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Pharmacophore identification by molecular modeling and chemometrics: The case of HMG-CoA reductase inhibitors

https://doi.org/10.1007/bf00124386
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jcc.540110403openalex-snapshot
Comparative study of the molecular electrostatic potential obtained from different wavefunctions. Reliability of the semiempirical MNDO wavefunction
inferredcites →https://doi.org/10.1002/jcc.540110405openalex-snapshot
Macromodel—an integrated software system for modeling organic and bioorganic molecules using molecular mechanics
inferredcites →https://doi.org/10.1002/jcc.540111004openalex-snapshot
The application of molecular similarity calculations
inferredcites →https://doi.org/10.1002/qsar.19900090303openalex-snapshot
Pharmacophore Identification in Amnesia‐Reversal Compounds Using Conformational Analysis and Chemometric Methods
inferredcites →https://doi.org/10.1007/bf00126669openalex-snapshot
Automatic search for maximum similarity between molecular electrostatic potential distributions
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/10.1016/0169-7439(87)80084-9openalex-snapshot
Principal component analysis
inferredcites →https://doi.org/10.1016/0223-5234(91)90019-jopenalex-snapshot
QSAR: Rational approaches to the design of bioactive compounds
inferredcites →https://doi.org/10.1016/0300-9629(90)90262-qopenalex-snapshot
Trends in medicinal chemistry '88
inferredcites →https://doi.org/10.1016/s0040-4039(00)82484-3openalex-snapshot
Synthesis of a novel HMG-COA reductase inhibitor
inferredcites →https://doi.org/10.1021/jm00152a001openalex-snapshot
3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 2. Structural modification of 7-(substituted aryl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives
inferredcites →https://doi.org/10.1021/jm00152a002openalex-snapshot
3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 3. 7-(3,5-Disubstituted-[1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives
inferredcites →https://doi.org/10.1021/jm00155a041openalex-snapshot
3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 5. 6-(Fluoren-9-yl)- and 6-(fluoren-9-ylidene)-3,5-dihydroxyhexanoic acids and their lactone derivatives
inferredcites →https://doi.org/10.1021/jm00163a005openalex-snapshot
Inhibitors of cholesterol biosynthesis. 1. trans-6-(2-Pyrrol-1-ylethyl)-4-hydroxypyran-2-ones, a novel series of HMG-CoA reductase inhibitors. 1. Effects of structural modifications at the 2- and 5-positions of the pyrrole nucleus
inferredcites →https://doi.org/10.1021/jm00163a010openalex-snapshot
Synthesis and biological activity of new HMG-CoA reductase inhibitors. 1. Lactones of pyridine- and pyrimidine-substituted 3,5-dihydroxy-6-heptenoic (-heptanoic) acids
inferredcites →https://doi.org/10.1021/jm00173a013openalex-snapshot
Synthesis, biological profile, and quantitative structure-activity relationship of a series of novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors
inferredcites →https://doi.org/10.1021/jm00381a014openalex-snapshot
3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. I. Structural modification of 5-substituted 3,5-dihydroxypentanoic acids and their lactone derivatives
inferredcites →https://doi.org/10.1088/0031-9112/32/3/038openalex-snapshot
Molecular Interactions Vol 1
inferredcites →https://doi.org/10.1109/t-c.1973.223640openalex-snapshot
Clustering Using a Similarity Measure Based on Shared Near Neighbors
inferredcites →https://doi.org/10.5860/choice.27-0916openalex-snapshot
Distance geometry and molecular conformation

What points at this work

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

inferred← citeshttps://doi.org/10.1002/0470845015.cta005openalex-snapshot
Three‐dimensional Structure Searching
inferred← citeshttps://doi.org/10.1002/9780470125847.ch2openalex-snapshot
Three‐Dimensional Structure Database Searches
inferred← citeshttps://doi.org/10.1002/9783527615674.ch2openalex-snapshot
3D QSAR The Integration of QSAR with Molecular Modeling
inferred← citeshttps://doi.org/10.1002/9783527628766.biblioopenalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1002/ejoc.200400828openalex-snapshot
Coupling–Isomerization–Enamine Addition–Cyclocondensation Sequences:A Multicomponent Approach to Substituted and Annelated Pyridines
inferred← citeshttps://doi.org/10.1007/978-94-011-5686-8_8openalex-snapshot
A Mechanistic Approach to Deriving Quantitative Structure Biodegradablity Relationships
inferred← citeshttps://doi.org/10.1007/bf00119868openalex-snapshot
A 3D QSAR approach to the search for geometrical similarity in a series of nonpeptide angiotensin II receptor antagonists
inferred← citeshttps://doi.org/10.1016/0166-1280(93)87170-iopenalex-snapshot
The role of electronic and conformational properties in the activity of 5-HT3 receptor antagonists
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/b978-012744481-9/50028-3openalex-snapshot
PHARMACOPHORE IDENTIFICATION AND RECEPTOR MAPPING
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01615-5openalex-snapshot
A novel four component one-pot access to pyrindines and tetrahydroquinolines
inferred← citeshttps://doi.org/10.1039/a815653yopenalex-snapshot
The biosynthesis of steroids and triterpenoids
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