Unknown

Dataset Information

0

New Arylethanolimidazole Derivatives as HO-1 Inhibitors with Cytotoxicity against MCF-7 Breast Cancer Cells.


ABSTRACT: In this paper, a novel series of imidazole-based heme oxygenase-1 (HO-1) inhibitors is reported. These compounds were obtained by modifications of previously described high potent and selective arylethanolimidazoles. In particular, simplification of the central linker and repositioning of the hydrophobic portion were carried out. Results indicate that a hydroxyl group in the central region is crucial for the potency as well as the spatial distribution of the hydrophobic portion. Docking studies revealed a similar interaction of the classical HO-1 inhibitors with the active site of the protein. The most potent and selective compound (5a) was tested for its potential cytotoxic activity against hormone-sensitive and hormone-resistant breast cancer cell lines (MCF-7 and MDA-MB-231).

SUBMITTER: Ciaffaglione V 

PROVIDER: S-EPMC7139504 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

New Arylethanolimidazole Derivatives as HO-1 Inhibitors with Cytotoxicity against MCF-7 Breast Cancer Cells.

Ciaffaglione Valeria V   Intagliata Sebastiano S   Pittalà Valeria V   Marrazzo Agostino A   Sorrenti Valeria V   Vanella Luca L   Rescifina Antonio A   Floresta Giuseppe G   Sultan Ameera A   Greish Khaled K   Salerno Loredana L  

International journal of molecular sciences 20200311 6


In this paper, a novel series of imidazole-based heme oxygenase-1 (HO-1) inhibitors is reported. These compounds were obtained by modifications of previously described high potent and selective arylethanolimidazoles. In particular, simplification of the central linker and repositioning of the hydrophobic portion were carried out. Results indicate that a hydroxyl group in the central region is crucial for the potency as well as the spatial distribution of the hydrophobic portion. Docking studies  ...[more]

Similar Datasets

| S-EPMC6780817 | biostudies-other
| S-EPMC8508995 | biostudies-literature
| S-EPMC3894702 | biostudies-literature
| S-EPMC5509251 | biostudies-literature
| S-EPMC8118639 | biostudies-literature
| S-EPMC6766798 | biostudies-other
| S-ECPF-GEOD-64430 | biostudies-other
| S-EPMC4957127 | biostudies-literature
| S-EPMC7428194 | biostudies-literature
| S-EPMC6274052 | biostudies-literature