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A System for Encoding and Searching Markush Structures
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-60761-274-2_6openalex-snapshot
Database Systems for Knowledge-Based Discovery
inferredcites →https://doi.org/10.1007/978-1-60761-931-4_13openalex-snapshot
LEAP into the Pfizer Global Virtual Library (PGVL) Space: Creation of Readily Synthesizable Design Ideas Automatically
inferredcites →https://doi.org/10.1007/bf02288323openalex-snapshot
Algorithms and codes for the assignment problem
inferredcites →https://doi.org/10.1016/j.wpi.2008.09.012openalex-snapshot
Towards in-house searching of Markush structures from patents
inferredcites →https://doi.org/10.1021/ci00001a004openalex-snapshot
The Chemical Abstracts Service generic chemical (Markush) structure storage and retrieval capability. 2. The MARPAT file
inferredcites →https://doi.org/10.1021/ci100261uopenalex-snapshot
Intuitive Patent Markush Structure Visualization Tool for Medicinal Chemists
inferredcites →https://doi.org/10.1021/ci100427jopenalex-snapshot
Molecular Dynamics Simulation, Free Energy Calculation and Structure-Based 3D-QSAR Studies of B-RAF Kinase Inhibitors
inferredcites →https://doi.org/10.1021/ci8002123openalex-snapshot
Chemical Markup, XML and the World-Wide Web. 8. Polymer Markup Language
inferredcites →https://doi.org/10.1021/ci950173lopenalex-snapshot
The Sheffield Generic Structures Projecta Retrospective Review
inferredcites →https://doi.org/10.1021/ci9600364openalex-snapshot
Handling Genericity in Chemical Structures Using the Markush Darc Software
inferredcites →https://doi.org/10.1021/ci990052bopenalex-snapshot
Chemical Markup, XML, and the Worldwide Web. 1. Basic Principles
inferredcites →https://doi.org/10.1021/jm00334a001openalex-snapshot
A Mathematical Contribution to Structure-Activity Studies
inferredcites →https://doi.org/10.1021/jm801070qopenalex-snapshot
Assessment of Additive/Nonadditive Effects in Structure−Activity Relationships: Implications for Iterative Drug Design
inferredcites →https://doi.org/10.1093/comjnl/45.6.631openalex-snapshot
RASCAL: Calculation of Graph Similarity using Maximum Common Edge Subgraphs
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9783527665143.ch02openalex-snapshot
Markush Structures and Chemical Patents
inferred← citeshttps://doi.org/10.1002/9783527677016.ch14openalex-snapshot
Coping with Combinatorial Space in Molecular Design
inferred← citeshttps://doi.org/10.1002/minf.70040openalex-snapshot
SpaceExpander: An Automated System for Drafting Markush Claims to Expand Chemical Space
inferred← citeshttps://doi.org/10.1007/978-3-031-10094-9_4openalex-snapshot
Interactions Between Systems, Their Differences and Environments
inferred← citeshttps://doi.org/10.1007/978-3-642-19231-9_17openalex-snapshot
Representation and Searching of Chemical-Structure Information in Patents
inferred← citeshttps://doi.org/10.1007/978-3-662-53817-3_15openalex-snapshot
Representation and Searching of Chemical Structure Information in Patents
inferred← citeshttps://doi.org/10.1007/s12293-024-00414-6openalex-snapshot
Molecular representations in bio-cheminformatics
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12345-5openalex-snapshot
Chemical Data Formats, Fingerprints, and Other Molecular Descriptions for Database Analysis and Searching
inferred← citeshttps://doi.org/10.1016/j.drudis.2014.09.021openalex-snapshot
The Pistoia Alliance Controlled Substance Compliance Service Project: from start to finish
inferred← citeshttps://doi.org/10.1016/j.wpi.2013.05.002openalex-snapshot
Markush structure searching by information professionals in the chemical industry – Our views and expectations
inferred← citeshttps://doi.org/10.1016/j.wpi.2019.03.006openalex-snapshot
Automatic generation of Markush structures from specific compounds
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.2c00403openalex-snapshot
A New CSRML Structure-Based Fingerprint Method for Profiling and Categorizing Per- and Polyfluoroalkyl Substances (PFAS)
inferred← citeshttps://doi.org/10.1021/acs.jcim.6b00082openalex-snapshot
A Novel Concept for the Search and Retrieval of the Derwent Markush Resource Database
inferred← citeshttps://doi.org/10.1021/ci400107kopenalex-snapshot
Searching for Recursively Defined Generic Chemical Patterns in Nonenumerated Fragment Spaces
inferred← citeshttps://doi.org/10.1124/dmd.115.067850openalex-snapshot
Database Extraction of Metabolite Information of Drug Candidates: Analysis of 27 AstraZeneca Compounds with Human Absorption, Distribution, Metabolism, and Excretion Data
inferred← citeshttps://doi.org/10.1186/s13321-019-0401-4openalex-snapshot
IntelliPatent: a web-based intelligent system for fast chemical patent claim drafting
inferred← citeshttps://doi.org/10.64898/2026.04.09.716825openalex-snapshot
SpaceExpander: Automated Drafting and Evaluation of Markush Claims for Chemical Space Expansion
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