Nature of Luminescence and Pharmacological Activity of Sulfaguanidine.


Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
18 May 2023
Historique:
received: 18 04 2023
revised: 15 05 2023
accepted: 16 05 2023
medline: 29 5 2023
pubmed: 27 5 2023
entrez: 27 5 2023
Statut: epublish

Résumé

Sulfonamides are one of the oldest groups of veterinary chemotherapeutic agents. Physico-chemical properties, the concentration and the nature of the environment are the factors responsible for the distribution of sulfonamides in the living organism. Although these drug compounds have been in use for more than half a century, knowledge about their behavior is still limited. Physiological activity is currently attributed to the sulfanyl radical. Our study is devoted to the spectral properties of aqueous solutions of sulfaguanidine, in which the formation of complexes with an H-bond and a protonated form takes place. The nature of the fluorescent state of sulfaguanidine was interpreted using computational chemistry, the electronic absorption method and the luminescence method. The structure of sulfaguanidine includes several active fragments: aniline, sulfonic and guanidine. To reveal the role of fragments in the physiological activity of the studied antibiotic, we calculated and compared the effective charges of the fragments of aniline and sulfaguanidine molecules. Chromophore groups were identified in molecules, which determine the intermolecular interaction between a molecule and a proton-donor solvent. The study also revealed the impact of sulfone and guanidine groups, as well as complexation, on the effective charge of the antibiotic fragment responsible for physiological activity and luminescent ability.

Identifiants

pubmed: 37241901
pii: molecules28104159
doi: 10.3390/molecules28104159
pmc: PMC10224513
pii:
doi:

Substances chimiques

Sulfaguanidine 15XQ8043FN
Anti-Bacterial Agents 0
Sulfonamides 0
Sulfanilamide 21240MF57M
aniline SIR7XX2F1K
Aniline Compounds 0
Guanidines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Russian Foundation for Basic Research
ID : 20-32-90116
Organisme : Russian Development Program of Tomsk State University (Priority-2030).
ID : NU 2.0.7.22 ML

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Auteurs

Olga Tchaikovskaya (O)

Quantum Electronics Laboratory, Institute of Electrophysics, Ural Branch of the Russian Academy of Sciences, 620146 Yekaterinburg, Russia.
Laboratory of Photophysics and Photochemistry of Molecules, Faculty of Physics, Tomsk State University, 634050 Tomsk, Russia.

Elena Bocharnikova (E)

Laboratory of Photophysics and Photochemistry of Molecules, Faculty of Physics, Tomsk State University, 634050 Tomsk, Russia.

Olga Bazyl (O)

Laboratory of Photophysics and Photochemistry of Molecules, Faculty of Physics, Tomsk State University, 634050 Tomsk, Russia.

Vlada Chaidonova (V)

Laboratory of Photophysics and Photochemistry of Molecules, Faculty of Physics, Tomsk State University, 634050 Tomsk, Russia.
Hygienic and Epidemiological Center in Republic of Khakassia, 655017 Abakan, Russia.

George Mayer (G)

Laboratory of Photophysics and Photochemistry of Molecules, Faculty of Physics, Tomsk State University, 634050 Tomsk, Russia.

Paul Avramov (P)

Department of Chemistry and Green-Nano Materials Research Center, Kyungpook National University, 80 Daehak-ro, Buk-gu, Daegu 41566, Republic of Korea.

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Classifications MeSH