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Electronic Structure of Tetrahydropteridine Derivatives

Electronic Structure of Tetrahydropteridine Derivatives Summary Recently; the 4-amino analogue of tetrahydrobiopterin was found to be a strong inhibitor of nitric oxide synthase while being bound to the enzyme in a manner similar to the natural cofactor tetrahydrobiopterin. We were interested in the electronic properties of these and similar compounds and studied therefore the following model tetrahydropteridine structures: tetrahydrolumazine, tetrahydropterin, 4-amino-analogue of tetrahydropterin and N5-methyl-tetrahydropterin. Ab initio quantum chemical computations used the Hartree- Fode method with basis set 6-31G** after geometry optimization with basis set 3-21G*. Results reveal dramatic differences in distribution of electronic charge and all the molecular properties derived thereof~ between a) the lumazine system, b) the normal pterin system, and c) the 4-amino analogue. In contrast, differences of electronic properties between tetrahydropterin and its N5-methyl-derivative are negligible. Our results are compatible with recent speculations that the striking differences between the effects of the tetrahydropterin struculrc and its 4-amino analogue on cnznllatic activity may be due to electronic interaction between the pyrimidine moiety of the ptcrin ring systcm and the heme group. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Pteridines de Gruyter

Electronic Structure of Tetrahydropteridine Derivatives

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Publisher
de Gruyter
Copyright
Copyright © 1999 by the
ISSN
0933-4807
eISSN
2195-4720
DOI
10.1515/pteridines.1999.10.3.91
Publisher site
See Article on Publisher Site

Abstract

Summary Recently; the 4-amino analogue of tetrahydrobiopterin was found to be a strong inhibitor of nitric oxide synthase while being bound to the enzyme in a manner similar to the natural cofactor tetrahydrobiopterin. We were interested in the electronic properties of these and similar compounds and studied therefore the following model tetrahydropteridine structures: tetrahydrolumazine, tetrahydropterin, 4-amino-analogue of tetrahydropterin and N5-methyl-tetrahydropterin. Ab initio quantum chemical computations used the Hartree- Fode method with basis set 6-31G** after geometry optimization with basis set 3-21G*. Results reveal dramatic differences in distribution of electronic charge and all the molecular properties derived thereof~ between a) the lumazine system, b) the normal pterin system, and c) the 4-amino analogue. In contrast, differences of electronic properties between tetrahydropterin and its N5-methyl-derivative are negligible. Our results are compatible with recent speculations that the striking differences between the effects of the tetrahydropterin struculrc and its 4-amino analogue on cnznllatic activity may be due to electronic interaction between the pyrimidine moiety of the ptcrin ring systcm and the heme group.

Journal

Pteridines – de Gruyter

Published: Aug 1, 1999

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