MétaCan
Menu
Back to cohort
Record W4301503045 · doi:10.1016/j.ejmcr.2022.100075

Design, synthesis and structure-activity relationship studies of 3-phenylpyrazino[1,2-a]indol-1(2H)-ones as amyloid aggregation and cholinesterase inhibitors with antioxidant activity

2022· article· en· W4301503045 on OpenAlexafffund
Sarbjeet Singh Gujral, Arash Shakeri, Leila Hejazi, Praveen P. N. Rao

Bibliographic record

VenueEuropean Journal of Medicinal Chemistry Reports · 2022
Typearticle
Languageen
FieldMedicine
TopicCholinesterase and Neurodegenerative Diseases
Canadian institutionsUniversity of Waterloo
FundersFaculty of Science, Prince of Songkla UniversityNatural Sciences and Engineering Research Council of CanadaGovernment of OntarioUniversity of WaterlooCanada Foundation for InnovationOntario Research Foundation
KeywordsButyrylcholinesteraseChemistryCholinesteraseIC50AntioxidantAcetylcholinesteraseCytotoxicityPharmacologyBiochemistryAchéViability assayEnzymeIn vitroBiology

Abstract

fetched live from OpenAlex

A group of novel fused tricyclic derivatives based on a pyrazino[1,2-a]indol-1(2H)-one ring scaffold possessing a C3 phenyl substituent were designed, synthesized and evaluated as multi-target-directed-ligands (MTDLs) for Alzheimer's disease (AD). The biochemical assays were carried out to determine their inhibition activity toward i) amyloid peptide aggregation (Aβ40 and Aβ42), ii) acetyl and butyrylcholinesterase (AChE and BuChE) enzyme inhibition and iii) evaluation of their antioxidant properties. These studies identified several 3-phenylpyrazino[1,2-a]indol-1(2H)-one derivatives that exhibited multi-targeting activity capable of preventing amyloid aggregation (Aβ40 and Aβ42 inhibition range ​= ​10–89.5% at 25 ​μM), inhibition of cholinesterase enzymes (AChE and BuChE IC50 range ​= ​1.6–21 ​μM) and antioxidant activity (24–55% inhibition at 25 ​μM). The lead compound 5i (3-(3,4-dimethoxyphenyl)pyrazino[1,2-a]indol-1(2H)-one), exhibited multi-targeting activity with excellent inhibition of Aβ40 and Aβ42 aggregation (85% and 90% inhibition at 25 ​μM), dual inhibition of human cholinesterase enzymes (hAChE IC50 ​= ​7.5 ​μM; hBuChE IC50 ∼ 15 ​μM) and antioxidant property (∼39% inhibition at 25 ​μM). Compound 5i did not exhibit toxicity in mouse HT22 mouse hippocampal neuronal cells at 25 ​μM. In addition, 5i was able to prevent Aβ42 mediated cytotoxicity in the mouse hippocampal neuronal HT22 ​cells (77% cell viability). In the in vitro PAMPA-BBB permeation assay, compound 5i and 5a showed permeability values Pe ​= ​2.25 ​× ​10−6 ​cm/s and 6.20 ​× ​10−6 ​cm/s respectively, suggesting their ability to get into brain. These structure-activity studies demonstrate that the fused tricyclic pyrazino[1,2-a]indol-1(2H)-one template is capable of binding to Aβ (Aβ40 and Aβ42), and human cholinesterase enzymes (hAChE and hBuChE), and that a C3 3,4-diOMe-phenyl is a novel Aβ-binding pharmacophore that can be incorporated in the design of anti-AD agents.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.002

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.041
GPT teacher head0.291
Teacher spread0.250 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations10
Published2022
Admission routes2
Has abstractyes

Explore more

Same venueEuropean Journal of Medicinal Chemistry ReportsSame topicCholinesterase and Neurodegenerative DiseasesFrench-language works237,207