Potential anti-obesity/inflammatory flavonoid-derived biomolecules against Obesity to prevent WAT differentiation by targeting a DNA-binding protein inhibitor, ID-1.


Journal

Cellular and molecular biology (Noisy-le-Grand, France)
ISSN: 1165-158X
Titre abrégé: Cell Mol Biol (Noisy-le-grand)
Pays: France
ID NLM: 9216789

Informations de publication

Date de publication:
31 May 2023
Historique:
received: 24 03 2023
medline: 14 8 2023
pubmed: 12 8 2023
entrez: 12 8 2023
Statut: epublish

Résumé

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 triglycerides in adipocytes, particularly white adipose tissue (WAT). In addition to modifying one's lifestyle, anti-obesity medicines are increasingly used as adjuvant therapy. Flavonoids are the major 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 that fight 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 study led to the identification of 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 bio-active molecule may be used as a lead for the development of 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.

Identifiants

pubmed: 37571884
doi: 10.14715/cmb/2023.69.5.23
doi:

Substances chimiques

DNA-Binding Proteins 0
Anti-Obesity Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

150-155

Auteurs

Jowaher S Alanazi (JS)

Department of Pharmacology and Toxicology, College of Pharmacy, University of Hail, Hail, KSA. jawaher.a@gmail.com.

Aziz Unnisa (A)

Department of Pharmaceutical Chemistry, College of Pharmacy, University of Ha'il, Ha'il, 81442, Saudi Arabia. Khushiazeez@yahoo.co.in.

Muteb S Alanazi (MS)

Department of Clinical Pharmacy, College of Pharmacy, University of Ha'il, Ha'il, 81442, Saudi Arabia. Alanazi.m@gmail.com.

Tareq N Alharby (TN)

Department of Clinical Pharmacy, College of Pharmacy, University of Ha'il, Ha'il, 81442, Saudi Arabia. mdth.ah@yahoo.com.

Rama Devi Patel (RD)

Department of Biology, College of Sciences, University of Ha'il, Ha'il, 81442, Saudi Arabia. R.PATEL@UOH.EDU.SA.

Ramaiah Itumalla (R)

Department of Health Management, College of Public Health and Health Informatics, University of Ha'il, Ha'il, 81442, Saudi Arabia. R.ITUMALLA@UOH.EDU.SA.

Kareem M Younes (KM)

Department of Pharmaceutical Chemistry, College of Pharmacy, University of Ha'il, Ha'il, 81442, Saudi Arabia. Khushiazeez@yahoo.co.in.

Amr S Abouzied (AS)

Department of Pharmaceutical Chemistry, College of Pharmacy, University of Ha'il, Ha'il, 81442, Saudi Arabia. Khushiazeez@yahoo.co.in.

N V C Lakshmi K (NVC)

Department of Pharmaceutical Chemistry, K.V.S.R. Siddhartha College of Pharmaceutical Sciences, Andhra Pradesh, India. chenchu_lakshmi@gmail.com.

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Classifications MeSH