Boc-protected benzimidazole-pyrrole, benzimidazole-imidazole, and benzimidazole-methoxypyrrole amino acids were synthesized and incorporated into DNA binding polyamides, comprised of N-methyl pyrrole and N-methyl imidazole amino acids, by means of solid-phase synthesis on an oxime resin. These hairpin polyamides were designed to determine the DNA recognition profile of a side-by-side benzimidaz...

A series of novel 2-substituted benzimidazole derivatives were synthesized and their antibacterial activity was assessed against selected Gram-positive and Gram-negative bacteria. The specific moiety at the 2-position of the benzimidazole was extensively modified with several fused heterocyclic functional groups containing nitrogen and sulfur heteroatoms. In addition, the influence of different...

The properties of benzimidazole and its derivatives have been studied over more than one hundred years. Benzimidazole derivatives are useful intermediates/subunits for the development of molecules of pharmaceutical or biological interest. Substituted benzimidazole derivatives have found applications in diverse therapeutic areas such as antiulcer, anticancer agents, and anthelmintic species to n...

Abstract This study evaluated the resistance status of Haemonchus contortus from sheep flocks in state São Paulo, Brazil, through comparison between fecal egg count reduction test (FECRT) and larval development (LDT). For FECRT, 35 were selected each five divided into groups treated with: benzimidazole, levamisole, ivermectin, monepantel control. Feces collected for EPG cultures. The LDT was pe...

Benzimidazole (BZ) resistance is widespread and appears to be readily selected in a variety of nematode parasites of animals. There have been reports of a lack of efficacy of BZ anthelmintics against soil transmitted nematode parasites of humans. However, resistance to BZs in nematodes of humans has not been confirmed. It is difficult to perform tests to confirm anthelmintic resistance in human...

(EC 9o) mycelial inhibition (Y) were ABSTRACT examined by analysis of variance. Northover, J., and Matteoni, J. A. 1986. Resistance of Botrytis cinerea to benomyl and iprodione in Differences between means were evaluated vineyards and greenhouses after exposure to the fungicides alone or mixed with captan. Plant using the Student-Newman-Keuls multiple Disease 70:398-402. range test. A discrimin...

Recently, due to active development of the pharmaceutical industry, an acute problem environmental pollution with synthetic biologically compounds has arisen. Benzimidazole cycle is one most frequently encountered pharmacophores in drugs. Substances containing even microquantities benzimidazole have a toxic effect on living systems. Besides, being alien nature, benzimidazoles are not included m...

In an endeavor to find a novel series of antihyperglycemic agents, new benzimidazole and pyrimidine derivatives were successfully synthesized efficiently in high yield with high purity, starting from amino acids in the presence of phosphorus oxychloride (POCl3). The synthesized compounds were identified by 1H-NMR, 13C-NMR, FT-IR spectroscopic techniques and elemental analysis. All products were...

Bu(3)SnH/1,1'-azobis(cyclohexanecarbonitrile) (ACN)-mediated five, six, and seven-membered double alkyl radical cyclizations onto imidazo[5,4-f]benzimidazole and imidazo[4,5-f]benzimidazole are described. The quinone derivatives evaluated show selective toxicity towards human cervical (HeLa) and prostate (DU145) cancer cell lines (with negligible toxicity towards a normal human cell line, GM006...

A series of 4-amino-6-benzimidazole-pyrimidines was designed to target lymphocyte-specific tyrosine kinase (Lck), a member of the Src kinase family. Highly efficient parallel syntheses were devised to prepare analogues for SAR studies. A number of these 4-amino-6-benzimidazole-pyrimidines exhibited single-digit nanomolar IC(50)s against Lck in biochemical and cellular assays. These 4-amino-6-be...