| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Pansuriya, K. | - |
| dc.contributor.author | Lalpara, J. N. | - |
| dc.contributor.author | Hadiyal, S. D. | - |
| dc.contributor.author | Dhaduk, B. B. | - |
| dc.contributor.author | Dubal, G. G | - |
| dc.date.accessioned | 2024-11-18T11:29:57Z | - |
| dc.date.available | 2024-11-18T11:29:57Z | - |
| dc.date.issued | 2022 | - |
| dc.identifier.citation | Pansuriya, K., Lalpara, J. N., Hadiyal, S. D., Dhaduk, B. B., & Dubal, G. G. (2022). Phenylboronic acid catalyzed synthesis of polysubstituted 1, 4-dihydropyridine derivatives as promising antioxidant agents correlated with molecular docking. Chemical Data Collections, 42, 100946. | en_US |
| dc.identifier.uri | http://10.9.150.37:8080/dspace//handle/atmiyauni/1649 | - |
| dc.description.abstract | A series of polysubstituted 1, 4-dihydropyridines (4a-i) were designed and developed using Ph-B (OH) 2 catalyst. Further, compounds were confirmed by various spectroscopic techniques. After that all compounds were studied for molecular docking against the human peroxidase enzyme (1PRX). Results of docking revealed that many compounds exhibited low binding score. To get a reference from the docking study, all synthesized molecules were evaluated for in vitro antioxidant assay using DPPH, H 2 O 2 … | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Chemical Data Collections | en_US |
| dc.subject | 1,4-dihydropyridine | en_US |
| dc.subject | Boronic acid catalyzed | en_US |
| dc.subject | Antioxidants | en_US |
| dc.subject | Molecular docking | en_US |
| dc.subject | Hantzsch synthesis | en_US |
| dc.title | Phenylboronic acid catalyzed synthesis of polysubstituted 1,4-dihydropyridine derivatives as promising antioxidant agents correlated with molecular docking | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | 01. Journal Articles | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Phenylboronic acid catalyzed synthesis of polysubstituted.pdf | 1.71 MB | Adobe PDF | View/Open |
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