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
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

Auteurs

Olga Książkiewicz (O)

Department of Physical Chemistry, Faculty of Chemistry, University of Lodz, Pomorska 163/165, Lodz 91-236, Poland.

Classifications MeSH