Facultad de Farmacia y Nutrición (FFN)
Centro académico
Jesús Manuel
Peregrina García
Publikationen, an denen er mitarbeitet Jesús Manuel Peregrina García (25)
2024
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Structure-Guided Approach for the Development of MUC1-Glycopeptide-Based Cancer Vaccines with Predictable Responses
JACS Au, Vol. 4, Núm. 1, pp. 150-163
2017
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Principles of mucin structure: Implications for the rational design of cancer vaccines derived from MUC1-glycopeptides
Chemical Society Reviews, Vol. 46, Núm. 23, pp. 7154-7175
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The Use of Fluoroproline in MUC1 Antigen Enables Efficient Detection of Antibodies in Patients with Prostate Cancer
Journal of the American Chemical Society, Vol. 139, Núm. 50, pp. 18255-18261
2016
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Bifunctional Chiral Dehydroalanines for Peptide Coupling and Stereoselective S-Michael Addition
Organic Letters, Vol. 18, Núm. 12, pp. 2796-2799
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Design of α-S-Neoglycopeptides Derived from MUC1 with a Flexible and Solvent-Exposed Sugar Moiety
Journal of Organic Chemistry, Vol. 81, Núm. 14, pp. 5929-5941
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Mucin Architecture behind the Immune Response: Design and Evaluation of an Antitumor Vaccine Derived from an Unnatural MUC1 Fragment
Chemical Science, Vol. 7, Núm. 3, pp. 2294
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Tn Antigen Mimics Based on sp2-Iminosugars with Affinity for an anti-MUC1 Antibody
Organic Letters, Vol. 18, Núm. 15, pp. 3890-3893
2015
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Deciphering the Non-Equivalence of Serine and Threonine O-glycosylation Points: Implications for Molecular Recognition of the Tn Antigen by an anti-MUC1 Antibody
Angewandte Chemie International, Vol. 54, Núm. 34, pp. 9830
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Detection of tumor-associated glycopeptides by Lectins: The peptide context modulates carbohydrate recognition
ACS chemical biology, Vol. 10, Núm. 3, pp. 747-756
2014
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A double diastereoselective Michael-type addition as an entry to Tn antigen mimics and analogs of Thiamet-G
XI Carbohydrate Symposium
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Conformational analysis of peptides and glycopeptides derived from the consensus sequence for β-O-glucosylation
Current Topics in Medicinal Chemistry, Vol. 14, Núm. 23, pp. 2712-2721
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Designing non-natural cancer vaccines by replacing the methyl group of Thr-10 in MUC1 derivatives
XI Carbohydrate Symposium
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Glycopeptides incorporating sulfur-based Tn antigen mimics
XI Carbohydrate Symposium
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Influence of amino acid stereocenters on the formation of bicyclic N, O -acetals
Journal of Organic Chemistry, Vol. 79, Núm. 6, pp. 2556-2563
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S-Michael additions to chiral dehydroalanines as an entry to glycosylated cysteines and a sulfa-tn antigen mimic
Journal of the American Chemical Society, Vol. 136, Núm. 2, pp. 789-800
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Serine versus Threonine Glycosylation witha-O-GalNAc: Unexpected Selectivity in Their Molecular Recognition with Lectins
Chemistry - A European Journal, Vol. 20, Núm. 39, pp. 12616-12627
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Synthesis, conformational analysis and biological evaluation of an antitumor vaccine derived from a non-natural MUC1 fragment
XI Carbohydrate Symposium
2013
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A double diastereoselective michael-type addition as an entry to conformationally restricted Tn antigen mimics
Journal of Organic Chemistry, Vol. 78, Núm. 21, pp. 10968-10977
2012
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A Biomimetic Approach to Lanthionines
Organic Letters, Vol. 14, Núm. 1, pp. 334-337
2011
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A Domino Michael/Dieckmann Process as an Entry to alpha-(Hydroxymethyl)glutamic Acid
Journal of Organic Chemistry, Vol. 76, Núm. 17, pp. 6990-6996