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Molecular docking analysis of aspirin analogues with β-catenin

Canonical Wnt signaling pathway plays a crucial role in cancer cell proliferation, which links by the growth of β-catenin in cell due to inactivation of glycogen synthetase kinase-3. Therefore, it is of interest to design novel candidates to bind with β-catenin. Hence, we document the molecular dock...

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Autores principales: Selvaraj, Jayaraman, Sardar, Hussain, Vishnupriya, Veeraraghavan, Balakrishna, Janardhana Papayya, Mohan, Surapaneni Krishna, Nivedha, Rajamanickam Pon, Vijayalakshmi, Periyasamy, Ponnulakshmi, Rajagopal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457021/
https://www.ncbi.nlm.nih.gov/pubmed/34621119
http://dx.doi.org/10.6026/97320630016725
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author Selvaraj, Jayaraman
Sardar, Hussain
Vishnupriya, Veeraraghavan
Balakrishna, Janardhana Papayya
Mohan, Surapaneni Krishna
Nivedha, Rajamanickam Pon
Vijayalakshmi, Periyasamy
Ponnulakshmi, Rajagopal
author_facet Selvaraj, Jayaraman
Sardar, Hussain
Vishnupriya, Veeraraghavan
Balakrishna, Janardhana Papayya
Mohan, Surapaneni Krishna
Nivedha, Rajamanickam Pon
Vijayalakshmi, Periyasamy
Ponnulakshmi, Rajagopal
author_sort Selvaraj, Jayaraman
collection PubMed
description Canonical Wnt signaling pathway plays a crucial role in cancer cell proliferation, which links by the growth of β-catenin in cell due to inactivation of glycogen synthetase kinase-3. Therefore, it is of interest to design novel candidates to bind with β-catenin. Hence, we document the molecular docking analysis data of aspirin analogues with β-catenin for further consideration.
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spelling pubmed-84570212021-10-06 Molecular docking analysis of aspirin analogues with β-catenin Selvaraj, Jayaraman Sardar, Hussain Vishnupriya, Veeraraghavan Balakrishna, Janardhana Papayya Mohan, Surapaneni Krishna Nivedha, Rajamanickam Pon Vijayalakshmi, Periyasamy Ponnulakshmi, Rajagopal Bioinformation Research Article Canonical Wnt signaling pathway plays a crucial role in cancer cell proliferation, which links by the growth of β-catenin in cell due to inactivation of glycogen synthetase kinase-3. Therefore, it is of interest to design novel candidates to bind with β-catenin. Hence, we document the molecular docking analysis data of aspirin analogues with β-catenin for further consideration. Biomedical Informatics 2020-09-30 /pmc/articles/PMC8457021/ /pubmed/34621119 http://dx.doi.org/10.6026/97320630016725 Text en © 2020 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
Selvaraj, Jayaraman
Sardar, Hussain
Vishnupriya, Veeraraghavan
Balakrishna, Janardhana Papayya
Mohan, Surapaneni Krishna
Nivedha, Rajamanickam Pon
Vijayalakshmi, Periyasamy
Ponnulakshmi, Rajagopal
Molecular docking analysis of aspirin analogues with β-catenin
title Molecular docking analysis of aspirin analogues with β-catenin
title_full Molecular docking analysis of aspirin analogues with β-catenin
title_fullStr Molecular docking analysis of aspirin analogues with β-catenin
title_full_unstemmed Molecular docking analysis of aspirin analogues with β-catenin
title_short Molecular docking analysis of aspirin analogues with β-catenin
title_sort molecular docking analysis of aspirin analogues with β-catenin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457021/
https://www.ncbi.nlm.nih.gov/pubmed/34621119
http://dx.doi.org/10.6026/97320630016725
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