H. Tristán

发表

Differential regulation of rat peripheral 5-HT2A and 5-HT2B receptor systems: influence of drug treatment

M. Loza, J. Brea, M. Cadavid, 2003, Naunyn-Schmiedeberg's Archives of Pharmacology.

Different pharmacological properties of two equipotent antagonists (clozapine and rauwolscine) for 5-HT2B receptors in rat stomach fundus.

M. Loza, J. Brea, M. Cadavid, 2003, Biochemical pharmacology.

Butyrophenone analogues in the carbazole series as potential atypical antipsychotics: synthesis and determination of affinities at D(2), 5-HT(2A), 5-HT(2B) and 5-HT(2C) receptors.

M. Loza, J. Brea, C. Masaguer, 2000, European journal of medicinal chemistry.

Butyrophenone analogues in the carbazole series: synthesis and determination of affinities at D2 and 5-HT2A receptors.

M. Loza, C. Masaguer, H. Tristán, 1998, Bioorganic & medicinal chemistry letters.

Study of the in vivo and in vitro cardiovascular effects of four new analogues of ketanserin: implication of 5-HT2A and alpha1 adrenergic antagonism in their hypotensive effect.

M. Loza, J. Calleja, F. Orallo, 2000, Biological & pharmaceutical bulletin.

In vivo and in vitro pharmacological studies of a new hypotensive compound (QF0301B) in rat: comparison with prazosin, a known α1-adrenoceptor antagonist

M. Loza, F. Orallo, C. Masaguer, 2003 .

Synthesis and affinities for dopamine (D2) and 5-hydroxytryptamine (5-HT2A) receptors of 1-(benzoylpropyl)-4-(1-oxocycloalkyl-2-ethyl)-piperazines as cyclic butyrophenone derivatives.

M. L. de Ceballos, J. Calleja, C. Masaguer, 1996, Chemical & pharmaceutical bulletin.

In vivo and in vitro pharmacological studies of a new hypotensive compound (QF0301B) in rat: comparison with prazosin, a known alpha1-adrenoceptor antagonist.

M. Loza, F. Orallo, M. J. Enguix, 2003, Vascular pharmacology.

Functional characterization of serotonin receptors in rat isolated aorta.

M. Loza, M. Cadavid, F. Orallo, 2002, Biological & pharmaceutical bulletin.