Results 171 to 180 of about 636,119 (261)

Cell Cycle Arrest and Apoptosis-Inducing Ability of Benzimidazole Derivatives: Design, Synthesis, Docking, and Biological Evaluation. [PDF]

Molecules, 2022
Nazreen S, Almalki ASA, Elbehairi SEI, Shati AA, Alfaifi MY, Elhenawy AA, Alsenani NI, Alfarsi A, Alhadhrami A, Alqurashi EA, Alam MM.   +10 more
europepmc   +1 more source

Progress in Synthesis and Pharmacology of Telmisartan

Chemistry &Biodiversity, Volume 23, Issue 9, September 2026.
Telmisartan is a benzimidazole derivative and a well‐known drug to treat hypertension. This review provides synthesis and understanding of telmisartan as an antihypertensive drug through two mechanisms of actions: RAAS inhibitor and PPARγ receptor. Effective repurposing of this drug for various diseases like chronic kidney illness, diabetes, fatty ...
Megha, Richa Srivastava, Ram Singh
wiley   +1 more source

Experimental and theoretical evaluation of the corrosion inhibition performance of two benzimidazole derivatives for low carbon steel in acidic solution. [PDF]

RSC Adv
Xhanari K, Farruku M, Berisha A, Xhaxhiu K, Canaj J, Seiti B, Kokalari E, Lame A.   +7 more
europepmc   +1 more source

Benzimidazole Derivatives as Energetic Materials: A Theoretical Study. [PDF]

Materials (Basel), 2021
Sarlauskas J, Tamuliene J, Bekesiene S, Kravcov A.   +3 more
europepmc   +1 more source

Heterocyclic‐Based Fungicides: Emerging Strategies for Viable Plant Disease Control

Chemistry &Biodiversity, Volume 23, Issue 9, September 2026.
Heterocyclic compounds have attracted considerable attention because of their structural diversity, potent antifungal activity, and ability to interact with multiple fungal targets, offering broad‐spectrum protection against phytopathogens. Synthetic and semisynthetic/part‐natural scaffolds, particularly azole, quinoline, indole, cyclotryptamine, and ...
Sumit Tahlan, Meenakshi Kaira, Sucheta Singh, Hrithik Dey, Kailash C. Pandey   +4 more
wiley   +1 more source

Introduction of new quinolone-2-thio-acetamide-propane hydrazide-benzimidazole derivatives as new α-glucosidase and α-amylase inhibitors. [PDF]

Sci Rep
Nikfar P, Karimian S, Safapoor S, Noori M, Noori M, Dastyafteh N, Ghafouri SN, Mohammadi-Khanaposhtani M, Larijani B, Taslimi P, Mahdavi M.   +10 more
europepmc   +1 more source

Computational, In Vitro, and In Vivo Evaluation of Benzimidazole–Pyrazole Hybrid Scaffolds as Multi‐Target Anti‐Ulcer Agents

Chemistry &Biodiversity, Volume 23, Issue 9, September 2026.
The hybrid pharmacophore approach involves the combination of benzimidazole‐pyrazole moieties to form multi‐functional anti‐ulcer compounds. Molecular modeling and biological evaluations show significant proton pump inhibition, anti‐inflammatory action, antioxidant property, and remarkable prevention of gastric ulcers.
Hafiz Aamir Ali Kharl, Abdul Malik, Humaira Nadeem, Mohammad Shamsul Ola, Sara Aiman, Arif Ullah Khan, Muhammad Akmal Farooq, Humaira Muzaffar, Syed Muzzammil Masaud   +8 more
wiley   +1 more source

Benzimidazole derivatives as potent <i>α</i>-amylase inhibitors: synthesis, characterization and <i>in vitro α</i>-amylase inhibition. [PDF]

Future Med Chem
Kangad SK, Sitapara SM, Maliwal D, Somaiya C, Pissurlenkar RRS, Patolia VN.   +5 more
europepmc   +1 more source

Co‐Acid Free Nitration of N,N‐Dimethylanilines Using Traditional and Nontraditional Activation Methods

Chemistry–Methods, Volume 6, Issue 9, September 2026.
Selective mono‐ and dinitration of dimethylanilines by co‐acid‐free dilute aqueous nitric acid using nontraditional activation methods, such as microwave, ultrasound, and high hydrostatic pressure. The nitration of aromatic compounds is a highly important transformation, contributing to the synthesis of dyes, agrochemicals, explosives, pharmaceuticals,
Kelsey M. Plasse, Lyah K. Esplana, Béla Török   +2 more
wiley   +1 more source

2-(Cyanomethyl)benzimidazole Derivatives as 1,3-Dicarbonyl Analogues for a Kinetically Controlled Diastereo- and Enantioselective Mannich-Type Reaction Catalyzed by Chiral Phosphoric Acid. [PDF]

Org Lett
Ye H, Hou L, Takeda A, Sato T, Yadav J, Kikuchi J, Bao M, Terada M.   +7 more
europepmc   +1 more source