Results 1 to 10 of about 4,804 (192)

Structural elucidation and Hirshfeld surface analysis of a fused thiophene ester: methyl 3-[(naphtho[2,1-b]thiophen-5-yl)methyl]-1-benzothiophene-2-carboxylate [PDF]

open access: yesActa Crystallographica Section E: Crystallographic Communications
The title compound, C23H16O2S2, is a benzo[b]thiophene-2-carboxylate derivative and consists of naphthothiophene and benzothiophene moieties bridged by a methylene group.
Sekaran Ranjith   +3 more
doaj   +2 more sources

Antimalarials with Benzothiophene Moieties as Aminoquinoline Partners

open access: yesMolecules, 2017
Malaria is a severe and life-threatening disease caused by Plasmodium parasites that are spread to humans through bites of infected Anopheles mosquitoes.
Milica Selakovic   +2 more
exaly   +3 more sources

Novel Insights on Benzo[b]thiophene Analogues for MAO-B Inhibition and Neuroprotection: Design, Synthesis, Molecular Modelling Studies and Biological Activity [PDF]

open access: yesAntioxidants
Neurodegenerative disorders (NDs), such as Alzheimer’s disease and Parkinson’s disease (PD), represent a significant challenge for ageing populations, with their prevalence increasing worldwide.
Francesca Arrighi   +21 more
doaj   +2 more sources

Structure-Guided Discovery of Benzoic-Acid-Based TRPC6 Ligands: An Integrated Docking, MD, and MM-GBSA SAR Study: Potential Therapeutic Molecules for Autism Spectrum Disorder [PDF]

open access: yesPharmaceuticals
Background: TRPC6 is recognized as a therapeutically relevant cation channel, whose activation is governed by specific ligand–pocket interactions. Methods: An integrated in silico workflow was employed, comprising structure-based docking, 100-nanosecond ...
Nicolás Ignacio Silva   +10 more
doaj   +2 more sources

A New Class of Benzo[b]thiophene-chalcones as Cholinesterase Inhibitors: Synthesis, Biological Evaluation, Molecular Docking and ADME Studies [PDF]

open access: yesMolecules
In this study, heterocyclic compounds containing a benzothiophene scaffold were designed and synthetized, and their inhibitory activity against cholinesterases (ChE) and the viability of SH-SY5Y cells have been evaluated.
Giovanna Lucia Delogu   +6 more
doaj   +2 more sources

Benzothiophene Adsorptive Desulfurization onto trihexYl(tetradecyl)phosphonium Dicyanamide Ionic-Liquid-Modified Renewable Carbon: Kinetic, Equilibrium and UV Spectroscopy Investigations

open access: yesMolecules, 2022
The negative environmental and industrial impacts of the presence of sulfur compounds such as benzothiophene in fuels have led to a greater interest in desulfurization research.
Mohamed A. Habila   +3 more
doaj   +1 more source

Synthesis of novel artesunate-benzothiophene and artemisinin-benzothiophene derivatives

open access: yesNatural Product Research, 2021
Natural products are used for the treatment of a variety of diseases for many years. Last decades, design and synthesis of novel biologically active hybrid molecules including natural product is gained big importance due to their unique and new biological properties.
Omruye Ozok, Emrah Kavak, Arif Kivrak
openaire   +4 more sources

Hetero-Type Benzannulation Leading to Substituted Benzothio-Phenes

open access: yesMolecules, 2021
TiCl4 (or SnCl4)-promoted hetero-type benzannulation reactions using various (2,2-dichlorocyclopropyl)(thiophen-2-yl)methanols proceeded smoothly to produce uniquely substituted 4-chlorobenzothiophenes (five examples).
Taro Kono   +4 more
doaj   +1 more source

Hydrodesulfurization of benzothiophene on Ni2P surface

open access: yesEnergy Exploration & Exploitation, 2020
The study of benzothiophene hydrodesulfurization reaction path contribute to clarifying the mechanism of hydrodesulfurization (HDS) of heavy oil. In this work, experiments and simulations were combined to study the reaction pathway of benzothiophene ...
Riyi Lin   +6 more
doaj   +1 more source

Metal‐Free Arylation of Benzothiophenes at C4 by Activation as their Benzothiophene S‐Oxides

open access: yesAngewandte Chemie International Edition, 2023
AbstractBenzothiophenes, activated by oxidation to the corresponding S‐oxides, undergo C−H/C−H‐type coupling with phenols to give C4 arylation products. While an electron‐withdrawing group at C3 of the benzothiophene is important, the process operates without a directing group and a metal catalyst, thus rendering it compatible with sensitive ...
Ranjana Bisht   +6 more
openaire   +3 more sources

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