MARÍA LUZ
LÓPEZ RODRÍGUEZ
Investigadora hasta 2022
Instituto de Química Orgánica General
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Instituto de Química Orgánica General (11)
2017
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Development of a Nucleotide Exchange Inhibitor That Impairs Ras Oncogenic Signaling
Chemistry - A European Journal, Vol. 23, Núm. 7, pp. 1676-1685
2010
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Development of fluorescent ligands for the human 5-HT1A receptor
ACS Medicinal Chemistry Letters, Vol. 1, Núm. 6, pp. 249-253
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Development of molecular probes for the human 5-HT6 receptor
Journal of Medicinal Chemistry, Vol. 53, Núm. 19, pp. 7095-7106
2006
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Synthesis of highly substituted enantiopure piperazines and ketopiperazines from vicinal N-sulfinyl diamines
Journal of Organic Chemistry, Vol. 71, Núm. 4, pp. 1442-1448
2005
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Activation of the endocannabinoid system as therapeutic approach in a murine model of multiple sclerosis
FASEB Journal, Vol. 19, Núm. 10, pp. 1338-1340
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Highly diastereoselective [3+2] cycloadditions between non-racemic p-tolylsulfinimines and iminoesters: An efficient entry to enantiopure imidazolidines and vicinal diaminoalcohols
Phosphorus, Sulfur and Silicon and the Related Elements
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Involvement of cannabinoids in cellular proliferation
Mini-Reviews in Medicinal Chemistry
2004
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Comparison of anandamide transport in FAAH wild-type and knockout neurons: Evidence for contributions by both FAAH and the CB1 receptor to anandamide uptake
Biochemistry, Vol. 43, Núm. 25, pp. 8184-8190
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Fine-Tuned Aminal Cleavage: A Concise Route to Differentially Protected Enantiopure syn-α,β-Diamino Esters
Journal of Organic Chemistry, Vol. 69, Núm. 5, pp. 1542-1547
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Synthesis and structure-activity relationships of a new model of arylpiperazines. Part 7: Study of the influence of lipophilic factors at the terminal amide fragment on 5-HT1A affinity/selectivity
Bioorganic and Medicinal Chemistry, Vol. 12, Núm. 6, pp. 1551-1557