On the public citation graph

In Silico Fragment Screening by Replica Generation (FSRG) Method for Fragment-Based Drug Design

https://doi.org/10.1021/ci800435x
0 signed · 47 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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)1097-0134(19981115)33:3<367::aid-prot6>3.0.co;2-wopenalex-snapshot
Flexible docking using tabu search and an empirical estimate of binding affinity
inferredcites →https://doi.org/10.1002/jcc.20035openalex-snapshot
Development and testing of a general amber force field
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/10.1002/prot.10232openalex-snapshot
A new test set for validating predictions of protein–ligand interaction
inferredcites →https://doi.org/10.1002/prot.340080302openalex-snapshot
Automated docking of substrates to proteins by simulated annealing
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.1996.0897openalex-snapshot
Development and validation of a genetic algorithm for flexible docking 1 1Edited by F. E. Cohen
inferredcites →https://doi.org/10.1016/0022-2836(82)90153-xopenalex-snapshot
A geometric approach to macromolecule-ligand interactions
inferredcites →https://doi.org/10.1016/0040-4020(80)80168-2openalex-snapshot
Iterative partial equalization of orbital electronegativity—a rapid access to atomic charges
inferredcites →https://doi.org/10.1016/0898-5529(88)90006-1openalex-snapshot
Computer-assisted organic synthesis design and reaction prediction system, “AIPHOS”
inferredcites →https://doi.org/10.1016/0959-440x(94)90268-2openalex-snapshot
Structure-based drug design
inferredcites →https://doi.org/10.1016/j.jmgm.2004.11.007openalex-snapshot
LigScore: a novel scoring function for predicting binding affinities
inferredcites →https://doi.org/10.1016/j.jmgm.2005.04.004openalex-snapshot
Similarities among receptor pockets and among compounds: Analysis and application to in silico ligand screening
inferredcites →https://doi.org/10.1016/j.jmgm.2005.11.006openalex-snapshot
Multiple target screening method for robust and accurate in silico ligand screening
inferredcites →https://doi.org/10.1016/s0040-4039(01)94977-9openalex-snapshot
A new model for calculating atomic charges in molecules
inferredcites →https://doi.org/10.1021/ci060152zopenalex-snapshot
Noise Reduction Method for Molecular Interaction Energy: Application to in Silico Drug Screening and in Silico Target Protein Screening
inferredcites →https://doi.org/10.1021/jm040031vopenalex-snapshot
Fragment-Based Drug Discovery
inferredcites →https://doi.org/10.1021/jm049131ropenalex-snapshot
Druggability Indices for Protein Targets Derived from NMR-Based Screening Data
inferredcites →https://doi.org/10.1021/jm049314dopenalex-snapshot
A Knowledge-Based Energy Function for Protein−Ligand, Protein−Protein, and Protein−DNA Complexes
inferredcites →https://doi.org/10.1021/jm049939bopenalex-snapshot
Design, Synthesis, and Structure−Activity Relationship Studies of 3,4,6-Triphenylpyran-2-ones as Selective Cyclooxygenase-2 Inhibitors
inferredcites →https://doi.org/10.1021/jm050362nopenalex-snapshot
A Critical Assessment of Docking Programs and Scoring Functions
inferredcites →https://doi.org/10.1021/jm0608356openalex-snapshot
Benchmarking Sets for Molecular Docking
inferredcites →https://doi.org/10.1021/jm8000373openalex-snapshot
Recent Developments in Fragment-Based Drug Discovery
inferredcites →https://doi.org/10.1021/jm980536jopenalex-snapshot
A General and Fast Scoring Function for Protein−Ligand Interactions: A Simplified Potential Approach
inferredcites →https://doi.org/10.1021/jo01299a001openalex-snapshot
Computer-assisted mechanistic evaluation of organic reactions. 1. Overview
inferredcites →https://doi.org/10.1021/jp035478eopenalex-snapshot
The Filling Potential Method: A Method for Estimating the Free Energy Surface for Protein−Ligand Docking
inferredcites →https://doi.org/10.1038/nrd2220openalex-snapshot
A decade of fragment-based drug design: strategic advances and lessons learned
inferredcites →https://doi.org/10.1038/nsb1196-927openalex-snapshot
Flexibility of the NSAID binding site in the structure of human cyclooxygenase-2
inferredcites →https://doi.org/10.1073/pnas.96.13.7563openalex-snapshot
Nonsteroid drug selectivities for cyclo-oxygenase-1 rather than cyclo-oxygenase-2 are associated with human gastrointestinal toxicity: A full in vitro analysis
inferredcites →https://doi.org/10.1126/science.166.3902.178openalex-snapshot
Computer-Assisted Design of Complex Organic Syntheses
inferredcites →https://doi.org/10.2174/0929867003374417openalex-snapshot
Recent Advances in Inducible Cyclooxygenase (COX-2) Inhibition.
inferredcites →https://doi.org/10.2174/156802607782341082openalex-snapshot
Fragment-Based Drug Discovery: What has it Achieved so Far?
inferredcites →https://doi.org/10.2174/156802607782341091openalex-snapshot
An Integrated Approach to Fragment-Based Lead Generation:Philosophy, Strategy and Case Studies from AstraZenecas Drug Discovery Programmes

What points at this work

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

inferred← citeshttps://doi.org/10.1002/9783527633326.ch17openalex-snapshot
Fragment‐Based Approaches in Virtual Screening
inferred← citeshttps://doi.org/10.1002/9783527633326.ch6openalex-snapshot
Docking Methods for Virtual Screening: Principles and Recent Advances
inferred← citeshttps://doi.org/10.1002/cem.2556openalex-snapshot
Multitarget fragment‐based design of novel inhibitors for AChE and SSAO/VAP‐1 enzymes
inferred← citeshttps://doi.org/10.1002/jmr.1077openalex-snapshot
Challenges and advances in computational docking: 2009 in review
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/10.1007/128_2011_182openalex-snapshot
Fragment-Based Approaches and Computer-Aided Drug Discovery
inferred← citeshttps://doi.org/10.1007/7653_2015_51openalex-snapshot
Computational Fragment-Based Drug Design
inferred← citeshttps://doi.org/10.1021/ci100108popenalex-snapshot
Selection of In Silico Drug Screening Results by Using Universal Active Probes (UAPs)
inferred← citeshttps://doi.org/10.1021/ci200236xopenalex-snapshot
Selection of In Silico Drug Screening Results for G-Protein-Coupled Receptors by Using Universal Active Probes
inferred← citeshttps://doi.org/10.1039/c6cp02914kopenalex-snapshot
Vibrational dynamics (IR, Raman, NRVS) and a DFT study of a new antitumor tetranuclearstannoxane cluster, Sn( iv )-oxo-{di-o-vanillin} dimethyl dichloride
inferred← citeshttps://doi.org/10.1517/17425255.2010.486399openalex-snapshot
Structural ensemble in computational drug screening
inferred← citeshttps://doi.org/10.2142/biophys.51.252openalex-snapshot
Prediction of Protein-compound Complex Structures by Docking Simulation
inferred← citeshttps://doi.org/10.2174/092986712803530467openalex-snapshot
Fragment Based Drug Design: From Experimental to Computational Approaches
inferred← citeshttps://doi.org/10.3390/ph4050758openalex-snapshot
Prediction of Positions of Active Compounds Makes It Possible To Increase Activity in Fragment-Based Drug Development
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.