Withanolides from Datura ceratocaula and Datura discolor and their acetylcholinesterase inhibitory activity.

Acetylcholinesterase inhibitors Datura ceratocaula Datura discolor Solanaceae Withanolides

Journal

Fitoterapia
ISSN: 1873-6971
Titre abrégé: Fitoterapia
Pays: Netherlands
ID NLM: 16930290R

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 01 06 2023
revised: 14 08 2023
accepted: 15 08 2023
medline: 23 10 2023
pubmed: 19 8 2023
entrez: 18 8 2023
Statut: ppublish

Résumé

The investigation of the chemical constituents of Datura ceratocaula and D. discolor allowed to isolate three new withanolides, datucerolide A (1) from the first species, and datudiscolides A (8) and B (9) from the second. In addition, seven known withanolides and five ubiquitous compounds were isolated from these plants, along with 27-O-β-d-glucopyranosyl dinnoxolide A (5), which was obtained as the tetraacetyl derivative 4. All the structures were elucidated by analyses of their spectroscopic and spectrometric data and that of dinnoxolide A (6) was confirmed by X-ray diffraction analysis. The structure 4 was assigned earlier to daturametelin G-Ac and that of 5 to datinolide B, therefore, it will be discussed whether these assignments are correct. On the other hand, the structure of datudiscolide A (8) was previously assigned to the aglycone of dinoxin B (14), however, a revision of its reported NMR data showed inconsistencies with the proposed structure. The inhibitory activity of withanolides 2, 3, 6-8, 12, and 13 against acetylcholinesterase enzyme (AChE) was evaluated. Compounds 6, 7, 12, and 13 exhibited the best activity with IC

Identifiants

pubmed: 37595646
pii: S0367-326X(23)00230-7
doi: 10.1016/j.fitote.2023.105655
pii:
doi:

Substances chimiques

Withanolides 0
Acetylcholinesterase EC 3.1.1.7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105655

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Ulises González (U)

Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Coyoacán, 04510, Cd. Mx., Mexico. Electronic address: gm_ulises@hotmail.com.

Antonio Nieto-Camacho (A)

Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Coyoacán, 04510, Cd. Mx., Mexico. Electronic address: anieto@unam.mx.

Simón Hernández-Ortega (S)

Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Coyoacán, 04510, Cd. Mx., Mexico. Electronic address: simonho@iquimica.unam.mx.

Mahinda Martínez (M)

Facultad de Ciencias Naturales, Universidad Autónoma de Querétaro, Avenida de las Ciencias s/n, Col. Juriquilla 76230, Querétaro, Qro, Mexico. Electronic address: mahinda@uaq.mx.

Emma Maldonado (E)

Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Coyoacán, 04510, Cd. Mx., Mexico. Electronic address: emmaldon@unam.mx.

Articles similaires

Pesticide Exposure and Its Association with Parkinson's Disease: A Case-Control Analysis.

Ali Samareh, Hossein Pourghadamyari, Mohammad Hadi Nemtollahi et al.
1.00
Humans Pesticides Case-Control Studies Male Female
Withanolides Animals Microglia Autophagy Mice
Animals Anopheles Insecticide Resistance Insecticides Pyrethrins

Expanding the antiprotozoal activity and the mechanism of action of n-butyl and iso-butyl ester of quinoxaline-1,4-di-

Alonzo González-González, Oscar Sánchez-Sánchez, Lilián Yépez-Mulia et al.
1.00
Giardia lamblia Trichomonas vaginalis Entamoeba histolytica Antiprotozoal Agents Quinoxalines

Classifications MeSH