Evidence map›Paper›PMID 40715238›Full record

ArticleScientific reports2025

In vitro and in silico neuroprotective evaluation of new biotransformation metabolites of (-)-α-bisabolol.

Reham Mansour, Ramadan A Eldomany, Amira Mira, Mohamed A Sabry, Saleh H El-Sharkawy, Amal F Soliman

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Reham MansourDepartment of Pharmacognosy, Faculty of Pharmacy, Kafr El-Sheikh University, Kafr El-Sheikh, 33516, Egypt.
Ramadan A EldomanyDepartment of Microbiology and Immunology, Faculty of Pharmacy, Kafr El-Sheikh University, Kafr El-Sheikh, 33156, Egypt.
Amira MiraDepartment of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt. amira_mera2006@mans.edu.eg.
Mohamed A SabryDepartment of Medicinal Chemistry, Faculty of Pharmacy, Mansoura National University, Gamasa, 7731168, Egypt.
Saleh H El-SharkawyDepartment of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt.
Amal F SolimanDepartment of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biotransformation of (-)-α-bisabolol (1) was investigated by screening twenty-two fungal strains in an effort to produce new more polar and potentially bioactive metabolites. Three fungi were selected for scale-up biotransformation: Cordyceps sinensis, Alternaria alternata and Aspergillus flavus. Five metabolites were isolated: 10β,11-dihydroxy-α-bisabolol (2), Hamanasic acid A (3), 2,3-dihydro-α-bisabolol (4), 7-dehydroxy-10,11-epoxy-3-methylcarboxy-α-bisabolol (5) and 10β,11,15-trihydroxy-α-bisabolol (6), with metabolites 4, 5, and 6 being newly identified. Structural elucidation was performed using spectroscopic methods. α-bisabolol and its metabolites were evaluated for their cyclooxygenase (COX) and acetylcholinesterase (AChE) inhibitory activities, as well as neuroprotective effects against H

Indexed as

Neuroprotective AgentsSesquiterpenesAcetylcholinesteraseAmyloid beta-PeptidesAspergillus flavusBiotransformationCell Line, TumorCholinesterase InhibitorsCyclooxygenase 2HumansHydrogen PeroxideMolecular Docking SimulationMonocyclic SesquiterpenesPeptide FragmentsAcetylcholinesteraseAmyloid beta-PeptidesbisabololCholinesterase InhibitorsCyclooxygenase 2Hydrogen PeroxideMonocyclic SesquiterpenesNeuroprotective AgentsPeptide FragmentsSesquiterpenesBiotransformationBisabololCholinesterase inhibitorsCOX inhibitorsHamanasic acid ANeuroprotective

Identifiers

PMID40715238
PMCPMC12297533

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.