2-(3-trifluoromethylphenyl)octahydropyrrolo<3,4-c>pyrrole | 86732-26-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: 2-(3-trifluoromethylphenyl)octahydropyrrolo<3,4-c>pyrrole
• 英文别名: 5-[3-(trifluoromethyl)phenyl]-2,3,3a,4,6,6a-hexahydro-1H-pyrrolo[3,4-c]pyrrole
• CAS: 86732-26-5
• 化学式: C₁₃H₁₅F₃N₂
• 分子量: 256.271
• InChiKey: RGSDEZYYVWBVSL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  15.3
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-(3-trifluoromethylphenyl)octahydropyrrolo<3,4-c>pyrrole 以 二氯甲烷 为溶剂， 反应 1.25h， 生成 N-(4-methylpyridin-2-yl)-5-(3-(trifluoromethyl)phenyl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carbothioamide trifluoroacetate
  参考文献：
  名称：

  4-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)-N-(4-methoxypyridin-2-yl)piperazine-1-carbothioamide (ML267), a Potent Inhibitor of Bacterial Phosphopantetheinyl Transferase That Attenuates Secondary Metabolism and Thwarts Bacterial Growth

  摘要：

  4'-Phosphopantetheinyl transferases (PPTases) catalyze a post-translational modification essential to bacterial cell viability and virulence. We present the discovery and medicinal chemistry optimization of 2-pyridinyl-N-(4-aryl)-piperazine-1-carbothioamides, which exhibit submicromolar inhibition of bacterial Sfp-PPTase with no activity toward the human orthologue. Moreover, compounds within this class possess antibacterial activity in the absence of a rapid cytotoxic response in human cells. An advanced analogue of this series, ML267 (55), was found to attenuate production of an Sfp-PPTase-dependent metabolite when applied to Bacillus subtilis at sublethal doses. Additional testing revealed antibacterial activity against methicillin-resistant Staphylococcus aureus, and chemical genetic studies implicated efflux as a mechanism for resistance in Escherichia coli. Additionally, we highlight the in vitro absorption, distribution, metabolism; and excretion and in vivo pharmacokinetic profiles of compound 55 to further demonstrate the potential utility of this small-molecule inhibitor.

  DOI：

  10.1021/jm401752p
• 作为产物：
  描述：

  1-benzyl-1H-pyrrole-3,4-dicarboxylic anhydride 在 palladium on activated charcoal lithium aluminium tetrahydride 、 氯化亚砜 、 氢气 作用下， 以 四氢呋喃 、 乙醚 、 溶剂黄146 为溶剂， 55.0~180.0 ℃ 、344.73 kPa 条件下， 反应 19.5h， 生成 2-(3-trifluoromethylphenyl)octahydropyrrolo<3,4-c>pyrrole
  参考文献：
  名称：

  Ohnmacht, Cyrus J.; Draper, Clyde W.; Dedinas, Robert F., Journal of Heterocyclic Chemistry, 1983, vol. 20, p. 321 - 329

  摘要：

  DOI：

文献信息

• 4-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)-<i>N</i>-(4-methoxypyridin-2-yl)piperazine-1-carbothioamide (ML267), a Potent Inhibitor of Bacterial Phosphopantetheinyl Transferase That Attenuates Secondary Metabolism and Thwarts Bacterial Growth
  作者：Timothy L. Foley、Ganesha Rai、Adam Yasgar、Thomas Daniel、Heather L. Baker、Matias Attene-Ramos、Nicolas M. Kosa、William Leister、Michael D. Burkart、Ajit Jadhav、Anton Simeonov、David J. Maloney

  DOI：10.1021/jm401752p

  日期：2014.2.13

  4'-Phosphopantetheinyl transferases (PPTases) catalyze a post-translational modification essential to bacterial cell viability and virulence. We present the discovery and medicinal chemistry optimization of 2-pyridinyl-N-(4-aryl)-piperazine-1-carbothioamides, which exhibit submicromolar inhibition of bacterial Sfp-PPTase with no activity toward the human orthologue. Moreover, compounds within this class possess antibacterial activity in the absence of a rapid cytotoxic response in human cells. An advanced analogue of this series, ML267 (55), was found to attenuate production of an Sfp-PPTase-dependent metabolite when applied to Bacillus subtilis at sublethal doses. Additional testing revealed antibacterial activity against methicillin-resistant Staphylococcus aureus, and chemical genetic studies implicated efflux as a mechanism for resistance in Escherichia coli. Additionally, we highlight the in vitro absorption, distribution, metabolism; and excretion and in vivo pharmacokinetic profiles of compound 55 to further demonstrate the potential utility of this small-molecule inhibitor.
• Ohnmacht, Cyrus J.; Draper, Clyde W.; Dedinas, Robert F., Journal of Heterocyclic Chemistry, 1983, vol. 20, p. 321 - 329
  作者：Ohnmacht, Cyrus J.、Draper, Clyde W.、Dedinas, Robert F.、Loftus, Philip、Wong, J. J.

  DOI：——

  日期：——