Cristina Nogueira

Dr. Cristina Nogueira


Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 November 2004 in Chemical Reviews
Verified
Journal Article
Closed access
CNCristina Nogueira
Cristina Nogueira
GZGilson Zeni
Gilson Zeni
João RochaJoão Rocha
João Rocha

1 July 2011 in Archives of Toxicology
Verified
Journal Article
Closed access
PDF file
CNCristina Nogueira
Cristina Nogueira
João RochaJoão Rocha
João Rocha

1 February 2005 in Neurochemical Research
Verified
Journal Article
Closed access
PDF file
RPRobson L. Puntel
Robson L. Puntel
CNCristina Nogueira
Cristina Nogueira
João RochaJoão Rocha
João Rocha

1 April 2021 in Archives of Toxicology
Verified
Journal Article
Closed access
PDF file
CNCristina Nogueira
Cristina Nogueira
NBNilda V. Barbosa
Nilda V. Barbosa
João RochaJoão Rocha
João Rocha

1 February 2003 in Inflammation Research
Verified
Journal Article
Closed access
PDF file
CNCristina Nogueira
Cristina Nogueira
EQE. B. Quinhones
E. B. Quinhones
EJE. A. C. Jung
E. A. C. Jung
GZG. Zeni
G. Zeni
João RochaJoão Rocha
João Rocha

1 January 2010 in Journal of the Brazilian Chemical Society
Verified
Journal Article
Open access
PDF file
CNCristina Nogueira
Cristina Nogueira
João RochaJoão Rocha
João Rocha
In this review, we summarized the potential role of synthetic organoseleno compounds as therapeutic or toxic agents, giving emphasis almost exclusively to diphenyl diselenide, the simplest of the diaryl diselenides, and some of its analogs. We presented the main molecular aspects related to the in vitro toxicity and pharmacology of diphenyl diselenide and also provided in vivo data indicating that the interaction of diphenyl diselenide with thiols can dictate either its toxicological or pharmacological property. The papers covered in this review indicate that a limited activation of the "toxic pathway", i.e., a controlled oxidation of specific high molecular weight thiol-containing molecules could contribute to the pharmacological effects of diphenyl diselenide. In conclusion, this review reinforces the necessity of developing new diorganoyl diselenides that could interact with specific molecular targets.