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Synthesis, biological activity and molecular modeling of a new series of condensed 1,2,4-triazoles.
El Bakri, Youness; Marmouzi, Ilias; El Jemli, Meryem; Anouar, El Hassane; Karthikeyan, Subramani; Harmaoui, Abdallah; Faouzi, My El Abbes; Mague, Joel T; Essassi, El Mokhtar.
Afiliación
  • El Bakri Y; Laboratoire de Chimie Organique Hétérocyclique, Centre de Recherche des Sciences des Médicaments, Pôle de Compétences Pharmacochimie, URAC 21, Faculté des Sciences, Université Mohammed V Rabat, Avenue Ibn Battouta, BP 10014 Rabat, Morocco; Organic Chemistry Department, Science Faculty, RUDN Universi
  • Marmouzi I; University Mohammed V in Rabat, Faculté de Médicine et de Pharmacie, Laboratoire de Pharmacologie et Toxicologie, équipe de Pharmacocinétique, BP 6203, Rabat Instituts, Rabat, Morocco.
  • El Jemli M; University Mohammed V in Rabat, Faculté de Médicine et de Pharmacie, Laboratoire de Pharmacologie et Toxicologie, équipe de Pharmacocinétique, BP 6203, Rabat Instituts, Rabat, Morocco.
  • Anouar EH; Department of Chemistry, College of Sciences and Humanities, Prince Sattam bin Abdulaziz University, P.O. Box 83, Al Kharj 11942, Saudi Arabia. Electronic address: anouarelhassane@yahoo.fr.
  • Karthikeyan S; Organic Chemistry Department, Science Faculty, RUDN University Miklukho-Maklaya st. 6, 117198 Moscow, Russian Federation. Electronic address: 92karthy@gmail.com.
  • Harmaoui A; Laboratoire de Chimie Organique Hétérocyclique, Centre de Recherche des Sciences des Médicaments, Pôle de Compétences Pharmacochimie, URAC 21, Faculté des Sciences, Université Mohammed V Rabat, Avenue Ibn Battouta, BP 10014 Rabat, Morocco.
  • Faouzi MEA; University Mohammed V in Rabat, Faculté de Médicine et de Pharmacie, Laboratoire de Pharmacologie et Toxicologie, équipe de Pharmacocinétique, BP 6203, Rabat Instituts, Rabat, Morocco.
  • Mague JT; Department of Chemistry, Tulane University, New Orleans, LA 70118, USA.
  • Essassi EM; Laboratoire de Chimie Organique Hétérocyclique, Centre de Recherche des Sciences des Médicaments, Pôle de Compétences Pharmacochimie, URAC 21, Faculté des Sciences, Université Mohammed V Rabat, Avenue Ibn Battouta, BP 10014 Rabat, Morocco.
Bioorg Chem ; 92: 103193, 2019 11.
Article en En | MEDLINE | ID: mdl-31445196
A ring transformation of 6-methyl-7H[1,2,4]triazolo [4,3-b][1,2,4] triazepine-8(9H)-ones (thiones) in the presence of acetic anhydride give rise to a new series of 17 condensed 1,2,4-triazole derivatives (1-17). Plausible mechanisms are proposed and show the formation of a beta fused ß-lactam moiety. The compounds were tested for their (i) inhibitory potential on digestive enzymes (α-amylase and α-glucosidase), and (ii) antioxidant activity using radical scavenging (DPPH and ABTS radicals) and ferric reducing power assays. The compounds showed interesting and promising antidiabetic activities compared to the reference drug Acarbose. Molecular docking study has been carried out to determine the binding mode interactions between these derivatives and the targeted enzymes. The results showed the strength of intermolecular hydrogen bonding in ligand-receptor complexes as an important descriptor in rationalizing the observed inhibition results. Moreover, molecular dynamics simulations are also performed for the best protein-ligand complex to understand the stability of small molecule in a protein environment. To shed light on the antioxidant activity of the synthesized compounds and the mechanism involved in DPPH free radical, DFT calculations were performed at the B3P86/6-311++G(d,p) level using the polarizable continuum model. The effect of aprotic solvent on bond dissociation enthalpies (BDEs) is investigated by calculating and comparing BDEs of 1 in methanol and dimethylsulfoxide as solvents using PCM. The obtained results show that the mechanism of action depends on the basic skeleton and the presence of substituted functional groups in these derivatives. BDEs are found to be slightly influenced by the aprotic solvent of less than 0.01 kcal/mol compared with those obtained in methanol.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Triazoles / Alfa-Amilasas / Alfa-Glucosidasas / Hipoglucemiantes / Antioxidantes Idioma: En Revista: Bioorg Chem Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Triazoles / Alfa-Amilasas / Alfa-Glucosidasas / Hipoglucemiantes / Antioxidantes Idioma: En Revista: Bioorg Chem Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos