Preparation and Biological Evaluation of 10B-Enriched 3-[5-{2-(2,3-Dihydroxyprop-1-yl)-o-carboran-1-yl}pentan-1-yl]thymidine (N5-2OH), a New Boron Delivery Agent for Boron Neutron Capture Therapy of Brain Tumors

Youngjoo Byun,* B. T. S. Thirumamagal, Weilian Yang,§ Staffan Eriksson, Rolf F. Barth,§ and Werner Tjarks
Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, and Department of Pathology, The Ohio State University, Columbus, OH, and Department of Molecular Biosciences, Division of Veterinary Medical Biochemistry, Swedish University of Agricultural Sciences, The Biomedical Center, Uppsala, Sweden
J. Med. Chem., 2006, 49 (18), pp 5513–5523
DOI: 10.1021/jm060413w
Publication Date (Web): August 11, 2006
Copyright © 2006 American Chemical Society
*

 To whom correspondence should be addressed. Phone:  +1-614-688-3149. Fax:  +1-614-292-2435. E-mail:  byun.12@osu.edu.

,

 Division of Medicinal Chemistry and Pharmacognosy, The Ohio State University.

,
§

 Department of Pathology, The Ohio State University.

,

 Swedish University of Agricultural Sciences.

Abstract

Abstract Image

3-[5-{2-(2,3-Dihydroxyprop-1-yl)-o-carboran-1-yl}pentan-1-yl]thymidine (compound 1, N5-2OH) belongs to a novel class of boron delivery agents for neutron capture therapy, which was designated 3-carboranylthymidine analogue (3CTAs). Two shorter and more convenient synthetic routes were developed for the synthesis of 1 in the 10B-enriched form, which is necessary for its preclinical and clinical evaluation in neutron irradiation studies. For more insight on structure−activity relationships, various stereochemical and geometrical isomers of 1 were synthesized and their specificities as substrate for human thymidine kinase 1 (hTK1) were evaluated. A computational model for the binding of various isomers of 1 to the active site of hTK1 was developed. Preliminary studies carried out in F98 glioma bearing rats that had received a 10B-enriched form of 1 followed by neutron irradiation demonstrated a significant prolongation in survival times compared to control animals, suggesting that further studies are warranted to evaluate the therapeutic potential of 1.

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History

  • Published In Issue September 07, 2006
  • Received April 7, 2006

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