Semi-synthesis, α-amylase inhibition, and kinetic and molecular docking studies of arylidene-based sesquiterpene coumarins isolated from Ferula tunetana Pomel ex Batt
| dc.rights.license | open | en_US |
| dc.contributor.author | BACCARI, Wiem | |
| dc.contributor.author | SAIDI, Ilyes | |
| dc.contributor.author | FILALI, Insaf | |
| dc.contributor.author | ZNATI, Mansour | |
| dc.contributor.author | LAZRAG, Houda | |
| dc.contributor.author | TOUNSI, Moncef | |
| hal.structure.identifier | Unité de Recherche Œnologie [Villenave d'Ornon] [OENO] | |
| dc.contributor.author | MARCHAL, Axel
IDREF: 150146477 | |
| hal.structure.identifier | Unité de Recherche Œnologie [Villenave d'Ornon] [OENO] | |
| dc.contributor.author | WAFFO TEGUO, Pierre | |
| dc.contributor.author | BEN JANNET, Hichem | |
| dc.date.accessioned | 2024-02-07T13:46:11Z | |
| dc.date.available | 2024-02-07T13:46:11Z | |
| dc.date.issued | 2024-02-05 | |
| dc.identifier.issn | 2046-2069 | en_US |
| dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/187980 | |
| dc.description.abstractEn | Despite all the significant progresses made to enhance the efficacy of the existing bank of drugs used to manage and cure type II diabetes mellitus, there is still a need to search and develop novel bioactive compounds with superior efficacy and minimal adverse effects. This study describes the valorization of the natural bioactive sesquiterpene coumarin via the semi-synthesis of new analogs and the study of their α-amylase inhibition activity. The sesquiterpene coumarin named coladonin (1) was quantitatively isolated from the chloroform extract of endemic Ferula tunetana roots. Subsequently, the oxidation of 1 via the Jones oxidation reaction, used as a key reaction, afforded precursor 2. The condensation of oxidized coladonin (2) with various aryl aldehydes provided a series of new arylidene-based sesquiterpene coumarin derivatives (3a–m), which were characterized by NMR and ESI-HRMS experiments. All derivatives evaluated in vitro for their α-amylase inhibitory potential showed interesting α-amylase inhibition with IC50 values ranging from 7.24 to 28.98 μM. Notably, compounds 3k and 3m exhibited lower IC50 values (7.24 μM and 8.38 μM, respectively) compared to the standard (acarbose: IC50 = 9.83 μM). In addition, the structure–activity relationship (SAR) for all the compounds was studied. The most active compounds were found to be mixed-type inhibitors, which was revealed by kinetic studies. Furthermore, molecular in silico docking studies were established for all synthesized analogs with the binding site for the α-amylase enzyme. | |
| dc.language.iso | EN | en_US |
| dc.rights | Attribution 3.0 United States | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
| dc.subject.en | Semi-synthesis | |
| dc.subject.en | α-amylase inhibition | |
| dc.subject.en | Sesquiterpene coumarins | |
| dc.subject.en | Ferula tunetana | |
| dc.title.en | Semi-synthesis, α-amylase inhibition, and kinetic and molecular docking studies of arylidene-based sesquiterpene coumarins isolated from Ferula tunetana Pomel ex Batt | |
| dc.title.alternative | RSC Adv. | en_US |
| dc.type | Article de revue | en_US |
| dc.identifier.doi | 10.1039/D3RA07540K | en_US |
| dc.subject.hal | Sciences du Vivant [q-bio] | en_US |
| bordeaux.journal | RSC Advances | en_US |
| bordeaux.page | 4654-4665 | en_US |
| bordeaux.volume | 7 | en_US |
| bordeaux.hal.laboratories | Oenologie - UMR 1366 | en_US |
| bordeaux.institution | Université de Bordeaux | en_US |
| bordeaux.institution | Bordeaux INP | en_US |
| bordeaux.institution | INRAE | en_US |
| bordeaux.peerReviewed | oui | en_US |
| bordeaux.inpress | non | en_US |
| hal.identifier | hal-04444202 | |
| hal.version | 1 | |
| hal.date.transferred | 2024-02-07T13:46:14Z | |
| hal.popular | non | en_US |
| hal.audience | Internationale | en_US |
| hal.export | true | |
| workflow.import.source | hal | |
| dc.rights.cc | CC BY-NC | en_US |
| bordeaux.COinS | ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=RSC%20Advances&rft.date=2024-02-05&rft.volume=7&rft.spage=4654-4665&rft.epage=4654-4665&rft.eissn=2046-2069&rft.issn=2046-2069&rft.au=BACCARI,%20Wiem&SAIDI,%20Ilyes&FILALI,%20Insaf&ZNATI,%20Mansour&LAZRAG,%20Houda&rft.genre=article |
