Conformation-Independent QSAR Study on Human Epidermal Growth Factor Receptor-2 (HER2) Inhibitors
Inhibition of HER2 (human epidermal growth factor receptor 2) expression and function is required in several cancer treatments. Numerous compounds with very different molecular structures have been suggested as HER2 inhibitors. Here we perform quantitative structure-activity relationship (QSAR) anal...
Guardado en:
Autores principales: | , , , , , |
---|---|
Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_23656549_v2_n13_p3725_Duchowicz |
Aporte de: |
id |
todo:paper_23656549_v2_n13_p3725_Duchowicz |
---|---|
record_format |
dspace |
spelling |
todo:paper_23656549_v2_n13_p3725_Duchowicz2023-10-03T16:41:16Z Conformation-Independent QSAR Study on Human Epidermal Growth Factor Receptor-2 (HER2) Inhibitors Duchowicz, P.R. Fioressi, S.E. Castro, E. Wróbel, K. Ibezim, N.E. Bacelo, D.E. Cancer HER2 QSAR Tyrosine kinase protein Inhibition of HER2 (human epidermal growth factor receptor 2) expression and function is required in several cancer treatments. Numerous compounds with very different molecular structures have been suggested as HER2 inhibitors. Here we perform quantitative structure-activity relationship (QSAR) analysis on 444 of such compounds to investigate the molecular properties that may influence its efficiency. Models based on 1D and 2D flexible molecular descriptors are proposed to develop simple models based solely on constitutional and topological molecular features. A large number of non-conformational descriptors (17974) was used to thoroughly explore the structural characteristics that influence the HER2 inhibitory activity. Three different approaches were explored using: 1) Molecular Descriptors, 2) Flexible Molecular Descriptors, and 3) Hybrid Descriptors. A QSAR model for HER2 inhibitors was successfully developed. Some properties such as electronegativity, aromatic character, and the presence of amino groups appear as molecular characteristics that may have influence in the HER2 inhibitory activity. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_23656549_v2_n13_p3725_Duchowicz |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Cancer HER2 QSAR Tyrosine kinase protein |
spellingShingle |
Cancer HER2 QSAR Tyrosine kinase protein Duchowicz, P.R. Fioressi, S.E. Castro, E. Wróbel, K. Ibezim, N.E. Bacelo, D.E. Conformation-Independent QSAR Study on Human Epidermal Growth Factor Receptor-2 (HER2) Inhibitors |
topic_facet |
Cancer HER2 QSAR Tyrosine kinase protein |
description |
Inhibition of HER2 (human epidermal growth factor receptor 2) expression and function is required in several cancer treatments. Numerous compounds with very different molecular structures have been suggested as HER2 inhibitors. Here we perform quantitative structure-activity relationship (QSAR) analysis on 444 of such compounds to investigate the molecular properties that may influence its efficiency. Models based on 1D and 2D flexible molecular descriptors are proposed to develop simple models based solely on constitutional and topological molecular features. A large number of non-conformational descriptors (17974) was used to thoroughly explore the structural characteristics that influence the HER2 inhibitory activity. Three different approaches were explored using: 1) Molecular Descriptors, 2) Flexible Molecular Descriptors, and 3) Hybrid Descriptors. A QSAR model for HER2 inhibitors was successfully developed. Some properties such as electronegativity, aromatic character, and the presence of amino groups appear as molecular characteristics that may have influence in the HER2 inhibitory activity. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim |
format |
JOUR |
author |
Duchowicz, P.R. Fioressi, S.E. Castro, E. Wróbel, K. Ibezim, N.E. Bacelo, D.E. |
author_facet |
Duchowicz, P.R. Fioressi, S.E. Castro, E. Wróbel, K. Ibezim, N.E. Bacelo, D.E. |
author_sort |
Duchowicz, P.R. |
title |
Conformation-Independent QSAR Study on Human Epidermal Growth Factor Receptor-2 (HER2) Inhibitors |
title_short |
Conformation-Independent QSAR Study on Human Epidermal Growth Factor Receptor-2 (HER2) Inhibitors |
title_full |
Conformation-Independent QSAR Study on Human Epidermal Growth Factor Receptor-2 (HER2) Inhibitors |
title_fullStr |
Conformation-Independent QSAR Study on Human Epidermal Growth Factor Receptor-2 (HER2) Inhibitors |
title_full_unstemmed |
Conformation-Independent QSAR Study on Human Epidermal Growth Factor Receptor-2 (HER2) Inhibitors |
title_sort |
conformation-independent qsar study on human epidermal growth factor receptor-2 (her2) inhibitors |
url |
http://hdl.handle.net/20.500.12110/paper_23656549_v2_n13_p3725_Duchowicz |
work_keys_str_mv |
AT duchowiczpr conformationindependentqsarstudyonhumanepidermalgrowthfactorreceptor2her2inhibitors AT fioressise conformationindependentqsarstudyonhumanepidermalgrowthfactorreceptor2her2inhibitors AT castroe conformationindependentqsarstudyonhumanepidermalgrowthfactorreceptor2her2inhibitors AT wrobelk conformationindependentqsarstudyonhumanepidermalgrowthfactorreceptor2her2inhibitors AT ibezimne conformationindependentqsarstudyonhumanepidermalgrowthfactorreceptor2her2inhibitors AT bacelode conformationindependentqsarstudyonhumanepidermalgrowthfactorreceptor2her2inhibitors |
_version_ |
1782029037594476544 |