Marta Barniol-Xicota
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Parents
Sign in to add mentorSantiago Vazquez | grad student | 2011-2017 | Universitat Pompeu Fabra |
Matthew Bogyo | post-doc | 2021-2023 | Stanford Medical School |
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Publications
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Codony S, Entrena JM, Calvó-Tusell C, et al. (2022) Synthesis, In Vitro Profiling, and In Vivo Evaluation of Benzohomoadamantane-Based Ureas for Visceral Pain: A New Indication for Soluble Epoxide Hydrolase Inhibitors. Journal of Medicinal Chemistry |
Pérez-Areales FJ, Turcu AL, Barniol-Xicota M, et al. (2019) A novel class of multitarget anti-Alzheimer benzohomoadamantane‒chlorotacrine hybrids modulating cholinesterases and glutamate NMDA receptors. European Journal of Medicinal Chemistry. 180: 613-626 |
Alonso JM, Quiroga S, Codony S, et al. (2018) Palladium-catalyzed cocyclotrimerization of arynes with a pyramidalized alkene. Chemical Communications (Cambridge, England) |
Karoutzou O, Kwak SH, Lee SD, et al. (2018) Towards a Novel Class of Multitarget-Directed Ligands: Dual P2X7-NMDA Receptor Antagonists. Molecules (Basel, Switzerland). 23 |
Leiva R, Barniol-Xicota M, Codony S, et al. (2017) Aniline-Based Inhibitors of Influenza H1N1 Virus Acting on Hemagglutinin-Mediated Fusion. Journal of Medicinal Chemistry |
Barniol-Xicota M, Gazzarrini S, Torres E, et al. (2017) Slow but steady wins the race: dissimilarities among new dual inhibitors of the wild-type and the V27A mutant M2 channels of influenza A virus. Journal of Medicinal Chemistry |
Barniol-Xicota M, Kwak SH, Lee SD, et al. (2017) Escape from adamantane: Scaffold optimization of novel P2X7 antagonists featuring complex polycycles. Bioorganic & Medicinal Chemistry Letters |
Zarei M, Barroso E, Leiva R, et al. (2016) Heme-Regulated eIF2α Kinase Modulates Hepatic FGF21 and is Activated by PPARβ/δ Deficiency. Diabetes |
Barniol-Xicota M, Escandell A, Valverde E, et al. (2014) Antibacterial activity of novel benzopolycyclic amines. Bioorganic & Medicinal Chemistry. 23: 290-6 |
Rey-Carrizo M, Barniol-Xicota M, Ma C, et al. (2014) Easily accessible polycyclic amines that inhibit the wild-type and amantadine-resistant mutants of the M2 channel of influenza A virus. Journal of Medicinal Chemistry. 57: 5738-47 |