# Structural Descriptors and Antioxidant Activity Markers of 4-[4-(2-Aminoethoxy)benzyl]aniline

**Authors:** Dmitry A. Filimonov, Alexander B. Eresko, Nadezhda N. Trubnikova, Irina A. Kisilenko, Margarita A. Belotserkovskaya, Elena V. Raksha, Roman V. Ishchenko, Dorota M. Chudoba

PMC · DOI: 10.3390/antiox15020256 · Antioxidants · 2026-02-17

## TL;DR

This study explores how a thyronamine analogue, ABA, affects antioxidant activity and neurological outcomes in a rat model of brain ischemia.

## Contribution

The paper introduces new insights into the antioxidant and neuroprotective mechanisms of ABA in acute cerebral ischemia.

## Key findings

- ABA administration significantly altered redox markers like malondialdehyde and superoxide dismutase in ischemic brain regions.
- ABA reduced neurological deficits in rats compared to untreated controls.
- DFT calculations were used to model ABA's structural forms and their antioxidant properties.

## Abstract

The release of reactive oxygen species accompanying oxidative stress is one of the most significant damaging mechanisms during brain ischemia. Some aspects of the neuroprotective activity of the thyronamine T0AM synthetic analogue, 4-[4-(2-aminoethoxy)benzyl]aniline (ABA), were studied and discussed in two independent experiments using a model of acute cerebral ischemia. Antioxidant effects were evaluated in adult male and female Wistar rats (Rattus norvegicus), while neurological outcomes were assessed in adult male outbred white rats. Administration of the ABA in a rat brain hemisphere ischemia model was associated with significant changes in redox markers: malondialdehyde, glutathione peroxidase and superoxide dismutase levels in the ischemic hemisphere. Also, the introduction of ABA into the model of acute cerebral ischemia contributed to a reduction in neurological deficit compared to untreated controls. It was revealed that the considered thyronamine T0AM analogue could control redox status in acute brain ischemia. Mono protonated form of ABA (ABA-H+) is considered to be the main species at pH 6.9–7.2. Structural models of the neutral (ABA), protonated (ABA-H+) thyronamine and its solvate (DMSO…ABA-H+) were used in DFT calculations, followed by estimation of molecular and supramolecular level descriptors.

## Linked entities

- **Chemicals:** 4-[4-(2-aminoethoxy)benzyl]aniline (PubChem CID 91938080), ABA (PubChem CID 287291), malondialdehyde (PubChem CID 10964), DMSO (PubChem CID 679)
- **Diseases:** brain ischemia (MONDO:0005299)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, Sod1 (superoxide dismutase 1, soluble) [NCBI Gene 20655] {aka B430204E11Rik, Cu/Zn-SOD, CuZnSOD, Ipo-1, Ipo1, SODC}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, Sod2 (superoxide dismutase 2, mitochondrial) [NCBI Gene 20656] {aka MnSOD, Sod-2}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, Aifm1 (apoptosis inducing factor, mitochondria associated 1) [NCBI Gene 83533] {aka Aif, Pdcd8}, Parp1 (poly (ADP-ribose) polymerase 1) [NCBI Gene 25591] {aka ARTD1, Adprt, Parp-1}
- **Diseases:** Alzheimer's-type dementia (MESH:D000544), Acute cerebral ischemia (MESH:D002545), neuroinflammation (MESH:D000090862), injury to (MESH:D014947), neurodegeneration (MESH:D019636), inflammatory (MESH:D007249), pain (MESH:D010146), ischemia (MESH:D007511), Neurological Deficit (MESH:D009461), acute (MESH:D000208), acute ischemic stroke (MESH:D000083242), muscle status (MESH:D013226), hypothermic effect (MESH:D065606), Stroke (MESH:D020521), ischemic injury (MESH:D017202), IS (MESH:D002544), toxicity (MESH:D064420), OS (MESH:D000079225), ischemic brain injury (MESH:D001930), ischemic brain damage (MESH:D001925), cognitive decline (MESH:D003072), Neuronal (MESH:D009410), abnormal movement (MESH:D004409)
- **Chemicals:** tert-butyl hydroperoxide (MESH:D020122), choline (MESH:D002794), TMS (MESH:C073196), quercetin (MESH:D011794), N (MESH:D009584), HOCl (MESH:D006997), carbon (MESH:D002244), lipid hydroperoxides (MESH:D008054), adrenaline (MESH:D004837), selenols (MESH:C442270), 3-Iodothyronamine (MESH:C487948), ABA (MESH:D000040), NaCl (MESH:D012965), thyronamine (MESH:C004547), O (MESH:D010100), NH3 (MESH:D000641), 5,5'-dithiobis-2-nitrobenzoic acid (MESH:D004228), 13C (MESH:C000615229), hydroxyl (MESH:D017665), aniline (MESH:C023650), H2O (MESH:D014867), ethylamine (MESH:C041564), TBA (MESH:C029684), acetylcholine (MESH:D000109), peroxide (MESH:D010545), adrenochrome (MESH:D000323), Cl (MESH:D002713), MDA (MESH:D008315), superoxide (MESH:D013481), ( OH) (-), H2O2 (MESH:D006861), polyunsaturated fatty acids (MESH:D005231), thiobarbituric acid reactive substances (MESH:D017392), RNS (MESH:D011886), H (MESH:D006859), chlorogenic acid (MESH:D002726), DMSO (MESH:D004121), ROS (MESH:D017382), GSH (MESH:D005978), 3-iodothyroacetic acid (MESH:C000597002), CO2 (MESH:D002245), Lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus (rat, genus) [taxon 10114], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Gerbillinae (gerbils, subfamily) [taxon 10045]

## Full text

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## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938765/full.md

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Source: https://tomesphere.com/paper/PMC12938765