Unraveling effective extracellular signal-regulated kinase 2 inhibitors: a

Caffeic acid extracellular signal-regulated kinase 2 molecular docking molecular dynamics

Journal

Journal of biomolecular structure & dynamics
ISSN: 1538-0254
Titre abrégé: J Biomol Struct Dyn
Pays: England
ID NLM: 8404176

Informations de publication

Date de publication:
16 Aug 2023
Historique:
pubmed: 16 8 2023
medline: 16 8 2023
entrez: 16 8 2023
Statut: aheadofprint

Résumé

Extracellular signal-regulated kinase 2 (ERK-2) is a serine/threonine protein kinase in eukaryotic cells and belongs to the mitogen-activated protein kinase (MAPK) family. An activated form of ERK-2 phosphorylates substrates in the nucleus or cytoplasm and causes specific proteins to be expressed or activated, regulating cell proliferation, differentiation and other functions. Caffeic acid (3,4 - dihydroxy cinnamic acid), as previously reported, directly interacts with ERK-2 and reduces its effects

Identifiants

pubmed: 37584104
doi: 10.1080/07391102.2023.2246563
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-11

Auteurs

Heba Ali Hassan (HA)

Department of Pharmacognosy, Faculty of Pharmacy, Sohag University, Sohag, Egypt.

Sara S Muhammed (SS)

Faculty of Pharmacy for girls, AlAzhar University, Banha, Egypt.

Ahmad Al-Khdhairawi (A)

Department of Biological Science and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia.

Sayed F Abdelwahab (SF)

Department of Pharmaceutics and Industrial Pharmacy, College of Pharmacy, Taif University, Taif, Saudi Arabia.

Islam M Abdel-Rahman (IM)

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Deraya University, New-Minia, Egypt.

Mahmoud M Abdelhamid (MM)

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Al-Azhar University, Assiut, Egypt.

Classifications MeSH