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Three-dimensional models of non-steroidal ligands: a comparative molecular field analysis.
- Source :
-
Steroids [Steroids] 2006 Jun; Vol. 71 (6), pp. 417-28. Date of Electronic Publication: 2006 Feb 14. - Publication Year :
- 2006
-
Abstract
- The estrogen receptor, ER, is an important biological target whose inhibition is known to be therapeutically relevant in the treatment of postmenopausal osteoporosis. In the present study, two prediction methods (CoMFA and GRIND (Almond)) were used to describe the binding modes of a set of estrogen receptor ligands. The critical alignment step presented in CoMFA was solved by using the information of the molecular descriptors space generated by grid-independent descriptors (GRIND). Then, it was possible to build robust and high predictive models based on the alignment-independent model. Since the structure of estrogen receptor is solved, the results of the present 3D QSAR models, given by the PLS maps based on molecular interaction fields (MIF) were compared to ligand-binding ER domains and showed good agreement.
- Subjects :
- Binding Sites
Binding, Competitive
Breast Neoplasms pathology
Cell Line, Tumor
Computer Simulation
Estrogens chemistry
Estrogens metabolism
Female
Humans
Hydrogen Bonding
Inhibitory Concentration 50
Ligands
Models, Molecular
Molecular Conformation
Molecular Structure
Raloxifene Hydrochloride chemistry
Raloxifene Hydrochloride metabolism
Reproducibility of Results
Tamoxifen analogs & derivatives
Tamoxifen chemistry
Tamoxifen metabolism
Quantitative Structure-Activity Relationship
Receptors, Estrogen chemistry
Receptors, Estrogen metabolism
Selective Estrogen Receptor Modulators chemistry
Selective Estrogen Receptor Modulators metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0039-128X
- Volume :
- 71
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Steroids
- Publication Type :
- Academic Journal
- Accession number :
- 16481019
- Full Text :
- https://doi.org/10.1016/j.steroids.2006.01.001