Pineda de las Infantas MJ - Search Results

1

Synthesis, chemical solvolytic stability and preliminary biological evaluation of (+/-)-N-Boc-CPzI: a pyrazole analog of the left-hand segment of the antitumor agent CC-1065.

Baraldi PG, Cacciari B, Pineda de las Infantas MJ, Romagnoli R, Spalluto G, Cozzi P, Mongelli N. Baraldi PG, et al. Among authors: pineda de las infantas mj. Anticancer Drug Des. 1997 Jan;12(1):67-74. Anticancer Drug Des. 1997. PMID: 9051115 No abstract available.

2

Design, synthesis, and biological activity of hybrid compounds between uramustine and DNA minor groove binder distamycin A.

Baraldi PG, Romagnoli R, Guadix AE, Pineda de las Infantas MJ, Gallo MA, Espinosa A, Martinez A, Bingham JP, Hartley JA. Baraldi PG, et al. Among authors: pineda de las infantas mj. J Med Chem. 2002 Aug 15;45(17):3630-8. doi: 10.1021/jm011113b. J Med Chem. 2002. PMID: 12166936

3

Synthesis and biological activity of a new series of N6-arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-carboxamido derivatives of adenosine-5'-N-ethyluronamide as A1 and A3 adenosine receptor agonists.

Baraldi PG, Cacciari B, Pineda de Las Infantas MJ, Romagnoli R, Spalluto G, Volpini R, Costanzi S, Vittori S, Cristalli G, Melman N, Park KS, Ji XD, Jacobson KA. Baraldi PG, et al. Among authors: pineda de las infantas mj. J Med Chem. 1998 Aug 13;41(17):3174-85. doi: 10.1021/jm980147p. J Med Chem. 1998. PMID: 9703463 Free PMC article.

4

Synthesis and biological evaluation of novel N6-[4-(substituted)sulfonamidophenylcarbamoyl]adenosine-5'-uronamides as A3 adenosine receptor agonists.

Baraldi PG, Fruttarolo F, Tabrizi MA, Romagnoli R, Preti D, Bovero A, Pineda de Las Infantas MJ, Moorman A, Varani K, Borea PA. Baraldi PG, et al. Among authors: pineda de las infantas mj. J Med Chem. 2004 Oct 21;47(22):5535-40. doi: 10.1021/jm0408161. J Med Chem. 2004. PMID: 15481989

5

1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one and 5H-pyrazolo[4,3-d] 1,2,3-triazin-4(3H)-one derivatives. Synthesis and in vitro biological activity at adenosine A1 and A2a receptors.

Baraldi PG, Cacciari B, Dalpiaz A, Dionisotti S, Zocchi C, Pineda de las Infantas MJ, Spalluto G, Varani K. Baraldi PG, et al. Among authors: pineda de las infantas mj. Arzneimittelforschung. 1996 Apr;46(4):365-8. Arzneimittelforschung. 1996. PMID: 8740079

6

Regioselective one-pot synthesis of 9-alkyl-6-chloropyrido[3,2-e][1,2,4]triazolo[4,3-a]pyrazines. Reactivity of aliphatic and aromatic hydrazides.

Unciti-Broceta A, Pineda-de-las-Infantas MJ, Díaz-Mochón JJ, Romagnoli R, Baraldi PG, Gallo MA, Espinosa A. Unciti-Broceta A, et al. Among authors: pineda de las infantas mj. J Org Chem. 2005 Apr 1;70(7):2878-80. doi: 10.1021/jo0478398. J Org Chem. 2005. PMID: 15787593

7

Synthesis of 6,8,9 poly-substituted purine analogue libraries as pro-apoptotic inducers of human leukemic lymphocytes and DAPK-1 inhibitors.

Pineda de las Infantas MJ, Torres-Rusillo S, Unciti-Broceta JD, Fernandez-Rubio P, Luque-Gonzalez MA, Gallo MA, Unciti-Broceta A, Molina IJ, Diaz-Mochon JJ. Pineda de las Infantas MJ, et al. Org Biomol Chem. 2015 May 14;13(18):5224-34. doi: 10.1039/c5ob00230c. Org Biomol Chem. 2015. PMID: 25856731

8

NMR and conformational studies of new 5-phenylpyrrole-carboxamide derivatives.

López-Cara LC, Pineda de las Infantas MJ, Carrión MD, Camacho ME, Gallo MA, Espinosa A, Entrena A. López-Cara LC, et al. Among authors: pineda de las infantas mj. Magn Reson Chem. 2009 Dec;47(12):1101-9. doi: 10.1002/mrc.2524. Magn Reson Chem. 2009. PMID: 19821470

9

Reduction of different electron-poor N-heteroarylhydrazines in strong basic conditions.

Unciti-Broceta A, Pineda de las Infantas MJ, Gallo MA, Espinosa A. Unciti-Broceta A, et al. Among authors: pineda de las infantas mj. Chemistry. 2007;13(6):1754-62. doi: 10.1002/chem.200600282. Chemistry. 2007. PMID: 17146826

10

Anticancer pyrimidine acyclonucleosides.

Gallo-Mezo MA, Espinosa A, Campos J, Entrena A, Pineda de las Infantas MJ, Gómez JA. Gallo-Mezo MA, et al. Among authors: pineda de las infantas mj. Farmaco. 1995 Jun;50(6):395-400. Farmaco. 1995. PMID: 7669177 Review.

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