Synthesis and Comparative Toxicology of a Series of Polyhedral Borane Anion-Substituted Tetraphenyl Porphyrins

Myoung-Seo Koo, Tomoko Ozawa, Raquel A. Santos, Kathleen R. Lamborn, Andrew W. Bollen,§ Dennis F. Deen, and Stephen B. Kahl*
Departments of Pharmaceutical Chemistry, Neurological Surgery, Pathology, and Radiation Oncology, University of California, San Francisco, San Francisco, California 94143
J. Med. Chem., 2007, 50 (4), pp 820–827
DOI: 10.1021/jm060895b
Publication Date (Web): January 25, 2007
Copyright © 2007 American Chemical Society

 Department of Pharmaceutical Chemistry.

,

 Department of Neurological Surgery.

,
§

 Department of Pathology.

,

 Department of Radiation Oncology.

,
*

 To whom correspondence should be addressed:  Tel.:  415-476-4684. Fax:  415-476-0688. E-mail:  sbkahl@picasso.ucsf.edu.

Abstract

Abstract Image

Three structurally similar tetraphenylporphyrins bearing polyhedral borane anions have been synthesized and their toxicological profiles obtained in rats. These conjugates were found to have quite different acute toxicities as manifested at the maximum tolerated dose (MTD). When given at the MTD and observed over 28 days, the most acutely toxic porphyrin was found to be devoid of toxicity, as measured by blood chemistry panels. The remaining two less acutely toxic compounds both elicited significant changes, characterized by moderate to severe thrombocytopenia, failure to gain weight normally and changes in liver enzymes indicative of mild hepatotoxicity. All toxic effects were transient, with platelets rebounding to above normal levels at day 28. We conclude that thrombocytopenia is the dose limiting toxicity for boronated porphyrins in mammals and suggest that these effects may be due to the porphyrin, not the borane or carborane.

Tools

History

  • Published In Issue February 22, 2007
  • Received July 27, 2006

Recommend & Share

Related Content

Other ACS content by these authors: