On the public citation graph
Improved FlexX Docking Using FlexS-Determined Base Fragment Placement
0 signed · 57 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.
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known work and none has been retracted — and get a dated CiteStamped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/jcc.540150503openalex-snapshot
ICM—A new method for protein modeling and design: Applications to docking and structure prediction from the distorted native conformation
inferredcites →https://doi.org/10.1006/jmbi.1996.0477openalex-snapshot
A Fast Flexible Docking Method using an Incremental Construction Algorithm
inferredcites →https://doi.org/10.1006/jmbi.1996.0776openalex-snapshot
Molecular docking to ensembles of protein structures 1 1Edited by B. Honig
inferredcites →https://doi.org/10.1006/jmbi.1996.0897openalex-snapshot
Development and validation of a genetic algorithm for flexible docking 1 1Edited by F. E. Cohen
inferredcites →https://doi.org/10.1006/jmbi.1999.3371openalex-snapshot
Knowledge-based scoring function to predict protein-ligand interactions
inferredcites →https://doi.org/10.1006/jmbi.2001.4551openalex-snapshot
FlexE: efficient molecular docking considering protein structure variations
inferredcites →https://doi.org/10.1016/0022-2836(82)90153-xopenalex-snapshot
A geometric approach to macromolecule-ligand interactions
inferredcites →https://doi.org/10.1016/s1093-3263(01)00125-5openalex-snapshot
Consensus scoring for ligand/protein interactions
inferredcites →https://doi.org/10.1016/s1093-3263(02)00164-xopenalex-snapshot
LigandFit: a novel method for the shape-directed rapid docking of ligands to protein active sites
inferredcites →https://doi.org/10.1021/jm0003992openalex-snapshot
Detailed Analysis of Scoring Functions for Virtual Screening
inferredcites →https://doi.org/10.1021/jm011112jopenalex-snapshot
Successful Virtual Screening for Novel Inhibitors of Human Carbonic Anhydrase: Strategy and Experimental Confirmation
inferredcites →https://doi.org/10.1021/jm0302997openalex-snapshot
Evaluation of Docking Performance: Comparative Data on Docking Algorithms
inferredcites →https://doi.org/10.1021/jm0306430openalex-snapshot
Glide: A New Approach for Rapid, Accurate Docking and Scoring. 1. Method and Assessment of Docking Accuracy
inferredcites →https://doi.org/10.1021/jm981037lopenalex-snapshot
F lex S: A Method for Fast Flexible Ligand Superposition
inferredcites →https://doi.org/10.1023/a:1007913026166openalex-snapshot
Multiple automatic base selection: Protein–ligand docking based on incremental construction without manual intervention
inferredcites →https://doi.org/10.1023/a:1007959729800openalex-snapshot
Time-efficient flexible superposition of medium-sized molecules
inferredcites →https://doi.org/10.1023/a:1008027706830openalex-snapshot
RigFit: A new approach to superimposing ligand molecules
inferredcites →https://doi.org/10.1023/a:1016399411208openalex-snapshot
Flexible docking under pharmacophore type constraints
inferredcites →https://doi.org/10.1089/cmb.1998.5.631openalex-snapshot
A Method for Biomolecular Structural Recognition and Docking Allowing Conformational Flexibility
inferredcites →https://doi.org/10.2174/1568026043451104openalex-snapshot
Guided Docking Approaches to Structure-Based Design and Screening
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781119654803.ch15openalex-snapshot
Prospects of Covalent Approaches in Drug Discovery: An Overview
inferred← citeshttps://doi.org/10.1002/jcc.21565openalex-snapshot
SDOVS: A solvent dipole ordering‐based method for virtual screening
inferred← citeshttps://doi.org/10.1007/978-1-0716-1406-8_3openalex-snapshot
Methods for Molecular Modelling of Protein Complexes
inferred← citeshttps://doi.org/10.1007/978-1-0716-5190-2_15openalex-snapshot
Computational Study of Enzyme Inhibition
inferred← citeshttps://doi.org/10.1007/978-1-60761-839-3_16openalex-snapshot
Methods for Combinatorial and Parallel Library Design
inferred← citeshttps://doi.org/10.1007/s13738-026-03481-3openalex-snapshot
Emerging computational tools and advanced technologies in chemical and medical research: applications in bioinformatics, drug discovery, and precision healthcare: a review
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11519-3openalex-snapshot
Modeling Covalent Protein-Ligand Interactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.20661-4openalex-snapshot
Protein-Carbohydrate Interactions
inferred← citeshttps://doi.org/10.1016/b978-0-443-43974-2.00007-0openalex-snapshot
Computational approaches for kinase inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-443-49253-2.00012-xopenalex-snapshot
Correlation of computational molecular docking predictions with experimental outcomes
inferred← citeshttps://doi.org/10.1016/j.aac.2022.11.006openalex-snapshot
Pesticide informatics expands the opportunity for structure-based molecular design and optimization
inferred← citeshttps://doi.org/10.1016/j.drudis.2008.12.006openalex-snapshot
Molecular fields in drug discovery: getting old or reaching maturity?
inferred← citeshttps://doi.org/10.1016/j.rechem.2025.102317openalex-snapshot
Role of structure-based drug design (SBDD) in the repurposing and discovery of anti-viral leads against Monkeypox virus disease
inferred← citeshttps://doi.org/10.1021/acs.jcim.5b00275openalex-snapshot
HybridDock: A Hybrid Protein–Ligand Docking Protocol Integrating Protein- and Ligand-Based Approaches
inferred← citeshttps://doi.org/10.1021/acs.jcim.9b00686openalex-snapshot
CANDOCK: Chemical Atomic Network-Based Hierarchical Flexible Docking Algorithm Using Generalized Statistical Potentials
inferred← citeshttps://doi.org/10.1021/ci100221gopenalex-snapshot
FLAP: GRID Molecular Interaction Fields in Virtual Screening. Validation using the DUD Data Set
inferred← citeshttps://doi.org/10.1021/ci600342eopenalex-snapshot
Optimizing Fragment and Scaffold Docking by Use of Molecular Interaction Fingerprints
inferred← citeshttps://doi.org/10.1021/ci700368popenalex-snapshot
Novel Approach to Structure-Based Pharmacophore Search Using Computational Geometry and Shape Matching Techniques
inferred← citeshttps://doi.org/10.1039/d0ra01483dopenalex-snapshot
Developing an effective polarizable bond method for small molecules with application to optimized molecular docking
inferred← citeshttps://doi.org/10.1080/14756366.2025.2600746openalex-snapshot
Identification and biological evaluation of benzimidazole-based compounds as novel TGFβR1 inhibitors
inferred← citeshttps://doi.org/10.1093/bib/bbaf697openalex-snapshot
The covalent docking software landscape: features and applications in drug design
inferred← citeshttps://doi.org/10.1109/escience.2008.56openalex-snapshot
Classification of Different Approaches for e-Science Applications in Next Generation Computing Infrastructures
inferred← citeshttps://doi.org/10.1155/2013/138012openalex-snapshot
Cloud Infrastructures for In Silico Drug Discovery: Economic and Practical Aspects
inferred← citeshttps://doi.org/10.1186/s12859-018-2449-yopenalex-snapshot
Benchmarking of different molecular docking methods for protein-peptide docking
inferred← citeshttps://doi.org/10.13040/ijpsr.0975-8232.7(2).554-72openalex-snapshot
3D-QSAR AND CONTOUR MAP ANALYSIS OF TARIQUIDAR ANALOGUES AS MULTIDRUG RESISTANCE PROTEIN-1 (MRP1) INHIBITORS.
inferred← citeshttps://doi.org/10.18052/www.scipress.com/ilns.57.18openalex-snapshot
Understanding the Exacerbating Role of the Metalloproteinase Meprin during AKI, an In Silico Approach
inferred← citeshttps://doi.org/10.21203/rs.3.rs-33294/v1openalex-snapshot
Search for therapeutics against COVID 19 targeting SARS-CoV-2 papain-like protease: an in silico study
inferred← citeshttps://doi.org/10.2174/138620711797537148openalex-snapshot
Integration of Virtual and High Throughput Screening in Lead Discovery Settings
inferred← citeshttps://doi.org/10.2174/1573409919666230112170025openalex-snapshot
Exploring Potential Non-steroidal Aromatase Inhibitors for Therapeutic Application against Estrogen-dependent Breast Cancer
inferred← citeshttps://doi.org/10.26434/chemrxiv.12478568openalex-snapshot
In Silico Screening of Some Antiviral Phytochemicals as Drug Leads Against Covid-19
inferred← citeshttps://doi.org/10.26434/chemrxiv.12478568.v1openalex-snapshot
In Silico Screening of Some Antiviral Phytochemicals as Drug Leads Against Covid-19
inferred← citeshttps://doi.org/10.3389/fchem.2025.1597454openalex-snapshot
Computational advances in the design and discovery of artemis inhibitors for radiosensitization in cancer therapy
inferred← citeshttps://doi.org/10.3390/ecsoc-27-16112openalex-snapshot
Comparative Molecular Docking Studies of Selected Phytoconstituents on the Dopamine D3 Receptor (PDB ID: 3PBL) as Potential Anti-Parkinson’s Agents
inferred← citeshttps://doi.org/10.3390/ijms24054401openalex-snapshot
Lessons Learnt from COVID-19: Computational Strategies for Facing Present and Future Pandemics
inferred← citeshttps://doi.org/10.3390/ijms241813831openalex-snapshot
Construction of Histone–Protein Complex Structures by Peptide Growing
inferred← citeshttps://doi.org/10.5772/intechopen.1005527openalex-snapshot
In Silico Docking: Protocols for Computational Exploration of Molecular Interactions
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.