Lucía Castillo
Spanish National Research Council
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Featured researches published by Lucía Castillo.
Journal of Chemical Ecology | 2008
Eleuterio Burgueño-Tapia; Lucía Castillo; Azucena González-Coloma; Pedro Joseph-Nathan
The sesquiterpene p-benzoquinone perezone (1), isolated from Perezia adnata var. alamani (Asteraceae), and its non-natural derivatives isoperezone (2), dihydroperezone (3), dihydroisoperezone (4), and anilidoperezone (5) were tested as antifeedants against the herbivorous insects Spodoptera littoralis, Leptinotarsa decemlineata, and Myzus persicae. Compounds 1–5 exhibited strong antifeedant activity against L. decemlineata and M. persicae, and elicited a low response by S. littoralis. Antifeedant activity on L. decemlineata and M. persicae increased when the hydroxyl group at C-3 in perezone (1) was changed to C-6 to give isoperezone (2). The same effect was found with hydrogenation of the double bond of the alkyl chain of (1) to yield dihydroperezone (3). In contrast, hydrogenation of this double bond in isoperezone (2) to give dihydroisoperezone (4) led to a reduction in antifeedant activity. Determination of the phytotoxic activity of 1–5 revealed that 3 had a significant inhibition effect on Lactuca sativa radicle length growth.
Phytochemistry Reviews | 2007
Carmen Rossini; Lucía Castillo; Andrés González
The head lice, Pediculus humanus capitis (Phthiraptera:Pediculidae), is an obligate ectoparasite of humans that causes pediculosis capitis, a nuisance for millions of people worldwide, with high prevalence in children. Pediculosis capitis has been treated by methods that include the physical remotion of lice, various domestic treatments and conventional insecticides. None of these methods render complete protection, and there is clear evidence for the evolution of resistance and cross-resistance to conventional insecticides. Non-toxic alternative options are hence needed for head lice treatment and/or prevention, and natural products from plants, especially essential oils (EOs), are good candidates for safer control agents that may provide good anti-lice activity and low levels of evolved resistance. A few EOs have been tested as repellents with promissory results, although often in vitro tests and clinical trials produce contradictory results. A handful of fixed extracts and several EOs and their individual components have also been tested as contact pediculicides or fumigants. The studies have focused mainly on plant families characterized for the production of EOs. While many EOs and individual compounds showed pediculicide activity, comparing results is difficult due to the diverse bioassay methodologies. Studies of anti-lice activity of individual EO components provide the basis for preliminary conclusions of structure–activity relationships, although no clear patterns can yet be drawn. We here attempt to provide a concise compilation of the available information on anti-lice activity of plant extracts and plant-derived compounds, which we hope may be of help for future developments in this area.
Phytochemistry | 2010
Lucía Castillo; Martina Díaz; Azucena González-Coloma; Andrés González; Eduardo Alonso-Paz; María Julia Bassagoda; Carmen Rossini
A bioassay-guided fractionation of leaf extracts from Clytostoma callistegioides (Cham.) Bureau ex Griseb. (Bignoniaceae) led to isolation of a natural mixture of four fatty acids with anti-insect activity against aphids. The compounds were identified by GC-MS as palmitic, stearic, linoleic and linolenic acids and quantified as their methyl esters. The anti-aphid activity of the natural mixture was traced to linolenic and linoleic acids, as shown by the settling inhibition activity of synthetic samples. Interestingly, the saturated acids (palmitic and stearic) tested alone stimulated settling on one of the tested aphids (Myzus persicae), but not on the other tested species (Rhopalosiphum padi). Although ubiquitous, none of these free acids have been previously reported in this Bignoniaceae species. The leaf surface chemistry, which is likely involved in modulating aphid settling behavior, was further investigated for the occurrence of lipophilic substances by histochemical staining. Short, stalked glandular trichomes, previously undescribed for this species, stained with osmium tetroxide and Sudan III, suggesting that the secretion of the defensive acids is related to these surface trichomes.
The Natural Products Journal | 2012
Martina Díaz; Lucía Castillo; Carmen E. Díaz; Azucena González-Coloma; Carmen Rossini
This work was supported by grants from Faculty of Chemistry (FQ), Uruguayan Technological Laboratory (LATU), CSIC-UR, Program for the Development of Basic Sciences (PEDECIBA) (grant PNUD- URU/06/004). Facundo Ibanez and Roberto Zoppolo from the Instituto Nacional de Investigacion Agropecuaria (INIA, Uruguay) provided de limonin standard.
Zeitschrift für Naturforschung C | 2008
Eleuterio Burgueño-Tapia; Azucena González-Coloma; Lucía Castillo; Pedro Joseph-Nathan
The insect antifeedant and toxic activity of hydroxyperezone (1), its derivatives 2-9, along with 3-hydroxy- (10) and 6-hydroxythymoquinone (11) were studied against Spodoptera littoralis, Leptinotarsa decemlineata, and Myzus persicae. The antifeedant tests showed that L. decemlineata was the most sensitive insect, followed by M. persicae, while S. littoralis was not deterred by compounds 1-11. Leucohydroxyperezone tetraacetate (3), oxoperezinone (6), dihydroleucoperezinone diacetate (7), 3-hydroxy- (10) and 6-hydroxythymoquinone (11) showed strong activity against L. decemlineata. 1 and 7 exhibited moderate deterrent activity against M. persicae, while 1 and dihydroleucohydroxyperezone tetraacetate (4) acted as postingestive antifeedants to S. littoralis. The phytotoxic activity of compounds 1-11 was also evaluated. Hydroxyperezone (1) strongly inhibited seed germination at 24 h, while the activity of 3-8 and 10 was moderate. The level of radicle growth inhibition obtained with compounds 1-5 and 8-11 was significant (< 50%)
Biochemical Systematics and Ecology | 2008
Jesús M. Rodilla; Maria Teresa Tinoco; Julio Cruz Morais; Cristina Giménez; Raimundo Cabrera; Darío Martín-Benito; Lucía Castillo; Azucena González-Coloma
Industrial Crops and Products | 2011
Jesús M. Rodilla; Lúcia Silva; N. Martinez; D. Lorenzo; D. Davyt; Lucía Castillo; Cristina Giménez; Raimundo Cabrera; Azucena González-Coloma; J. Zrostlíková; E. Dellacassa
Journal of Plant Protection Research | 2015
Martina Díaz; Carmen E. Díaz; Ricardo Guillermo Álvarez; Andrés González; Lucía Castillo; Azucena González-Coloma; Gustavo Seoane; Carmen Rossini
Advances in Biological Chemistry | 2014
Martina Díaz; Lucía Castillo; Carmen E. Díaz; Ricardo Guillermo Álvarez; Azucena González-Coloma; Carmen Rossini
Industrial Crops and Products | 2013
Lucía Castillo; Martina Díaz; Azucena González-Coloma; Carmen Rossini