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11,22,35-trimethyl-14,32-dithia-2,8,12,21,25,34,37,38-octaazatetracyclo[31.3.19,13.121,25]nonatriaconta-1(37),9(38),10,12,22,33,35-heptaene-24,39-dione | 658041-90-8

中文名称
——
中文别名
——
英文名称
11,22,35-trimethyl-14,32-dithia-2,8,12,21,25,34,37,38-octaazatetracyclo[31.3.19,13.121,25]nonatriaconta-1(37),9(38),10,12,22,33,35-heptaene-24,39-dione
英文别名
11,23,36-trimethyl-8,26-dithia-1,10,14,20,24,33,38,39-octazatetracyclo[31.3.1.19,13.121,25]nonatriaconta-9,11,13(39),21(38),22,24,35-heptaene-34,37-dione
11,22,35-trimethyl-14,32-dithia-2,8,12,21,25,34,37,38-octaazatetracyclo[31.3.1<sup>9,13</sup>.1<sup>21,25</sup>]nonatriaconta-1(37),9(38),10,12,22,33,35-heptaene-24,39-dione化学式
CAS
658041-90-8
化学式
C32H48N8O2S2
mdl
——
分子量
640.918
InChiKey
ARQPSUWQCPLTTN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.23
  • 重原子数:
    44.0
  • 可旋转键数:
    0.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    119.62
  • 氢给体数:
    2.0
  • 氢受体数:
    12.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    对甲苯磺酸甲酯11,22,35-trimethyl-14,32-dithia-2,8,12,21,25,34,37,38-octaazatetracyclo[31.3.19,13.121,25]nonatriaconta-1(37),9(38),10,12,22,33,35-heptaene-24,39-dione 反应 7.0h, 以92%的产率得到10,11,23,24,34-pentamethyl-36,37-dioxo-8,26-dithia-1,14,20,33,38,39-hexaaza-10,24-diazoniatetracyclo[31.3.1.1(9,13).1(21,25)]nonatriaconta-9(39),10,12,21(38),22,24,34-heptaene bis(p-toluenesulfonate)
    参考文献:
    名称:
    Pyrimidinophane p-toluenesulfonate—Water-soluble pyrimidine-containing macrocycles
    摘要:
    Reactions of pyrimidinophanes containing two 6-methylthiocytosine and one 6-methyluracil fragments with methyl p-toluenesulfonate gave amphiphilic macrocyclic bis-p-toluenesulfonates. Despite the presence of several reaction centers in the initial pyrimidinophane molecules, methylation occurred only at the N-1 atom (with quaternization) of the 6-methylthiocytosine fragments. Bacteriostatic and fungistatic activity of the products was estimated.
    DOI:
    10.1134/s1070363209010216
  • 作为产物:
    参考文献:
    名称:
    Pyrimidinophane p-toluenesulfonate—Water-soluble pyrimidine-containing macrocycles
    摘要:
    Reactions of pyrimidinophanes containing two 6-methylthiocytosine and one 6-methyluracil fragments with methyl p-toluenesulfonate gave amphiphilic macrocyclic bis-p-toluenesulfonates. Despite the presence of several reaction centers in the initial pyrimidinophane molecules, methylation occurred only at the N-1 atom (with quaternization) of the 6-methylthiocytosine fragments. Bacteriostatic and fungistatic activity of the products was estimated.
    DOI:
    10.1134/s1070363209010216
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文献信息

  • Metal binding properties of pyrimidinophanes and their acyclic counterparts
    作者:Sergey N. Podyachev、Vyacheslav E. Semenov、Victor V. Syakaev、Nadezda E. Kashapova、Svetlana N. Sudakova、Julia K. Voronina、Anatoly S. Mikhailov、Alexandra D. Voloshina、Vladimir S. Reznik、Alexander I. Konovalov
    DOI:10.1039/c3ra47571a
    日期:——
    A series of acyclic and macrocyclic nucleobase derivatives that contain uracil and 2-thiocytosine units linked by polymethylene spacers was prepared. The length of spacers as well as the oxidation number of sulfur atoms entering into the structure of the compounds was varied. The crystal structure of pyrimidinophane with hexa- and heptamethylene linkers was established by X-ray analysis. The metal ion-binding properties of pyrimidinophanes and their acyclic counterparts were investigated by liquid extraction and 1H NMR titration experiments. The compounds with 2-thiocytosine fragments revealed a high selectivity of extraction towards Ag+ ions. The stoichiometry of silver complexes and the binding constants have been determined. The antibacterial activity of these complexes was also discussed.
    一系列含有尿嘧啶和2-胞嘧啶单元并通过聚亚甲基间隔相连的非环和宏环核碱衍生物被制备出来。间隔的长度以及进入化合物结构的原子的氧化数被改变。通过X射线分析确定了含有六亚甲基和七亚甲基连接体的嘧啶冠醚的晶体结构。通过液体萃取和1H NMR滴定实验研究了嘧啶冠醚及其非环对应物的属离子结合性质。含有2-胞嘧啶片段的化合物显示出对Ag+离子的高选择性萃取。确定络合物的化学计量比和结合常数。这些络合物的抗菌活性也进行了讨论。
  • Antimicrobial activity of pyrimidinophanes with thiocytosine and uracil moieties
    作者:Vyacheslav E. Semenov、Anatoly S. Mikhailov、Alexandra D. Voloshina、Natalia V. Kulik、Alexandra D. Nikitashina、Vladimir V. Zobov、Sergey V. Kharlamov、Shamil K. Latypov、Vladimir S. Reznik
    DOI:10.1016/j.ejmech.2011.05.034
    日期:2011.9
    Reactions of pyrimidinophanes with two 6-methylthiocytosine and one 5(6)-alkyluracil moieties bridged with each other by polymethylene spacers with methyl or nonyl p-toluenesulfonate, p-toluenesulfonic acid, methanesulfonate and trifluorosulfonate afforded amphiphilic macrocyclic bis-p-toluene-, methane- and trifluorosulfonates. Despite the presence of several reaction centers in the initial pyrimidinophane molecules, protonation and methylation occurred only at the N-1 atom (with quaternization) of the 6-methylthiocytosine moieties. The bacteriostatic and fungistatic activity of the products was estimated. Macrocyclic tosylates exhibit a remarkable selectivity towards Staphylococcus aureus, with MIC values comparable with a reference drug. Bacteriostatic activity of the amphiphilic pyrimiclinophanes depends on the size of the macrocycles, and the highest activity corresponds to definite lengths of polymethylene bridges. Besides, the antimicrobial activity of the screened pyrimidine derivatives depends on their topology. While macrocyclic tosylates are more active against bacteria than against fungi, acyclic tosylate with the same structural fragments shows a dramatical decrease of MIC towards mold and yeast with respect to the corresponding macrocycle. It is found that macrocyclic and acyclic tosylates in high dilutions decrease the extracellular lipase activity. (C) 2011 Elsevier Masson SAS. All rights reserved.
  • ——
    作者:A. S. Mikhailov、R. Kh. Giniyatullin、V. E. Semenov、V. S. Reznik、A. A. Nafikova、Sh. K. Latypov、Yu. Ya. Efremov、D. R. Sharafutdinova
    DOI:10.1023/a:1024839513846
    日期:——
    The reactions of disodium salts of N,N'-bis(2-mercapto-6-methylpyrimidin-4-yl)alkylenediamines with 1,3-bis(omega-bromoalkyl)-6-methyluracils afforded a series of macrocyclic compounds containing three pyrimidine fragments with different numbers of methylene groups in linking bridges.
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