Antiviral activity of benzimidazole derivatives. II. Antiviral activity of 2-phenylbenzimidazole derivatives

M Tonelli, M Simone, B Tasso, F Novelli, V Boido… - Bioorganic & medicinal …, 2010 - Elsevier
Seventy-six 2-phenylbenzimidazole derivatives were synthesized and evaluated in cell-
based assays for cytotoxicity and antiviral activity against a panel of 10 RNA and DNA …

75 years of bovine viral diarrhea virus: Current status and future applications of the use of directed antivirals

BW Newcomer - Antiviral Research, 2021 - Elsevier
Bovine viral diarrhea virus (BVDV) was first reported 75 years ago and remains a source of
major financial and production losses in the North American cattle industry. Currently …

Discovery of benzimidazole derivatives as novel multi-target EGFR, VEGFR-2 and PDGFR kinase inhibitors

Y Li, C Tan, C Gao, C Zhang, X Luan, X Chen… - Bioorganic & medicinal …, 2011 - Elsevier
Multi-target EGFR, VEGFR-2 and PDGFR inhibitors are highly useful anticancer agents with
improved therapeutic efficacies. In this work, we used two virtual screening methods, support …

Approved and experimental countermeasures against pestiviral diseases: Bovine viral diarrhea, classical swine fever and border disease

BW Newcomer, MD Givens - Antiviral research, 2013 - Elsevier
The pestiviruses, bovine viral diarrhea virus (BVDV), classical swine fever (CSFV) and
border disease virus, are important livestock pathogens in many countries, but current …

New benzimidazole-1, 2, 4-triazole hybrid compounds: Synthesis, anticandidal activity and cytotoxicity evaluation

H Karaca Gençer, U Acar Çevik, S Levent, BN Sağlık… - Molecules, 2017 - mdpi.com
Owing to the growing need for antifungal agents, we synthesized a new series 2-((5-(4-(5-
substituted-1 H-benzimidazol-2-yl) phenyl)-4-substituted-4 H-1, 2, 4-triazol-3-yl) thio)-1 …

Rapid Generation and Molecular Docking Analysis of Single-Chain Fragment Variable (scFv) Antibody Selected by Ribosome Display Targeting Cholecystokinin B …

A Kunamneni, MA Montera, R Durvasula… - International journal of …, 2023 - mdpi.com
A robust cell-free platform technology, ribosome display in combination with cloning,
expression, and purification was utilized to develop single chain Fragment variable (scFv) …

Molecular docking and molecular dynamics (MD) simulation of human anti-complement factor H (CFH) antibody Ab42 and CFH polypeptide

B Yang, SJ Lin, JY Ren, T Liu, YM Wang, CM Li… - International Journal of …, 2019 - mdpi.com
An understanding of the interaction between the antibody and its targeted antigen and
knowing of the epitopes are critical for the development of monoclonal antibody drugs …

Template entrance channel as possible allosteric inhibition and resistance site for quinolines tricyclic derivatives in RNA dependent RNA polymerase of bovine viral …

M Srivastava, L Mittal, D Sarmadhikari, VK Singh… - Pharmaceuticals, 2023 - mdpi.com
The development of potent non-nucleoside inhibitors (NNIs) could be an alternate strategy
to combating infectious bovine viral diarrhea virus (BVDV), other than the traditional …

Synthesis, cytotoxicity and antiviral evaluation of new series of imidazo [4, 5-g] quinoline and pyrido [2, 3-g] quinoxalinone derivatives

I Briguglio, R Loddo, E Laurini, M Fermeglia… - European Journal of …, 2015 - Elsevier
Linear aromatic N-tricyclic compounds with promising antiviral activity and minimal
cytotoxicity were prepared and analyzed in the last years. Specifically, the pyrido [2, 3-g] …

Pd-Catalyzed Direct C–H Bond Functionalization of Spirocyclic σ1 Ligands: Generation of a Pharmacophore Model and Analysis of the Reverse Binding Mode by Docking into a …

C Meyer, D Schepmann, S Yanagisawa… - Journal of medicinal …, 2012 - ACS Publications
To explore the hydrophobic binding region of the σ1 receptor protein, regioisomeric
spirocyclic thiophenes 9–11 were developed as versatile building blocks. Regioselective α …