(6-methoxy-quinolin-4-yl)-hydrazine | 49612-21-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: (6-methoxy-quinolin-4-yl)-hydrazine
• 英文别名: 4-Hydrazinyl-6-methoxyquinoline；(6-methoxyquinolin-4-yl)hydrazine
• CAS: 49612-21-7
• 化学式: C₁₀H₁₁N₃O
• mdl: MFCD12403193
• 分子量: 189.217
• InChiKey: JMSTXGKKPCBKCO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  60.2
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (6-methoxy-quinolin-4-yl)-hydrazine 在 盐酸 、 sodium cyanoborohydride 、 对甲苯磺酸 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 乙腈 为溶剂， 生成 (2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-[2-(6-methoxy-quinolin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-5-yl]-amine
  参考文献：
  名称：

  Tetrahydroindazole inhibitors of bacterial type II topoisomerases. Part 2: SAR development and potency against multidrug-resistant strains

  摘要：

  We have previously reported a novel class of tetrahydroindazoles that display potency against a variety of Gram-positive and Gram-negative bacteria, potentially via interaction with type II bacterial topoisomerases. Herein are reported SAR investigations of this new series. Several compounds possessing broad-spectrum potency were prepared. Further, these compounds exhibit activity against multidrug-resistant Gram-positive microorganisms equivalent to that against susceptible strains. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.03.004
• 作为产物：
  描述：

  4-氯-6-甲氧基喹啉 在 一水合肼 作用下， 生成 (6-methoxy-quinolin-4-yl)-hydrazine
  参考文献：
  名称：

  John, Journal fur praktische Chemie (Leipzig 1954), 1930, vol. <2> 128, p. 201,206

  摘要：

  DOI：

文献信息

• Bicyclic pyrazole compounds as antibacterial agents
  申请人：Allison D. Brett

  公开号：US20060223810A1

  公开（公告）日：2006-10-05

  Antibacterial compounds, compositions containing them, and methods of use for the inhibition of bacterial activity and the treatment, prevention or inhibition of bacterial infection.

  抗菌化合物、含有它们的组合物以及用于抑制细菌活性以及治疗、预防或抑制细菌感染的方法。
• Design, Synthesis, and Structure–Activity Relationship Studies of 4-Quinolinyl- and 9-Acrydinylhydrazones as Potent Antimalarial Agents
  作者：Caterina Fattorusso、Giuseppe Campiani、Gagan Kukreja、Marco Persico、Stefania Butini、Maria Pia Romano、Maria Altarelli、Sindu Ros、Margherita Brindisi、Luisa Savini、Ettore Novellino、Vito Nacci、Ernesto Fattorusso、Silvia Parapini、Nicoletta Basilico、Donatella Taramelli、Vanessa Yardley、Simon Croft、Marianna Borriello、Sandra Gemma

  DOI：10.1021/jm7012375

  日期：2008.3.13

  synthesis, and biological investigation of novel antimalarial agents with low potential to develop resistance and structurally based on a highly conjugated scaffold. Starting from a new hit, the designed modifications were performed hypothesizing a specific interaction with free heme and generation of radical intermediates. This approach provided antimalarials with improved potency against chloroquine-resistant

  疟疾是贫困地区的主要健康问题，在这些地区，人们迫切需要以负担得起的价格购买新的抗寄生虫药。我们在此报告了新型抗疟疾药物的设计，合成和生物学研究，这些药物具有发展抗药性的低潜力，并且在结构上基于高度偶联的支架。从新的命中开始，进行设计的修饰，假设与游离血红素发生特定的相互作用并产生自由基中间体。与已知药物相比，该方法为抗疟药提供了增强的抗氯喹抗疟原虫能力。确定了许多结构-活性关系（SAR）趋势，在合成的类似物中，吡咯烷基甲基亚芳基和咪唑衍生物5r，5t，发现8b和8b是新系列中最有效的抗疟药。研究了新化合物的作用机理，并评估了它们的体内活性。
• BICYCLIC PYRAZOLE COMPOUNDS AS ANTIBACTERIAL AGENTS
  申请人：Allison Brett D.

  公开号：US20100280240A1

  公开（公告）日：2010-11-04

  Antibacterial compounds, compositions containing them, and methods of use for the inhibition of bacterial activity and the treatment, prevention or inhibition of bacterial infection.

  抗菌化合物，含有它们的组合物，以及用于抑制细菌活性和治疗、预防或抑制细菌感染的使用方法。
• BICYCLIC PIRAZOLE COMPOUNDS AS ANTIBACTERIAL AGENTS
  申请人：Allison Brett D.

  公开号：US20100274004A1

  公开（公告）日：2010-10-28

  Antibacterial compounds, compositions containing them, and methods of use for the inhibition of bacterial activity and the treatment, prevention or inhibition of bacterial infection.

  抗菌化合物，含有它们的组合物以及使用方法，用于抑制细菌活动和治疗、预防或抑制细菌感染。
• Bartolucci; Cellai; Di Filippo, Il Farmaco, 1992, vol. 47, # 11, p. 1367 - 1383
  作者：Bartolucci、Cellai、Di Filippo、Segre、Brufani、Filocamo、Bianco、Guiso、Brizzi、Benedetto、Di Caro、Elia

  DOI：——

  日期：——