Discovering some novel 7-chloroquinolines carrying a biologically active benzenesulfonamide moiety as a new class of anticancer agents.

Abstract

Based on the reported anticancer activity of quinolines, a new series of 7-chloroquinoline derivatives bearing the biologically active benzenesulfonamide moiety 2-17 and 19-25 were synthesized starting with 4,7-dichloroquinolne 1. Compound 17 was the most active compound with IC(50) value 64.41, 75.05 and 30.71 µM compared with Doxorubicin as reference drug with IC(50) values 82.53, 88.32 and 73.72 µM on breast cancer cells, skin cancer cells and neuroblastoma, respectively. All the synthesized compounds were evaluated for their in vitro anticancer activity on breast cancer cells, skin cancer cells and neuroblastoma cells. Most of the synthesized compounds showed moderate activity. In order to suggest the mechanism of action for their cytotoxic activity, molecular docking for all synthesized compounds was done on the active site of phosphoinositide kinase (PI3K) and good results were obtained.

• Authors: Mohammed Salem Al-Dosari, Mostafa Mohamed Ghorab, Mansour Sulaiman Al-Said, Yassin Mohammed Nissan
• Journal: Chemical & pharmaceutical bulletin (Chem Pharm Bull (Tokyo)) Vol. 61 Issue 1 Pg. 50-8 ( 2013) ISSN: 1347-5223 [Electronic] Japan
• PMID: 23302586 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• Quinolines
• Sulfonamides
• benzenesulfonamide
• 2-chloroquinoline

Topics

• Antineoplastic Agents (chemistry, pharmacology)
• Cell Line, Tumor
• Humans
• Models, Molecular
• Neoplasms (drug therapy)
• Quinolines (chemistry, pharmacology)
• Sulfonamides (chemistry, pharmacology)