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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 102 (1999), S. 147-160 
    ISSN: 1432-2234
    Keywords: Key words: Flavin ; Deprenyl ; Irreversible inhibitor ; Acyclic adduct ; Cyclic adduct ; Hydrogen migration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract. Possible inhibition mechanisms of flavin (isoalloxazine) with (−)-deprenyl as an acetylenic irreversible inhibitor have been investigated in detail by ab initio methods with the 6-31G* basis set through the simplified model compounds 3-formyl-2-imino-1-hydropyrazine and propargylamine. The resulting compounds have been verified by calculations with the 3-21G basis set using flavin itself and the model of (−)-deprenyl for confirmation of the reactions through the simplified models. Two cyclic O4,N5- and C4a,N5-covalent adducts have been found. The latter was the most stable and was considered to be the final irreversible product. The intermediates in the reaction, the acyclic C4a- or N5-allenic compounds and their hydrogen-transferred cyanine-type compounds, are in agreement with the results of experimental photochemical reactions. In most of the reaction processes, hydrogen migration played an important role.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 103 (1999), S. 109-116 
    ISSN: 1432-2234
    Keywords: Key words: Flavin ring ; Isoalloxazine ; Electron transfer ; Twist motion and butterfly motion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract. The dynamic aspects along the normal vibrational motions of the lowest frequencies in the oxidized, radical, and reduced states of flavin (isoalloxazine) have been studied. In comparison with the twist motions in the oxidized state, the butterfly motions in the radical and reduced states turned out to bring more significant variations to the frontier molecular orbital energies and to the charge distributions on the atoms of the pyrazine ring in isoalloxazine. It can be considered that the electron transfers from and to the isoalloxazine ring can be adjusted or controlled by these variations. In the reduced states the electron release from the molecule, and in the radical states the electron release from or acceptance by the molecule, could be impelled by the butterfly motions, while in the oxidized state the electron acceptance by the molecule could be accelerated slightly by the twist motion.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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