CO-ENZYME PROPERTIES OF SOME ADE-1-SUBSTITUTED AND ADE-N6-SUBSTITUTED NADAND DERIVATIVES
- 1 January 1976
- journal article
- research article
- Vol. 357 (6) , 887-891
Abstract
By reaction of NAD+ with different oxiranes or with aziridine, derivatives of the coenzyme are obtained with substituents in position 1 or on the amino group in position 6 of the adenine ring. While the Adenine-1-substituted derivatives show high Km values with different dehydrogenases and are reduced only very slowly by these enzymes, the coenzyme derivatives substituted at the amino group behave very similarly to NAD+. Correlations were found between coenzyme efficiency of the compounds and the lipophilic character of their substituents. The results can be interpreted from the structure of the active site of the dehydrogenases investigated.This publication has 3 references indexed in Scilit:
- The Preparation and Properties of N-Hydroxyethyl Derivatives of Adenosine, Adenosine Triphosphate, and Nicotinamide Adenine DinucleotideJournal of Biological Chemistry, 1961
- THE SPECTROPHOTOMETRIC DETERMINATION OF AMINE, AMINO ACID AND PEPTIDE WITH 2,4,6- TRINITROBENZENE 1-SULFONIC ACID*The Journal of Biochemistry, 1960
- Phosphorus Assay in Column ChromatographyJournal of Biological Chemistry, 1959