5-(hydroxymethyl)-3-(4-methylacridin-9-ylamino)aniline | 740787-40-0

• 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: 5-(hydroxymethyl)-3-(4-methylacridin-9-ylamino)aniline
• 英文别名: [3-amino-5-(4-methylacridin-9-ylamino)phenyl]methanol；3-(4-methylacridin-9-yl)amino-5-hydroxymethylaniline；[3-Amino-5-[(4-methylacridin-9-yl)amino]phenyl]methanol
• CAS: 740787-40-0
• 化学式: C₂₁H₁₉N₃O
• 分子量: 329.401
• InChiKey: XHBYURUZBMRTPH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  25
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  71.2
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  p-isocyanophenyl mustard 、 5-(hydroxymethyl)-3-(4-methylacridin-9-ylamino)aniline 在 吡啶 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 以55.2%的产率得到1-{4-[Bis(2-chloroethyl)-amino]phenyl}-3-[3-hydroxymethyl-5-(4-methylacridin-9-ylamino)phenyl]urea
  参考文献：
  名称：

  稳定和有效的抗肿瘤药苯胺氮芥的合成及其生物学活性，其通过尿素键与9-苯胺基cr啶连接。

  摘要：

  为了提高N-芥末的化学稳定性和治疗效果，合成了一系列通过尿素接头与DNA亲和性9-苯胺基cr啶和​​and啶连接的苯基N-芥末，并进行了抗肿瘤研究。通过使4-双（2-氯乙基）氨基苯基异氰酸酯与各种9-苯胺基cr啶或9-氨基ac啶反应制备新的N-芥末衍生物。抗肿瘤研究表明，这些药物在体外显示出有效的细胞毒性，而对紫杉醇或长春碱没有交叉耐药性，并且在裸鼠中对人肿瘤异种移植物显示出有效的抗肿瘤治疗功效。还表明24d通过彗星试验能够诱导明显的剂量依赖性DNA交联水平，并且在大鼠血浆中具有长的半衰期。

  DOI：

  10.1016/j.bmc.2008.04.024

文献信息

• Aniline or phenol mustards linked to DNA-affinic molecules or water-soluble aromatic rings and their use as cancer therapeutic agents
  申请人：Su Tsann-Long

  公开号：US20080171765A1

  公开（公告）日：2008-07-17

  New aniline or phenol N-mustards linked to DNA-affinity carriers (such as 9-anilinoacridines, acridines and quinolines), aminobenzamides or aminophenol ethers by a urea, carbamic acid, carbanic acid ester, hydrazineurea, hydrazinecarbamic acid ester, phenoxyurea, phenoxycarbamic acid ester linkage with improved chemical stability and anti-tumor therapeutic efficacy are provided.

  提供了与DNA亲和载体（如9-苯胺基吖啶、吖啶和喹啉）、氨基苯甲酰胺或氨基酚醚通过脲、碳酸酯、碳酸酯、叠氮脲、叠氮碳酸酯、苯氧基脲、苯氧基碳酸酯链接的新苯胺或酚N-芥子素，具有改善的化学稳定性和抗肿瘤治疗效果。
• Novel DNA-directed alkylating agents: Design, synthesis and potent antitumor effect of phenyl N-mustard-9-anilinoacridine conjugates via a carbamate or carbonate linker
  作者：Naval Kapuriya、Kalpana Kapuriya、Huajin Dong、Xiuguo Zhang、Ting-Chao Chou、Yu-Ting Chen、Te-Chang Lee、Wen-Chuan Lee、Tung-Hu Tsai、Yogesh Naliapara、Tsann-Long Su

  DOI：10.1016/j.bmc.2008.12.022

  日期：2009.2

  A series of phenyl N-mustard-9-anilinoacridine conjugates via a carbamate or carbonate linker was synthesized for antitumor evaluation. The carbamate or carbonate linker is able to lower the reactivity of the phenyl N-mustard pharmacophore and thus, these conjugates are rather chemically stable. The in vitro studies revealed that these derivatives possessed significant cytotoxicity with IC50 in sub-micromolar range in inhibiting human lymphoblastic leukemia (CCRF-CEM), breast carcinoma (MX-1), colon carcinoma (HCT-116) and human non-small cell lung cancer (H1299) cell growth in vitro. Compounds 10a, 10b, 10e, 10i, and 15a were selected for evaluating their antitumor activity in nude mice bearing MX1 and HCT-116 xenografts. Remarkably, total tumor remission was achieved by these agents with only one cycle of treatment. Interestingly, no tumor relapse was found in mice treated with 10a over 129 days. This agent is capable of inducing DNA interstrand cross-linking in human non-small lung cancer H1299 cells in a dose dependent manner by modified comet assay and has a long half-life in rat plasma. (c) 2008 Elsevier Ltd. All rights reserved.
• US5939428A
  申请人：——

  公开号：US5939428A

  公开（公告）日：1999-08-17
• Synthesis and biological activity of stable and potent antitumor agents, aniline nitrogen mustards linked to 9-anilinoacridines via a urea linkage
  作者：Naval Kapuriya、Kalpana Kapuriya、Xiuguo Zhang、Ting-Chao Chou、Rajesh Kakadiya、Yu-Tse Wu、Tung-Hu Tsai、Yu-Ting Chen、Te-Chang Lee、Anamik Shah、Yogesh Naliapara、Tsann-Long Su

  DOI：10.1016/j.bmc.2008.04.024

  日期：2008.5

  synthesized and evaluated for antitumor studies. The new N-mustard derivatives were prepared by the reaction of 4-bis(2-chloroethyl)aminophenyl isocyanate with a variety of 9-anilinoacridines or 9-aminoacridine. The antitumor studies revealed that these agents exhibited potent cytotoxicity in vitro without cross-resistance to taxol or vinblastine and showed potent antitumor therapeutic efficacy in nude

  为了提高N-芥末的化学稳定性和治疗效果，合成了一系列通过尿素接头与DNA亲和性9-苯胺基cr啶和​​and啶连接的苯基N-芥末，并进行了抗肿瘤研究。通过使4-双（2-氯乙基）氨基苯基异氰酸酯与各种9-苯胺基cr啶或9-氨基ac啶反应制备新的N-芥末衍生物。抗肿瘤研究表明，这些药物在体外显示出有效的细胞毒性，而对紫杉醇或长春碱没有交叉耐药性，并且在裸鼠中对人肿瘤异种移植物显示出有效的抗肿瘤治疗功效。还表明24d通过彗星试验能够诱导明显的剂量依赖性DNA交联水平，并且在大鼠血浆中具有长的半衰期。