The interaction of calf thymus DNA (ct DNA) with anastrozole, which is acknowledged as an
antineoplastic drug, has been enquired into in the absence and presence of histone H1 …

The main mechanism for drug-drug interaction is displacement reaction of ligands from their
protein binding sites. The aim of this study was to evaluate anticancer drug sorafenib …

Twenty different cold gels were made by adding transglutaminase enzyme and using soy
protein isolate (SPI) powders from different manufacturers to investigate their potential as an …

The organochlorine pesticide dicofol (DCF), a persistent organic pollutant, is used as
acaricide worldwide. Considering its large consumption in the agriculture sector and …

Drug-drug interactions are due to the binding of a drug to plasma proteins displacing
another plasma protein-bound drug. Two ligands, olmutinib (OLM) and colchicine (COL) …

Binding of toxic ligands to DNA could result in undesirable biological processes, such as
carcinogenesis or mutagenesis. Binding mode of Abiraterone (ABR), a steroid drug and calf …

The presence of the p-aryl/cyclohexyl ring in the N-(4-aryl/cyclohexyl)-2-(pyridine-4-yl
carbonyl) hydrazine carbothioamide derivative (2C) is reported to enhance the antifungal …

Flavonoid-containing food supplements are widely used as antioxidants, and the continuous
use of these supplements with other drugs can lead to clinically significant interactions …

This study was designed to examine the interaction of neratinib (NRB) with human serum
albumin (HSA) in presence of flavonoids quercetin and rutin. Both quercetin and rutin can …

The interaction between erlotinib (ERL) and bovine serum albumin (BSA) was studied in the
presence of quercetin (QUR), a flavonoid with antioxidant properties. Ligands bind to the …