Novel derivatives of 6-mercaptopurine: synthesis, characterization and antiproliferative activities of S-allylthio-mercaptopurines.

Abstract

Biologically active S-allylthio derivatives of 6-mercaptopurine (6-MP) and 6-mercaptopurine riboside (6-MPR) were synthesized. The products, S-allylthio-6-mercaptopurine (SA-6MP) and S-allylthio-6-mercaptopurine riboside (SA-6MPR) were characterized. The antiproliferative activity of the new prodrugs was tested on human leukemia and monolayer cell lines, and compared to that of their parent reactants. The new prodrugs acted by a concentration-dependent mechanism. They inhibited cell proliferation and induced-apoptosis more efficiently than the parent molecules. Leukemia cell lines were more sensitive to the new prodrugs than monolayer cell lines. Higher hydrophobicity of the derivatives improves their penetration into cells, where upon reaction with glutathione, S-allylthioglutathione (GSSA) is formed, and 6-MP or 6-MPR is released for further processing.

• Authors: T Miron, F Arditti, L Konstantinovski, A Rabinkov, D Mirelman, A Berrebi, M Wilchek
• Journal: European journal of medicinal chemistry (Eur J Med Chem) Vol. 44 Issue 2 Pg. 541-50 (Feb 2009) ISSN: 1768-3254 [Electronic] France
• PMID: 18467007 (Publication Type: Journal Article)

Chemical References

• Antineoplastic Agents
• Prodrugs
• Mercaptopurine

Topics

• Antineoplastic Agents (chemical synthesis, pharmacology)
• Apoptosis (drug effects)
• Cell Line, Tumor
• Cell Proliferation (drug effects)
• Drug Screening Assays, Antitumor
• Humans
• Mercaptopurine (chemical synthesis, pharmacology)
• Prodrugs (chemical synthesis)
• Structure-Activity Relationship