Facultad de Ciencias de la Salud
Facultades


Eli Lilly and Company
Indianapolis, EE. UU.Publications in collaboration with researchers from Eli Lilly and Company (11)
2013
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GluK1 antagonists from 6-(tetrazolyl)phenyl decahydroisoquinoline derivatives: In vitro profile and in vivo analgesic efficacy
Bioorganic and Medicinal Chemistry Letters, Vol. 23, Núm. 23, pp. 6463-6466
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GluK1 antagonists from 6-(carboxy)phenyl decahydroisoquinoline derivatives. SAR and evaluation of a prodrug strategy for oral efficacy in pain models
Bioorganic and Medicinal Chemistry Letters, Vol. 23, Núm. 23, pp. 6459-6462
2006
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Antiallodynic and antihyperalgesic effects of selective competitive GLUK5 (GluR5) ionotropic glutamate receptor antagonists in the capsaicin and carrageenan models in rats
Journal of Pharmacology and Experimental Therapeutics, Vol. 319, Núm. 1, pp. 396-404
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A novel class of positive allosteric modulators of AMPA receptors: Design, synthesis, and structure-activity relationships of 3-biphenyl-4-yl-4-cyano-5-ethyl-1-methyl-1H-pyrrole-2-carboxylic acid, LY2059346
Bioorganic and Medicinal Chemistry Letters, Vol. 16, Núm. 19, pp. 5203-5206
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A novel class of AMPA receptor allosteric modulators. Part 1: Design, synthesis, and SAR of 3-aryl-4-cyano-5-substituted-heteroaryl-2-carboxylic acid derivatives
Bioorganic and Medicinal Chemistry Letters, Vol. 16, Núm. 19, pp. 5057-5061
2005
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Two prodrugs of potent and selective GluR5 kainate receptor antagonists actives in three animal models of pain
Journal of Medicinal Chemistry, Vol. 48, Núm. 13, pp. 4200-4203
2002
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Ethyl (3s,4aR,6S,8aR)-6-(4-ethoxycar-bonylimidazol-1-ylmethyl) decahydroiso-quinoline-3-carboxylic ester: A prodrug of a GluR5 kainate receptor antagonist active in two animal models of acute migraine
Journal of Medicinal Chemistry, Vol. 45, Núm. 20, pp. 4383-4386
2001
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Enantioselective solution- and solid-phase synthesis of glutamic acid derivatives via Michael addition reactions
Tetrahedron Asymmetry, Vol. 12, Núm. 6, pp. 821-828
2000
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Solid phase synthesis of glutamic acid derivatives via nucleophilic ring opening of N-Boc pyroglutamate with heteronucleophiles
Tetrahedron Letters, Vol. 41, Núm. 23, pp. 4567-4571
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Efficient synthesis of 4,4-disubstituted-3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2-dioxides
Tetrahedron Letters, Vol. 41, Núm. 50, pp. 9825-9828
1998
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Solid-phase synthesis of substituted glutamic acid derivatives via Michael addition reactions
Tetrahedron Letters, Vol. 39, Núm. 15, pp. 2167-2170