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Molecular docking analysis of PARγ with compounds from Ocimum tenuiflorum

The ligand-activated transcription factor peroxisome proliferator-activated receptor (PPAR) has become a major target for type 2 diabetes. It belongs to the nuclear receptor superfamily, which controls the expression of proteins involved in glucose metabolism, lipid metabolism, adipocyte proliferati...

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Detalles Bibliográficos
Autores principales: Rajagopal, Ponnulakshmi, Jayaraman, Selvaraj, JH, Shazia Fathima, Radhakrishnan, Saravanan, Laxman, Patil Ashlesh, Krishnan Muthaiah, Vijaya Prakash, Tripathi, Satyendra Chandra, Gugapriya, TS, Tarnekar, Aaditya Madhusudan, Girish Muthiyan, Gayatri, Deshmukh, Vishwajit Ravindra, Sontakke, Bharat Ramrao, Chandrashekar, Kirubhanand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148598/
https://www.ncbi.nlm.nih.gov/pubmed/35655905
http://dx.doi.org/10.6026/97320630017928
Descripción
Sumario:The ligand-activated transcription factor peroxisome proliferator-activated receptor (PPAR) has become a major target for type 2 diabetes. It belongs to the nuclear receptor superfamily, which controls the expression of proteins involved in glucose metabolism, lipid metabolism, adipocyte proliferation and differentiation, and insulin sensitivity. Ocimum tenuiflorum, often known as Krishna tulsi, is the most sacred herb in India. It was utilized for a variety of medicinal purposes. Therefore, it is of interest to document the molecular docking analysis data of PARγ modulators from Ocimum tenuiflorum. Four of the twenty substances (rosmarinic acid, permethrin, luteolin, and isosakuranetin) have a considerable binding affinity for the PPARγ. These phytochemicals are a source of potential anti-diabetic medicines.