1-Amino-4-[2-(dimethylamino)ethylamino]anthracene-9,10-dione | 102650-26-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 蒽
• 英文名称: 1-Amino-4-[2-(dimethylamino)ethylamino]anthracene-9,10-dione
• CAS: 102650-26-0
• 化学式: C₁₈H₁₉N₃O₂
• 分子量: 309.368
• InChiKey: ROQCOWGVQIQPFM-UHFFFAOYSA-N

物化性质

• 熔点：
  135-136 °C(Solv: ligroine (8032-32-4))
• 沸点：
  554.3±50.0 °C(Predicted)
• 密度：
  1.302±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  75.4
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  烟酰氯 、 1-Amino-4-[2-(dimethylamino)ethylamino]anthracene-9,10-dione 以 甲苯 为溶剂， 反应 24.0h， 以45%的产率得到N-[4-[2-(dimethylamino)ethylamino]-9,10-dioxoanthracen-1-yl]pyridine-3-carboxamide
  参考文献：
  名称：

  Novel anthraquinone derivatives with redox-active functional groups capable of producing free radicals by metabolism: are free radicals essential for cytotoxicity?

  摘要：

  The mode of action of antitumour anthraquinone derivatives (i.e. mitoxantrone) is not clearly established yet. It includes, among others, intercalation and binding to DNA, bioreduction and aerobic redox cycling. A series of anthraquinone derivatives, with potentially bioreducible groups sited in the side chain, have been synthesized and biologically evaluated. Their redox and cytotoxic activities were screened. Derivatives which bear a 2-(dimethylamino)ethylamino substituent, known to confer high DNA affinity, demonstrated cytotoxicity but not redox activity (beside the anthraquinone reduction). Conversely, derivatives which showed redox activity were not cytotoxic toward the P388 cell line. The results suggest that bioreduction is not the main mode of action in the cytotoxicity of anthraquinones. (C) 1999 Editions scientifiques et medicales Elsevier SAS.

  DOI：

  10.1016/s0223-5234(00)80029-x
• 作为产物：
  描述：

  1,4-Dinitroanthracene-9,10-dione 在 乙二胺 作用下， 反应 24.0h， 生成 1-Amino-4-[2-(dimethylamino)ethylamino]anthracene-9,10-dione
  参考文献：
  名称：

  Synthesis of 1,4-dinitroanthracene-9,10-dione. Stepwise substitution of the nitro groups by diamines leading to 1-[(aminoalkyl)amino]-4-nitroanthracene-9,10-diones and unsymmetrical 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones

  摘要：

  DOI：

  10.1021/jo00308a030

文献信息

• A Facile Method for Preparing Substituted 1-Aminoanthraquinones
  作者：Henry C. Wormser、Manik S. Sardessai、Hanley N. Abramson

  DOI：10.1080/00397919308011182

  日期：1993.12

  Abstract An efficient and simple preparation of α - substituted aminoanthraquinones using 2,2-dialkoxyethylamines is described.

  摘要 描述了使用 2,2-二烷氧基乙胺有效且简单地制备 α - 取代的氨基蒽醌。
• Synthesis and antitumor activities of unsymmetrically substituted 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones and related systems
  作者：A. Paul Krapcho、John J. Landi、Kenneth J. Shaw、Donald G. Phinney、Miles P. Hacker、John J. McCormack

  DOI：10.1021/jm00158a008

  日期：1986.8

  A number of unsymmetrically substituted 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones have been synthesized and evaluated for their antitumor activity against L1210 in vitro and in vivo. The high activity of several compounds observed in vitro was not paralleled by comparable activity in vivo. The activities of the substituted 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones as inhibitors of cell

  已合成了许多不对称取代的1,4-双[（氨基烷基）氨基]蒽-9,10-二酮，并在体外和体内评估了它们对L1210的抗肿瘤活性。体外观察到的几种化合物的高活性与体内可比的活性无法比拟。取代的1,4-双[（氨基烷基）氨基]蒽-9,10-二酮作为细胞生长抑制剂的活性通常比相关的1-[（氨基烷基）氨基] -4-甲氧基蒽-的活性高得多。 9,10-二酮，这与两种化合物与小牛胸腺DNA相互作用的相对能力有关。
• KRAPCHO, A. PAUL;AVERY, KENNETH L. (JR), J. ORG. CHEM., 55,(1990) N1, C. 5662-5664
  作者：KRAPCHO, A. PAUL、AVERY, KENNETH L. (JR)

  DOI：——

  日期：——
• KRAPCHO A. P.; LANDI J. J., JR.; SHAW K. J.; PHINNEY D. G.; HACKER M. P.;+, J. MED. CHEM., 29,(1986) N 8, 1370-1373
  作者：KRAPCHO A. P.、 LANDI J. J., JR.、 SHAW K. J.、 PHINNEY D. G.、 HACKER M. P.、+

  DOI：——

  日期：——
• Novel anthraquinone derivatives with redox-active functional groups capable of producing free radicals by metabolism: are free radicals essential for cytotoxicity?
  作者：Dinorah Barasch、Omer Zipori、Israel Ringel、Isaac Ginsburg、Amram Samuni、Jehoshua Katzhendler

  DOI：10.1016/s0223-5234(00)80029-x

  日期：1999.7

  The mode of action of antitumour anthraquinone derivatives (i.e. mitoxantrone) is not clearly established yet. It includes, among others, intercalation and binding to DNA, bioreduction and aerobic redox cycling. A series of anthraquinone derivatives, with potentially bioreducible groups sited in the side chain, have been synthesized and biologically evaluated. Their redox and cytotoxic activities were screened. Derivatives which bear a 2-(dimethylamino)ethylamino substituent, known to confer high DNA affinity, demonstrated cytotoxicity but not redox activity (beside the anthraquinone reduction). Conversely, derivatives which showed redox activity were not cytotoxic toward the P388 cell line. The results suggest that bioreduction is not the main mode of action in the cytotoxicity of anthraquinones. (C) 1999 Editions scientifiques et medicales Elsevier SAS.