F. Gómez-Contreras

发表

A NEW DIAZA HETEROAROMATIC CROWN OF 3,5-DISUBSTITUTED 1H-PYRAZOLE WHICH FORMS SOLID DINUCLEAR COMPLEXES WITH LIPOPHILIC PHENETHYLAMINES

A. Samat, A. Sanz, P. Navarro, 1998 .

The influence of A steric interactions on the conformational features of benzo[g]pyridazino[1,2-b]phthalazine-6,13-dione derivatives

F. Gómez-Contreras, M. C. Cano, M. Lora-Tamayo, 1991 .

Phthalazine derivatives containing imidazole rings behave as Fe-SOD inhibitors and show remarkable anti-T. cruzi activity in immunodeficient-mouse mode of infection.

M. J. Yunta, F. Olmo, A. Sanz, 2012, Journal of medicinal chemistry.

Synthesis and evaluation of in vitro and in vivo trypanocidal properties of a new imidazole-containing nitrophthalazine derivative.

M. J. Yunta, F. Olmo, P. Navarro, 2015, European journal of medicinal chemistry.

Synthesis and cytotoxic activity of N,N-bis-(3-[N-(4-chlorobenzo[g]-phthalazin-1-yl)]aminopropyl)-N-methylamine: a new potential DNA bisintercalator.

M. J. Yunta, A. Sanz, P. Navarro, 2003, Bioorganic & medicinal chemistry.

In vitro leishmanicidal activity of imidazole- or pyrazole-based benzo[g]phthalazine derivatives against Leishmania infantum and Leishmania braziliensis species.

M. J. Yunta, F. Olmo, A. Sanz, 2012, The Journal of antimicrobial chemotherapy.

In Search of New Tyrosinase Mimetics: Acyclic Polyaminic Ligands of Benzo[g]Phthalazine Able to Form Dinuclear Complexes with Cu(II)

M. J. Yunta, A. Sanz, P. Navarro, 1998 .

1,4-Bis(alkylamino)benzo[g]phthalazines able to form dinuclear complexes of Cu(II) which as free ligands behave as SOD inhibitors and show efficient in vitro activity against Trypanosoma cruzi.

M. J. Yunta, A. Osuna, A. Sanz, 2007, Bioorganic & medicinal chemistry.

The steric course of some electrophilic additions to the tetrahydropyridazine ring moiety of benzo[g]phthalazino[1,2-b]pyridazine-6,13-dione derivatives. I.

M. J. Yunta, A. Sanz, F. Gómez-Contreras, 1993 .

Efficient inhibition of iron superoxide dismutase and of Trypanosoma cruzi growth by benzo[g]phthalazine derivatives functionalized with one or two imidazole rings.

M. J. Yunta, A. Osuna, A. Sanz, 2008, Journal of medicinal chemistry.

A new series of heteroaromatic receptors containing the 1,3-bis(6-oxopyridazin-1-yl)propane unit: their selective transport ability towards NH4+ in relation to Na+, K+ and Ca2+

M. J. Yunta, A. Sanz, P. Navarro, 2004 .

Imidazole-containing phthalazine derivatives inhibit Fe-SOD performance in Leishmania species and are active in vitro against visceral and mucosal leishmaniasis

M. J. Yunta, A. Sanz, P. Navarro, 2015, Parasitology.

In vitro leishmanicidal activity of pyrazole-containing polyamine macrocycles which inhibit the Fe-SOD enzyme of Leishmania infantum and Leishmania braziliensis species

M. J. Yunta, E. Garcı́a-España, R. Gutiérrez-Sánchez, 2014, Parasitology.

New acyclic receptors containing pyridazine units. The influence of π-stacking on the selective transport of lipophilic phenethylamines

M. J. Yunta, A. Sanz, P. Navarro, 2005 .

Essential oil of Santolina rosmarinifolia L. ssp. rosmarinifolia: first isolation of capillene, a diacetylene derivative

J. Palá-Paúl, A. Velasco-Negueruela, M. Pérez-Alonso, 1999 .

In vitro and in vivo trypanosomicidal activity of pyrazole-containing macrocyclic and macrobicyclic polyamines: their action on acute and chronic phases of Chagas disease.

L. Lamarque, E. Garcı́a-España, F. Olmo, 2012, Journal of medicinal chemistry.

Acid–base behaviour and binding to double stranded DNA/RNA of benzo[g]phthalazine-based ligands

M. J. Yunta, C. Galiana-Roselló, E. Garcı́a-España, 2019, New Journal of Chemistry.

Synthesis and cytotoxic activity of a new potential DNA bisintercalator: 1,4-Bis{3-[N-(4-chlorobenzo[g]phthalazin-1-yl)aminopropyl]}piperazine.

M. J. Yunta, E. Garcı́a-España, F. Mollinedo, 2010, Bioorganic & medicinal chemistry.