On the public citation graph

Assessment of Molecular Similarity from the Analysis of Randomly Generated Structural Fragment Populations

0 signed · 53 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/(sici)1521-3773(19991004)38:19<2894::aid-anie2894>3.0.co;2-fopenalex-snapshot
“Scaffold-Hopping” by Topological Pharmacophore Search: A Contribution to Virtual Screening
inferredcites →https://doi.org/10.1002/(sici)1521-3773(19991004)38:19<2896::aid-anie2896>3.0.co;2-3openalex-snapshot
Cascade Reactions in Quantitative Solid-State Syntheses
inferredcites →https://doi.org/10.1002/j.1538-7305.1948.tb01338.xopenalex-snapshot
A Mathematical Theory of Communication
inferredcites →https://doi.org/10.1002/mas.20072openalex-snapshot
Processing and classification of protein mass spectra
inferredcites →https://doi.org/10.1016/s1359-6446(03)02740-5openalex-snapshot
Chemical substructures in drug discovery
inferredcites →https://doi.org/10.1021/ci0001482openalex-snapshot
Selected Concepts and Investigations in Compound Classification, Molecular Descriptor Analysis, and Virtual Screening
inferredcites →https://doi.org/10.1021/ci00046a002openalex-snapshot
Atom pairs as molecular features in structure-activity studies: definition and applications
inferredcites →https://doi.org/10.1021/ci00046a003openalex-snapshot
Computer code for producing Eh-pH plots of equilibrium chemical systems
inferredcites →https://doi.org/10.1021/ci00057a005openalex-snapshot
SMILES, a chemical language and information system. 1. Introduction to methodology and encoding rules
inferredcites →https://doi.org/10.1021/ci0102867openalex-snapshot
Differential Shannon Entropy as a Sensitive Measure of Differences in Database Variability of Molecular Descriptors
inferredcites →https://doi.org/10.1021/ci025592eopenalex-snapshot
Similarity Searching Using Reduced Graphs
inferredcites →https://doi.org/10.1021/ci034006uopenalex-snapshot
Prediction of Aqueous Solubility and Partition Coefficient Optimized by a Genetic Algorithm Based Descriptor Selection Method
inferredcites →https://doi.org/10.1021/ci9800211openalex-snapshot
Chemical Similarity Searching
inferredcites →https://doi.org/10.1021/ci990182kopenalex-snapshot
Base Information Content in Organic Formulas
inferredcites →https://doi.org/10.1021/cr990076hopenalex-snapshot
Mass Spectrometry in Proteomics
inferredcites →https://doi.org/10.1021/es00001a734openalex-snapshot
MDL Information Systems, Inc.
inferredcites →https://doi.org/10.1021/jm9602928openalex-snapshot
The Properties of Known Drugs. 1. Molecular Frameworks
inferredcites →https://doi.org/10.1023/a:1008184403558openalex-snapshot
De novo design of molecular architectures by evolutionary assembly of drug-derived building blocks
inferredcites →https://doi.org/10.1038/nrd941openalex-snapshot
Integration of virtual and high-throughput screening
inferredcites →https://doi.org/10.1063/1.95082openalex-snapshot
Ultrasensitive fingerprint detection of organometallic compounds by laser multiphoton ionization mass spectrometry

What points at this work

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

inferred← citeshttps://doi.org/10.1002/chin.200649214openalex-snapshot
Assessment of Molecular Similarity from the Analysis of Randomly Generated Structural Fragment Populations.
inferred← citeshttps://doi.org/10.1002/cmdc.200700199openalex-snapshot
Similarity Searching using Compound Class‐Specific Combinations of Substructures Found in Randomly Generated Molecular Fragment Populations
inferred← citeshttps://doi.org/10.1002/cmdc.200900035openalex-snapshot
Fragment Formal Concept Analysis Accurately Classifies Compounds with Closely Related Biological Activities
inferred← citeshttps://doi.org/10.1002/med.21255openalex-snapshot
Fragment Informatics and Computational Fragment‐Based Drug Design: An Overview and Update
inferred← citeshttps://doi.org/10.1007/7653_2015_51openalex-snapshot
Computational Fragment-Based Drug Design
inferred← citeshttps://doi.org/10.1007/978-0-8176-4904-3_9openalex-snapshot
Markov Entropy Centrality: Chemical, Biological, Crime, and Legislative Networks
inferred← citeshttps://doi.org/10.1007/978-1-4939-2486-8_10openalex-snapshot
Computational Methods for Fragment-Based Ligand Design: Growing and Linking
inferred← citeshttps://doi.org/10.1007/978-1-60761-839-3_9openalex-snapshot
Fragment Descriptors in Structure–Property Modeling and Virtual Screening
inferred← citeshttps://doi.org/10.1007/s00894-008-0335-7openalex-snapshot
Data mining using template-based molecular docking on tetrahydroimidazo-[4,5,1-jk][1,4]-benzodiazepinone (TIBO) derivatives as HIV-1RT inhibitors
inferred← citeshttps://doi.org/10.1007/s11030-008-9078-8openalex-snapshot
Distribution of randomly generated activity class characteristic substructures in diverse active and database compounds
inferred← citeshttps://doi.org/10.1016/j.drudis.2007.01.011openalex-snapshot
Molecular similarity analysis in virtual screening: foundations, limitations and novel approaches
inferred← citeshttps://doi.org/10.1021/ci200472sopenalex-snapshot
Improving Classical Substructure-Based Virtual Screening to Handle Extrapolation Challenges
inferred← citeshttps://doi.org/10.1021/ci400324uopenalex-snapshot
Noncontiguous Atom Matching Structural Similarity Function
inferred← citeshttps://doi.org/10.1021/ci600377mopenalex-snapshot
Chemical Database Mining through Entropy-Based Molecular Similarity Assessment of Randomly Generated Structural Fragment Populations
inferred← citeshttps://doi.org/10.1021/ci600488xopenalex-snapshot
Information Content in Organic Molecules: Brownian Processing at Low Levels
inferred← citeshttps://doi.org/10.1021/ci700108qopenalex-snapshot
Mining of Randomly Generated Molecular Fragment Populations Uncovers Activity-Specific Fragment Hierarchies
inferred← citeshttps://doi.org/10.1021/ci700251bopenalex-snapshot
Mapping of Activity-Specific Fragment Pathways Isolated from Random Fragment Populations Reveals the Formation of Coherent Molecular Cores
inferred← citeshttps://doi.org/10.1021/ci800020sopenalex-snapshot
Core Trees and Consensus Fragment Sequences for Molecular Representation and Similarity Analysis
inferred← citeshttps://doi.org/10.1021/ci8003896openalex-snapshot
Substructure Mining of GPCR Ligands Reveals Activity-Class Specific Functional Groups in an Unbiased Manner
inferred← citeshttps://doi.org/10.1021/jp7119526openalex-snapshot
Information and Classical Thermodynamic Transformations
inferred← citeshttps://doi.org/10.1021/jp711953ropenalex-snapshot
Experimental Investigation of Information Processing under Irreversible Brownian Conditions: Work/Time Analysis of Paper Chromatograms
inferred← citeshttps://doi.org/10.1039/9781847558879-00001openalex-snapshot
Fragment Descriptors in SAR/QSAR/QSPR Studies, Molecular Similarity Analysis and in Virtual Screening
inferred← citeshttps://doi.org/10.1039/9781847558879-00120openalex-snapshot
Molecular Similarity Analysis in Virtual Screening
inferred← citeshttps://doi.org/10.1039/9781849732093-00301openalex-snapshot
Developing the Applicability Domain of In Silico Models: Relevance, Importance and Methods
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2008.00723.xopenalex-snapshot
RelACCS‐FP: A Structural Minimalist Approach to Fingerprint Design
inferred← citeshttps://doi.org/10.1177/026119290903700510openalex-snapshot
Definition of the Applicability Domains of Knowledge-based Predictive Toxicology Expert Systems by Using a Structural Fragment-based Approach
inferred← citeshttps://doi.org/10.1186/1758-2946-2-s1-o12openalex-snapshot
Random molecular substructures as fragment-type descriptors
inferred← citeshttps://doi.org/10.1186/s13321-019-0386-zopenalex-snapshot
A visual approach for analysis and inference of molecular activity spaces
inferred← citeshttps://doi.org/10.2174/092986712800167356openalex-snapshot
Privileged Structures - Dream or Reality: Preferential Organization of Azanaphthalene Scaffold
inferred← citeshttps://doi.org/10.2174/9781608057450113010005openalex-snapshot
Building a Chemical Space Based on Fragment Descriptors
inferred← citeshttps://doi.org/10.4155/fmc.10.277openalex-snapshot
Computational Medicinal Chemistry in Fragment-Based Drug Discovery: What, How and When
inferred← citeshttps://doi.org/10.70675/763f9808zf2fez469ezba2cz56622b867580openalex-snapshot
Chimiothèque : vers une approche rationnelle pour la sélection de sous-chimiothèques
inferred← citeshttps://doi.org/10.70675/f0cedbe1z6c18z48e4z901cza22a3ae4e98aopenalex-snapshot
Les triplets pharmacophoriques flous : développement et applications
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.