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Target Family-Directed Exploration of Scaffolds with Different SAR Profiles
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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/(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/10.1002/1439-7633(20021004)3:10<928::aid-cbic928>3.0.co;2-5openalex-snapshot
Drug Design Strategies for Targeting G-Protein-Coupled Receptors
inferredcites →https://doi.org/10.1002/ange.200906555openalex-snapshot
A Scaffold‐Tree‐Merging Strategy for Prospective Bioactivity Annotation of γ‐Pyrones
inferredcites →https://doi.org/10.1002/cmdc.201000272openalex-snapshot
Structural and Potency Relationships between Scaffolds of Compounds Active against Human Targets
inferredcites →https://doi.org/10.1016/s1359-6446(03)02740-5openalex-snapshot
Chemical substructures in drug discovery
inferredcites →https://doi.org/10.1021/cc990047kopenalex-snapshot
Definition of Templates within Combinatorial Libraries
inferredcites →https://doi.org/10.1021/ci100059qopenalex-snapshot
Molecular Scaffolds with High Propensity to Form Multi-Target Activity Cliffs
inferredcites →https://doi.org/10.1021/ci1003637openalex-snapshot
Polypharmacology Directed Compound Data Mining: Identification of Promiscuous Chemotypes with Different Activity Profiles and Comparison to Approved Drugs
inferredcites →https://doi.org/10.1021/ci200179yopenalex-snapshot
Lessons Learned from Molecular Scaffold Analysis
inferredcites →https://doi.org/10.1021/ci600338xopenalex-snapshot
The Scaffold Tree − Visualization of the Scaffold Universe by Hierarchical Scaffold Classification
inferredcites →https://doi.org/10.1021/ci7003412openalex-snapshot
Scaffold Topologies. 1. Exhaustive Enumeration up to Eight Rings
inferredcites →https://doi.org/10.1021/jm049032dopenalex-snapshot
HierS: Hierarchical Scaffold Clustering Using Topological Chemical Graphs
inferredcites →https://doi.org/10.1021/jm060217popenalex-snapshot
Quest for the Rings. In Silico Exploration of Ring Universe To Identify Novel Bioactive Heteroaromatic Scaffolds
inferredcites →https://doi.org/10.1021/jm701021bopenalex-snapshot
Kinase-likeness and Kinase-Privileged Fragments: Toward Virtual Polypharmacology
inferredcites →https://doi.org/10.1021/jm9014229openalex-snapshot
Systematic Analysis of Public Domain Compound Potency Data Identifies Selective Molecular Scaffolds across Druggable Target Families
inferredcites →https://doi.org/10.1021/jm9602928openalex-snapshot
The Properties of Known Drugs. 1. Molecular Frameworks
inferredcites →https://doi.org/10.1038/nchembio.188openalex-snapshot
Bioactivity-guided mapping and navigation of chemical space
inferredcites →https://doi.org/10.1039/c0md00156bopenalex-snapshot
Global assessment of scaffold hopping potential for current pharmaceutical targets
inferredcites →https://doi.org/10.1101/gr.1239303openalex-snapshot
Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks
inferredcites →https://doi.org/10.2174/092986706775197999openalex-snapshot
Privileged Structures as Leads in Medicinal Chemistry
inferredcites →https://doi.org/10.2174/138955706778742768openalex-snapshot
On Scaffolds and Hopping in Medicinal Chemistry
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.ch03openalex-snapshot
Scaffold Diversity in Medicinal Chemistry Space
inferred← citeshttps://doi.org/10.1007/978-3-031-04998-9_14openalex-snapshot
Polypharmacology in Predicting Drug Toxicity: Drug Promiscuity
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2013.01.016openalex-snapshot
Structure and dynamics of molecular networks: A novel paradigm of drug discovery
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.7b00954openalex-snapshot
The Rise and Fall of a Scaffold: A Trend Analysis of Scaffolds in the Medicinal Chemistry Literature
inferred← citeshttps://doi.org/10.1186/s13321-021-00526-yopenalex-snapshot
“Molecular Anatomy”: a new multi-dimensional hierarchical scaffold analysis tool
inferred← citeshttps://doi.org/10.14233/ajchem.2023.28078openalex-snapshot
Synthesis, Characterization and Evaluation of Anticancer Activity of New Pyrazole-5-carboxamide Derivatives
inferred← citeshttps://doi.org/10.3390/molecules27103300openalex-snapshot
Quantitative and Qualitative Analysis of the Anti-Proliferative Potential of the Pyrazole Scaffold in the Design of Anticancer Agents
inferred← citeshttps://doi.org/10.3390/molecules28186584openalex-snapshot
NMR-Verified Dearomatization of 5,7-Substituted Pyrazolo[1,5-a]pyrimidines
inferred← citeshttps://doi.org/10.3390/ph18050714openalex-snapshot
Machine Learning-Driven Consensus Modeling for Activity Ranking and Chemical Landscape Analysis of HIV-1 Inhibitors
inferred← citeshttps://doi.org/10.6084/m9.figshare.15047880openalex-snapshot
Additional file 1 of “Molecular Anatomy”: a new multi-dimensional hierarchical scaffold analysis tool
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