Synthesis and Dihydropteridine Reductase [EC 1.6.99.10] (Human) Activity of Reduced 2,7-Dimethylpteridin-4(3H)-one, 2-Methyl-2-desaminoneopterin [6-(1' S,2' R-1' ,2' ,3' -trihydroxypropyl)-2-methylpteridin-4(3H)one] and 2-Methyl-2-desaminobiopterin [6-(1' R,2' S-1',2'-dihydroxypropyl)- 2-methylpteridin-4(3 H)-one]
Open Access
- 1 May 1989
- journal article
- Published by Walter de Gruyter GmbH in Pteridines
- Vol. 1 (2) , 73-82
- https://doi.org/10.1515/pteridines.1989.1.2.73
Abstract
Summary The syntheses of the title compounds have been achieved starting from 4,5-diamino-2-methylpyrimidin-6( 1 H)one. Sufficient amounts of the quinonoid 7,8-dihydropteridin-4(6H)-ones (12-14) were formed upon oxidation of the corresponding 5,6,7 ,8-tetrahydro derivatives (15 -17) to show that they are substrates of dihydroptcridine reductase (human). The apparent Km and Kcal values of (12-14) were determined. These provided evidence that the tautomeric form of the natural cofactor 7,8-dihydro(6H)biopterin has the endocyclic C2- N3 double bond structure (29).Keywords
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