Synthesis, modification and biological activity of 2,3-indoles of Glycyrrhetinic acid.

2 3-indoles Glycyrrhetinic acid antiulcer and anti-inflammatory activity modification synthesis

Journal

Natural product research
ISSN: 1478-6427
Titre abrégé: Nat Prod Res
Pays: England
ID NLM: 101167924

Informations de publication

Date de publication:
07 Mar 2024
Historique:
medline: 8 3 2024
pubmed: 8 3 2024
entrez: 8 3 2024
Statut: aheadofprint

Résumé

The synthesis of 2,3-indoles of Glycyrrhetinic acid (GLA) and its methyl ester was carried out by the Fischer reaction. Reductive transformations of GLA methyl ester 2,3-indole

Identifiants

DOI: 10.1080/14786419.2024.2326844 PMID: 38454327
pubmed: 38454327
doi: 10.1080/14786419.2024.2326844
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-6

Auteurs

Lidia Baltina (L)

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation.
ORCID: 0000-0002-6291-5260

Elza Karimova (E)

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation.

Timur Nugumanov (T)

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation.

Svetlana Petrova (S)

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation.

Svetlana Gabdrakhmanova (S)

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation.

Regina Khisamutdinova (R)

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation.

Classifications MeSH