D. T. Stanton

发表

Application of Nearest‐Neighbor and Cluster Analyses in Pharmaceutical Lead Discovery.

D. T. Stanton, T. Morris, S. Roychoudhury, 1999 .

Computer-assisted prediction of gas chromatographic retention indexes of pyrazines

P. Jurs, D. T. Stanton, 1989 .

Development and use of charged partial surface area structural descriptors in computer-assisted quantitative structure-property relationship studies

P. Jurs, D. T. Stanton, 1990 .

Understanding the underlying dimensions in perfumers’ odor perception space as a basis for developing meaningful odor maps

D. T. Stanton, M. Zarzo, 2009, Attention, perception & psychophysics.

Identification of latent variables in a semantic odor profile database using principal component analysis.

D. T. Stanton, M. Zarzo, 2006, Chemical Sensors.

6. Molecular Modeling of Formulated Consumer Products

Peter H. Koenig, D. T. Stanton, B. Murch, 2014 .

Molecular Modeling of Formulated Consumer Products

Peter H. Koenig, David M. Eike, D. T. Stanton, 2011 .

Discovery of novel SERCA inhibitors by virtual screening of a large compound library.

D. T. Stanton, S. Paula, M. Lape, 2011, European journal of medicinal chemistry.

Comparison of LC/MS and SFC/MS for screening of a large and diverse library of pharmaceutically relevant compounds.

D. T. Stanton, K. Morand, J. Pinkston, 2006, Analytical chemistry.

Novel phenolic inhibitors of the sarco/endoplasmic reticulum calcium ATPase: identification and characterization by quantitative structure–activity relationship modeling and virtual screening

D. T. Stanton, S. Paula, E. Hofmann, 2015, Journal of enzyme inhibition and medicinal chemistry.

A novel class of fungicides: (2-pyridylthio)methyl benzoate N-oxides

R. A. Davis, A. Doweyko, D. T. Stanton, 1983 .

Development and interpretation of a QSAR model for in vitro breast cancer (MCF-7) cytotoxicity of 2-phenylacrylonitriles

David T. Stanton, Adam McCluskey, Stefan Paula, 2021, Journal of Computer-Aided Molecular Design.

The Effect of Freeze/Thaw Cycles on the Stability of Compounds in DMSO

Sandra L. Nelson, David T. Stanton, Barbara R. Kuzmak, 2003, Journal of biomolecular screening.

On the importance of topological descriptors in understanding structure–property relationships

David T. Stanton, D. T. Stanton, 2008, J. Comput. Aided Mol. Des..

Effects of surfactants on the rotifer, Brachionus calyciflorus, in a chronic toxicity test and in the development of qsars

D. T. Stanton, D. Versteeg, Michael A. Pence, 1997 .

Development and Use of a High-Throughput Bacterial DNA Gyrase Assay to Identify Mammalian Topoisomerase II Inhibitors with Whole-Cell Anticancer Activity

D. T. Stanton, S. Roychoudhury, C. Catrenich, 2003, Journal of biomolecular screening.

Application of Nearest-Neighbor and Cluster Analyses in Pharmaceutical Lead Discovery

David T. Stanton, Timothy W. Morris, Christian N. Parker, 1999, J. Chem. Inf. Comput. Sci..

Evaluation and Use of BCUT Descriptors in QSAR and QSPR Studies

David T. Stanton, D. T. Stanton, 1999, J. Chem. Inf. Comput. Sci..

Elution and preliminary structure-retention modeling of polar and ionic substances in supercritical fluid chromatography using volatile ammonium salts as mobile phase additives.

D. T. Stanton, J. Pinkston, D. Wen, 2004, Journal of separation science.

The Effect of Room-Temperature Storage on the Stability of Compounds in DMSO

Sandra L. Nelson, David T. Stanton, Barbara R. Kuzmak, 2003, Journal of biomolecular screening.

Profiling of Drugs for Membrane Activity Using Liposomes as an In Vitro Model System

D. T. Stanton, A. Curnow, L. Grinius, 2002, Drug development and industrial pharmacy.

Computer-assisted prediction of normal boiling points of pyrans and pyrroles

David T. Stanton, Peter C. Jurs, Martin G. Hicks, 1992, J. Chem. Inf. Comput. Sci..

Charged partial surface area (CPSA) descriptors QSAR applications

S Dimitrov, D. T. Stanton, O. Mekenyan, 2002, SAR and QSAR in environmental research.

QSAR and QSPR model interpretation using partial least squares (PLS) analysis.

David T Stanton, D. T. Stanton, 2012, Current computer-aided drug design.

Development of a Quantitative Structure-Activity Relationship Model for Inhibition of Gram-positive Bacterial Cell Growth by Biarylamides

David T. Stanton, Prakash J. Madhav, Larry J. Wilson, 2004, J. Chem. Inf. Model..

Computer-assisted study of the relationship between molecular structure and surface tension of organic compounds

David T. Stanton, Peter C. Jurs, P. Jurs, 1992, J. Chem. Inf. Comput. Sci..

Structure–activity relationships for acute and chronic toxicity of alcohol ether sulfates

S. Dyer, D. T. Stanton, D. Cherry, 2000 .

Computer‐Assisted Prediction of Normal Boiling Points of Furans, Tetrahydrofurans, and Thiophenes.

David T. Stanton, Peter C. Jurs, Martin G. Hicks, 1991 .

Computer-assisted prediction of normal boiling points of furans, tetrahydrofurans, and thiophenes

David T. Stanton, Peter C. Jurs, Martin G. Hicks, 1991, J. Chem. Inf. Comput. Sci..

On the Physical Interpretation of QSAR Models

David T. Stanton, D. T. Stanton, 2003, J. Chem. Inf. Comput. Sci..