Binary Quantitative Structure−Activity Relationship (QSAR) Analysis of Estrogen Receptor Ligands
- 16 December 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Chemical Information and Computer Sciences
- Vol. 39 (1), 164-168
- https://doi.org/10.1021/ci980140g
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Can We Learn To Distinguish between “Drug-like” and “Nondrug-like” Molecules?Journal of Medicinal Chemistry, 1998
- Three-Dimensional Quantitative Structure−Activity Relationship Study of Nonsteroidal Estrogen Receptor Ligands Using the Comparative Molecular Field Analysis/Cross-Validated r2-Guided Region Selection ApproachJournal of Medicinal Chemistry, 1998
- Using Artificial Neural Networks To Classify the Activity of Capsaicin and Its AnaloguesJournal of Chemical Information and Computer Sciences, 1997
- Clustering of Large Databases of Compounds: Using the MDL “Keys” as Structural DescriptorsJournal of Chemical Information and Computer Sciences, 1997
- The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding siteSteroids, 1997
- Cloning of a novel receptor expressed in rat prostate and ovary.Proceedings of the National Academy of Sciences, 1996
- Erratum: A canonical structure for the ligand-binding domain of nuclear receptorsNature Structural & Molecular Biology, 1996
- Comparative QSAR: Toward a Deeper Understanding of Chemicobiological InteractionsChemical Reviews, 1996
- Crystal structure of the ligand-binding domain of the human nuclear receptor RXR-αNature, 1995
- Correlation of Biological Activity of Phenoxyacetic Acids with Hammett Substituent Constants and Partition CoefficientsNature, 1962