Heterocyclic Quinones. 4. A new highly cytotoxic drug: 6,7-bis(1-aziridinyl)-5,8-quinazolinedione.

Abstract

With the aim of obtaining new antitumoral agents, a series of 5,8-quinazolinediones was prepared. 5-Amino-6-methoxyquinazoline was oxidized by Fremy's salt to give 6-methoxy-5,8-quinazolinedione. Nucleophilic substitution reaction at C6, electrophilic substitution at C7, and synthesis of 7-amino-6-methoxy-5,8-quinazolinedione, the parent compound of streptonigrin, were studied. These compounds were tested for cytotoxic properties on L1210 leukemia cells in vitro. One of them, 6,7-bis(1-aziridinyl)-5,8-quinazolinedione, which exhibits a high cytotoxic activity (ID50 = 0.08 microM), was further screened in standard antitumor systems, including L1210 leukemia, P388 lymphocytic leukemia, sarcoma 180, and B16 melanocarcinoma. This drug gives a significant antitumoral effect on P388 leukemia but is inactive on other experimental models. Moreover, this compound was found to be highly mutagenic for Salmonella typhimurium TA98 and TA100 strains (Ames test), suggesting that DNA damage could be responsible for its cytotoxicity.

• Authors: J Renault, S Giorgi-Renault, M Baron, P Mailliet, C Paoletti, S Cros, E Voisin
• Journal: Journal of medicinal chemistry (J Med Chem) Vol. 26 Issue 12 Pg. 1715-9 (Dec 1983) ISSN: 0022-2623 [Print] United States
• PMID: 6644740 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• Quinazolines
• 6,7-bis(1-aziridinyl)-5,8-quinazolinedione

Topics

• Animals
• Antineoplastic Agents (chemical synthesis, therapeutic use)
• Leukemia L1210 (drug therapy)
• Leukemia P388 (drug therapy)
• Mice
• Mutagenicity Tests
• Quinazolines (chemical synthesis, therapeutic use)
• Sarcoma 180 (drug therapy)