Title:Discovery of Potent Natural-Product-Derived SIRT2 Inhibitors Using Structure- Based Exploration of SIRT2 Pharmacophoric Space Coupled With QSAR Analyses
Volume: 21
Issue: 16
Author(s): Mohammad A. Khanfar* Saja Alqtaishat
Affiliation:
- College of Pharmacy, Alfaisal University, Al Takhassusi Rd, Riyadh11533,Saudi Arabia
Keywords:
SIRT2, cancer, neurodegenerative diseases, pharmacophore, QSAR, virtual screening, natural products.
Abstract:
Background: SIRT2 belongs to a class III of Histone Deacetylase (HDAC) and has crucial roles in
neurodegeneration and malignancy.
Objective: The objective of this study is to discover structurally novel natural-product-derived SIRT2 inhibitors.
Methods: Structure-based pharmacophore modeling integrated with validated QSAR analysis was implemented
to discover structurally novel SIRT2 inhibitors from the natural products database. The targeted QSAR model
combined molecular descriptors with structure-based pharmacophore capable of explaining bioactivity variation
of structurally diverse SIRT2 inhibitors. Manually built pharmacophore model, validated with receiver operating
characteristic curve, and selected using the statistically optimum QSAR equation, was applied as a 3Dsearch
query to mine AnalytiCon Discovery database of natural products.
Results: Experimental in vitro testing of highest-ranked hits identified asperphenamate and salvianolic acid B
as active SIRT2 inhibitors with IC50 values in low micromolar range.
Conclusion: New chemical scaffolds of SIRT2 inhibitors have been identified that could serve as a starting
point for lead-structure optimization.
