On the public citation graph
Identification of New Fyn Kinase Inhibitors Using a FLAP-Based Approach
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.
1 of the 46 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-11): 10.1523/jneurosci.1858-12.2012 (notice 2025-03-12).
Dataset join, best-effort; this page does not check the publisher record.
Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0);
dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
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known work and none has been retracted — and get a dated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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ijc.23579openalex-snapshotLysophosphatidic acid induces ovarian cancer cell dispersal by activating Fyn kinase associated with p120‐catenin
inferredcites →https://doi.org/10.1002/ijc.24177openalex-snapshotA signature predictive of disease outcome in breast carcinomas, identified by quantitative immunocytochemical assays
inferredcites →https://doi.org/10.1007/s10822-012-9612-8openalex-snapshotLigand-, structure- and pharmacophore-based molecular fingerprints: a case study on adenosine A1, A2A, A2B, and A3 receptor antagonists
inferredcites →https://doi.org/10.1016/s0304-3940(02)01439-8openalex-snapshotTyrosine kinase and tyrosine phosphatase participate in regulation of interactions of NMDA receptor subunit 2A with Src and Fyn mediated by PSD-95 after transient brain ischemia
inferredcites →https://doi.org/10.1021/ci300153dopenalex-snapshotGRID-Based Three-Dimensional Pharmacophores I: FLAPpharm, a Novel Approach for Pharmacophore Elucidation
inferredcites →https://doi.org/10.1021/ci600253eopenalex-snapshotA Common Reference Framework for Analyzing/Comparing Proteins and Ligands. Fingerprints for Ligands And Proteins (FLAP): Theory and Application
inferredcites →https://doi.org/10.1021/jm060727jopenalex-snapshot2-Aminothiazole as a Novel Kinase Inhibitor Template. Structure−Activity Relationship Studies toward the Discovery of N -(2-Chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1- piperazinyl)]-2-methyl-4-pyrimidinyl]amino)]-1,3-thiazole-5-carboxamide (Dasatinib, BMS-354825) as a Potent pan -Src…
inferredcites →https://doi.org/10.1038/emboj.2009.289openalex-snapshotSynapse formation regulated by protein tyrosine phosphatase receptor T through interaction with cell adhesion molecules and Fyn
inferredcites →https://doi.org/10.1038/nn.3178openalex-snapshotAlzheimer amyloid-β oligomer bound to postsynaptic prion protein activates Fyn to impair neurons
inferredcites →https://doi.org/10.1042/bj20080909openalex-snapshotRegulation of microtubule nucleation from membranes by complexes of membrane-bound γ-tubulin with Fyn kinase and phosphoinositide 3-kinase
inferredcites →https://doi.org/10.1093/carcin/bgs109openalex-snapshotDeficiency of Fyn protein is prerequisite for apoptosis induced by Src family kinase inhibitors in human mesothelioma cells
inferredcites →https://doi.org/10.1124/jpet.102.038380openalex-snapshotInhibition of Human T Cell Activation by Novel Src Kinase Inhibitors Is Dependent upon the Complexity of the Signal Delivered to the Cell
inferredcites →https://doi.org/10.1124/mol.111.077149openalex-snapshotFyn Inhibition by Cycloalkane-Fused 1,2-Dithiole-3-thiones Enhances Antioxidant Capacity and Protects Mitochondria from Oxidative Injury
inferredcites →https://doi.org/10.1158/1535-7163.mct-05-0171openalex-snapshotAP23846, a novel and highly potent Src family kinase inhibitor, reduces vascular endothelial growth factor and interleukin-8 expression in human solid tumor cell lines and abrogates downstream angiogenic processes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s11030-024-10905-wopenalex-snapshotIn silico screening of Fyn kinase inhibitors using classification-based QSAR model, molecular docking, molecular dynamics and ADME study
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2014.06.001openalex-snapshotThe Interplay Between Molecular Modeling and Chemoinformatics to Characterize Protein–Ligand and Protein–Protein Interactions Landscapes for Drug Discovery
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00140openalex-snapshotStudies on the ATP Binding Site of Fyn Kinase for the Identification of New Inhibitors and Their Evaluation as Potential Agents against Tauopathies and Tumors
inferred← citeshttps://doi.org/10.1021/ci5006806openalex-snapshotApplication of a FLAP-Consensus Docking Mixed Strategy for the Identification of New Fatty Acid Amide Hydrolase Inhibitors
inferred← citeshttps://doi.org/10.3233/jad-230828openalex-snapshotUnveiling Phytoconstituents with Inhibitory Potential Against Tyrosine-Protein Kinase Fyn: A Comprehensive Virtual Screening Approach Targeting Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/molecules20058772openalex-snapshotDevelopment and Validation of a Docking-Based Virtual Screening Platform for the Identification of New Lactate Dehydrogenase Inhibitors
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.