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1.
Arch Pharm Res ; 35(11): 1953-9, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23212637

RESUMEN

Piperidine derivatives are known to exhibit analgesic activities and are likely to possess the ability to block the effects of prostaglandins through inhibition of downstream signaling pathways. The present study investigated the activity of five derivatives (PD2-6) of 4-(4'-bromophenyl)-4-piperidinol (PD1), against pain and platelet aggregation mediated by the release of prostaglandins and thromboxane A2, respectively. The results showed that compound PD1 and its two phenacyl derivatives PD3 and PD5 exhibited a highly significant analgesic effect (p < 0.01), whereas PD4 and PD6 also showed significant activity. PD3, the most active analgesic compound when docked to the opioid receptor, had interactions between the oxygen of its nitro group and the amino group of ARG 573, indicating a distance of 1.2563 Å. The antiplatelet data showed that compound PD5 (4-(4'-bromo-phenyl)-4-hydroxy-1-[2-(2″,4″-dimethoxyphenyl)-2-oxo-ethyl]-piperidinium bromide) had an IC(50) = 0.06 mM, which was the most active compound, whereas PD3 was the second most active compound against platelet aggregating factor-induced aggregation with an IC(50) = 80 mM. Acetyl salicylic acid (IC(50) = 150 µM) was used as a positive control.


Asunto(s)
Analgésicos/farmacología , Dolor/tratamiento farmacológico , Piperidinas/farmacología , Inhibidores de Agregación Plaquetaria/farmacología , Analgésicos/administración & dosificación , Analgésicos/química , Animales , Aspirina/administración & dosificación , Aspirina/farmacología , Femenino , Humanos , Concentración 50 Inhibidora , Masculino , Ratones , Piperidinas/administración & dosificación , Piperidinas/química , Agregación Plaquetaria/efectos de los fármacos , Inhibidores de Agregación Plaquetaria/administración & dosificación , Inhibidores de Agregación Plaquetaria/química , Prostaglandinas/metabolismo , Receptores Opioides/metabolismo , Relación Estructura-Actividad , Tromboxano A2/metabolismo
2.
Nat Prod Res ; 25(20): 1965-8, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22050275

RESUMEN

Piperidine derivatives are reported to exhibit a variety of pharmacological activities. In this article, synthesis and aspartic protease inhibitory activity of three nitrophenacyl derivatives of N-methyl-4-hydroxy piperidine are reported. Enzyme assays showed that the attachment of a nitro group in the benzene ring plays an important role in the inhibition of plasmepsin-II of Plasmodium falciparum. The compound 1-methyl-1-(4'-nitrophenacyl)-4-hydroxypiperidinium bromide (3), consisting of a nitro group at the para position, was the most active at the concentration of 1.0 µM. The activity of the compounds was evaluated through the observed orientation and diagrammatic representation of nitrophenacyl derivatives of 4-hydroxy piperidine.


Asunto(s)
Ácido Aspártico Endopeptidasas/antagonistas & inhibidores , Proteasas de Ácido Aspártico/antagonistas & inhibidores , Piperidinas/química , Piperidinas/farmacología , Plasmodium falciparum/enzimología , Proteínas Protozoarias/antagonistas & inhibidores , Nitrofenoles/química , Piperidinas/síntesis química , Unión Proteica
3.
Nat Prod Res ; 19(4): 337-46, 2005 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-15938139

RESUMEN

Wheat seeds were grown in the presence and absence of some trace elements like Co, Cu, Fe, Mn, Mo and Zn in non-toxic limits. The level of enzyme activities involved in nucleic acid metabolism were measured by spectrophotometric methods. The level of certain RNA metabolising enzymes increased manyfold in trace element-treated seeds, while the level of AMP-deaminase was increased manyfold in Co-treated seeds.


Asunto(s)
Desoxirribonucleasas/metabolismo , Ribonucleasas/metabolismo , Semillas/efectos de los fármacos , Semillas/enzimología , Oligoelementos/farmacología , Triticum/efectos de los fármacos , Triticum/enzimología , Germinación/fisiología , Proteínas de Plantas/metabolismo , Triticum/fisiología
4.
Nat Prod Res ; 18(1): 11-4, 2004 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-14974611

RESUMEN

Characteristic fragment ions obtained in Fast atom bombardment (FAB) mass spectroscopy of ribose alkylated Uridine 5'-monophosphate (5'-UMP) derivatives in negative ion mode are described. All the compounds examined exhibited either [M]- or quasimolecular ion [M - H]- the fragmentations can be used to characterize these nucleotides.


Asunto(s)
Ribosa/metabolismo , Uridina Monofosfato/análogos & derivados , Uridina Monofosfato/química , Alquilación , Espectrometría de Masa Bombardeada por Átomos Veloces
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