Synthesis and antitumor activity of 5-(9-acridinylamino)anisidine derivatives

Valeriy A. Bacherikov, Jang Yang Chang, Yi Wen Lin, Ching Huang Chen, Wen Yu Pan, Huajin Dong, Rong Zau Lee, Ting Chao Chou, Tsann Long Su

Research output: Contribution to journalArticlepeer-review

32 Citations (Scopus)


A series of 5-(9-acridinylamino)anisidines were synthesized by condensing methoxy-substituted 1,3-phenylenediamines (10 and 11) with 9-chloroacridine derivatives to form 5-(9-acridinylamino)-m-anisidines (AMAs, 14a-e) and 5-(9-acridinylamino)-o-anisidines (AOAs, 15a-e). 5-(9-Acridinylamino)-p- anisidines (APAs, 17a-e) were synthesized by reacting 2-methoxy-5-nitroaniline (12) with 9-anilinoacridines, followed by reduction. The cytotoxic inhibition of growth of various human tumor cells in culture, inhibitory effects against topoisomerase II, and DNA interaction of these agents were studied. The structure-activity relationship studies revealed the following degree of potency: AOAs > AMAs > APAs. They also revealed that the newly synthesized derivatives bearing CONH2NH2NMe2 and Me substituents at C4 and C5 positions of the acridine chromophore (i.e., AMA 14e, AOA 15e, and APA 17e) exhibited significant cytotoxicity against human tumor cell growth in vitro. AOA (15e) was the most potent among these derivatives, which resulted in 60% suppression of tumor volume at a dose of 20 mg/kg (Q2D × 9), intravenous injection on day 26 in nude mice bearing human breast carcinoma MX-1 xenografts.

Original languageEnglish
Pages (from-to)6513-6520
Number of pages8
JournalBioorganic and Medicinal Chemistry
Issue number23
Publication statusPublished - Dec 2005
Externally publishedYes


  • Acridines
  • Antitumor compounds
  • Chemotherapy
  • Substituent effects
  • Synthesis

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Pharmaceutical Science
  • Drug Discovery
  • Clinical Biochemistry
  • Organic Chemistry


Dive into the research topics of 'Synthesis and antitumor activity of 5-(9-acridinylamino)anisidine derivatives'. Together they form a unique fingerprint.

Cite this