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
Bibliographic record
Abstract
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.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot 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.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.001 | 0.000 |
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.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
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".