Miguel Carda
Affiliations: | Universitat Jaume I, Spain |
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Pla-López A, Carda M, Falomir E. (2023) Tetrazole derivatives as potent immunomodulatory agents in tumor microenvironment. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie. 169: 115668 |
Pla-López A, Martínez-Colomina P, Cañada-García L, et al. (2023) Aryl azoles based scaffolds for disrupting tumor microenvironment. Bioorganic & Medicinal Chemistry. 95: 117490 |
Gil-Edo R, Royo S, Carda M, et al. (2023) Unveiling the Potential of BenzylethyleneAryl-Urea Scaffolds for the Design of New Onco Immunomodulating Agents. Pharmaceuticals (Basel, Switzerland). 16 |
Gil-Edo R, Hernández-Ribelles G, Royo S, et al. (2023) Exploring BenzylethoxyAryl Urea Scaffolds for Multitarget Immunomodulation Therapies. International Journal of Molecular Sciences. 24 |
Gil-Edo R, Espejo S, Falomir E, et al. (2023) Synthesis and Biological Evaluation of Potential Oncoimmunomodulator Agents. International Journal of Molecular Sciences. 24 |
Pla-López A, Castillo R, Cejudo-Marín R, et al. (2022) Synthesis and Biological Evaluation of Small Molecules as Potential Anticancer Multitarget Agents. International Journal of Molecular Sciences. 23 |
Martín-Beltrán C, Gil-Edo R, Hernández-Ribelles G, et al. (2021) Aryl Urea Based Scaffolds for Multitarget Drug Discovery in Anticancer Immunotherapies. Pharmaceuticals (Basel, Switzerland). 14 |
Agut R, Falomir E, Murga J, et al. (2020) Synthesis of Combretastatin A-4 and 3'-Aminocombretastatin A-4 derivatives with Aminoacid Containing Pendants and Study of Their Interaction with Tubulin and as Downregulators of the VEGF, hTERT and c-Myc Gene Expression. Molecules (Basel, Switzerland). 25 |
Castrillón W, Herrera-R A, Prieto LJ, et al. (2019) Synthesis and Evaluation of S-allyl Cysteine Ester - Caffeic Acid Amide Hybrids as Potential Anticancer Agents. Iranian Journal of Pharmaceutical Research : Ijpr. 18: 1770-1789 |
Conesa-Milián L, Falomir E, Murga J, et al. (2019) Novel multitarget inhibitors with antiangiogenic and immunomodulator properties. European Journal of Medicinal Chemistry. 170: 87-98 |