Results 151 to 160 of about 35,659 (254)
This study assesses the presence, genotypes and clinical signs of E. cuniculi infection in pet rabbits in Slovenia. Molecular analysis reveals the presence of E. cuniculi DNA (Genotype I) in 14.98% rabbit urine samples, mostly in rabbits with signs of urinary tract disorders.
Maruša Škrbec +8 more
wiley +1 more source
Structural Modifications of Hybrid O-Alkylsulfonyl-β-(Benzimidazol-1-yl)propioamidoximes as a Pathway to the Antimicrobial, Antifungal and Antidiabetic Drugs. [PDF]
Kayukova L +6 more
europepmc +1 more source
This study evaluated the efficacy of widely used commercial anthelmintics and examined whether combining different drug classes enhances their effectiveness in naturally infected sheep in the Kaffa Zone. This study suggest the presence of emerging anthelmintic resistance to albendazole and tetramisole in the study area and highlight the potential ...
Nahom Belay, Asrat Arke, Lamrot Tesfaye
wiley +1 more source
Alveolar echinococcosis. [PDF]
Stojković M, Junghanss T, Gehling KG.
europepmc +1 more source
The first crystal structure of the telmisartan–tempol conjugate YK‐4‐250 is reported, revealing the intramolecular C–H…π interactions that stabilize the nitroxide radical while preserving the angiotensin AT1 receptor antagonist pharmacophore.We report the first crystal structure of the telmisartan–tempol conjugate 2,2,6,6‐tetramethyl‐1‐(λ′‐oxidaneyl ...
Simon Friedrich +4 more
wiley +1 more source
We explore covalent allosteric targeting of MGL regulatory cysteines using iso‐ and benzisothiazolinone scaffolds. Combining mechanism‐based warhead release with structure‐guided scaffold decoration to improve molecular recognition, this study probes strategies to achieve selective on‐target engagement beyond the catalytic site. Monoacylglycerol lipase
Edoardo Rocca +12 more
wiley +1 more source
From Scaffold to Therapy: Benzimidazole Pharmacophore Evolution in Breast Cancer Research. [PDF]
Kaur A, Singh G.
europepmc +1 more source
Human immunodeficiency virus (HIV) allosteric integrase inhibitors (ALLINIs) offer a vital alternative to standard therapies by targeting noncatalytic sites. By inducing aberrant integrase multimerization, they disrupt viral maturation. This review explores their medicinal chemistry evolution, detailing structural insights, structure–activity ...
Francesco Saccoliti +10 more
wiley +1 more source
A metal‐free PIII/PV redox organocatalytic aza‐Wittig reaction enables the efficient cyclization of azide‐functionalized imides into pharmaceutically relevant amidine‐containing heterocycles. Using only 2 mol% of a methanophosphocine catalyst and a Brønsted acid additive, a broad range of substrates is converted in up to 96% yield, including ...
Raphael El Bekri Saudain +3 more
wiley +1 more source
Design, Synthesis, <i>In Silico</i> ADME, Toxicity Prediction and Molecular Docking Studies of Benzimidazole-Oxadiazole Derivatives for α-Glucosidase and Aldose Reductase Pathways as Potent Anti-Diabetic Agents. [PDF]
Işık M +8 more
europepmc +1 more source

