A. J. Kaye

The British Steel Corporation-integrated digital network

A. J. Kaye, 1988 .

Ring-substituted 11-oxo-11H-indeno[1,2-b]quinoline-6-carboxamides with similar patterns of cytotoxicity to the dual topo I/II inhibitor DACA.

A. J. Kaye, W. Denny, M. Thompson, 1999, Bioorganic & medicinal chemistry.

Synthesis and antitumor properties of N-[2-(dimethylamino)ethyl]carboxamide derivatives of fused tetracyclic quinolines and quinoxalines: a new class of putative topoisomerase inhibitors.

A. J. Kaye, W. Denny, B. Baguley, 1997, Journal of medicinal chemistry.

Synthesis and antitumor activity of some indeno[1,2-b]quinoline-based bis carboxamides.

A. J. Kaye, W. Denny, B. Baguley, 2000, Bioorganic & medicinal chemistry.

Positioning of the carboxamide side chain in 11-oxo-11H-indeno[1,2-b]quinolinecarboxamide anticancer agents: effects on cytotoxicity.

A. J. Kaye, W. Denny, B. Baguley, 2001, Bioorganic & medicinal chemistry.

Synthesis and cytotoxic activity of N-(2-diethylamino)ethylcarboxamide and other derivatives of 10H-quindoline.

A. J. Kaye, W. Denny, B. Baguley, 2002, Bioorganic & medicinal chemistry.

Synthesis of substituted indeno[1,2-b]quinoline-6-carboxamides, [1]benzothieno[3,2-b]quinoline-4-carboxamides and 10H-quindoline-4-carboxamides: evaluation of structure-activity relationships for cytotoxicity.

A. J. Kaye, W. Denny, B. Baguley, 2000, Bioorganic & medicinal chemistry.