Identification of human IKK-2 inhibitors of natural origin (Part II): in Silico prediction of IKK-2 inhibitors in natural extracts with known anti-inflammatory activity.

Détails

ID Serval
serval:BIB_BB86FECE9C1E
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Identification of human IKK-2 inhibitors of natural origin (Part II): in Silico prediction of IKK-2 inhibitors in natural extracts with known anti-inflammatory activity.
Périodique
European Journal of Medicinal Chemistry
Auteur⸱e⸱s
Sala E., Guasch L., Iwaszkiewicz J., Mulero M., Salvadó M.J., Bladé C., Ceballos M., Valls C., Zoete V., Grosdidier A., Garcia-Vallvé S., Michielin O., Pujadas G.
ISSN
1768-3254 (Electronic)
ISSN-L
0223-5234
Statut éditorial
Publié
Date de publication
2011
Volume
46
Numéro
12
Pages
6098-6103
Langue
anglais
Résumé
Human inhibitor NF-κB kinase 2 (hIKK-2) is the primary component responsible for activating NF-κB in response to various inflammatory stimuli. Thus, synthetic ATP-competitive inhibitors for hIKK-2 have been developed as anti-inflammatory compounds. We recently reported a virtual screening protocol (doi:10.1371/journal.pone.0016903) that is able to identify hIKK-2 inhibitors that are not structurally related to any known molecule that inhibits hIKK-2 and that have never been reported to have anti-inflammatory activity. In this study, a stricter version of this protocol was applied to an in-house database of 29,779 natural products annotated with their natural source. The search identified 274 molecules (isolated from 453 different natural extracts) predicted to inhibit hIKK-2. An exhaustive bibliographic search revealed that anti-inflammatory activity has been previously described for: (a) 36 out of these 453 extracts; and (b) 17 out of 30 virtual screening hits present in these 36 extracts. Only one of the remaining 13 hit molecules in these extracts shows chemical similarity with known synthetic hIKK-2 inhibitors. Therefore, it is plausible that a significant portion of the remaining 12 hit molecules are lead-hopping candidates for the development of new hIKK-2 inhibitors.
Mots-clé
Anti-Inflammatory Agents/chemistry, Anti-Inflammatory Agents/pharmacology, Biological Agents/chemistry, Biological Agents/pharmacology, Databases, Factual, Drug Discovery/methods, Humans, I-kappa B Kinase/antagonists & inhibitors, I-kappa B Kinase/metabolism, Plant Extracts/chemistry, Plant Extracts/pharmacology, Plants, Medicinal/chemistry, Protein Kinase Inhibitors/chemistry, Protein Kinase Inhibitors/pharmacology, Workflow
Pubmed
Web of science
Création de la notice
25/10/2011 9:30
Dernière modification de la notice
20/08/2019 16:29
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