Derivados selenados como terapia frente a cáncer, tripanosomas y otras patologías
SECALE
Instituto de Química Orgánica General
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Instituto de Química Orgánica General (13)
2022
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Pharmaceutical and Safety Profile Evaluation of Novel Selenocompounds with Noteworthy Anticancer Activity
Pharmaceutics, Vol. 14, Núm. 2
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Synthesis of novel organic selenium compounds and speciation of their metabolites in biofortified kale sprouts
Microchemical Journal, Vol. 172
2020
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Phenothiazines and selenocompounds: A potential novel combination therapy of multidrug resistant cancer
Anticancer Research, Vol. 40, Núm. 9, pp. 4921-4928
2019
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Antiviral, antimicrobial and antibiofilm activity of selenoesters and selenoanhydrides
Molecules, Vol. 24, Núm. 23
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Organoselenium compounds as novel adjuvants of chemotherapy drugs—a promising approach to fight cancer drug resistance
Molecules, Vol. 24, Núm. 2
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Selenocompounds as novel antibacterial agents and bacterial efflux pump inhibitors
Molecules, Vol. 24, Núm. 8
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Selenoesters and selenoanhydrides as novel agents against resistant breast cancer
Anticancer Research, Vol. 39, Núm. 7, pp. 3777-3783
2017
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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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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
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
2014
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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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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
1989
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2-Arylamino-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidines: synthesis and diuretic activity
European Journal of Medicinal Chemistry, Vol. 24, Núm. 3, pp. 209-216