：10.1021/jm0201518

  日期：2002.8.1

  As a continuation of our project aimed at the search for new and safe chemotherapeutic and chemoprophylactic agents against American trypanosomiasis (Chagas' disease), several drugs structurally related to 4-phenoxyphenoxyethyl thiocyanate (4) were designed, synthesized, and evaluated as antiproliferative agents against the parasite responsible for this disease, the hemoflagellated protozoan Trypanosoma cruzi. This thiocyanate derivative was previously shown to be an effective and potent agent against T. cruzi proliferation. Several drugs possessing thiocyanate groups proved to be effective growth inhibitors of T. cruzi growth. Among the designed compounds, it is important to point out the extremely potent activity shown by 11, 23, 38, 53, 90, 99, and 117 against the epimastigote forms of the parasite. All of them exhibited IC50 values in the low micromolar range, and these values were comparable with those presented by our lead drug 4 and ketokonazole, a well-known antiparasitic agent. The activity displayed by the nitrogen-containing derivative 90 was very promising with IC50 values of 3.3 muM. Several other thiocyanate derivatives also proved to be very potent inhibitors of the multiplication of T. cruzi epimastigotes, such as compounds 28, 33, 43, 48, 56, 61, 66, 71, 76, and 124. Compound 43 resulted in being a promising drug because it was also very effective against amastigotes, the clinically more relevant form of the parasite. This compound was Mold more potent than 4, while 11 showed nearly the same activity as our lead drug against intracellular T. cruzi. It was very surprising that the experimental juvenoid 124, although fairly devoid of activity against epimastigotes, was very effective against intracellular amastigotes growing in myoblasts. The rest of the designed compounds showed a broad degree of inhibitory action, from moderately active drugs to drugs almost devoid of antiparasitic activity. Compound 43 is an interesting example of an effective antichagasic agent that presents excellent prospectives not only as a lead drug but also to be used for further in vivo studies.
• KISIDA, XIROSI;XATA, KOSINOBU
  作者：KISIDA, XIROSI、XATA, KOSINOBU

  DOI：——

  日期：——
• US4486449A
  申请人：——

  公开号：US4486449A

  公开（公告）日：1984-12-04
• Activity of Fluorine-Containing Analogues of WC-9 and Structurally Related Analogues against Two Intracellular Parasites:<i>Trypanosoma cruzi</i>and<i>Toxoplasma gondii</i>
  作者：María N. Chao、Catherine Li、Melissa Storey、Bruno N. Falcone、Sergio H. Szajnman、Sergio M. Bonesi、Roberto Docampo、Silvia N. J. Moreno、Juan B. Rodriguez

  DOI：10.1002/cmdc.201600505

  日期：2016.12.16

  evaluated for their effect on T. cruzi and T. gondii growth in tissue culture cells. Two fluorine‐containing derivatives, the 3‐(3‐fluorophenoxy)‐ and 3‐(4‐fluorophenoxy)phenoxyethyl thiocyanates, exhibited half‐maximal effective concentration (EC50) values of 1.6 and 4.9 μm, respectively, against tachyzoites of T. gondii, whereas they showed similar potency to WC‐9 against intracellular T. cruzi (EC50 values

  两种专性细胞内寄生虫，克氏锥虫（恰加斯病的病原体）和弓形虫（弓形虫病的病原体），在感染后上调宿主细胞的甲羟戊酸途径，这表明该宿主途径可能是潜在的药物靶点。在这项工作中，设计、合成了许多结构与WC-9 （4-苯氧基苯氧基乙基硫氰酸酯）（一种已知的角鲨烯合酶抑制剂）相关的化合物，并评估了它们对组织培养细胞中克氏弓形虫和刚地弓形虫生长的影响。两种含氟衍生物，3-(3-氟苯氧基)-和3-(4-氟苯氧基)苯氧基乙基硫氰酸盐，针对T的速殖子表现出半最大有效浓度(EC 50 )值分别为1.6和4.9μm 。 .​​​​此外，2-[3-（苯氧基）苯氧基乙硫基]乙基-1,1-二膦酸酯是一种含有 3-苯氧基苯氧基和二膦酸酯基团的混合抑制剂，具有亚微摩尔水平的抗弓形虫增殖活性（EC 50 = 0.7 μ m ），这表明两个官能团的联合抑制作用。