Synthesis and evaluation of quinonoid compounds against tumor cell lines.
| dc.Type | Article | pt_BR |
| dc.contributor.author | Silva Júnior, Eufrânio Nunes da | |
| dc.contributor.author | Cavalcanti, Bruno Coelho | |
| dc.contributor.author | Guimarães, Tiago Teixeira | |
| dc.contributor.author | Pinto, Maria do Carmo Freire Ribeiro | |
| dc.contributor.author | Cabral, Igor | |
| dc.contributor.author | Pessoa, Claudia do Ó | |
| dc.contributor.author | Lotufo, Leticia Veras Costa | |
| dc.contributor.author | Moraes Filho, Manoel Odorico de | |
| dc.contributor.author | Andrade, Carlos Kleber Zago de | |
| dc.contributor.author | Santos, Marcelo Rodrigues dos | |
| dc.contributor.author | Simone, Carlos Alberto de | |
| dc.contributor.author | Pinto, Antonio Ventura | |
| dc.contributor.author | Goulart, Marilia Oliveira Fonseca | |
| dc.date.accessioned | 2022-07-05T17:07:01Z | |
| dc.date.available | 2022-07-05T17:07:01Z | |
| dc.date.issued | 2011 | |
| dc.description | p. 399-410.: il. p&b. | |
| dc.description.abstract | Thirty two compounds were synthesized in moderate to high yields and showed activity against cancer cells HL-60 (leukemia), MDA-MB435 (melanoma), HCT-8 (colon) and SF295 (central nervous system), with IC50 below 2 mM for some compounds. The b-lapachone-based 1,2,3-triazoles showed the best cytoxicity profile and emerge as promising anticancer prototypes. Insights about the reactive oxygen species (ROS) mechanism of anticancer action for some compounds were obtained by addition of 1-bromoheptane that deplete reduced glutathione (GSH) content and by using N-acetylcysteine that protects cells against apoptotic cellular death, as well by analysis of thiobarbituric acid reactive substances (TBARS) formation, and oxidative DNA damage after treatment detected by the comet assay with the bacterial enzymes formamidopyrimidine DNA-glycosylase (FPG) and endonuclease III (ENDOIII). | |
| dc.identifier.citation | SILVA JÚNIOR, Eufrânio Nunes da et al. Synthesis and evaluation of quinonoid compounds against tumor cell lines. European Journal of Medicinal Chemistry, v. 46, p. 399-410, 2011. | |
| dc.identifier.uri | http://sr-vmlxaph03:8080/jspui/handle/123456789/8658 | |
| dc.publisher | European Journal of Medicinal Chemistry | pt_BR |
| dc.subject | Naftoquinonas | pt_BR |
| dc.subject | Naphthoquinones | pt_BR |
| dc.subject | Neoplasias | pt_BR |
| dc.subject | Neoplasms | pt_BR |
| dc.subject | Linhagem Celular Tumoral | pt_BR |
| dc.subject | Cell Line, Tumor | pt_BR |
| dc.subject | Citotoxinas | pt_BR |
| dc.subject | Cytotoxins | pt_BR |
| dc.subject | Línea Celular Tumoral | |
| dc.title | Synthesis and evaluation of quinonoid compounds against tumor cell lines. | pt_BR |
Files
Original bundle
1 - 1 of 1
Loading...
- Name:
- Synthesis and evaluation of quinonoid compounds against tumor cell lines..pdf
- Size:
- 1.05 MB
- Format:
- Adobe Portable Document Format
- Description:
License bundle
1 - 1 of 1
Loading...
- Name:
- license.txt
- Size:
- 1.6 KB
- Format:
- Item-specific license agreed upon to submission
- Description: