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Molecular docking analysis of penta-galloyl-glucose with VEGF signaling molecules
It is of interest to document the molecular docking analysis data of penta-galloyl-glucose with VEGF signaling molecules in the context of cancer. Data shows that penta-galloyl-glucose have optimal binding affinities with VEGF-A,VEGFR-2, PKC, RAF, MEK, ERK and AKT with binding affinity of -7.9,-8.3,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148596/ https://www.ncbi.nlm.nih.gov/pubmed/35655912 http://dx.doi.org/10.6026/97320630017924 |
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author | Dharmalingam, Karthick Dharmalingam, Velvizhi Durairaj, Satheesh Sharma, Praveen Jayaraman, Selvaraj |
author_facet | Dharmalingam, Karthick Dharmalingam, Velvizhi Durairaj, Satheesh Sharma, Praveen Jayaraman, Selvaraj |
author_sort | Dharmalingam, Karthick |
collection | PubMed |
description | It is of interest to document the molecular docking analysis data of penta-galloyl-glucose with VEGF signaling molecules in the context of cancer. Data shows that penta-galloyl-glucose have optimal binding affinities with VEGF-A,VEGFR-2, PKC, RAF, MEK, ERK and AKT with binding affinity of -7.9,-8.3,-8.6, -3.7,10.1,-9 and -10.8 kcal/mol respectively for further consideration in this context. |
format | Online Article Text |
id | pubmed-9148596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-91485962022-06-01 Molecular docking analysis of penta-galloyl-glucose with VEGF signaling molecules Dharmalingam, Karthick Dharmalingam, Velvizhi Durairaj, Satheesh Sharma, Praveen Jayaraman, Selvaraj Bioinformation Research Article It is of interest to document the molecular docking analysis data of penta-galloyl-glucose with VEGF signaling molecules in the context of cancer. Data shows that penta-galloyl-glucose have optimal binding affinities with VEGF-A,VEGFR-2, PKC, RAF, MEK, ERK and AKT with binding affinity of -7.9,-8.3,-8.6, -3.7,10.1,-9 and -10.8 kcal/mol respectively for further consideration in this context. Biomedical Informatics 2021-11-30 /pmc/articles/PMC9148596/ /pubmed/35655912 http://dx.doi.org/10.6026/97320630017924 Text en © 2021 Biomedical Informatics https://creativecommons.org/licenses/by/3.0/This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License. |
spellingShingle | Research Article Dharmalingam, Karthick Dharmalingam, Velvizhi Durairaj, Satheesh Sharma, Praveen Jayaraman, Selvaraj Molecular docking analysis of penta-galloyl-glucose with VEGF signaling molecules |
title | Molecular docking analysis of penta-galloyl-glucose with VEGF signaling molecules |
title_full | Molecular docking analysis of penta-galloyl-glucose with VEGF signaling molecules |
title_fullStr | Molecular docking analysis of penta-galloyl-glucose with VEGF signaling molecules |
title_full_unstemmed | Molecular docking analysis of penta-galloyl-glucose with VEGF signaling molecules |
title_short | Molecular docking analysis of penta-galloyl-glucose with VEGF signaling molecules |
title_sort | molecular docking analysis of penta-galloyl-glucose with vegf signaling molecules |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148596/ https://www.ncbi.nlm.nih.gov/pubmed/35655912 http://dx.doi.org/10.6026/97320630017924 |
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