5-methylphenylene-1,3-diamine dihydrochloride | 26067-68-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 5-methylphenylene-1,3-diamine dihydrochloride
• 英文别名: 5-methyl-m-phenylenediamine; dihydrochloride；5-Methyl-m-phenylendiamin; Dihydrochlorid；3,5-Diaminotoluene hydrochloride；5-methylbenzene-1,3-diamine;hydrochloride
• CAS: 26067-68-5；26346-38-3
• 化学式: C₇H₁₀N₂*2ClH
• 分子量: 195.092
• InChiKey: WDJDWSHAZKRYFN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.58
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  52
• 氢给体数：
  3
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-{2-[bis(2-chloroethyl)-amino]ethoxy}-9-chloro acridine 、 5-methylphenylene-1,3-diamine dihydrochloride 在 N-甲基吗啉 作用下， 以 乙醇 为溶剂， 生成 3-N-[4-[2-[bis(2-chloroethyl)amino]ethoxy]acridin-9-yl]-5-methylbenzene-1,3-diamine
  参考文献：
  名称：

  Potent Antitumor 9-Anilinoacridines and Acridines Bearing an Alkylating N-Mustard Residue on the Acridine Chromophore:  Synthesis and Biological Activity

  摘要：

  A series of 9-anilinoacridine and acridine derivatives bearing an alkylating N-mustard residue at C4 of the acridine chromophore were synthesized. The N-mustard pharmacophore was linked to the C4 of the acridine ring with an O-ethyl ( O-C-2), O-propyl ( O-C-3), or O-butyl ( O-C-4) spacer. It revealed that all newly synthesized compounds were very potent cytotoxic agents against human leukemia and various solid tumors in vitro. These agents did not exhibit cross-resistance against vinblastine-resistant ( CCRF-CEM/VBL) or taxol-resistant ( CCRF-CEM/taxol) cells. It also showed that these agents were DNA cross-linking agents rather than topoisomerase II inhibitors. Of these agents, compounds 27a and 27c were shown to have potent antitumor activity in nude mice bearing the human breast carcinoma MX-1 xenograft. The therapeutic efficacies of these two agents are comparable to that of taxol.

  DOI：

  10.1021/jm060197r

文献信息

• 5-(9-ACRIDINYLAMINO)-TOLUIDINE COMPOUNDS
  申请人：——

  公开号：US20040198765A1

  公开（公告）日：2004-10-07

  This invention relates to 9-anilinoacridine compounds, and more particularly to their synthesis and their use in pharmaceutical compositions for treating diseases.

  这项发明涉及9-苯胺基吖啶化合物，更具体地涉及它们的合成以及它们在制备治疗疾病的药物组合物中的应用。
• US6821983B2
  申请人：——

  公开号：US6821983B2

  公开（公告）日：2004-11-23
• Potent Antitumor 9-Anilinoacridines and Acridines Bearing an Alkylating <i>N</i>-Mustard Residue on the Acridine Chromophore:  Synthesis and Biological Activity
  作者：Tsann-Long Su、Yi-Wen Lin、Ting-Chao Chou、Xiuguo Zhang、Valeriy A. Bacherikov、Ching-Huang Chen、Leroy F. Liu、Tsong-Jen Tsai

  DOI：10.1021/jm060197r

  日期：2006.6.1

  A series of 9-anilinoacridine and acridine derivatives bearing an alkylating N-mustard residue at C4 of the acridine chromophore were synthesized. The N-mustard pharmacophore was linked to the C4 of the acridine ring with an O-ethyl ( O-C-2), O-propyl ( O-C-3), or O-butyl ( O-C-4) spacer. It revealed that all newly synthesized compounds were very potent cytotoxic agents against human leukemia and various solid tumors in vitro. These agents did not exhibit cross-resistance against vinblastine-resistant ( CCRF-CEM/VBL) or taxol-resistant ( CCRF-CEM/taxol) cells. It also showed that these agents were DNA cross-linking agents rather than topoisomerase II inhibitors. Of these agents, compounds 27a and 27c were shown to have potent antitumor activity in nude mice bearing the human breast carcinoma MX-1 xenograft. The therapeutic efficacies of these two agents are comparable to that of taxol.