Abstract
A concoction of unhealthy eating, inactivity, and the adverse effects of specific drugs brings on obesity. The primary cause of Obesity is the storage of too much energy and triglycérides in adipocytes, mainly white adipose tissue (WAT). In addition to modifying one's lifestyle, anti-obesity medicines are increasingly used as adjuvant therapy. Flavonoids are the primary class of compounds having significant biological impacts and health-improving properties. To find novel flavonoid compounds that fight obesity using computational drug design techniques. This work targets 1DI protein to predict new flavonoid compounds against obesity. The study uses computational approaches to anticipate potential anti-obesity, inflammatory flavonoid compounds against obesity to prevent WAT differentiation by targeting ID-1, a DNA-binding protein inhibitor. Our investigation led to identifying the protein target inhibitor lead CID: 5280443, which was found to be a potent inhibitor of the receptor. According to the findings of this study, this bioactive molecule may be used as a lead for developing drugs that preferentially fight obesity without interfering with the functions of the human proteasome. The scientific community will benefit from these discoveries, which could aid in the creation of new medications that treat obesity more successfully.
Author supplied keywords
Cite
CITATION STYLE
Alanazi, J. S., Unnisa, A., Alanazi, M. S., Alharby, T. N., Patel, R. D., Itumalla, R., … Lakshmi, N. V. C. K. (2023). Potential anti-obesity/inflammatory flavonoid-derived biomolecules against Obesity to prevent WAT differentiation by targeting a DNA-binding protein inhibitor, ID-1. Cellular and Molecular Biology, 69(5), 150–155. https://doi.org/10.14715/cmb/2023.69.5.23
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.