On the public citation graph

Three-Dimensional Quantitative Structure−Activity Relationship of Interleukin 1-β Converting Enzyme Inhibitors: A Comparative Molecular Field Analysis Study

https://doi.org/10.1021/jm9708442
0 signed · 86 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/jcc.540100804openalex-snapshot
Validation of the general purpose tripos 5.2 force field
inferredcites →https://doi.org/10.1007/bf00126215openalex-snapshot
A comparison of progestin and androgen receptor binding using the CoMFA technique
inferredcites →https://doi.org/10.1007/bf00130399openalex-snapshot
QSAR of conformationally flexible molecules: Comparative Molecular Field Analysis of protein-tyrosine kinase inhibitors
inferredcites →https://doi.org/10.1007/s008940050062openalex-snapshot
Docking of a Series of Peptide-Based Interleukin-1� Converting Enzyme Inhibitors with Aspartyl Hemiacetals, a-((2,6-Dichlorobenzoyl)oxy)methyl and (Acyloxy)methyl Ketone Moieties
inferredcites →https://doi.org/10.1016/0014-5793(89)81376-6openalex-snapshot
Activation of interleukin‐ 1β by a co‐induced protease
inferredcites →https://doi.org/10.1016/0092-8674(93)90486-aopenalex-snapshot
Induction of apoptosis in fibroblasts by IL-1β-converting enzyme, a mammalian homolog of the C. elegans cell death gene ced-3
inferredcites →https://doi.org/10.1016/0898-5529(90)90120-wopenalex-snapshot
Comparative molecular field analysis (CoMFA). 2. Toward its use with 3D-structural databases
inferredcites →https://doi.org/10.1016/s0021-9258(18)77334-1openalex-snapshot
Substrate specificity of the protease that processes human interleukin-1 beta.
inferredcites →https://doi.org/10.1016/s0960-894x(01)81209-9openalex-snapshot
Synthesis of a potent, reversible inhibitor of interleukin-1β converting enzyme
inferredcites →https://doi.org/10.1021/bi00179a020openalex-snapshot
Inactivation of Interleukin-1.beta. Converting Enzyme by Peptide (Acyloxy)methyl Ketones
inferredcites →https://doi.org/10.1021/bi00233a007openalex-snapshot
Peptidyl (acyloxy)methyl ketones and the quiescent affinity label concept: the departing group as a variable structural element in the design of inactivators of cysteine proteinases
inferredcites →https://doi.org/10.1021/bi00233a008openalex-snapshot
Deuterium nuclear magnetic resonance of the gramicidin A backbone in a phospholipid bilayer
inferredcites →https://doi.org/10.1021/ja00014a033openalex-snapshot
Bis-heteroannulation. 15. Enantiospecific syntheses of (+)- and (-)-norsecurinine
inferredcites →https://doi.org/10.1021/jm00006a006openalex-snapshot
Three-Dimensional Quantitative Structure-Activity Relationship (QSAR) of HIV Integrase Inhibitors: A Comparative Molecular Field Analysis (CoMFA) Study
inferredcites →https://doi.org/10.1021/jm00053a009openalex-snapshot
On the prediction of binding properties of drug molecules by comparative molecular field analysis
inferredcites →https://doi.org/10.1021/jm00075a004openalex-snapshot
Comparative molecular field analysis of in vitro growth inhibition of L1210 and HCT-8 cells by some pyrazoloacridines
inferredcites →https://doi.org/10.1021/jm00098a010openalex-snapshot
Comparative molecular field analysis of polyhalogenated dibenzo-p-dioxins, dibenzofurans, and biphenyls
inferredcites →https://doi.org/10.1021/jm00112a004openalex-snapshot
Comparative molecular field analysis of some clodronic acid esters
inferredcites →https://doi.org/10.1021/jm950704xopenalex-snapshot
A Comparative Molecular Field Analysis Study of N-Benzylpiperidines as Acetylcholinesterase Inhibitors
inferredcites →https://doi.org/10.1021/jm9601516openalex-snapshot
First Examples of Peptidomimetic Inhibitors of Interleukin-1β Converting Enzyme
inferredcites →https://doi.org/10.1021/jm9701637openalex-snapshot
Pyridazinodiazepines as a High-Affinity, P 2 −P 3 Peptidomimetic Class of Interleukin-1β-Converting Enzyme Inhibitor
inferredcites →https://doi.org/10.1038/356768a0openalex-snapshot
A novel heterodimeric cysteine protease is required for interleukin-1βprocessing in monocytes
inferredcites →https://doi.org/10.1038/370270a0openalex-snapshot
Structure and mechanism of interleukin-lβ converting enzyme
inferredcites →https://doi.org/10.1073/pnas.86.14.5227openalex-snapshot
Identification of a monocyte specific pre-interleukin 1 beta convertase activity.
inferredcites →https://doi.org/10.1073/pnas.88.19.8485openalex-snapshot
Interleukin 1 is processed and released during apoptosis.
inferredcites →https://doi.org/10.1111/j.1399-3011.1994.tb00573.xopenalex-snapshot
Preparation and evaluation of peptidic aspartyl hemiacetals as reversible inhibitors of interleukin‐l β converting enzyme (ICE)
inferredcites →https://doi.org/10.1137/0905052openalex-snapshot
The Collinearity Problem in Linear Regression. The Partial Least Squares (PLS) Approach to Generalized Inverses
inferredcites →https://doi.org/10.4049/jimmunol.147.9.2964openalex-snapshot
IL-1-converting enzyme requires aspartic acid residues for processing of the IL-1 beta precursor at two distinct sites and does not cleave 31-kDa IL-1 alpha

What points at this work

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

inferred← citeshttps://doi.org/10.1002/med.20042openalex-snapshot
Small molecular anti-cytokine agents
inferred← citeshttps://doi.org/10.1002/qsar.200510161openalex-snapshot
On Selection of Training and Test Sets for the Development of Predictive QSAR models
inferred← citeshttps://doi.org/10.1002/qsar.200510211openalex-snapshot
QSTR with Extended Topochemical Atom (ETA) Indices 8.aQSAR for the inhibition of substituted phenols on germination rate ofCucumis sativususing chemometric tools
inferred← citeshttps://doi.org/10.1002/qsar.200630131openalex-snapshot
Three‐Dimensional Quantitative Structure–Activity Relationship of MT3 Melatonin Binding Site Ligands: A Comparative Molecular Field Analysis
inferred← citeshttps://doi.org/10.1007/s00044-010-9546-4openalex-snapshot
QSAR study of a series of 2,3-dihydroimidazo[1,2-c]pyrimidines as antibacterial agents
inferred← citeshttps://doi.org/10.1007/s00044-012-0110-2openalex-snapshot
Comprehensive two and three-dimensional QSAR studies of 3-substituted 6-butyl-1,2dihydropyridin-2-ones derivatives as angiotensin II receptor antagonists
inferred← citeshttps://doi.org/10.1007/s00044-014-1290-8openalex-snapshot
Inhibition of microsomal prostaglandin E synthase-1 by phenanthrene imidazoles: a QSAR study
inferred← citeshttps://doi.org/10.1007/s00894-018-3791-8openalex-snapshot
Virtual screening to identify Leishmania braziliensis N-myristoyltransferase inhibitors: pharmacophore models, docking, and molecular dynamics
inferred← citeshttps://doi.org/10.1007/s10822-008-9195-6openalex-snapshot
Quantitative Series Enrichment Analysis (QSEA): a novel procedure for 3D-QSAR analysis
inferred← citeshttps://doi.org/10.1007/s11030-018-9825-4openalex-snapshot
Probing the opportunities for designing anthelmintic leads by sub-structural topology-based QSAR modelling
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.02.005openalex-snapshot
De novo design and synthesis of HIV-1 integrase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.09.022openalex-snapshot
QSAR by LFER model of HIV protease inhibitor mannitol derivatives using FA-MLR, PCRA, and PLS techniques
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.07.031openalex-snapshot
Inhibition of interleukin-1β converting enzyme (ICE or caspase 1) by aspartyl acyloxyalkyl ketones and aspartyl amidooxyalkyl ketones
inferred← citeshttps://doi.org/10.1016/j.ces.2012.01.005openalex-snapshot
QSPR with extended topochemical atom (ETA) indices: Modeling of critical micelle concentration of non-ionic surfactants
inferred← citeshttps://doi.org/10.1016/j.ces.2012.07.008openalex-snapshot
QSPR with extended topochemical atom (ETA) indices, 3: Modeling of critical micelle concentration of cationic surfactants
inferred← citeshttps://doi.org/10.1016/j.chemolab.2007.07.004openalex-snapshot
Exploring the impact of size of training sets for the development of predictive QSAR models
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2007.07.037openalex-snapshot
QSTR with extended topochemical atom (ETA) indices. 9. Comparative QSAR for the toxicity of diverse functional organic compounds to Chlorella vulgaris using chemometric tools
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2009.07.072openalex-snapshot
QSTR with extended topochemical atom (ETA) indices. 12. QSAR for the toxicity of diverse aromatic compounds to Tetrahymena pyriformis using chemometric tools
inferred← citeshttps://doi.org/10.1016/j.ejmech.2004.10.014openalex-snapshot
Ligand-based assessment of factor Xa binding site flexibility via elaborate pharmacophore exploration and genetic algorithm-based QSAR modeling
inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.02.021openalex-snapshot
Exploring molecular shape analysis of styrylquinoline derivatives as HIV-1 integrase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2008.12.004openalex-snapshot
Comparative chemometric modeling of cytochrome 3A4 inhibitory activity of structurally diverse compounds using stepwise MLR, FA-MLR, PLS, GFA, G/PLS and ANN techniques
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2010.07.116openalex-snapshot
QSTR with extended topochemical atom (ETA) indices. 14. QSAR modeling of toxicity of aromatic aldehydes to Tetrahymena pyriformis
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.03.012openalex-snapshot
QSAR studies of some substituted imidazolinones angiotensin II receptor antagonists using Partial Least Squares Regression (PLSR) method based feature selection
inferred← citeshttps://doi.org/10.1016/s0223-5234(00)01202-2openalex-snapshot
A feature based pharmacophore for Candida albicans MyristoylCoA: protein N-myristoyltransferase inhibitors
inferred← citeshttps://doi.org/10.1016/s0968-0896(01)00186-9openalex-snapshot
Three-dimensional quantitative structure–activity relationship (3D-QSAR) of 3-aryloxazolidin-2-one antibacterials
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00056-1openalex-snapshot
3D-QSAR CoMFA and CoMSIA on protein tyrosine phosphatase 1B inhibitors
inferred← citeshttps://doi.org/10.1016/s0968-0896(03)00305-5openalex-snapshot
3D-QSAR of N-myristoyltransferase inhibiting antifungal agents by CoMFA and CoMSIA methods
inferred← citeshttps://doi.org/10.1016/s0968-0896(99)00063-2openalex-snapshot
Three-dimensional quantitative structure activity relationships (3-D-QSAR) of antihyperglycemic agents
inferred← citeshttps://doi.org/10.1016/s1093-3263(01)00110-3openalex-snapshot
Automatic generation of alignments for 3D QSAR analyses
inferred← citeshttps://doi.org/10.1021/ci0001334openalex-snapshot
Eigen Value Analysis of HIV-1 Integrase Inhibitors
inferred← citeshttps://doi.org/10.1021/ci900144xopenalex-snapshot
Docking and 3D-QSAR Studies on Isatin Sulfonamide Analogues as Caspase-3 Inhibitors
inferred← citeshttps://doi.org/10.1021/ci990019popenalex-snapshot
Structure Based Prediction of Binding Affinity of Human Immunodeficiency Virus-1 Protease Inhibitors
inferred← citeshttps://doi.org/10.1021/ci990020oopenalex-snapshot
Development of Pharmacophore Alignment Models as Input for Comparative Molecular Field Analysis of a Diverse Set of Azole Antifungal Agents
inferred← citeshttps://doi.org/10.1021/jm0101343openalex-snapshot
Three-Dimensional Quantitative Structure−Activity Relationships of Cyclo-oxygenase-2 (COX-2) Inhibitors: A Comparative Molecular Field Analysis
inferred← citeshttps://doi.org/10.1021/jm020194oopenalex-snapshot
Topomer CoMFA: A Design Methodology for Rapid Lead Optimization
inferred← citeshttps://doi.org/10.1021/jm020217zopenalex-snapshot
Three-Dimensional Quantitative Structure−Activity Relationship of 1,4-Dihydropyridines As Antitubercular Agents
inferred← citeshttps://doi.org/10.1021/jm030016aopenalex-snapshot
Understanding the Antitumor Activity of Novel Hydroxysemicarbazide Derivatives as Ribonucleotide Reductase Inhibitors Using CoMFA and CoMSIA
inferred← citeshttps://doi.org/10.1021/jm050260xopenalex-snapshot
Development of Quantitative Structure−Binding Affinity Relationship Models Based on Novel Geometrical Chemical Descriptors of the Protein−Ligand Interfaces
inferred← citeshttps://doi.org/10.1021/jm9806852openalex-snapshot
Comparative Molecular Field Analysis of Fungal Squalene Epoxidase Inhibitors
inferred← citeshttps://doi.org/10.1023/a:1011140723828openalex-snapshot
Comparative molecular field analysis (CoMFA) study of epothilones – tubulin depolymerization inhibitors: Pharmacophore development using 3D QSAR methods
inferred← citeshttps://doi.org/10.1023/a:1014888730876openalex-snapshot
Molecular electrostatic potentials as input for the alignment of HIV-1 integrase inhibitors in 3D QSAR
inferred← citeshttps://doi.org/10.1023/a:1020137802155openalex-snapshot
3D-QSAR and molecular modeling of HIV-1 integrase inhibitors
inferred← citeshttps://doi.org/10.1039/b606365aopenalex-snapshot
3D-QSAR of histone deacetylase inhibitors: hydroxamate analogues
inferred← citeshttps://doi.org/10.1080/08927020902744664openalex-snapshot
QSTR with extended topochemical atom (ETA) indices. 11. Comparative QSAR of acute NSAID cytotoxicity in rat hepatocytes using chemometric tools
inferred← citeshttps://doi.org/10.1080/08927020903015379openalex-snapshot
QSTR with extended topochemical atom (ETA) indices. 13. Modelling of hERG K+channel blocking activity of diverse functional drugs using different chemometric tools
inferred← citeshttps://doi.org/10.1080/08927020903033141openalex-snapshot
Comparative QSAR studies of nitrofuranyl amide derivatives using theoretical structural properties
inferred← citeshttps://doi.org/10.1080/08927022.2010.492835openalex-snapshot
Chemometric modelling of antimalarial activity of aryltriazolylhydroxamates
inferred← citeshttps://doi.org/10.1080/17568919.2025.2527596openalex-snapshot
Ribonucleotide reductase (RNR) inhibitors as target-based weapon for future cancer drug development
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2008.00686.xopenalex-snapshot
On Application of Constitutional Descriptors for Merging of Quinoxaline Data Sets Using Linear Statistical Methods
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2008.00712.xopenalex-snapshot
QSTR with Extended Topochemical Atom Indices. 10. Modeling of Toxicity of Organic Chemicals to Humans Using Different Chemometric Tools
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2008.00717.xopenalex-snapshot
Comparative QSAR Studies of CYP1A2 Inhibitor Flavonoids Using 2D and 3D Descriptors
inferred← citeshttps://doi.org/10.1177/1091581812444140openalex-snapshot
In Silico Predicative Studies for Cytotoxic Potential of NSAIDs Using Self-Organizing Molecular Field Analysis
inferred← citeshttps://doi.org/10.1186/s43094-024-00701-6openalex-snapshot
Exhaustive computational studies on pyrimidine derivatives as GPR119 agonist for the development of compounds against NIDDM
inferred← citeshttps://doi.org/10.18052/www.scipress.com/ilcpa.85.23openalex-snapshot
Molecular Docking and QSAR Study of Chalcone and Pyrimidine Derivatives as Potent Anti-Malarial Agents against Plasmodium falciparum
inferred← citeshttps://doi.org/10.2147/rrmc.s50737openalex-snapshot
3D-QSAR of p38-α mitogen-activated protein kinase inhibitors: pyridopyridazin-6-ones (part 1)
inferred← citeshttps://doi.org/10.2174/092986709789352303openalex-snapshot
QSAR Modeling for Quinoxaline Derivatives using Genetic Algorithm and Simulated Annealing Based Feature Selection
inferred← citeshttps://doi.org/10.2174/157340909789054702openalex-snapshot
Recent Studies of QSAR on Inhibitors of Estrogen Receptor and Human Eosinophil Phosphodiesterase
inferred← citeshttps://doi.org/10.22270/jddt.v2i1.52openalex-snapshot
A NOVEL QSAR MODEL FOR EVALUATING AND PREDICTING THE INHIBITION ACTIVITY OF H1-RECEPTOR ANTAGONISTS: A SERIES OF THIENOPYRIMIDINE DERIVATIVES
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.