Wood, Hamish C. S. published the artcileSpecific enzyme inhibitors in vitamin biosynthesis. II. Revised structures for 8-substituted pyrido[2,3d]pyrimidines, Formula: C8H7N3O2, the main research area is structure pyridopyrimidine; inhibition riboflavin synthetase pyridopyrimidine.
Condensation of 6-D-ribitylaminouracil (I) with MeCH:CMeCHO and MeCOCHMeCHO gave the pyridopyrimidines II and III resp. and not, as previously stated by T. Paterson and H. C. S. Wood, 1972, III and II resp. The structures were determined by nuclear Overhauser and photochem. degradation studies. The structures originally proposed were shown to be incorrect byenzyme inhibition studies.
Journal of the Chemical Society, Perkin Transactions 16: Organic and Bio-Organic Chemistry published new progress about Doebner-Miller cyclization. 36075-35-1 belongs to class pyrimidines, name is 7-Methylpyrido[2,3-d]pyrimidine-2,4-diol, and the molecular formula is C8H7N3O2, Formula: C8H7N3O2.
Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia