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A Steroids QSAR Approach Based on Approximate Similarity Measurements

https://doi.org/10.1021/ci0600511
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What this work says

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

inferredcites →https://doi.org/10.1002/0471678856openalex-snapshot
Reviews in Computational Chemistry
inferredcites →https://doi.org/10.1002/1521-3838(200006)19:3<237::aid-qsar237>3.0.co;2-aopenalex-snapshot
The Thirty-one Benchmark Steroids Revisited: Comparative Molecular Moment Analysis (CoMMA) with Principal Component Regression
inferredcites →https://doi.org/10.1002/9783527613106openalex-snapshot
Handbook of Molecular Descriptors
inferredcites →https://doi.org/10.1002/9783527616824openalex-snapshot
QSAR: Hansch Analysis and Related Approaches
inferredcites →https://doi.org/10.1007/0-306-46858-1_13openalex-snapshot
The CoMFA Steroids as a Benchmark Dataset for Development of 3D QSAR Methods
inferredcites →https://doi.org/10.1007/s0089490050141openalex-snapshot
Encyclopedia of Computational Chemistry
inferredcites →https://doi.org/10.1016/s0165-6147(00)89046-xopenalex-snapshot
QSAR: Hansch analysis and related approaches
inferredcites →https://doi.org/10.1016/s0169-7439(96)00063-9openalex-snapshot
Modeling and prediction of molecular properties. Theory of grid-weighted holistic invariant molecular (G-WHIM) descriptors
inferredcites →https://doi.org/10.1021/ar50020a002openalex-snapshot
Quantitative approach to biochemical structure-activity relationships
inferredcites →https://doi.org/10.1021/ci00001a026openalex-snapshot
Topological organic chemistry. 3. Graph theory, binary and decimal adjacency matrices, and topological indices of alkanes
inferredcites →https://doi.org/10.1021/ci00001a027openalex-snapshot
Chemical Abstracts ONLINE: a study of the quality of controlled terms
inferredcites →https://doi.org/10.1021/ci00005a012openalex-snapshot
Notes on fully benzenoid hydrocarbons and their constant-isomer series
inferredcites →https://doi.org/10.1021/ci00021a022openalex-snapshot
Topological Organic Chemistry. 8. Graph Theory and Topological Indexes of Heteronuclear Systems
inferredcites →https://doi.org/10.1021/ci00027a011openalex-snapshot
Topological Organic Chemistry. 9. Graph Theory and Molecular Topological Indices of Stereoisomeric Organic Compounds
inferredcites →https://doi.org/10.1021/ci00063a012openalex-snapshot
Topological organic chemistry. 1. Graph theory and topological indices of alkanes
inferredcites →https://doi.org/10.1021/ci00065a007openalex-snapshot
Topological organic chemistry. 2. Graph theory, matrix determinants and eigenvalues, and topological indexes of alkanes
inferredcites →https://doi.org/10.1021/ci0103469openalex-snapshot
Novel ZE-Isomerism Descriptors Derived from Molecular Topology and Their Application to QSAR Analysis
inferredcites →https://doi.org/10.1021/ci025516bopenalex-snapshot
QSAR Modeling Using Chirality Descriptors Derived from Molecular Topology
inferredcites →https://doi.org/10.1021/ci9800211openalex-snapshot
Chemical Similarity Searching
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/jm00050a010openalex-snapshot
Molecular Similarity Indices in a Comparative Analysis (CoMSIA) of Drug Molecules to Correlate and Predict Their Biological Activity
inferredcites →https://doi.org/10.1021/jm950589qopenalex-snapshot
Comparative Molecular Moment Analysis (CoMMA): 3D-QSAR without Molecular Superposition
inferredcites →https://doi.org/10.1021/jo0267697openalex-snapshot
Computational Studies of Chiral Catalysts: A Comparative Molecular Field Analysis of an Asymmetric Diels−Alder Reaction with Catalysts Containing Bisoxazoline or Phosphinooxazoline Ligands
inferredcites →https://doi.org/10.1201/9781482296945openalex-snapshot
Topological Indices and Related Descriptors in QSAR and QSPR

What points at this work

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

inferred← citeshttps://doi.org/10.1002/9783527645121.ch7openalex-snapshot
Structural‐Similarity‐Based Approaches for the Development of Clustering and QSPR/QSAR Models in Chemical Databases
inferred← citeshttps://doi.org/10.1002/chin.200641212openalex-snapshot
A Steroids QSAR Approach Based on Approximate Similarity Measurements.
inferred← citeshttps://doi.org/10.1002/jcc.20671openalex-snapshot
QSAR models based on isomorphic and nonisomorphic data fusion for predicting the blood brain barrier permeability
inferred← citeshttps://doi.org/10.1002/jssc.201200423openalex-snapshot
Structure‐retention relationship study of polyoxygenated steroids
inferred← citeshttps://doi.org/10.1002/qsar.200730048openalex-snapshot
Description and Application of Similarity‐Based Methods for Fast and Simple QSAR Model Development
inferred← citeshttps://doi.org/10.1007/s10822-013-9637-7openalex-snapshot
QSAR model based on weighted MCS trees approach for the representation of molecule data sets
inferred← citeshttps://doi.org/10.1007/s10910-007-9283-1openalex-snapshot
Approximate similarity and QSAR in the study of spirosuccinimide type aldose reductase inhibitors
inferred← citeshttps://doi.org/10.1016/j.chemolab.2018.03.007openalex-snapshot
A new data representation based on relative measurements and fingerprint patterns for the development of QSAR regression models
inferred← citeshttps://doi.org/10.1021/acs.jcim.7b00492openalex-snapshot
Advantages of Relative versus Absolute Data for the Development of Quantitative Structure–Activity Relationship Classification Models
inferred← citeshttps://doi.org/10.1021/ci100484zopenalex-snapshot
Analysis and Study of Molecule Data Sets Using Snowflake Diagrams of Weighted Maximum Common Subgraph Trees
inferred← citeshttps://doi.org/10.1021/ci300182popenalex-snapshot
Similarity Boosted Quantitative Structure–Activity Relationship—A Systematic Study of Enhancing Structural Descriptors by Molecular Similarity
inferred← citeshttps://doi.org/10.1080/1062936x.2012.719543openalex-snapshot
Comparison of representational spaces based on structural information in the development of QSAR models for benzylamino enaminone derivatives
inferred← citeshttps://doi.org/10.1080/1062936x.2018.1442879openalex-snapshot
QSAR classification and regression models for β-secretase inhibitors using relative distance matrices
inferred← citeshttps://doi.org/10.1080/1062936x.2018.1494038openalex-snapshot
Robust QSAR prediction models for volume of distribution at steady state in humans using relative distance measurements
inferred← citeshttps://doi.org/10.2174/1573409911309020010openalex-snapshot
Structural Similarity and Descriptor Spaces for Clustering and Development of QSAR Models§
inferred← citeshttps://doi.org/10.3390/molecules24091698openalex-snapshot
Analysis and Comparison of Vector Space and Metric Space Representations in QSAR Modeling
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