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A 3D QSAR CoMFA study of non-peptide angiotensin II receptor antagonists
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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/chin.199152175openalex-snapshot
ChemInform Abstract: Conformationally Restricted Polysubstituted Biphenyl Derivatives with Angiotensin II Receptor Antagonist Properties.
inferredcites →https://doi.org/10.1002/chin.199426185openalex-snapshot
ChemInform Abstract: Imidazo(4,5‐b)pyridine‐Based AT1/AT2 Angiotensin II Receptor Antagonists.
inferredcites →https://doi.org/10.1002/jcc.540080710openalex-snapshot
An efficient newton‐like method for molecular mechanics energy minimization of large molecules
inferredcites →https://doi.org/10.1002/jcc.540110404openalex-snapshot
Atomic charges derived from semiempirical methods
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/qsar.19930120103openalex-snapshot
Generating Optimal Linear PLS Estimations (GOLPE): An Advanced Chemometric Tool for Handling 3D‐QSAR Problems
inferredcites →https://doi.org/10.1007/978-1-4757-1904-8openalex-snapshot
Principal Component Analysis
inferredcites →https://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
inferredcites →https://doi.org/10.1007/bf00123662openalex-snapshot
Derivation of a 3D pharmacophore model for the angiotensin-II site one receptor
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/10.1016/0165-6147(87)90013-7openalex-snapshot
The renin-angiotensin system
inferredcites →https://doi.org/10.1016/0166-1280(93)87080-wopenalex-snapshot
On the role of the molecular electrostatic potential in modelling the activity of non-peptide angiotensin II receptor antagonists
inferredcites →https://doi.org/10.1021/ja00194a035openalex-snapshot
An internal-coordinate Monte Carlo method for searching conformational space
inferredcites →https://doi.org/10.1021/ja00226a005openalex-snapshot
Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins
inferredcites →https://doi.org/10.1021/jm00049a012openalex-snapshot
Nonpeptide Angiotensin II Receptor Antagonists. Synthesis, in vitro Activity, and Molecular Modeling Studies of N-[(Heterobiaryl)methyl]imidazoles
inferredcites →https://doi.org/10.1021/jm00053a013openalex-snapshot
Nonpeptide angiotensin II antagonists: N-phenyl-1H-pyrrole derivatives are angiotensin II receptor antagonists
inferredcites →https://doi.org/10.1021/jm00061a016openalex-snapshot
New nonpeptide angiotensin II receptor antagonists. 3. Synthesis, biological properties, and structure-activity relationships of 2-alkyl-4-(biphenylylmethoxy)pyridine derivatives
inferredcites →https://doi.org/10.1021/jm00083a011openalex-snapshot
New nonpeptide angiotensin II receptor antagonists. 1. Synthesis, biological properties and structure-activity relationships of 2-alkylbenzimidazole derivatives
inferredcites →https://doi.org/10.1021/jm00100a007openalex-snapshot
New nonpeptide angiotensin II receptor antagonists. 2. Synthesis, biological properties, and structure-activity relationships of 2-alkyl-4-(biphenylylmethoxy)quinoline derivatives
inferredcites →https://doi.org/10.1021/jm00112a015openalex-snapshot
Conformationally restricted polysubstituted biphenyl derivatives with angiotensin II receptors antagonist properties
inferredcites →https://doi.org/10.1021/jm00112a031openalex-snapshot
Nonpeptide angiotensin II receptor antagonists: the discovery of a series of N-(biphenylylmethyl)imidazoles as potent, orally active antihypertensives
inferredcites →https://doi.org/10.1021/jm00167a008openalex-snapshot
Part VI. Nonpeptide angiotensin II receptor antagonists: N-[(benzyloxy)benzyl]imidazoles and related compounds as potent antihypertensives
inferredcites →https://doi.org/10.1080/00401706.1988.10488412openalex-snapshot
Principal Component Analysis
inferredcites →https://doi.org/10.1152/physrev.1987.67.3.725openalex-snapshot
Peptides and central neural regulation of the circulation.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/cmdc.70460openalex-snapshot
Oxadiazolone‐Triazole Derivatives as a New Scaffold for Modulation of Angiotensin II‐Induced Vascular Contraction
inferred← citeshttps://doi.org/10.1002/qsar.200860128openalex-snapshot
The Effect of Molecular Fields, Lattice Spacing and Analysis Options on CoMFA Predictive Ability
inferred← citeshttps://doi.org/10.1007/s00044-009-9197-5openalex-snapshot
Structural insights for 3H-1, -2, -4 triazolinones as angiotensin II receptor antagonists using QSAR techniques
inferred← citeshttps://doi.org/10.1007/s00044-011-9622-4openalex-snapshot
Predicting 3H-1,2,4-triazolinones as angiotensin II receptor antagonists: 2D and 3D QSAR by kNN-molecular field analysis approach
inferred← citeshttps://doi.org/10.1007/s00044-011-9815-xopenalex-snapshot
Insight into the structural requirement of aryltriazolinone derivatives as angiotensin II AT1 receptor: 2D and 3D-QSAR k-Nearest Neighbor Molecular Field Analysis approach
inferred← citeshttps://doi.org/10.1007/s00044-012-0462-7openalex-snapshot
A rational design, synthesis, characterization, and antihypertensive activities of some new substituted benzimidazoles
inferred← citeshttps://doi.org/10.1007/s00894-007-0252-1openalex-snapshot
Effect of steric molecular field settings on CoMFA predictivity
inferred← citeshttps://doi.org/10.1007/s10822-019-00231-xopenalex-snapshot
www.3d-qsar.com: a web portal that brings 3-D QSAR to all electronic devices—the Py-CoMFA web application as tool to build models from pre-aligned datasets
inferred← citeshttps://doi.org/10.1007/s13721-017-0160-yopenalex-snapshot
Prediction of structural requirements of AT1 receptor through application of pharmacophore-based 3D-QSAR studies
inferred← citeshttps://doi.org/10.1016/j.arabjc.2011.04.016openalex-snapshot
WITHDRAWN: An approach to design antihypertensive agents by 2D QSAR studies on series of substituted benzimidazoles derivatives as angiotensin II receptor antagonists
inferred← citeshttps://doi.org/10.1016/j.arabjc.2011.05.015openalex-snapshot
WITHDRAWN: QSAR studies on substituted benzimidazoles as angiotensin II receptor antagonists: kNN-MFA approach
inferred← citeshttps://doi.org/10.1016/j.arabjc.2011.07.008openalex-snapshot
WITHDRAWN: QSAR analysis and 3D QSAR kNN-MFA approach on a series of substituted quinolines derivatives as angiotensin II receptor antagonists
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.10.043openalex-snapshot
Angiotensin II receptor type 1 (AT1) selective nonpeptidic antagonists—A perspective
inferred← citeshttps://doi.org/10.1016/j.ejmech.2009.12.063openalex-snapshot
A comparison of different electrostatic potentials on prediction accuracy in CoMFA and CoMSIA studies
inferred← citeshttps://doi.org/10.1016/j.jmgm.2006.10.004openalex-snapshot
Development of CoMFA models of affinity and selectivity to angiotensin II type-1 and type-2 receptors
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.03.005openalex-snapshot
3D QSAR kNN-MFA studies on 6-substituted benzimidazoles derivatives as Nonpeptide Angiotensin II Receptor Antagonists: A rational approach to antihypertensive agents
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/j.jscs.2011.05.011openalex-snapshot
Insight into the structural requirement of substituted quinazolinone biphenyl acylsulfonamides derivatives as Angiotensin II AT1 receptor antagonist: 2D and 3D QSAR approach
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.07.013openalex-snapshot
WITHDRAWN: QSAR analysis of imidazo[4,5-b]pyridine substituted α-Phenoxyphenylacetic acids as angiotensin II AT1 receptor antagonists
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.08.005openalex-snapshot
WITHDRAWN: QSAR studies of a series of angiotensin II receptor substituted benzimidazole bearing acidic heterocycles derivatives
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.09.001openalex-snapshot
WITHDRAWN: Predicting substituted 2-butylbenzimidazoles derivatives as angiotensin II receptor antagonists: 3D-QSAR and pharmacophore modeling
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.10.008openalex-snapshot
WITHDRAWN: Two dimensional and k-nearest neighbor molecular field analysis approach on substituted Triazolone derivatives: An insight into the structural requirement for the angiotensin II receptor antagonist
inferred← citeshttps://doi.org/10.1016/s0968-0896(98)00160-6openalex-snapshot
Design and synthesis of nonpeptide angiotensin II receptor antagonists featuring acyclic imidazole-mimicking structural units
inferred← citeshttps://doi.org/10.1021/ci049612jopenalex-snapshot
Improved CoMFA Modeling by Optimization of Settings
inferred← citeshttps://doi.org/10.1021/ci600214bopenalex-snapshot
Systematic Statistical Comparison of Comparative Molecular Similarity Indices Analysis Molecular Fields for Computer-Aided Lead Optimization
inferred← citeshttps://doi.org/10.1021/ci800390mopenalex-snapshot
Partial Charge Calculation Method Affects CoMFA QSAR Prediction Accuracy
inferred← citeshttps://doi.org/10.1021/ci900117mopenalex-snapshot
Comparison Data Sets for Benchmarking QSAR Methodologies in Lead Optimization
inferred← citeshttps://doi.org/10.1021/cr000025gopenalex-snapshot
Comparative QSAR: Angiotensin II Antagonists
inferred← citeshttps://doi.org/10.1021/jm060338popenalex-snapshot
Proposal of a New Binding Orientation for Non-Peptide AT1 Antagonists: Homology Modeling, Docking and Three-Dimensional Quantitative Structure−Activity Relationship Analysis
inferred← citeshttps://doi.org/10.1023/a:1017015028419openalex-snapshot
List of CoMFA references, 1993-1996
inferred← citeshttps://doi.org/10.1080/1062936021000058782openalex-snapshot
Selection of data sets for qsars: Analyses of tetrahymena toxicity from aromatic compounds
inferred← citeshttps://doi.org/10.3390/ecsoc-1-02064openalex-snapshot
HQSAR: A New, Highly Predictive QSAR Technique
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