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vol.53 issue1THE STEREOSELECTIVE SYNTHESIS OF THE WERNER COMPLEX WITH SUBSTOICHIOMETRIC SUGARSCONFORMATIONAL PREFERENCE IN 4,6-DIMETHYL-l,3-THIOXANE author indexsubject indexarticles search
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Journal of the Chilean Chemical Society

On-line version ISSN 0717-9707

Abstract

GOMEZ-JERIA, JUAN S; SOTO-MORALES, FRANCISCO; RIVAS, JORGE  and  SOTOMAYOR, ALEJANDRA. A THEORETICAL STRUCTURE-AFFINITY RELATIONSHIP STUDY OF SOME CANNABINOID DERIVATIVES. J. Chil. Chem. Soc. [online]. 2008, vol.53, n.1, pp.1382-1388. ISSN 0717-9707.  http://dx.doi.org/10.4067/S0717-97072008000100013.

A ZINDO/1 quantum-chemical structure-affinity relationship study with the KPG model is presented for the in vitro interaction of a group of classical, indole-derived and aminoalkylindole-derived cannabinoids with CB and CB2 receptors. From this work the following conclusions are obtained. CB and CB2 CB2 receptor affinities are regulated by different mechanisms involving orbital and charge control. Nevertheless CB and CB2 classical ligands share three common features: a hydrogen bond to a lysine (for CB ) or serine (for CB), a fully aromatic ring and a branched carbon side chain. In the case of indole-derived and aminoalkylindole-derived cannabinoids orientation and alignment rules have been defined as a basis for the comparison of noncongeneric molecules. In this way it was possible to associate the location of molecular fragments of these systems with known molecular systems such as classical cannabinoids. For aminoalkyhndoles we have proposed the locus with which they bind to a second receptor site that is available to WIN-55212-2 but not to classical cannabinoids. On the basis of our results we propose a new molecule that should help to discriminate between the above two receptor sites

Keywords : Structure-affinity relationships; QSAR; cannabinoid receptors; ZINDO/1; quantum pharmacology.

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