Jahan, Humera et al. published their research in Medicinal Chemistry (Sharjah, United Arab Emirates) in 2017 |CAS: 5709-67-1

The Article related to fibroblast cell proliferation ros protein glycation 6 nitrobenzimidazole derivative, 6-nitrobenzimidazole derivatives, advanced glycation end products, fructose-derived ages, intracellular oxidative stress, protein glycation and other aspects.Recommanded Product: 2-Nitro-1H-benzo[d]imidazole

On September 30, 2017, Jahan, Humera; Choudhary, Muhammad I.; Shah, Zarbad; Khan, Khalid M.; Atta-ur-Rahman published an article.Recommanded Product: 2-Nitro-1H-benzo[d]imidazole The title of the article was Derivatives of 6-Nitrobenzimidazole Inhibit Fructose-Mediated Protein Glycation and Intracellular Reactive Oxygen Species Production. And the article contained the following:

Background: Benzimidazoles are important pharmacophores in drug discovery, and currently its derivatives such as flubendazole, omeprazole, and astemizole are used for the treatment of anthelmintic, ulcerative, and histaminic diseases, resp.

Objectives: The aim of the current study was to investigate the antiglycation activity of nitrobenzimidazole derivatives against fructose-mediated human serum albumin (HSA) glycation. The study was also aimed at investigating the effects of newly identified antiglycation inhibitors on AGEsinduced intracellular reactive oxygen species (ROS) production, and associated impaired proliferation of the hepatocytes.

Methods: The present study focuses on the antiglycation activity of 6-nitrobenzimidazole derivatives 1-13 in in-vitro human serum albumin (HSA)- fructose model. These derivatives were also identified as non-toxic against 3T3 mouse fibroblast cell-line in MTT-based assay. The effect of the most promising derivative 5, 4-(6-nitro-1H-benzimidazol-2-yl)-1,2,3-benzenetriol, was studied in a dose dependent manner, co-incubated with fructose-derived AGEs (0- 200 g/mL) on rat hepatocytes proliferation and associated intracellular generation of ROS via MTT-based assay and DCFHDA technique, resp.

Results: We found that derivative 5 ameliorates the elevated intracellular oxidative stress and associated diminished proliferation of the hepatocytes in response to AGEs.

Conclusion: In conclusion, we identified novel 6-nitrobenzimidazole derivatives as antiglycation agents through in-vitro, and cell-based models. The experimental process involved the reaction of 2-Nitro-1H-benzo[d]imidazole(cas: 5709-67-1).Recommanded Product: 2-Nitro-1H-benzo[d]imidazole

The Article related to fibroblast cell proliferation ros protein glycation 6 nitrobenzimidazole derivative, 6-nitrobenzimidazole derivatives, advanced glycation end products, fructose-derived ages, intracellular oxidative stress, protein glycation and other aspects.Recommanded Product: 2-Nitro-1H-benzo[d]imidazole

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem