Francisco
Orallo Cambeiro
Publicaciones en las que colabora con Francisco Orallo Cambeiro (70)
2013
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Cyclic AMP relaxation of rat aortic smooth muscle is mediated in part by decrease of depletion of intracellular Ca2+ stores and inhibition of capacitative calcium entry
Vascular Pharmacology, Vol. 58, Núm. 1-2, pp. 98-104
2011
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Chromone, a privileged scaffold for the development of monoamine oxidase inhibitors
Journal of Medicinal Chemistry, Vol. 54, Núm. 14, pp. 5165-5173
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New butyrolactone from a marine-derived fungus aspergillus SP
Journal of the Chilean Chemical Society, Vol. 56, Núm. 1, pp. 625-627
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Trans-resveratrol simultaneously increases cytoplasmic Ca 2+ levels and nitric oxide release in human endothelial cells
Molecular Nutrition and Food Research, Vol. 55, Núm. 8, pp. 1237-1248
2010
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Antidepressant-like profile and MAO-A inhibitory activity of 4-propyl-2H-benzo[h]-chromen-2-one
Life Sciences, Vol. 86, Núm. 21-22, pp. 819-824
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New pyridazinone derivatives with vasorelaxant and platelet antiaggregatory activities
Bioorganic and Medicinal Chemistry Letters, Vol. 20, Núm. 22, pp. 6624-6627
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Synthesis and vasorelaxant and platelet antiaggregatory activities of a new series of 6-Halo-3-phenylcoumarins
Molecules, Vol. 15, Núm. 1, pp. 270-279
2009
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A new series of 3-phenylcoumarins as potent and selective MAO-B inhibitors
Bioorganic and Medicinal Chemistry Letters, Vol. 19, Núm. 12, pp. 3268-3270
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Alignment-free prediction of a drug-target complex network based on parameters of drug connectivity and protein sequence of receptors
Molecular Pharmaceutics, Vol. 6, Núm. 3, pp. 825-835
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Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors
Bioorganic and Medicinal Chemistry Letters, Vol. 19, Núm. 17, pp. 5053-5055
2008
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Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors
Journal of Medicinal Chemistry, Vol. 51, Núm. 21, pp. 6740-6751
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Short-term or long-term treatments with a phosphodiesterase-4 (PDE4) inhibitor result in opposing agonist-induced Ca 2+ responses in endothelial cells
British Journal of Pharmacology, Vol. 154, Núm. 1, pp. 82-92
2007
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Effects of (-)-epigallocatechin-3-gallate in Ca2+-permeable non-selective cation channels and voltage-operated Ca2+ channels in vascular smooth muscle cells
Life Sciences, Vol. 80, Núm. 23, pp. 2147-2153
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Effects of trans- and cis-resveratrol on Ca2+ handling in A7r5 vascular myocytes
European Journal of Pharmacology, Vol. 577, Núm. 1-3, pp. 91-99
2006
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(-)-Trans-ε-viniferin, a polyphenol present in wines, is an inhibitor of noradrenaline and 5-hydroxytryptamine uptake and of monoamine oxidase activity
European Journal of Pharmacology, Vol. 542, Núm. 1-3, pp. 54-60
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Design, synthesis, and vasorelaxant and platelet antiaggregatory activities of coumarin-resveratrol hybrids
Bioorganic and Medicinal Chemistry Letters, Vol. 16, Núm. 2, pp. 257-261
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Inhibitory effects of cis- and trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity
Biochemical and Biophysical Research Communications, Vol. 344, Núm. 2, pp. 688-695
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Study of the mechanisms involved in the vasorelaxation induced by (-)-epigallocatechin-3-gallate in rat aorta
British Journal of Pharmacology, Vol. 147, Núm. 3, pp. 269-280
2005
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Hydralazine decreases sodium nitroprusside-induced rat aortic ring relaxation and increased cGMP production by rat aortic myocytes
Life Sciences, Vol. 77, Núm. 24, pp. 3105-3116
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Implication of cyclic nucleotide phosphodiesterase inhibition in the vasorelaxant activity of the citrus-fruits flavonoid (±)-naringenin
Planta Medica, Vol. 71, Núm. 2, pp. 99-107