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1.
Plants (Basel) ; 11(22)2022 Nov 09.
Article in English | MEDLINE | ID: mdl-36432757

ABSTRACT

This field study aimed to assess the baseline conditions of a long-term shooting range in Argentina polluted with 428 mg kg-1 lead (Pb) to evaluate the establishment and development of Helianthus petiolaris plants and address the efficacy of the phytomanagement strategy through: (i) element accumulation in plant tissues; (ii) rhizosphere bacterial diversity changes by Illumina Miseq™, and (iii) floral water and essential oil yield, composition, and element concentration by GC-MS and ICP. After one life cycle growing in the polluted sites, in the roots of Helianthus petiolaris plants, Pb concentration was between 195 and 304 mg kg-1 Pb. Only a limited fraction of the Pb was translocated to the aerial parts. The predominance of the genus Serratia in the rhizosphere of Helianthus petiolaris plants cultivated in the polluted sites and the decrease in the essential oil yield were some effects significantly associated with soil Pb concentration. No detectable Pb concentration was found in the floral water and essential oil obtained. Extractable Pb concentration in the soil reduced between 28% and 45% after the harvest.

2.
Molecules ; 10(11): 1369-76, 2005 Nov 30.
Article in English | MEDLINE | ID: mdl-18007532

ABSTRACT

R,R'-disubstituted sulfoximines were phosphorylated with O,O-diethylchloro phosphate and phosphorothionate to obtain new organophosphorus compounds. After purification they were characterized by GC-MS and (1)H-NMR. The toxicity of the synthesized O,O-diethyl N-(R,R'-disubstituted sulfoximine) phosphoro-amidothionates was assayed on Musca domestica. It was found that the methyl phenyl derivative was the most toxic compound, followed by the dipropyl and dibutyl derivatives. The dihexyl compound was the less toxic of all the assayed compounds, being one hundred times less toxic than a paraoxon standard The anticholinesterasic activity of the corresponding phosphoramidates was assayed on homogenates of house flies' heads, giving values similar to paraoxon for the methyl phenyl derivative.


Subject(s)
Buthionine Sulfoximine/chemistry , Enzyme Inhibitors/pharmacology , Methionine Sulfoximine/chemistry , Organophosphorus Compounds/chemical synthesis , Acetylcholinesterase/chemistry , Acetylcholinesterase/metabolism , Animals , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/chemistry , Gas Chromatography-Mass Spectrometry , Houseflies , Magnetic Resonance Spectroscopy , Models, Molecular , Molecular Structure , Organophosphorus Compounds/chemistry , Organophosphorus Compounds/pharmacology , Phosphorylation , Structure-Activity Relationship
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