A 5-HT1A pharmacophore has been obtained employing a set of rigid temp
lates encompassing the 5-HT structure. The use of rigid templates allo
wed us to overcome the discrepancy found when flexible structures wher
e the energy of the active conformers are sometimes higher than the gl
obal minimum energy are used. On the basis of the results herein repor
ted the three-dimensional requirements necessary for the binding inter
action have been defined within this set of molecules. In this study f
orbidden zones of the receptor have been characterised. The pharmacoph
ore model derived places some agonist/antagonist pharmacophore models
appeared in the literature in question.