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Page 1
Unraveling the Multistimuli Responses of a Complex Dynamic System of Pseudopeptidic Macrocycles.
Chemistry. 2017 Aug 10;23(45):10789-10799. doi: 10.1002/chem.201701294. Epub 2017 Jun 12.
Chemistry. 2017.
PMID: 28480991
Synthesis and antitumoral evaluation of indole alkaloid analogues containing an hexahydropyrrolo[1',2',3':1,9a,9]imidazo[1,2-a]indole skeleton.
Ventosa-Andrés P, González-Vera JA, Valdivielso AM, Teresa García-López M, Herranz R.
Ventosa-Andrés P, et al. Among authors: valdivielso am.
Bioorg Med Chem. 2008 Oct 15;16(20):9313-22. doi: 10.1016/j.bmc.2008.08.070. Epub 2008 Aug 31.
Bioorg Med Chem. 2008.
PMID: 18818089
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Highly functionalized 2-oxopiperazine-based peptidomimetics: an approach to PAR1 antagonists.
Valdivielso ÁM, Ventosa-Andrés P, Tato F, Fernández-Ibañez MÁ, Pappos I, Tsopanoglou NE, García-López MT, Gutiérrez-Rodríguez M, Herranz R.
Valdivielso ÁM, et al.
Eur J Med Chem. 2013;70:199-224. doi: 10.1016/j.ejmech.2013.09.058. Epub 2013 Oct 10.
Eur J Med Chem. 2013.
PMID: 24158013
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Exploring the Phe-Gly dipeptide-derived piperazinone scaffold in the search for antagonists of the thrombin receptor PAR1.
Valdivielso ÁM, García-López MT, Gutiérrez-Rodríguez M, Herranz R.
Valdivielso ÁM, et al.
Molecules. 2014 Apr 16;19(4):4814-46. doi: 10.3390/molecules19044814.
Molecules. 2014.
PMID: 24743938
Free PMC article.
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Design, synthesis and biological evaluation of new peptide-based ureas and thioureas as potential antagonists of the thrombin receptor PAR1.
Ventosa-Andrés P, Valdivielso AM, Pappos I, García-López MT, Tsopanoglou NE, Herranz R.
Ventosa-Andrés P, et al. Among authors: valdivielso am.
Eur J Med Chem. 2012 Dec;58:98-111. doi: 10.1016/j.ejmech.2012.10.015. Epub 2012 Oct 17.
Eur J Med Chem. 2012.
PMID: 23123726
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