A comprehensive account on recent progress in pharmacological activities of benzimidazole derivatives

SR Brishty, MJ Hossain, MU Khandaker… - Frontiers in …, 2021 - frontiersin.org
Nowadays, nitrogenous heterocyclic molecules have attracted a great deal of interest
among medicinal chemists. Among these potential heterocyclic drugs, benzimidazole …

Cannabinoids: structures, effects, and classification

VA Shevyrin, YY Morzherin - Russian Chemical Bulletin, 2015 - Springer
The data on the chemical structures, biological effects, and use of cannabinoids on the
illegal market of new psychoactive substances were generalized. An extended classification …

Discovery of high-affinity cannabinoid receptors ligands through a 3D-QSAR ushered by scaffold-hopping analysis

G Floresta, O Apirakkan, A Rescifina, V Abbate - Molecules, 2018 - mdpi.com
Two 3D quantitative structure–activity relationships (3D-QSAR) models for predicting
Cannabinoid receptor 1 and 2 (CB1 and CB2) ligands have been produced by way of …

Synthesis, binding assays, cytotoxic activity and docking studies of benzimidazole and benzothiophene derivatives with selective affinity for the CB2 cannabinoid …

J Romero-Parra, J Mella-Raipán, V Palmieri… - European Journal of …, 2016 - Elsevier
Herein we report the design, synthesis, bioinformatic and biological studies of
benzimidazole and benzothiophene derivatives as new cannabinoid receptor ligands. To …

QSAR Modelling of Biological Activity in Cannabinoids with Quantum Similarity Combinations of Charge Fitting Schemes and 3D‐QSAR

D Navarro‐Acosta, L Coba‐Jimenez… - Chemistry & …, 2023 - Wiley Online Library
Quantitative structure− activity relationship (QSAR) modeled the biological activities of 30
cannabinoids with quantum similarity descriptors (QSD) and Comparative Molecular Field …

Combined CoMFA and CoMSIA 3D-QSAR study of benzimidazole and benzothiophene derivatives with selective affinity for the CB2 cannabinoid receptor

J Romero-Parra, H Chung, RA Tapia… - European Journal of …, 2017 - Elsevier
The preceding years have brought an exponential increase in our understanding of the
endocannabinoid system (ECS), including the knowledge of CB1 and CB2 cannabinoid …

Cannabis and bioactive cannabinoids

F Messina, O Rosati, M Curini… - Studies in natural products …, 2015 - Elsevier
The therapeutic use of Cannabis dates back to ancient times and this plant has been used
for centuries as remedy for a large number of diseases. Today it is well known that biological …

Trichloroisocyanuric Acid/Triphenylphosphine-Mediated Synthesis of Benzimidazoles, Benzoxazoles, and Benzothiazoles

S Rezazadeh, B Akhlaghinia… - Australian Journal of …, 2014 - CSIRO Publishing
A new and efficient method for preparation of benzimidazoles, benzoxazoles, and
benzothiazoles from reactions of different carboxylic acids with o-phenylenediamine, o …

Three-dimensional quantitative structure-activity relationships (3D-QSAR) on a series of piperazine-carboxamides fatty acid amide hydrolase (FAAH) inhibitors as a …

M Lorca, Y Valdes, H Chung, J Romero-Parra… - International Journal of …, 2019 - mdpi.com
Fatty Acid Amide Hydrolase (FAAH) is one of the main enzymes responsible for
endocannabinoid metabolism. Inhibition of FAAH increases endogenous levels of fatty acid …

In-silico designing and characterization of binding modes of two novel inhibitors for CB1 receptor against obesity by classical 3D-QSAR approach

N Khan, SA Halim, W Khan, SK Zafar… - Journal of Molecular …, 2019 - Elsevier
Obesity is the fifth primary hazard for mortality in the world; hence different therapeutic
targets are explored to overcome this problem. Endocannabinoid is identified as the …