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Métodos Terapéuticos y Terapias MTCI
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1.
Nat Prod Commun ; 4(1): 109-14, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19370886

RESUMEN

The essential oil from the aerial parts of Stachys cretica L. subsp. smyrnaea Rech. fil. (Lamiaceae), endemic to Turkey, was investigated by using GC and GC-MS. Thirty-four of 37 components, represented 99.7% of the total oil, were identified. The major components of the essential oil were trans-beta-caryophyllene (51.0%), germacrene-D (32.8%), a-humulene (3.1%), delta-cadinene (2.1%) and delta-elemene (2.1%). The antimicrobial activity of the essential oil, trans-beta-caryophyllene and five different extracts of the aerial parts of S. cretica L. subsp. smyrnaea were investigated by the standard disc diffusion method. The essential oil and trans-beta-caryophyllene exhibited antibacterial and antifungal activities. The activity increased with increasing concentrations of the essential oil and the extracts. The essential oil showed antimicrobial activity, particularly against Pseudomonas aeruginosa and Bacillus subtilis. The extracts exhibited either moderate or no activity.


Asunto(s)
Antibacterianos/química , Antibacterianos/farmacología , Aceites Volátiles/química , Aceites Volátiles/farmacología , Aceites de Plantas/química , Aceites de Plantas/farmacología , Stachys/química , Bacterias/efectos de los fármacos , Cromatografía de Gases y Espectrometría de Masas
2.
Phytochemistry ; 67(19): 2170-5, 2006 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16860354

RESUMEN

From the roots of Delphinium linearilobum (Trautv.) N. Busch two new norditerpene alkaloids linearilobin and linearilin, and the known alkaloids lycoctonine, 14-acetyltalatizamine, browniine, cammaconine, talatizamine, and cochlearenine were isolated. Spectroscopic techniques were used for structure determination. Antioxidant activity was performed by DPPH and metal chelating activity assays.


Asunto(s)
Alcaloides/química , Delphinium/química , Diterpenos/química , Alcaloides/aislamiento & purificación , Quelantes/química , Quelantes/aislamiento & purificación , Diterpenos/aislamiento & purificación , Depuradores de Radicales Libres/química , Depuradores de Radicales Libres/aislamiento & purificación , Hierro/química , Espectroscopía de Resonancia Magnética/métodos , Estructura Molecular , Raíces de Plantas/química , Plantas Medicinales/química
3.
J Nat Prod ; 67(1): 118-21, 2004 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-14738403

RESUMEN

The three new triterpenes (1-3) and five known triterpenes and a sterol were isolated from the acetone extract of a Turkish collection of Salvia kronenburgii. The structures of the new triterpenes were established as 1beta,2alpha-dihydroxy-3beta-acetoxy-11-oxours-12-ene (1), 2alpha,20beta-dihydroxy-3beta-acetoxyurs-9(11),12-diene (2), and 1beta,2alpha-dihydroxy-3beta-acetoxyurs-9(11),12-diene (3) on the basis of spectral analyses, including 1D and 2D NMR and mass spectroscopy. It is probable that compounds 2 and 3 are artifacts from dehydration of the corresponding allylic alcohols. 1beta,2alpha,3beta,11alpha-Tetrahydroxyurs-12-ene (5), the most abundant compound in the extract, was found to be highly cytotoxic to renal, non-small cell lung, and breast cancer cell lines.


Asunto(s)
Antineoplásicos Fitogénicos/aislamiento & purificación , Plantas Medicinales/química , Salvia/química , Triterpenos/aislamiento & purificación , Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/farmacología , Línea Celular Tumoral , Ensayos de Selección de Medicamentos Antitumorales , Femenino , Humanos , Concentración 50 Inhibidora , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Estereoisomerismo , Triterpenos/química , Triterpenos/farmacología , Turquía
4.
Planta Med ; 68(9): 818-21, 2002 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12357394

RESUMEN

From the roots of Salvia eriophora (Lamiaceae), a new compound, 4,14-dihydroxysaprorthoquinone, was isolated in addition to ten known diterpenoids. The structure of the new compound was established by spectroscopic analysis. The crude extract of the plant and the isolated diterpenoids were tested for their cardiovascular activities using Wistar Albino rats. Activity was demonstrated in the crude extract and in 4,14-dihydroxysaprorthoquinone, aethiopinone, ferruginol, 4,12-dihydroxysapriparaquinone, and 6,7-dehydroroyleanone.


Asunto(s)
Abietanos , Diterpenos/aislamiento & purificación , Diterpenos/farmacología , Quinonas/aislamiento & purificación , Salvia , Animales , Presión Sanguínea/efectos de los fármacos , Diterpenos/química , Frecuencia Cardíaca/efectos de los fármacos , Espectroscopía de Resonancia Magnética , Masculino , Estructura Molecular , Naftoquinonas/química , Naftoquinonas/aislamiento & purificación , Naftoquinonas/farmacología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Raíces de Plantas/química , Quinonas/química , Ratas , Ratas Wistar
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