Luis Miguel Bedoya

Prof. Dr. Luis Miguel Bedoya

Farmacologia, Farmacognosia y Botánica, Universidad Complutense de Madrid, Madrid, Spain
orcid

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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2 March 2012 in Molecules
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Journal Article
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MAMaria Jose Abad
Maria Jose Abad
LBLuis Miguel Bedoya
Luis Miguel Bedoya
Luis APAZA TICONALuis APAZA TICONA
Luis APAZA TICONA
PBPaulina Bermejo Benito
Paulina Bermejo Benito
Numerous members of the Anthemideae tribe are important as cut flowers and ornamental crops, as well as being medicinal and aromatic plants, many of which produce essential oils used in folk and modern medicine and in the cosmetics and pharmaceutical industry. Essential oils generally have a broad spectrum of bioactivity, owing to the presence of several active ingredients that work through various modes of action. Due to their mode of extraction, mostly by distillation from aromatic plants, they contain a variety of volatile molecules such as terpenes, phenol-derived aromatic and aliphatic components. The large genus Artemisia L., from the tribe Anthemideae, comprises important medicinal plants which are currently the subject of phytochemical attention due to their biological and chemical diversity. Artemisia species, widespread throughout the world, are one of the most popular plants in Chinese traditional preparations and are frequently used for the treatment of diseases such as malaria, hepatitis, cancer, inflammation and infections by fungi, bacteria and viruses. Extensive studies of the chemical components of Artemisia have led to the identification of many compounds as well as essentials oils. This review summarizes some of the main reports on the chemistry and anti-infective activities of Artemisia. Li. essential oils from the data in the recent literature (2000–2011).

1 May 2010 in Bioorganic & Medicinal Chemistry Letters
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Journal Article
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PGPaolo Di Gianvincenzo
Paolo Di Gianvincenzo
MMMarco Marradi
Marco Marradi
OMOlga María Martínez-Ávila
Olga María Martínez-Ávila
LBLuis Miguel Bedoya
Luis Miguel Bedoya
JAJosé Alcami
José Alcami
SPSoledad Penadés
Soledad Penadés

13 July 2009 in ChemBioChem
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Journal Article
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OMOlga Martínez‐Ávila
Olga Martínez‐Ávila
LBLuis Miguel Bedoya
Luis Miguel Bedoya
MMMarco Marradi
Marco Marradi
CCCaroline Clavel
Caroline Clavel
JAJosé Alcami
José Alcami
SPSoledad Penadés
Soledad Penadés

1 July 2008 in Mini-Reviews in Medicinal Chemistry
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Journal Article
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MAMaria Jose Abad
Maria Jose Abad
LBLuis Miguel Bedoya
Luis Miguel Bedoya
PBPaulina Bermejo Benito
Paulina Bermejo Benito
The marine environment has been shown to be the source of a great diversity of chemical structures with promising biological activities. The isolation, biological evaluation, chemical properties and synthetic elaborations of the products of marine organisms and microorganisms have attracted the attention of organic chemists, medicinal chemists, biologists and pharmacists. Marine organisms and microorganisms have provided a large proportion of the natural antiinflammatory products over the last years. Marine organisms include green algae, brown algae, red algae, sponges, coelenterates, bryozoans, molluscs, tunicates, echinoderms, miscellaneous marine organisms and marine microorganisms and phytoplankton. This review describes current progress in the development of a selection of new anti-inflammatory agents from marine sources. The chemistry and biological evaluation are discussed.

2 August 2012 in Molecules
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Journal Article
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DADionisio Antonio Olmedo Agudo
Dionisio Antonio Olmedo Agudo
RSRocío Sancho
Rocío Sancho
LBLuis Miguel Bedoya
Luis Miguel Bedoya
JLJosé Luis López-Pérez
José Luis López-Pérez
EOEsther Del Olmo
Esther Del Olmo
AFArturo San Feliciano
Arturo San Feliciano
We have synthesized fourteen 3-phenylcoumarin derivatives and evaluated their anti-HIV activity. Antiviral activity was assessed on MT-2 cells infected with viral clones carrying the luciferase gene as reporter. Inhibition of HIV transcription and Tat function were tested on cells stably transfected with the HIV-LTR and Tat protein. Six compounds displayed NF-κB inhibition, four resulted Tat antagonists and three of them showed both activities. Three compounds inhibited HIV replication with IC50 values < 25 µM. The antiviral effect of the 4-hydroxycoumarin derivative 19 correlates with its specific inhibition of Tat functions, while compound 8, 3-(2-chlorophenyl)coumarin, seems to act through a mechanism unrelated to the molecular targets considered in this research.

1 September 2010 in Antiviral Research
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Journal Article
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LBLuis Miguel Bedoya
Luis Miguel Bedoya
MAMaría José Abad
María José Abad
ECEsther Calonge
Esther Calonge
LSLuis Astudillo Saavedra
Luis Astudillo Saavedra
MCMargarita Gutierrez C.
Margarita Gutierrez C.
PBPaulina Bermejo Benito
Paulina Bermejo Benito