7-(Substituted-phenyl)amino-5,8-isoquinolinediones: Synthesis and cytotoxic activities on cancer cell lines

Chung Kyu Ryu, In Kyung Lee, Sung Hee Jung, Hye Young Kang, Chong Ock Lee

Research output: Contribution to journal › Article › peer-review

8 Citations (Scopus)

Abstract

6-Chloro-7-(substituted-phenyl)amino-5,8-isoquinolinediones (3a-3u) and 7-(substituted-phenyl)amino-5,8-isoquinolinediones (4a-4d) were synthesized by nucleophilic substitution of 6,7-dichloro-5,8-isoquinolinedione (8) and 5,8-isoquinolinedione (9) with appropriate arylamines. The quinones 3a-3u and 4a-4d were evaluated for in vitro cytotoxic activities against five solid tumor cell lines such as A549, SK-OV-3, SK-MEL-2, XF498 and HCT-15. Among them, 3c, 3d, 3f and 3h exhibited potent activities against the cell lines HCT-15 and SK-MEL-2.

Original languageEnglish
Pages (from-to)40-49
Number of pages10
JournalMedicinal Chemistry Research
Volume10
Issue number1
Publication statusPublished - 2000

All Science Journal Classification (ASJC) codes

  • Pharmacology, Toxicology and Pharmaceutics(all)
  • Organic Chemistry

UN SDGs

This output contributes to the following Sustainable Development Goal(s)

  • SDG 3 - Good Health and Well-being

Other files and links

Fingerprint Dive into the research topics of '7-(Substituted-phenyl)amino-5,8-isoquinolinediones: Synthesis and cytotoxic activities on cancer cell lines'. Together they form a unique fingerprint.

Cite this