On the public citation graph
Improved Electron-Conformational Method of Pharmacophore Identification and Bioactivity Prediction. Application to Angiotensin Converting Enzyme Inhibitors
0 signed · 60 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/9780470125793.ch10openalex-snapshot
The Electron‐Topological Approach to the QSAR Problem
inferredcites →https://doi.org/10.1002/med.2610050405openalex-snapshot
Recent developments in the design of angiotensin‐converting enzyme inhibitors
inferredcites →https://doi.org/10.1007/978-3-642-61917-5openalex-snapshot
Theory of Orientation and Stereoselection
inferredcites →https://doi.org/10.1007/bf01590992openalex-snapshot
Constrained search of conformational hyperspace
inferredcites →https://doi.org/10.1007/bf01676957openalex-snapshot
A theoretical study of angiotensin-converting enzyme inhibitors
inferredcites →https://doi.org/10.1007/bf01680553openalex-snapshot
A unique geometry of the active site of angiotensin-converting enzyme consistent with structure-activity studies
inferredcites →https://doi.org/10.1016/0263-7855(90)80092-topenalex-snapshot
Computer-aided drug design, methods and applications
inferredcites →https://doi.org/10.1016/s0065-7743(09)04434-0openalex-snapshot
Annual Reports in Medicinal Chemistry
inferredcites →https://doi.org/10.1016/s0166-1280(97)00069-9openalex-snapshot
Electron-topological (ET) investigation of structure-antagonist activity of a series of dibenzo[a,d]cycloalkenimines
inferredcites →https://doi.org/10.1016/s0190-9622(08)82060-9openalex-snapshot
Angiotensin-converting enzyme inhibitors
inferredcites →https://doi.org/10.1021/bi00277a040openalex-snapshot
Binding of hormones and neuropeptides by calmodulin
inferredcites →https://doi.org/10.1021/ci990327nopenalex-snapshot
Automated Pharmacophore Identification for Large Chemical Data Sets
inferredcites →https://doi.org/10.1021/ja00066a004openalex-snapshot
3D-QSAR of angiotensin-converting enzyme and thermolysin inhibitors: a comparison of CoMFA models based on deduced and experimentally determined active site geometries
inferredcites →https://doi.org/10.1021/ja950818yopenalex-snapshot
Three-Dimensional Models of ACE and NEP Inhibitors and Their Use in the Design of Potent Dual ACE/NEP Inhibitors
inferredcites →https://doi.org/10.1021/jm00076a010openalex-snapshot
Heterocyclic lactam derivatives as dual angiotensin converting enzyme and neutral endopeptidase 24.11 inhibitors
inferredcites →https://doi.org/10.1021/jm00106a030openalex-snapshot
Configuration and preferential solid-state conformations of perindoprilat (S-9780). Comparison with the crystal structures of other ACE inhibitors and conclusions related to structure-activity relationships
inferredcites →https://doi.org/10.1021/jm00106a031openalex-snapshot
Dual-action cephalosporins: cephalosporin 3'-quaternary ammonium quinolones
inferredcites →https://doi.org/10.1021/jm00345a011openalex-snapshot
Angiotensin-converting enzyme inhibitors: importance of the amide carbonyl of mercaptoacyl amino acids for hydrogen bonding to the enzyme
inferredcites →https://doi.org/10.1021/jm00345a012openalex-snapshot
Catechol O-methyltransferase. 10. 5-Substituted, 3-hydroxy-4-methoxybenzoic acids (isovanillic acids) and 5-substituted, 3-hydroxy-4-methoxybenzaldehydes (isovanillins) as potential inhibitors
inferredcites →https://doi.org/10.1021/jm00357a015openalex-snapshot
Antihypertensive activity of 6-arylpyrido[2,3-d]pyrimidin-7-amine derivatives. 2. 7-Acyl amide analogs
inferredcites →https://doi.org/10.1021/jm00363a012openalex-snapshot
Angiotensin converting enzyme inhibitors: 1-glutarylindoline-2-carboxylic acid derivatives
inferredcites →https://doi.org/10.1021/jm00363a013openalex-snapshot
Aromatic retinoic acid analogs. 2. Synthesis and pharmacological activity
inferredcites →https://doi.org/10.1021/jm00381a021openalex-snapshot
Conformational analysis and active site modeling of angiotensin-converting enzyme inhibitors
inferredcites →https://doi.org/10.1021/jm00381a022openalex-snapshot
The pKa of butaclamol and the mode of butaclamol binding to central dopamine receptors
inferredcites →https://doi.org/10.1021/jm00397a027openalex-snapshot
Angiotensin-converting enzyme inhibitors. 2. Perhydroazepin-2-one derivatives
inferredcites →https://doi.org/10.1021/jm00397a028openalex-snapshot
Synthesis of spin traps specific for hydroxyl radical
inferredcites →https://doi.org/10.1023/a:1008052914704openalex-snapshot
An electron-conformational method of identification of pharmacophore and anti-pharmacophore shielding: Application to rice blast activity
inferredcites →https://doi.org/10.1038/288283a0openalex-snapshot
3H-apomorphine labels both dopamine postsynaptic receptors and autoreceptors
inferredcites →https://doi.org/10.1080/10629369908039174openalex-snapshot
A Novel Electron-Conformational Approach to Molecular Modeling for QSAR by Identification of Pharmacophore and Anti-Pharmacophore Shielding
inferredcites →https://doi.org/10.1126/science.191908openalex-snapshot
Design of Specific Inhibitors of Angiotensin-Converting Enzyme: New Class of Orally Active Antihypertensive Agents
inferredcites →https://doi.org/10.1126/science.850788openalex-snapshot
Major Innervation of Newborn Rat Cortex by Monoaminergic Neurons
inferredcites →https://doi.org/10.5860/choice.34-0310openalex-snapshot
Electronic structure and properties of transition metal compounds: introduction to the theory
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/chin.200105250openalex-snapshot
ChemInform Abstract: Improved Electron‐Conformational Method of Pharmacophore Identification and Bioactivity Prediction. Application to Angiotensin Converting Enzyme Inhibitors.
inferred← citeshttps://doi.org/10.1007/s10822-008-9191-xopenalex-snapshot
QSAR without arbitrary descriptors: the electron-conformational method
inferred← citeshttps://doi.org/10.1007/s11030-023-10798-1openalex-snapshot
Clustering of atoms relative to vector space in the Z-matrix coordinate system and ‘graphical fingerprint’ analysis of 3D pharmacophore structure
inferred← citeshttps://doi.org/10.1007/s13738-019-01835-8openalex-snapshot
Molecular docking and 4D-QSAR model of methanone derivatives by electron conformational-genetic algorithm method
inferred← citeshttps://doi.org/10.1016/b0-08-045044-x/00247-9openalex-snapshot
Pharmacophore Modeling: 1 – Methods
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.02559-2openalex-snapshot
Pharmacophore Modeling: 1 – Methods
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.02.035openalex-snapshot
4D-QSAR analysis and pharmacophore modeling: Electron conformational-genetic algorithm approach for penicillins
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2019.107190openalex-snapshot
The effect of stereoisomerism on the 4D-QSAR study of some dipeptidyl boron derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2010.06.007openalex-snapshot
Pharmacophore identification and bioactivity prediction for triaminotriazine derivatives by electron conformational-genetic algorithm QSAR method
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.03.033openalex-snapshot
Synthesis, structure–activity relationships, and in vitro antibacterial and antifungal activity evaluations of novel pyrazole carboxylic and dicarboxylic acid derivatives
inferred← citeshttps://doi.org/10.1016/s0968-0896(03)00437-1openalex-snapshot
Electron-conformational study for the structure–hallucinogenic activity relationships of phenylalkylamines
inferred← citeshttps://doi.org/10.1021/ci700401popenalex-snapshot
Quantitative Antidiabetic Activity Prediction for the Class of Guanidino- and Aminoguanidinopropionic Acid Analogs Based on Electron-Conformational Studies
inferred← citeshttps://doi.org/10.1080/1062936x.2010.548341openalex-snapshot
Quantitative bioactivity prediction and pharmacophore identification for benzotriazine derivatives using the electron conformational–genetic algorithm in QSAR
inferred← citeshttps://doi.org/10.1080/1062936x.2012.665082openalex-snapshot
4D-QSAR study of HEPT derivatives by electron conformational–genetic algorithm method
inferred← citeshttps://doi.org/10.1080/1062936x.2016.1174152openalex-snapshot
4D-QSAR investigation and pharmacophore identification of pyrrolo[2,1-c][1,4]benzodiazepines using electron conformational–genetic algorithm method
inferred← citeshttps://doi.org/10.1097/00124363-200418020-00002openalex-snapshot
Quantitative Drug Activity Prediction for Inhibitors of Human Breast Carcinoma
inferred← citeshttps://doi.org/10.1109/bmei.2009.5305805openalex-snapshot
Is that Possible to Design the Versatile Inhibitors for H1N1, H5N1, H5N2, and H5N7?
inferred← citeshttps://doi.org/10.1109/cibcb.2004.1393959openalex-snapshot
Evolutionary optimization of interval rules for drug design
inferred← citeshttps://doi.org/10.1201/b19853-5openalex-snapshot
Considering the Molecular Conformational Flexibility in QSAR Studies
inferred← citeshttps://doi.org/10.19261/cjm.2008.03(1).13openalex-snapshot
Toxicophores and Quantitative Structure -Toxicity Relationships for Some Environmental Pollutants
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4091168/v1openalex-snapshot
Comprehensive 4D-QSAR Analysis for Predicting the Biological Activity of Quinazoline: Integrating Electron Conformational and Genetic Algorithm Approaches through a Unified Framework to Uncover Essential Pharmacophoric Features
inferred← citeshttps://doi.org/10.2174/1570180815666180926104319openalex-snapshot
DNA Cleavage Properties, Antimicrobial and Cytotoxic Activity and 4D-QSAR Analysis of Some Pyrazole Derivatives
inferred← citeshttps://doi.org/10.24218/vjpps.2016.13openalex-snapshot
Anti-pharmacophore Identification and Structure-Activity Relationships for the Inhibition of Cellular Protein and DNA Syntheses by a Series of Thiosemicarbazones and Thiosemicarbazides
inferred← citeshttps://doi.org/10.3109/14756366.2012.684051openalex-snapshot
Conformation depends on 4D-QSAR analysis using EC–GA method: pharmacophore identification and bioactivity prediction of TIBOs as non-nucleoside reverse transcriptase inhibitors
inferred← citeshttps://doi.org/10.3233/ifs-2006-00296openalex-snapshot
Optimization study with ligand-design interval rules
inferred← citeshttps://doi.org/10.3923/ajdd.2011.85.104openalex-snapshot
Quantitative Structure Activity Relationship Analysis of N-(mercaptoalkanoyl)- and [(acylthio)alkanoyl] Glycine Derivatives as ACE 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.