Química Orgánica
Department
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Hospital Ramón y Cajal
Madrid, EspañaPublications in collaboration with researchers from Hospital Ramón y Cajal (15)
2022
2020
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Characterization of a cholesteronitrone (ISQ-201), a novel drug candidate for the treatment of ischemic stroke
Antioxidants, Vol. 9, Núm. 4, pp. 1-21
2016
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A double-blind, randomized, cross-over, placebo-controlled, pilot trial with Sativex in Huntington’s disease
Journal of Neurology, Vol. 263, Núm. 7, pp. 1390-1400
2010
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Gentisic acid, a compound associated with plant defense and a metabolite of aspirin, heads a new class of in vivo fibroblast growth factor inhibitors
Journal of Biological Chemistry, Vol. 285, Núm. 15, pp. 11714-11729
2004
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Characterization of an anandamide degradation system in prostate epithelial PC-3 cells: Synthesis of new transporter inhibitors as tools for this study
British Journal of Pharmacology, Vol. 141, Núm. 3, pp. 457-467
2001
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Synthesis and structure-activity relationships of a new model of arylpiperazines. 5. Study of the physicochemical influence of the pharmacophore on 5-HT1A/α1-adrenergic receptor affinity: Synthesis of a new derivative with mixed 5-HT1A/D2 antagonist properties
Journal of Medicinal Chemistry, Vol. 44, Núm. 2, pp. 186-197
1999
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Benzimidazole derivatives. 2. Synthesis and structure-activity relationships of new azabicyclic benzimidazole-4-carboxylic acid derivatives with affinity for serotoninergic 5-HT3 receptors
Journal of Medicinal Chemistry, Vol. 42, Núm. 24, pp. 5020-5028
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Benzimidazole derivatives. Part 1: Synthesis and structure-activity relationships of new benzimidazole-4-carboxamides and carboxylates as potent and selective 5-HT4 receptor antagonists
Bioorganic and Medicinal Chemistry, Vol. 7, Núm. 11, pp. 2271-2281
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Design and synthesis of 2-[4-[4-(m-(ethylsulfonamido)-phenyl)piperazin- 1-yl]butyl]-1,3-dioxoperhydropyrrolo[1,2c]imidazole (EF-7412) using neural networks. A selective derivative with mixed 5-HT(1A)/D2 antagonist properties
Bioorganic and Medicinal Chemistry Letters, Vol. 9, Núm. 12, pp. 1679-1682
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Synthesis and structure-activity relationships of a new model of arylpiperazines 4. 1-[ω-(4-Arylpiperazin-1-yl)alkyl]-3-(diphenylmethylene)- 2,5-pyrrolidinediones and -3-(9h-fluoren-9-ylidene)-2,5-pyrrolidinediones: Study of the steric requirements of the terminal amide fragment on 5-HT(1A) affinity/selectivity
Journal of Medicinal Chemistry, Vol. 42, Núm. 1, pp. 36-49
1998
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1-[ω-(4-arylpiperazin-1-yl)alkyl]-3-diphenylmethylene-2,5-pyrrolidinediones as 5-HT(1A) receptor ligands: Study of the steric requirements of the terminal amide fragment on 5-HT(1A) affinity/selectivity
Bioorganic and Medicinal Chemistry Letters, Vol. 8, Núm. 6, pp. 581-586
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Preclinical pharmacology of B-20991, a 5-HT(1A) receptor agonist with anxiolytic activity
European Journal of Pharmacology, Vol. 344, Núm. 2-3, pp. 127-135
1996
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Synthesis and structure-activity relationships of a new model of arylpiperazines. 1. 2-[[4-(o-methoxyphenyl)piperazin-1-yl]methyl]-1,3- dioxoperhydroimidazo[1,5-a]pyridine: A selective 5-HT(1A) receptor agonist
Journal of Medicinal Chemistry, Vol. 39, Núm. 22, pp. 4439-4450
1995
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α1-Adrenoceptor Reagents. Synthesis of Some 5,6,11,11α-Tetrahydro-1H-imidazo[1’,5’: 1,6]pyrido and 5,6,11,11b-Tetrahydro-1H-imidazo-[l’,5’: 1,2] pyrido [3,4-b] indole-1,3(2H)-diones
Chemical and Pharmaceutical Bulletin, Vol. 43, Núm. 6, pp. 941-946
1994
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Reaction of 6-Hydroxy tetrahydro-β-carboline-3-carboxylic Acids with Isocyanates and Isothiocyanates
Chemical and Pharmaceutical Bulletin, Vol. 42, Núm. 10, pp. 2108-2112