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Refinement and Use of the Approximate Similarity in QSAR Models for Benzodiazepine Receptor Ligands

https://doi.org/10.1021/ci600216h
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What this work says

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

inferredcites →https://doi.org/10.1002/9780470125892openalex-snapshot
Reviews in Computational Chemistry
inferredcites →https://doi.org/10.1007/s0089490050141openalex-snapshot
Encyclopedia of Computational Chemistry
inferredcites →https://doi.org/10.1016/0009-2614(93)87094-jopenalex-snapshot
Novel molecular descriptor for structure—property studies
inferredcites →https://doi.org/10.1016/s0223-5234(02)01334-xopenalex-snapshot
Local intersection volume: a new 3D descriptor applied to develop a 3D-QSAR pharmacophore model for benzodiazepine receptor ligands
inferredcites →https://doi.org/10.1016/s1093-3263(01)00123-1openalex-snapshot
Beware of q2!
inferredcites →https://doi.org/10.1016/s1359-6446(97)01079-9openalex-snapshot
QSAR and 3D QSAR in drug design Part 1: methodology
inferredcites →https://doi.org/10.1016/s1359-6446(97)01084-2openalex-snapshot
QSAR and 3D QSAR in drug design Part 2: applications and problems
inferredcites →https://doi.org/10.1021/ar50020a002openalex-snapshot
Quantitative approach to biochemical structure-activity relationships
inferredcites →https://doi.org/10.1021/ci0000777openalex-snapshot
Distance-Related Indexes in the Quantitative Structure−Property Relationship Modeling
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/ci050139zopenalex-snapshot
A Multivariate Analysis of HIV-1 Protease Inhibitors and Resistance Induced by Mutation
inferredcites →https://doi.org/10.1021/ci0503208openalex-snapshot
Molecular Transformations as a Way of Finding and Exploiting Consistent Local QSAR
inferredcites →https://doi.org/10.1021/ci9800211openalex-snapshot
Chemical Similarity Searching
inferredcites →https://doi.org/10.1021/jm049228dopenalex-snapshot
A General Method for Exploiting QSAR Models in Lead Optimization
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.200649217openalex-snapshot
Refinement and Use of the Approximate Similarity in QSAR Models for Benzodiazepine Receptor Ligands.
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/qsar.200730048openalex-snapshot
Description and Application of Similarity‐Based Methods for Fast and Simple QSAR Model Development
inferred← citeshttps://doi.org/10.1007/s00044-010-9306-5openalex-snapshot
3D-QSAR studies of 4-quinolone derivatives as high-affinity ligands at the benzodiazepine site of brain GABAA receptors
inferred← citeshttps://doi.org/10.1007/s00210-026-05648-4openalex-snapshot
From molecular mechanisms to digital surveillance: the 2010–2025 evolution of benzodiazepine and Z-drug misuse research
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.2013.04.003openalex-snapshot
An Algorithm for Pattern Extraction in Fingerprints
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/10.1016/j.ejmech.2007.09.004openalex-snapshot
Quantitative structure–activity relationship studies of a series of non-benzodiazepine structural ligands binding to benzodiazepine receptor
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/np400501uopenalex-snapshot
Indolo[3,2-a]carbazoles from a Deep-Water Sponge of the Genus Asteropus
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/10.1111/j.1747-0285.2011.01183.xopenalex-snapshot
A Structure‐based QSAR and Docking Study on Imidazo[1,5‐a][1,2,4]‐triazolo[1,5‐d][1,4,]benzodiazepines as Selective GABAAα5 Inverse Agonists
inferred← citeshttps://doi.org/10.2174/157340609788681494openalex-snapshot
QSAR Studies on 4-Quinolone Derivatives as High-Affinity Ligands at the Benzodiazepine Site of Brain GABAA Receptors
inferred← citeshttps://doi.org/10.2174/1573409911309020010openalex-snapshot
Structural Similarity and Descriptor Spaces for Clustering and Development of QSAR Models§
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