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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Pingaew R. | |
dc.contributor.author | Worachartcheewan A. | |
dc.contributor.author | Prachayasittikul V. | |
dc.contributor.author | Prachayasittikul S. | |
dc.contributor.author | Ruchirawat S. | |
dc.contributor.author | Prachayasittikul V. | |
dc.date.accessioned | 2021-04-05T03:32:46Z | - |
dc.date.available | 2021-04-05T03:32:46Z | - |
dc.date.issued | 2013 | |
dc.identifier.issn | 15701808 | |
dc.identifier.other | 2-s2.0-84887864374 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13968 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84887864374&doi=10.2174%2f15701808113109990004&partnerID=40&md5=a3eee064f49f651dd797425acaef207d | |
dc.description.abstract | Metal complexes of 8-aminoquinoline (8AQ) derivatives were reported. This study presents a series of synthesized transition metal complexes of mixed ligands 8AQ-5-iodouracils (1-3) and 8AQ-5-nitrouracil (4-6) which have been investigated for their antioxidative and cytotoxic activities, as well as, powder X-ray diffraction patterns. Ni complex of 8AQ-5-nitrouracil (6) exerted significant cytotoxicity against MOLT-3 cell and superoxide scavenging activity. The results demonstrate an application of 8AQ molecule as a potential ligand for new bioactive compounds. ©2013 Bentham Science Publishers. | |
dc.subject | 8 aminoquinoline derivative | |
dc.subject | copper complex | |
dc.subject | doxorubicin | |
dc.subject | etoposide | |
dc.subject | ligand | |
dc.subject | manganese derivative | |
dc.subject | metal complex | |
dc.subject | nickel complex | |
dc.subject | reactive nitrogen species | |
dc.subject | reactive oxygen metabolite | |
dc.subject | superoxide | |
dc.subject | superoxide dismutase | |
dc.subject | transition element | |
dc.subject | uracil derivative | |
dc.subject | antioxidant activity | |
dc.subject | article | |
dc.subject | cancer cell culture | |
dc.subject | complex formation | |
dc.subject | controlled study | |
dc.subject | drug cytotoxicity | |
dc.subject | drug synthesis | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | IC 50 | |
dc.subject | infrared spectroscopy | |
dc.subject | priority journal | |
dc.subject | structure activity relation | |
dc.subject | X ray powder diffraction | |
dc.title | Transition metal complexes of 8-aminoquinoline-5-substituted uracils with antioxidative and cytotoxic activities | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Letters in Drug Design and Discovery. Vol 10, No.9 (2013), p.859-864 | |
dc.identifier.doi | 10.2174/15701808113109990004 | |
Appears in Collections: | Scopus 1983-2021 |
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