Espinosa-Bustos C - Search Results

1

Substituted Purines as High-Affinity Histamine H₃ Receptor Ligands.

Espinosa-Bustos C, Leitzbach L, Añazco T, Silva MJ, Campo AD, Castro-Alvarez A, Stark H, Salas CO. Espinosa-Bustos C, et al. Pharmaceuticals (Basel). 2022 May 4;15(5):573. doi: 10.3390/ph15050573. Pharmaceuticals (Basel). 2022. PMID: 35631399 Free PMC article.

2

New lead elements for histamine H₃ receptor ligands in the pyrrolo[2,3-d]pyrimidine class.

Espinosa-Bustos C, Frank A, Arancibia-Opazo S, Salas CO, Fierro A, Stark H. Espinosa-Bustos C, et al. Bioorg Med Chem Lett. 2018 Sep 15;28(17):2890-2893. doi: 10.1016/j.bmcl.2018.07.023. Epub 2018 Jul 17. Bioorg Med Chem Lett. 2018. PMID: 30025902

3

Nature-inspired pyrrolo[2,3-d]pyrimidines targeting the histamine H₃ receptor.

Frank A, Meza-Arriagada F, Salas CO, Espinosa-Bustos C, Stark H. Frank A, et al. Bioorg Med Chem. 2019 Jul 15;27(14):3194-3200. doi: 10.1016/j.bmc.2019.05.042. Epub 2019 May 29. Bioorg Med Chem. 2019. PMID: 31176569

4

Synthesis and pharmacophore modelling of 2,6,9-trisubstituted purine derivatives and their potential role as apoptosis-inducing agents in cancer cell lines.

Calderón-Arancibia J, Espinosa-Bustos C, Cañete-Molina Á, Tapia RA, Faúndez M, Torres MJ, Aguirre A, Paulino M, Salas CO. Calderón-Arancibia J, et al. Molecules. 2015 Apr 15;20(4):6808-26. doi: 10.3390/molecules20046808. Molecules. 2015. PMID: 25884555 Free PMC article.

5

Design, Synthesis, In Silico Studies and Inhibitory Activity towards Bcr-Abl, BTK and FLT3-ITD of New 2,6,9-Trisubstituted Purine Derivatives as Potential Agents for the Treatment of Leukaemia.

Bertrand J, Dostálová H, Kryštof V, Jorda R, Delgado T, Castro-Alvarez A, Mella J, Cabezas D, Faúndez M, Espinosa-Bustos C, Salas CO. Bertrand J, et al. Among authors: espinosa bustos c. Pharmaceutics. 2022 Jun 17;14(6):1294. doi: 10.3390/pharmaceutics14061294. Pharmaceutics. 2022. PMID: 35745866 Free PMC article.

6

New 2,6,9-trisubstituted purine derivatives as Bcr-Abl and Btk inhibitors and as promising agents against leukemia.

Bertrand J, Dostálová H, Krystof V, Jorda R, Castro A, Mella J, Espinosa-Bustos C, María Zarate A, Salas CO. Bertrand J, et al. Among authors: espinosa bustos c. Bioorg Chem. 2020 Jan;94:103361. doi: 10.1016/j.bioorg.2019.103361. Epub 2019 Oct 17. Bioorg Chem. 2020. PMID: 31699386

7

Fluorescence properties of aurone derivatives: an experimental and theoretical study with some preliminary biological applications.

Espinosa-Bustos C, Cortés-Arriagada D, Soto-Arriaza MA, Robinson-Duggon J, Pizarro N, Cabrera AR, Fuentealba D, Salas CO. Espinosa-Bustos C, et al. Photochem Photobiol Sci. 2017 Aug 9;16(8):1268-1276. doi: 10.1039/c7pp00078b. Photochem Photobiol Sci. 2017. PMID: 28636041

8

New imidoyl-indazole platinum (II) complexes as potential anticancer agents: Synthesis, evaluation of cytotoxicity, cell death and experimental-theoretical DNA interaction studies.

Cabrera AR, Espinosa-Bustos C, Faúndez M, Meléndez J, Jaque P, Daniliuc CG, Aguirre A, Rojas RS, Salas CO. Cabrera AR, et al. J Inorg Biochem. 2017 Sep;174:90-101. doi: 10.1016/j.jinorgbio.2017.06.001. Epub 2017 Jun 15. J Inorg Biochem. 2017. PMID: 28648925

9

State of the art of Smo antagonists for cancer therapy: advances in the target receptor and new ligand structures.

Espinosa-Bustos C, Mella J, Soto-Delgado J, Salas CO. Espinosa-Bustos C, et al. Future Med Chem. 2019 Mar;11(6):617-638. doi: 10.4155/fmc-2018-0497. Epub 2019 Mar 26. Future Med Chem. 2019. PMID: 30912670 Review.

10

New aryloxy-quinone derivatives with promising activity on Trypanosoma cruzi.

Espinosa-Bustos C, Vázquez K, Varela J, Cerecetto H, Paulino M, Segura R, Pizarro J, Vera B, González M, Zarate AM, Salas CO. Espinosa-Bustos C, et al. Arch Pharm (Weinheim). 2020 Jan;353(1):e1900213. doi: 10.1002/ardp.201900213. Epub 2019 Nov 11. Arch Pharm (Weinheim). 2020. PMID: 31709599

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