Unknown

Dataset Information

0

Synthesis, antioxidant activity, molecular docking and ADME studies of novel pyrrole-benzimidazole derivatives.


ABSTRACT: Several 5-(alkylsulfonyl)-1-substituted-2-(1H-pyrrol-2-yl)-1H-benzo[d]imidazole derivatives were synthesized and their antioxidant activities were investigated using lipid peroxidation (LPO) and 7-ethoxyresorufin O-deethylase (EROD) assays. Docking analysis with Human NAD[P]H-Quinone oxidoreductase 1 (NQO1) was also performed to gather thorough information about these compounds that have antioxidant activities. Moreover, their molecular descriptors and ADME properties were calculated using the SwissADME online program. As a result, most of our compounds possessed better affinity and created ample interactions with NQO1. The most potent compound 5j had LP inhibition value of 3.73 nmol/mg/min. Other compounds exhibited moderate activity on LP levels comparing to standard butylated hydroxy toluene (BHT). However, the inhibitory effect on EROD activity was not significant.

SUBMITTER: Zengin Karadayi F 

PROVIDER: S-EPMC10503985 | biostudies-literature | 2022

REPOSITORIES: biostudies-literature

altmetric image

Publications

Synthesis, antioxidant activity, molecular docking and ADME studies of novel pyrrole-benzimidazole derivatives.

Zengin Karadayi Fikriye F   Başaran Rahman R   Kişla Mehmet Murat MM   Can Eke Binay B   Ateş Alagöz Zeynep Z  

Turkish journal of chemistry 20210220 3


Several 5-(alkylsulfonyl)-1-substituted-2-(1H-pyrrol-2-yl)-1H-benzo[d]imidazole derivatives were synthesized and their antioxidant activities were investigated using lipid peroxidation (LPO) and 7-ethoxyresorufin O-deethylase (EROD) assays. Docking analysis with Human NAD[P]H-Quinone oxidoreductase 1 (NQO1) was also performed to gather thorough information about these compounds that have antioxidant activities. Moreover, their molecular descriptors and ADME properties were calculated using the S  ...[more]

Similar Datasets

| S-EPMC10994708 | biostudies-literature
| S-EPMC10219251 | biostudies-literature
| S-EPMC7180718 | biostudies-literature
| S-EPMC9000376 | biostudies-literature
| S-EPMC9609714 | biostudies-literature
| S-EPMC5362474 | biostudies-literature
| S-EPMC3425833 | biostudies-literature
| S-EPMC10421135 | biostudies-literature
| S-EPMC11391345 | biostudies-literature
| S-EPMC10276907 | biostudies-literature