Publication: Design, Stereoselective Synthesis, Computational Studies and Cholinesterase Inhibitory Activity of Novel Spiropyrrolidinoquinoxaline Tethered Indole Hybrid Heterocycle
| dc.authorscopusid | 8351597600 | |
| dc.authorscopusid | 6603003502 | |
| dc.authorscopusid | 36100384200 | |
| dc.authorscopusid | 57208244523 | |
| dc.authorscopusid | 7801614849 | |
| dc.authorscopusid | 40761083300 | |
| dc.authorscopusid | 57201886418 | |
| dc.authorwosid | N, Dege/B-2545-2016 | |
| dc.authorwosid | Kansız, Sevgi/Aaq-1908-2020 | |
| dc.authorwosid | Kumar, Yeswanth/Kii-9701-2024 | |
| dc.authorwosid | Dege, Necmi/B-2545-2016 | |
| dc.authorwosid | Thota, Sai Manohar/Aaz-9546-2021 | |
| dc.authorwosid | Kumar, Raju Suresh/Abc-7605-2020 | |
| dc.authorwosid | Almansour, Abdulrahman/Aay-8328-2021 | |
| dc.contributor.author | Arumugam, Natarajan | |
| dc.contributor.author | Almansour, Abdulrahman I. | |
| dc.contributor.author | Kumar, Raju Suresh | |
| dc.contributor.author | Yeswanthkumar, Santhakumar | |
| dc.contributor.author | Padmanaban, Ramanathan | |
| dc.contributor.author | Arun, Yuvaraj | |
| dc.contributor.author | Venketesh, S. | |
| dc.contributor.authorID | N, Dege/0000-0003-0660-4721 | |
| dc.contributor.authorID | Arun, Y/0000-0002-2258-9667 | |
| dc.contributor.authorID | Santhakumar, Yeswanth Kumar/0000-0003-3710-9205 | |
| dc.contributor.authorID | Ramanathan, Padmanaban/0000-0003-1947-1868 | |
| dc.contributor.authorID | Sivaramakrishnan, Venketesh/0000-0003-3094-5905 | |
| dc.contributor.authorID | Thota, Sai Manohar/0000-0003-1710-5645 | |
| dc.contributor.authorID | Sivaperumal, Sivaramakrishnan/0000-0002-1075-1014 | |
| dc.date.accessioned | 2025-12-11T01:40:23Z | |
| dc.date.issued | 2021 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Arumugam, Natarajan; Almansour, Abdulrahman I.; Kumar, Raju Suresh] King Saud Univ, Coll Sci, Dept Chem, POB 2455, Riyadh 11451, Saudi Arabia; [Yeswanthkumar, Santhakumar; Padmanaban, Ramanathan] Pondicherry Univ, Sch Phys Chem & Appl Sci, Dept Chem, Kalapet 605014, Puducherry, India; [Arun, Yuvaraj] CSIR Cent Leather Res Inst, Organ & Bioorgan Chem Lab, Chennai 600020, Tamil Nadu, India; [Kansiz, Sevgi] Samsun Univ, Fac Engn, Dept Fundamental Sci, TR-55420 Samsun, Turkey; [Dege, Necmi] Ondokuz Mayis Univ, Fac Arts & Sci, Dept Phys, TR-55139 Samsun, Turkey; [Manohar, Thota Sai; Venketesh, S.] Sri Sathya Sai Inst Higher Learning, Dept Biosci, Prasanthinilayam 515134, AP, India | en_US |
| dc.description | N, Dege/0000-0003-0660-4721; Arun, Y/0000-0002-2258-9667; Santhakumar, Yeswanth Kumar/0000-0003-3710-9205; Ramanathan, Padmanaban/0000-0003-1947-1868; Sivaramakrishnan, Venketesh/0000-0003-3094-5905; Thota, Sai Manohar/0000-0003-1710-5645; Arumugam, Natarajan/0000-0001-9073-155X; Raju, Suresh Kumar/0000-0003-3754-4223; Sivaperumal, Sivaramakrishnan/0000-0002-1075-1014 | en_US |
| dc.description.abstract | A facile eco-friendly approach for the regioand stereoselective synthesis of structurally intriguing novel spiropyrrolidinoquinoxaline tethered indole hybrid heterocycle has been accomplished via a cascade reaction sequence involving 1,3-dipolar cycloaddition as the key step. Structural elucidation of the synthesized spiroheterocycle was performed by NMR spectroscopy, mass spectrometric analysis and the stereochemistry of asymmetric carbons have been confirmed by single crystal X-ray diffraction analysis. The mechanistic rationalization for the formation of spiroheterocyclic hybrid was investigated through density functional theory (DFT) calculations. In addition, the synthesized spiroheterocyclic hybrid was tested for its cholinesterase inhibitory activity against ChEs and displayed good activity when compared to the standard drug galantamine. (C) 2020 Elsevier B.V. All rights reserved. | en_US |
| dc.description.sponsorship | King Saud University, Riyadh, Saudi Arabia [RSP-2020/231]; Ondokuz Mayis University [PYO.FEN.1906.19.001] | en_US |
| dc.description.sponsorship | The project was supported by Researchers Supporting Project number (RSP-2020/231), King Saud University, Riyadh, Saudi Arabia. This study was supported by Ondokuz Mayis University under project No. PYO.FEN.1906.19.001. | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded | |
| dc.identifier.doi | 10.1016/j.molstruc.2020.129165 | |
| dc.identifier.issn | 0022-2860 | |
| dc.identifier.issn | 1872-8014 | |
| dc.identifier.scopus | 2-s2.0-85090123827 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.uri | https://doi.org/10.1016/j.molstruc.2020.129165 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/45328 | |
| dc.identifier.volume | 1225 | en_US |
| dc.identifier.wos | WOS:000596475500001 | |
| dc.identifier.wosquality | Q2 | |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier | en_US |
| dc.relation.ispartof | Journal of Molecular Structure | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Spiropyrrolidines | en_US |
| dc.subject | Quinoxalinone | en_US |
| dc.subject | 1,3-Dipolar Cycloaddition, DFT Calculation | en_US |
| dc.subject | X-Ray Diffraction Analysis | en_US |
| dc.subject | Molecular Docking Simulation | en_US |
| dc.title | Design, Stereoselective Synthesis, Computational Studies and Cholinesterase Inhibitory Activity of Novel Spiropyrrolidinoquinoxaline Tethered Indole Hybrid Heterocycle | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
