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A 3D QSAR approach to the search for geometrical similarity in a series of nonpeptide 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/actp.1984.010350714openalex-snapshot
Molecular mechanics. Von U LRICH B URKERT und N ORMAN L. A LLINGER . ACS Monograph 177. Washington: American Chemical Society 1982. 430 S., US $ 77.95
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/10.1007/bf00124386openalex-snapshot
Pharmacophore identification by molecular modeling and chemometrics: The case of HMG-CoA reductase inhibitors
inferredcites →https://doi.org/10.1007/bf00135315openalex-snapshot
Structure-activity relationship of Ca2+ channel blockers: A study using conformational analysis and chemometric methods
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/10.1016/0169-7439(92)80075-fopenalex-snapshot
Linear discriminant classification tree: A user-driven multicriteria classification method
inferredcites →https://doi.org/10.1021/ja00194a035openalex-snapshot
An internal-coordinate Monte Carlo method for searching conformational space
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/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/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/jm00113a035openalex-snapshot
Potent, orally active imidazo[4,5-b]pyridine-based angiotensin II receptor antagonists
inferredcites →https://doi.org/10.1021/jm00167a007openalex-snapshot
The discovery of potent nonpeptide angiotensin II receptor antagonists: a new class of potent 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/10.1137/1.9781611970319openalex-snapshot
The Jackknife, the Bootstrap and Other Resampling Plans
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/10.1002/9783527615674.ch2openalex-snapshot
3D QSAR The Integration of QSAR with Molecular Modeling
inferred← citeshttps://doi.org/10.1007/978-1-62703-050-2_3openalex-snapshot
Role of Computational Methods in Pharmaceutical Sciences
inferred← citeshttps://doi.org/10.1007/bf00134180openalex-snapshot
A 3D QSAR CoMFA study of non-peptide angiotensin II receptor antagonists
inferred← citeshttps://doi.org/10.1016/0960-894x(96)00116-3openalex-snapshot
The design, binding affinity prediction and synthesis of macrocyclic angiotensin II AT1 and AT2 receptor antagonists
inferred← citeshttps://doi.org/10.1016/j.aca.2007.04.031openalex-snapshot
QSAR study of angiotensin II antagonists using robust boosting partial least squares regression
inferred← citeshttps://doi.org/10.1016/j.chemolab.2016.03.023openalex-snapshot
Variable-selection approaches to generate QSAR models for a set of antichagasic semicarbazones and analogues
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/10.1016/s1050-1738(96)00068-0openalex-snapshot
Computational Science New Horizons and Relevance to Pharmaceutical Design
inferred← citeshttps://doi.org/10.1021/jm9504722openalex-snapshot
Nonpeptide Angiotensin II Receptor Antagonists: The Next Generation in Antihypertensive Therapy
inferred← citeshttps://doi.org/10.1081/bip-100104193openalex-snapshot
BIOPHARMACEUTICAL STATISTICS BEYOND 2000
inferred← citeshttps://doi.org/10.1139/v04-160openalex-snapshot
A quantitative structure-activity relationship study for α-substituted acetamido-N-benzylacetamide derivatives A novel anticonvulsant drug class
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