A salt from biologically active compounds pyridine-2,3-dicarboxylic (quinolinic) acid and cytosine.
Hirshfeld surface analysis
crystal structure
cytosine
hydrogen bond
nitrogenous base
pyridine-2,3-dicarboxylic acid
quinolinic acid
Journal
Acta crystallographica. Section C, Structural chemistry
ISSN: 2053-2296
Titre abrégé: Acta Crystallogr C Struct Chem
Pays: England
ID NLM: 101620313
Informations de publication
Date de publication:
01 Nov 2024
01 Nov 2024
Historique:
medline:
11
10
2024
pubmed:
11
10
2024
entrez:
11
10
2024
Statut:
aheadofprint
Résumé
Biologically active compounds are highly sought-after materials for developing novel structures applicable to industry. Cytosine and pyridine-2,3-dicarboxylic acid (quinolinic acid) are notably significant environmentally. Cytosine, a pyrimidine derivative, features a six-membered ring with a ketone and an amino group, constituting a fundamental nitrogenous base found in deoxyribonucleic acid (DNA). The present synthesis yielded a salt of dipyridine-2,3-dicarboxylic acid with cytosine, wherein a proton was transferred from a carboxyl group of quinolinic acid to a ring N atom in the cytosine molecule giving the salt 6-amino-2-oxo-2,3-dihydropyrimidin-1-ium 3-carboxypyridine-2-carboxylate, C
Identifiants
pubmed: 39392458
pii: S2053229624009598
doi: 10.1107/S2053229624009598
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM