Acar Cevik U, Celik I, Gorgulu S, Sahin Inan Z, Bostanci H, Karayel A
ACS Omega. 2025; 10(7):6801-6813.
PMID: 40028103
PMC: 11866186.
DOI: 10.1021/acsomega.4c08885.
Muheyuddeen G, Khan M, Ahmad T, Srivastava S, Verma S, Ansari M
Sci Rep. 2024; 14(1):23121.
PMID: 39367036
PMC: 11452658.
DOI: 10.1038/s41598-024-72399-8.
Heine S, Alessandrini F, Grosch J, Grass C, Heldner A, Schnautz B
Front Immunol. 2024; 15:1397072.
PMID: 38915403
PMC: 11194380.
DOI: 10.3389/fimmu.2024.1397072.
Ichinose P, Miro M, Larsen K, Lanusse C, Lifschitz A, Virkel G
Vet Res Commun. 2022; 47(2):803-815.
PMID: 36542192
DOI: 10.1007/s11259-022-10041-6.
Qin S, Ma J, Wang Q, Xu W, Ye W, Jiang R
Molecules. 2022; 27(19).
PMID: 36234715
PMC: 9570981.
DOI: 10.3390/molecules27196179.
Aromatic heterobicycle-fused porphyrins: impact on aromaticity and excited state electron transfer leading to long-lived charge separation.
Moss A, Jang Y, Arvidson J, Nesterov V, DSouza F, Wang H
Chem Sci. 2022; 13(34):9880-9890.
PMID: 36199634
PMC: 9431455.
DOI: 10.1039/d2sc03238d.
CuI nanoparticle-catalyzed synthesis of tetracyclic benzo[]benzo[4,5]imidazo[1,2-][1,3]thiazin-6-imine heterocycles by SAr-type C-S, C-N bond formation from isothiocyanatobenzenes and benzimidazoles.
Guo X, Wang L, Hu J, Zhang M
RSC Adv. 2022; 8(39):22259-22267.
PMID: 35541714
PMC: 9081286.
DOI: 10.1039/c8ra02552e.
Novel benzimidazole derivatives; synthesis, bioactivity and molecular docking study as potent urease inhibitors.
Saeedian Moghadam E, Al-Sadi A, Talebi M, Amanlou M, Amini M, Abdel-Jalil R
Daru. 2022; 30(1):29-37.
PMID: 35040104
PMC: 9114190.
DOI: 10.1007/s40199-021-00427-3.
In vitro study of chlorine dioxide on porcine intestinal epithelial cell gene markers.
Palocz O, Noszticzius Z, Kaly-Kullai K, Bradley E, Csiko G
Vet Med Sci. 2021; 8(2):591-597.
PMID: 34672097
PMC: 8959260.
DOI: 10.1002/vms3.658.
Benzylic Methylene Functionalizations of Diarylmethanes.
Gulati U, Gandhi R, Laha J
Chem Asian J. 2020; 15(20):3135-3161.
PMID: 32794651
PMC: 7436909.
DOI: 10.1002/asia.202000730.
Development of 2-(4-pyridyl)-benzimidazoles as PKN2 chemical tools to probe cancer.
Scott F, Fala A, Pennicott L, Reuillon T, Massirer K, Elkins J
Bioorg Med Chem Lett. 2020; 30(8):127040.
PMID: 32085971
PMC: 7078758.
DOI: 10.1016/j.bmcl.2020.127040.
Alteration in Inflammatory Responses and Cytochrome P450 Expression of Porcine Jejunal Cells by Drinking Water Supplements.
Palocz O, Szita G, Csiko G
Mediators Inflamm. 2019; 2019:5420381.
PMID: 30718974
PMC: 6334367.
DOI: 10.1155/2019/5420381.
Oxibendazole inhibits prostate cancer cell growth.
Chen Q, Li Y, Zhou X, Li R
Oncol Lett. 2018; 15(2):2218-2226.
PMID: 29434928
PMC: 5776919.
DOI: 10.3892/ol.2017.7579.
Synthesis and Evaluation of Selected Benzimidazole Derivatives as Potential Antimicrobial Agents.
Alasmary F, Snelling A, Zain M, Alafeefy A, Awaad A, Karodia N
Molecules. 2015; 20(8):15206-23.
PMID: 26307956
PMC: 6332381.
DOI: 10.3390/molecules200815206.
Gene and protein expression and cellular localisation of cytochrome P450 enzymes of the 1A, 2A, 2C, 2D and 2E subfamilies in equine intestine and liver.
Tyden E, Tjalve H, Larsson P
Acta Vet Scand. 2014; 56:69.
PMID: 25288196
PMC: 4192735.
DOI: 10.1186/s13028-014-0069-8.
An experimental and theoretical NMR study of NH-benzimidazoles in solution and in the solid state: proton transfer and tautomerism.
Nieto C, Cabildo P, Garcia M, Claramunt R, Alkorta I, Elguero J
Beilstein J Org Chem. 2014; 10:1620-9.
PMID: 25161719
PMC: 4142846.
DOI: 10.3762/bjoc.10.168.
General one-pot, two-step protocol accessing a range of novel polycyclic heterocycles with high skeletal diversity.
Xu Z, Ayaz M, Cappelli A, Hulme C
ACS Comb Sci. 2012; 14(8):460-4.
PMID: 22746181
PMC: 3426865.
DOI: 10.1021/co300046r.
2-(4-Chloro-phen-yl)-1-phenyl-1H-benz-imidazole.
Kassim K, Hashim N, Fadzil A, Yusof M
Acta Crystallogr Sect E Struct Rep Online. 2012; 68(Pt 3):o799.
PMID: 22412669
PMC: 3297866.
DOI: 10.1107/S1600536812006678.
Facile, novel two-step syntheses of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines.
Xu Z, Shaw A, Dietrich J, Cappelli A, Nichol G, Hulme C
Mol Divers. 2012; 16(1):73-9.
PMID: 22237832
PMC: 3311162.
DOI: 10.1007/s11030-011-9354-x.
Exacerbation of acetaminophen hepatotoxicity by the anthelmentic drug fenbendazole.
Gardner C, Mishin V, Laskin J, Laskin D
Toxicol Sci. 2011; 125(2):607-12.
PMID: 22048645
PMC: 3262853.
DOI: 10.1093/toxsci/kfr301.