On the public citation graph

13C NMR Quantitative Spectrometric Data-Activity Relationship (QSDAR) Models of Steroids Binding the Aromatase Enzyme

https://doi.org/10.1021/ci010285e
0 signed · 52 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/qsar.19880070105openalex-snapshot
Crossvalidation, Bootstrapping, and Partial Least Squares Compared with Multiple Regression in Conventional QSAR Studies
inferredcites →https://doi.org/10.1002/qsar.19920110208openalex-snapshot
MULTICASE 1. A Hierarchical Computer Automated Structure Evaluation Program
inferredcites →https://doi.org/10.1006/taap.2000.9043openalex-snapshot
13C NMR and Electron Ionization Mass Spectrometric Data-Activity Relationship Model of Estrogen Receptor Binding
inferredcites →https://doi.org/10.1007/bf00134175openalex-snapshot
E-state fields: Applications to 3D QSAR
inferredcites →https://doi.org/10.1007/bf00355042openalex-snapshot
Three-dimensional quantitative structure-activity relationships of steroid aromatase inhibitors
inferredcites →https://doi.org/10.1007/bf00682736openalex-snapshot
Aromatase and its inhibitors in breast cancer treatment ? overview and perspective
inferredcites →https://doi.org/10.1016/0006-291x(91)91997-qopenalex-snapshot
6α,7 ga-Cyclopropane derivatives of androst-4-ene: A novel class of competitive aromatase inhibitors
inferredcites →https://doi.org/10.1016/0960-0760(94)90269-0openalex-snapshot
Aromatase inhibitors in the treatment of breast cancer
inferredcites →https://doi.org/10.1016/s0003-2670(01)83100-7openalex-snapshot
Hose — a novel substructure code
inferredcites →https://doi.org/10.1016/s0006-291x(89)80102-0openalex-snapshot
19-hydroxy-4-androsten-17-one: Potential competitive inhibitor of estrogen biosynthesis
inferredcites →https://doi.org/10.1021/ac00083a005openalex-snapshot
Prediction of Gas Chromatographic Retention Times and Response Factors Using a General Qualitative Structure-Property Relationships Treatment
inferredcites →https://doi.org/10.1021/ci000331vopenalex-snapshot
Producing 13C NMR, Infrared Absorption, and Electron Ionization Mass Spectrometric Data Models of the Monodechlorination of Chlorobenzenes, Chlorophenols, and Chloroanilines
inferredcites →https://doi.org/10.1021/ci990038zopenalex-snapshot
Comparative Spectra Analysis (CoSA): Spectra as Three-Dimensional Molecular Descriptors for the Prediction of Biological Activities
inferredcites →https://doi.org/10.1021/ja00226a005openalex-snapshot
Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins
inferredcites →https://doi.org/10.1021/ja00336a004openalex-snapshot
Artificial intelligence approach to structure-activity studies. Computer automated structure evaluation of biological activity of organic molecules
inferredcites →https://doi.org/10.1021/ja00336a005openalex-snapshot
Orbital interactions in some polycycloalkyl halides: a photoelectron spectroscopic study
inferredcites →https://doi.org/10.1021/ja01077a029openalex-snapshot
A Correlation of Chemical Shifts with Inductive Effect Parameters
inferredcites →https://doi.org/10.1021/jm00112a028openalex-snapshot
Synthesis and biochemical studies of 16- or 19-substituted androst-4-enes as aromatase inhibitors
inferredcites →https://doi.org/10.1021/jm00112a029openalex-snapshot
Syntheses of tolrestat analogs containing additional substituents in the ring and their evaluation as aldose reductase inhibitors. Identification of potent, orally active 2-fluoro derivatives
inferredcites →https://doi.org/10.1021/jp953224qopenalex-snapshot
Correlation of Boiling Points with Molecular Structure. 1. A Training Set of 298 Diverse Organics and a Test Set of 9 Simple Inorganics
inferredcites →https://doi.org/10.1023/a:1008048822117openalex-snapshot
QSAR modeling with the electrotopological state indices: Corticosteroids
inferredcites →https://doi.org/10.1210/endo.138.9.5487openalex-snapshot
QSAR Models for Binding of Estrogenic Compounds to Estrogen Receptor α and β Subtypes
inferredcites →https://doi.org/10.3109/03602538909103557openalex-snapshot
Human Aromatase
inferredcites →https://doi.org/10.7551/mitpress/5236.001.0001openalex-snapshot
Parallel Distributed Processing

What points at this work

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

inferred← citeshttps://doi.org/10.1002/9780470571224.pse007openalex-snapshot
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.200148238openalex-snapshot
ChemInform Abstract: 13C NMR Quantitative Spectrometric Data—Activity Relationship (QSDAR) Models of Steroids Binding the Aromatase Enzyme.
inferred← citeshttps://doi.org/10.1002/etc.5620220306openalex-snapshot
THE USE OF CARBON THIRTEEN NUCLEAR MAGNETIC RESONANCE SPECTRA TO PREDICT DIOXIN AND FURAN BINDING AFFINITIES TO THE ARYL HYDROCARBON RECEPTOR
inferred← citeshttps://doi.org/10.1002/jmr.570openalex-snapshot
Comparative structural connectivity spectra analysis (CoSCoSA) models of steroids binding to the aromatase enzyme
inferred← citeshttps://doi.org/10.1002/jps.21222openalex-snapshot
Topical Corticosteroids, Structure-Activity and the Glucocorticoid Receptor: Discovery and Development—A Process of ‘‘Planned Serendipity’’
inferred← citeshttps://doi.org/10.1002/minf.201300172openalex-snapshot
Global Model for Octanol‐Water Partition Coefficients from Proton Nuclear Magnetic Resonance Spectra
inferred← citeshttps://doi.org/10.1007/978-1-61779-965-5_10openalex-snapshot
Advances in Nuclear Magnetic Resonance for Drug Discovery
inferred← citeshttps://doi.org/10.1007/978-88-470-2409-0_3openalex-snapshot
Relazioni quantitative struttura-attività/proprietà
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.bmc.2007.12.055openalex-snapshot
A genetic algorithm optimized fuzzy neural network analysis of the affinity of inhibitors for HIV-1 protease
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/10.1016/j.jpba.2003.12.024openalex-snapshot
Prediction of anti-plasmodial activity of Artemisia annua extracts: application of NMR spectroscopy and chemometrics
inferred← citeshttps://doi.org/10.1021/ci0202842openalex-snapshot
Molecular Quantum Similarity-Based QSARs for Binding Affinities of Several Steroid Sets
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/10.1021/cr300314qopenalex-snapshot
Integrated Approach to Structure-Based Enzymatic Drug Design: Molecular Modeling, Spectroscopy, and Experimental Bioactivity
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/10.1023/b:modi.0000006536.02970.f0openalex-snapshot
Comparative molecular surface analysis: A novel tool for drug design and molecular diversity studies
inferred← citeshttps://doi.org/10.1039/c6gc00945jopenalex-snapshot
Predicting skin permeation rate from nuclear magnetic resonance spectra
inferred← citeshttps://doi.org/10.1080/10590501.2018.1537132openalex-snapshot
Computational prediction models for assessing endocrine disrupting potential of chemicals
inferred← citeshttps://doi.org/10.1289/ehp.1510267openalex-snapshot
CERAPP: Collaborative Estrogen Receptor Activity Prediction Project
inferred← citeshttps://doi.org/10.1385/1-59259-964-8:227openalex-snapshot
Nuclear Magnetic Resonance-Based Screening Methods for Drug Discovery
inferred← citeshttps://doi.org/10.17179/excli2018-1417openalex-snapshot
Towards understanding aromatase inhibitory activity via QSAR modeling
inferred← citeshttps://doi.org/10.3797/scipharm.0804-12openalex-snapshot
Chemical Structure Indices in In Silico Molecular Design
inferred← citeshttps://doi.org/10.4018/978-1-4666-8136-1.ch011openalex-snapshot
Ligand- and Structure-Based Drug Design of Non-Steroidal Aromatase Inhibitors (NSAIs) in Breast Cancer
inferred← citeshttps://doi.org/10.4018/978-1-5225-0549-5.ch004openalex-snapshot
Ligand- and Structure-Based Drug Design of Non-Steroidal Aromatase Inhibitors (NSAIs) in Breast Cancer
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.