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Comparative Structural Connectivity Spectra Analysis (CoSCoSA) Models of Steroid Binding to the Corticosteroid Binding Globulin

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/chin.198632064openalex-snapshot

ChemInform Abstract: 1H and 13C Assignments from Sensitivity‐Enhanced Detection of Heteronuclear Multiple‐Bond Connectivity by 2D Multiple Quantum NMR

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Crossvalidation, Bootstrapping, and Partial Least Squares Compared with Multiple Regression in Conventional QSAR Studies

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MULTICASE 1. A Hierarchical Computer Automated Structure Evaluation Program

inferredcites →https://doi.org/10.1002/qsar.19970160406openalex-snapshot

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E-state fields: Applications to 3D QSAR

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Natural abundance nitrogen-15 NMR by enhanced heteronuclear spectroscopy

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Highly discriminating distance-based topological index

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Quantitative structure-activity relationships and ecological risk assessment: an overview of predictive aquatic toxicology research

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Neural Networks in QSAR and Drug Design

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Hose — a novel substructure code

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[12] Chemical shifts as a tool for structure determination

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[13] Use of chemical shifts and coupling constants in nuclear magnetic resonance structural studies on peptides and proteins

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Steroid-protein interactions. Human corticosteroid binding globulin: some physicochemical properties and binding specificity

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The Receptor-like Neural Network for Modeling Corticosteroid and Testosterone Binding Globulins

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Comparative Spectra Analysis (CoSA): Spectra as Three-Dimensional Molecular Descriptors for the Prediction of Biological Activities

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Orbital interactions in some polycycloalkyl halides: a photoelectron spectroscopic study

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Importance of nonbonded attraction in the stereochemistry of the SN2' reaction

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Protein φ and ψ dihedral restraints determined from multidimensional hypersurface correlations of backbone chemical shifts and their use in the determination of protein tertiary structures

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High-resolution Nuclear Magnetic Resonance

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Parallel Distributed Processing

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Combining NMR Spectral Information with Associated Structural Features to form Computationally Nonintensive, Rugged, and Objective Models of Biological Activity

inferred← citeshttps://doi.org/10.1002/9783527628766.biblioopenalex-snapshot

Bibliography

inferred← citeshttps://doi.org/10.1002/ardp.201000029openalex-snapshot

NMR QSAR Model for the Analysis of 4‐(5‐Arylamino‐1,3,4‐thiadiazol‐2‐yl)benzene‐1,3‐diols

inferred← citeshttps://doi.org/10.1002/chin.200247212openalex-snapshot

Comparative Structural Connectivity Spectra Analysis (CoSCoSA) Models of Steroid Binding to the Corticosteroid Binding Globulin.

inferred← citeshttps://doi.org/10.1016/b978-0-12-822248-5.00001-2openalex-snapshot

In silico modeling of environmental toxicity of drugs

inferred← citeshttps://doi.org/10.1016/j.chemolab.2010.10.007openalex-snapshot

Quantitative structure–spectral property relationships for functional groups of novel 1,2,5-thiadiazole compounds

inferred← citeshttps://doi.org/10.1016/j.drudis.2006.03.014openalex-snapshot

Computational modeling of biologically active molecules using NMR spectra

inferred← citeshttps://doi.org/10.1021/acs.chemrev.5c00259openalex-snapshot

Exploring the Frontiers of Computational NMR: Methods, Applications, and Challenges

inferred← citeshttps://doi.org/10.1021/ci034110bopenalex-snapshot

Spectroscopic QSAR Methods and Self-Organizing Molecular Field Analysis for Relating Molecular Structure and Estrogenic Activity

inferred← citeshttps://doi.org/10.1021/ci0342829openalex-snapshot

Discriminant Function Analyses of Liver-Specific Carcinogens

inferred← citeshttps://doi.org/10.1021/ci049925eopenalex-snapshot

Models of Steroid Binding Based on the Minimum Deviation of Structurally Assigned 13C NMR Spectra Analysis (MiDSASA)

inferred← citeshttps://doi.org/10.1021/ci050087dopenalex-snapshot

Identifying Biologically Active Compound Classes Using Phenotypic Screening Data and Sampling Statistics

inferred← citeshttps://doi.org/10.1021/ci050282sopenalex-snapshot

On the Use of 1H and 13C 1D NMR Spectra as QSPR Descriptors

inferred← citeshttps://doi.org/10.1021/ci3001698openalex-snapshot

13C NMR–Distance Matrix Descriptors: Optimal Abstract 3D Space Granularity for Predicting Estrogen Binding

inferred← citeshttps://doi.org/10.1021/cr100125dopenalex-snapshot

Use of13C NMR Chemical Shift as QSAR/QSPR Descriptor

inferred← citeshttps://doi.org/10.1023/a:1022479510524openalex-snapshot

Combining NMR spectral and structural data to form models of polychlorinated dibenzodioxins, dibenzofurans, and biphenyls binding to the AhR

inferred← citeshttps://doi.org/10.1186/s13321-017-0211-5openalex-snapshot

QuBiLS-MAS, open source multi-platform software for atom- and bond-based topological (2D) and chiral (2.5D) algebraic molecular descriptors computations

inferred← citeshttps://doi.org/10.2174/1568026619666190510093651openalex-snapshot

Higher-Order and Mixed Discrete Derivatives such as a Novel Graph- Theoretical Invariant for Generating New Molecular Descriptors

inferred← citeshttps://doi.org/10.3390/molecules17033383openalex-snapshot

Modeling Chemical Interaction Profiles: I. Spectral Data-Activity Relationship and Structure-Activity Relationship Models for Inhibitors and Non-inhibitors of Cytochrome P450 CYP3A4 and CYP2D6 Isozymes

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