Examination of the pharmacophoric points of the pyrazolo[1,5-a]pyrimidine derivatives, ligands for BZR, previously published led us to the design of a novel class of 3,6-diaryl-4,7-dihydro-pyrazolo[1,5-a]pyrimidin-7-ones and to determine the groups involved in the BZR recognition.

Synthesis and BZR affinity of pyrazolo[1,5-a]pyrimidine derivatives. Part 1: Study of the structural features for BZR recognition / Selleri S.; Bruni F.; Costagli C.; Costanzo A.; Guerrini G.; Ciciani G.; Costa B.; Martini C.. - In: BIOORGANIC & MEDICINAL CHEMISTRY. - ISSN 0968-0896. - ELETTRONICO. - 7:(1999), pp. 2705-2711. [10.1016/S0968-0896(99)00232-1]

Synthesis and BZR affinity of pyrazolo[1,5-a]pyrimidine derivatives. Part 1: Study of the structural features for BZR recognition

Selleri S.;Bruni F.;COSTAGLI, CAMILLA;Costanzo A.;Ciciani G.;COSTA, BARBARA;
1999

Abstract

Examination of the pharmacophoric points of the pyrazolo[1,5-a]pyrimidine derivatives, ligands for BZR, previously published led us to the design of a novel class of 3,6-diaryl-4,7-dihydro-pyrazolo[1,5-a]pyrimidin-7-ones and to determine the groups involved in the BZR recognition.
1999
7
2705
2711
Selleri S.; Bruni F.; Costagli C.; Costanzo A.; Guerrini G.; Ciciani G.; Costa B.; Martini C.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1175695
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