W. Schulz

Structure-activity studies of benzimidazole-based DNA-cleaving agents. Comparison of benzimidazole, pyrrolobenzimidazole, and tetrahydropyridobenzimidazole analogues.

I. Islam, E. B. Skibo, M. J. Heileman, 1994, Journal of medicinal chemistry.

Synthesis and biological evaluation of a series of liver-selective phosphonic acid thyroid hormone receptor agonists and their prodrugs.

M. Erion, Wenyu Li, E. Cable, 2008, Journal of medicinal chemistry.

The Organic Chemistry of the Pyrrolo[1,2-a]benzimidazole Antitumor Agents. An Example of Rational Drug Design

I. Islam, E. B. Skibo, L. Bess, 1996 .

Pyrrolo[1,2-a]benzimidazole-based quinones and iminoquinones. The role of the 3-substituent on cytotoxicity.

I. Islam, E. B. Skibo, W. Schulz, 1995, Journal of medicinal chemistry.

Evidence for DNA phosphate backbone alkylation and cleavage by pyrrolo[1,2-a]benzimidazoles: small molecules capable of causing base-pair-specific phosphodiester bond hydrolysis.

R. Nieman, E. B. Skibo, W. Schulz, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Discovery of phosphonic diamide prodrugs and their use for the oral delivery of a series of fructose 1,6-bisphosphatase inhibitors.

M. Erion, Q. Dang, S. Kasibhatla, 2008, Journal of medicinal chemistry.

Pyrrolo(1,2-a)benzimidazole-Based Aziridinyl Quinones, e.g. (I). A New Class of DNA Cleaving Agent Exhibiting G and A Base Specificity.

E. B. Skibo, W. Schulz, 1995 .

Pyrrolo[1,2-a]benzimidazole-based aziridinyl quinones. A new class of DNA cleaving agent exhibiting G and A base specificity.

E. B. Skibo, W. Schulz, 1993, Journal of medicinal chemistry.