137856-21-4Relevant articles and documents
Bisbenzimidazole Derivatives as Potential Antimicrobial Agents: Design, Synthesis, Biological Evaluation and Pharmacophore Analysis
Ersan, Ronak Haj,Bolelli, Kayhan,Gonca, Serpil,Dogen, Aylin,Burmaoglu, Serdar,Algul, Oztekin
, p. 149 - 158 (2021)
In an attempt to design and synthesize a potent class of antimicrobials, 1,2-phenylenediamine derivatives were reacted with various aliphatic and heteroaliphatic dicarboxylic acids to generate a small library of 26 head-to-head bisbenzimidazole compounds (16 – 42) using the polyphosphoric acid method. These compounds were screened for their antibacterial activity and their antifungal activity. Compound 25 showed maximum potency against both Gram-positive and Gram-negative bacterial strains with minimum inhibitory concentration (MIC) values in the range of 7.81 – 31.25 μg/mL. In particular, it showed the maximum MIC values of 7.81 μg/mL against Gram-negative bacteria, which was four-fold more active than the standard drug ampicillin (MIC = 32.25 μg/mL). Compound 19 was found to be the most active against S. aureus with a MIC value of 3.90 μg/mL, whereas the remaining compounds showed only low-to-moderate activity. Furthermore, all compounds exhibited low activity against all fungal strains in comparison to the standard drug fluconazole. I addition, pharmacophore hypotheses were generated to analyze structure–activity relationships between the molecular structures and antimicrobial activities on E. coli. This pharmacophore model can be useful in order to design new antimicrobial drugs. It can be suggested that the substitution of a phenyl ring at the 5/6 and 5′/6′ positions in symmetric bisbenzimidazole derivatives produces compounds with promising antimicrobial activity.
Synthesis, X-ray structure, theoretical investigation, corrosion inhibition and antimicrobial activity of benzimidazole thioether and theirs metal complexes
Bouchouit, Mehdi,Said, Mohamed Elhadi,Kara Ali, Mounira,Bouacida, Sofiane,Merazig, Hocine,Kacem Chaouche, Noreddine,Chibani, Aissa,Zouchoune, Bachir,Belfaitah, Ali,Bouraiou, Abdelmalek
, p. 248 - 259 (2016)
Synthesis, characterization, corrosion inhibition as well as antimicrobial activity of the coordination compounds {Co(bbms)Cl2}, {Zn(bbms)Cl2}, {Co(btmb)Cl2} and {Zn(btmb)Cl2} containing benzimidazole thioether have been described. Co(bbms) and Zn(bbms) as well as Co(btmb) and Zn(btmb) are isostructural with space group Pbca and P21 respectively. The coordination polyhedron around the metal center for all complexes may be described as a quasi-regular tetragonal geometry. The corrosion inhibition study of these complexes for steel in 0.5?M H2SO4medium has been investigated using potentiodynamic polarization and EIS techniques. These later show the corrosion inhibition ability of the prepared complexes for steel in acid medium. A new procedure has been developed for antimicrobial assay using a solid tablet of the corresponding complexes. These later show moderate to significant antimicrobial activities against: Pseudomonas syringae, Staphylococcus aureus and Pichia caribbica. DFT/BP86 calculations have been carried out on the neutral complexes and on the monoanionic of (1) and (3) forms of singlet and triplet species. The optimized structures reproduce those observed experimentally, while the reduced ones undergo remarkable geometrical parameters variations.
Synthesis and antibacterial evaluation of some novel imidazole and benzimidazole sulfonamides
Al-Mohammed, Nassir N.,Alias, Yatimah,Abdullah, Zanariah,Shakir, Raied M.,Taha, Ekhlass M.,Hamid, Aidil Abdul
, p. 11978 - 11995 (2013/11/06)
Several new substituted sulfonamide compounds were synthesized and their structures were confirmed by 1H-NMR, 13C-NMR, FT-IR, and mass spectroscopy. The antibacterial activities of the synthesized compounds were screened against stan
