Novel synthesis of palladium (II) complexes derived from 3-arylsydnone-4-carbaldehyde N(4)-phenylthiosemicarbazones and biological activity. (25th October 2013)
- Record Type:
- Journal Article
- Title:
- Novel synthesis of palladium (II) complexes derived from 3-arylsydnone-4-carbaldehyde N(4)-phenylthiosemicarbazones and biological activity. (25th October 2013)
- Main Title:
- Novel synthesis of palladium (II) complexes derived from 3-arylsydnone-4-carbaldehyde N(4)-phenylthiosemicarbazones and biological activity
- Authors:
- Shih, Mei-Hsiu
Chen, Jian-Chyi
Lin, Guan-Ling
Lin, Tzu-Ting
Sun, Ming-Hsiang - Abstract:
- Abstract: Objectives: The aim of this research is to investigate whether the oxygen atom O(6) in the sydnone ring of 3-arylsydnone-4-carbaldehyde N(4)-phenylthiosemicarbazones (HArSYTSCs, 3a–d) is a good electron donor atom upon metal complexation. Furthermore, ligands 3a–d and the corresponding palladium complexes (Pd(ArSYTSC)Cl, 4a–d) would be expected to find their potent biological activities. Methods: The desired palladium complexes 4a–d were first synthesized from thiosemicarbazones 3a–d. Then, the antiproliferative activity of ligands 3a–d and complexes 4a-d were tested against human hepatocellular carcinoma and human cervical epithelioid carcinoma (HeLa) cells by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl trazolium bromide (MTT) assay. Key findings: According to X-ray analyses, ligands 3a–d are bonded to the Pd (II) center in an O, N, S-tridentate coordination mode through sydnone carbonyl oxygen O(6), azomethine nitrogen and the thiolate sulfur atom. The carbonyl oxygen of the sydnone ring is found to be a good electron donor site upon metal complexation. Moreover, MTT assay results reveal that the palladium complexes 4a–d have greater antiproliferative activity than 5-fluorouracil. In particular, the complexes exhibit obvious better activity than the corresponding ligands 3a–d against HeLa cell. Conclusions: The results indicate that the synthesized novel palladium complexes have greater antiproliferative activity than both 5-fluorouracil and the correspondingAbstract: Objectives: The aim of this research is to investigate whether the oxygen atom O(6) in the sydnone ring of 3-arylsydnone-4-carbaldehyde N(4)-phenylthiosemicarbazones (HArSYTSCs, 3a–d) is a good electron donor atom upon metal complexation. Furthermore, ligands 3a–d and the corresponding palladium complexes (Pd(ArSYTSC)Cl, 4a–d) would be expected to find their potent biological activities. Methods: The desired palladium complexes 4a–d were first synthesized from thiosemicarbazones 3a–d. Then, the antiproliferative activity of ligands 3a–d and complexes 4a-d were tested against human hepatocellular carcinoma and human cervical epithelioid carcinoma (HeLa) cells by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl trazolium bromide (MTT) assay. Key findings: According to X-ray analyses, ligands 3a–d are bonded to the Pd (II) center in an O, N, S-tridentate coordination mode through sydnone carbonyl oxygen O(6), azomethine nitrogen and the thiolate sulfur atom. The carbonyl oxygen of the sydnone ring is found to be a good electron donor site upon metal complexation. Moreover, MTT assay results reveal that the palladium complexes 4a–d have greater antiproliferative activity than 5-fluorouracil. In particular, the complexes exhibit obvious better activity than the corresponding ligands 3a–d against HeLa cell. Conclusions: The results indicate that the synthesized novel palladium complexes have greater antiproliferative activity than both 5-fluorouracil and the corresponding ligands against HeLa cell. Accordingly, the study of sydnonyl complexes bearing anticancer activities may support the development of coordination chemistry. … (more)
- Is Part Of:
- Journal of pharmacy and pharmacology. Volume 66:Number 1(2014:Jan.)
- Journal:
- Journal of pharmacy and pharmacology
- Issue:
- Volume 66:Number 1(2014:Jan.)
- Issue Display:
- Volume 66, Issue 1 (2014)
- Year:
- 2014
- Volume:
- 66
- Issue:
- 1
- Issue Sort Value:
- 2014-0066-0001-0000
- Page Start:
- 73
- Page End:
- 83
- Publication Date:
- 2013-10-25
- Subjects:
- biological activity -- palladium complexes -- sydnones -- thiosemicarbazides -- thiosemicarbazones
Pharmacy -- Periodicals
Pharmacology -- Periodicals
615.1 - Journal URLs:
- https://academic.oup.com/jpp ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)2042-7158 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.ingentaconnect.com/content/rpsgb/jpp ↗ - DOI:
- 10.1111/jphp.12157 ↗
- Languages:
- English
- ISSNs:
- 0022-3573
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5034.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22685.xml