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1.
Iquitos; s.n; 2016. 47 p. tab, graf.
Thesis in Spanish | LILACS, MOSAICO - Integrative health | ID: biblio-915218

ABSTRACT

Se evaluó la concentración de cadmio, plomo, mercurio y arsénico en la corteza de doce especies botánicas de la Amazonía Peruana, consideradas recursos terapéuticos, mediante absorción atómica. El cadmio y plomo fueron determinados por flama (SpectrAA,Varian AA 240); el mercurio con vapor frío (AAnalyst 300,Perkin Elmer) y el arsénicopor generación de hidruros (AAnalyst 300, Perkin Elmer).Los niveles encontrados en el caso de las especies: Tynanthuspanurensis (clavo huasca), Campsiandra angustifolia (Huacapurana) Abutarufescens (abuta), Anomospermunsp. (achunisanango) y Hymnaeaoblongfolia(azucarhuayro) sobrepasan los límites máximos permitidos para cadmio. Ninguna de las especies estudiadas sobrepasó los límites permitidos para plomo. De otro lado,Brosiunpotabile(tamamuri) fue la única de las especies estudiadas que sobrepasa los límites permitidos para mercurio. Para el caso del arsénico todas las especies registraron, concentraciones por encima de los límites máximos permitidos, en un rango entre1,07­ 8,19 µg/g.Se concluye que todas las cortezas vegetales estudiadas presentan mayores concentraciones de arsénico que lo permitido y el 50% de presentan un doble riesgo de toxicidad por su alto contenido de cadmio o mercurio.


Subject(s)
Plants, Medicinal , Metals, Heavy , Peru , Ethnobotany
2.
Nat Prod Commun ; 9(8): 1075-80, 2014 Aug.
Article in English | MEDLINE | ID: mdl-25233577

ABSTRACT

Twenty-three indole alkaloids were isolated from Aspidosperma desmanthum and A. spruceanum. Alkaloids 1-4 were isolated from the leaves, 5-8 from the stem bark and 9-15 from the root bark of A. desmanthum. Alkaloids 5, 11, 16, 17 and 19 were isolated from the stem bark, 18 and 20-22 from the root bark and 23 from the flowers of A. spruceanum. Compounds 4, 14, and 15 have not been previously reported as natural products while 16 and 20 have been isolated for the first time from the genus Aspidosperma. Their structures were determined by spectroscopic techniques including 1D and 2D NMR experiments (COSY, NOESY, HSQC, HMBC). The antiparasitic activity of these compounds was tested against Trypanosoma cruzi and Leishmania infantum and their non-specific cytotoxicity on mammalian cells. The most active compounds were 10, 12, 13, and 14 from A. desmanthum, and 19, 21 and 22 from A. spruceanum. Aspidolimine (10) aspidocarpine (12) and tubotaiwine (21) showed selective activity against L. infantum.


Subject(s)
Antiparasitic Agents , Aspidosperma , Plant Extracts , Secologanin Tryptamine Alkaloids , Animals , Humans , Antiparasitic Agents/chemistry , Antiparasitic Agents/isolation & purification , Antiparasitic Agents/pharmacology , Aspidosperma/chemistry , Brazil , Cell Line , CHO Cells , Cricetulus , Leishmania infantum/drug effects , Leishmaniasis, Visceral/parasitology , Magnetic Resonance Spectroscopy , Molecular Structure , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Secologanin Tryptamine Alkaloids/chemistry , Secologanin Tryptamine Alkaloids/isolation & purification , Secologanin Tryptamine Alkaloids/pharmacology
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