Asim_2026_J.Comput.Aided.Mol.Des_40_59

Reference

Title : Pistagremic acid from Pistacia integerrima as a natural multi-target candidate tackling crucial enzymes involved in Alzheimer's disease - Asim_2026_J.Comput.Aided.Mol.Des_40_59
Author(s) : Asim M , Marryum , Naz S , Rauf A , Aslam N , Rashid U , Akram Z , Alsanie WF , Alamri AS , Alshammary AF , Ribaudo G
Ref : J Comput Aided Mol Des , 40 :59 , 2026
Abstract :

Natural products have crucial relevance both in traditional medicine as well as in modern drug discovery. Indeed, they inspire currently developed drugs, emphasizing the importance of biodiversity and sustainability. Alzheimer's disease (AD), a complex neurodegenerative disorder marked by amyloid plaques and neurofibrillary tangles, involves dysregulation of molecular pathways including increased cholinesterases and monoamine oxidase-B (MAO-B) activities, with enzyme inhibition remaining a key therapeutic strategy. This study investigates pistagremic acid, a triterpene from Pistacia chinensis subsp. integerrima and its inhibitory effects on such crucial enzymes implicated in AD. The compound showed moderate inhibition of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) in vitro with selectivity for AChE, while a potent inhibition of MAO-B was noted, indicating potential neuroprotective effects by reducing oxidative stress. Molecular docking showed interactions with key enzyme residues, and off targets were studied with a ligand-based approach. The findings support its multi-target therapeutic potential, but also prompt future studies exploring selectivity profile.

PubMedSearch : Asim_2026_J.Comput.Aided.Mol.Des_40_59
PubMedID: 41639310

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Citations formats

Asim M, Marryum, Naz S, Rauf A, Aslam N, Rashid U, Akram Z, Alsanie WF, Alamri AS, Alshammary AF, Ribaudo G (2026)
Pistagremic acid from Pistacia integerrima as a natural multi-target candidate tackling crucial enzymes involved in Alzheimer's disease
J Comput Aided Mol Des 40 :59

Asim M, Marryum, Naz S, Rauf A, Aslam N, Rashid U, Akram Z, Alsanie WF, Alamri AS, Alshammary AF, Ribaudo G (2026)
J Comput Aided Mol Des 40 :59