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Range and Sensitivity as Descriptors of Molecular Property Spaces in Dynamic QSAR Analyses
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Selection criteria for drug‐like compounds
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Computer Modeling of Size and Shape Descriptors of α1-Adrenergic Receptor Antagonists and Quantitative Structure–Affinity/Selectivity Relationships
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Molecular Lipophilicity Potential, a tool in 3D QSAR: Method and applications
inferredcites →https://doi.org/10.1007/bf02158636openalex-snapshot
Fine tipped metal microelectrodes with glass insulation
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Quantitative structure?activity relationships of a 1 adrenergic antagonists
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Recent advances in α1-adrenoceptor pharmacology
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Prediction of ‘drug-likeness’
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Synthesis and biological activity of new 1,4-benzodioxan-arylpiperazine derivatives. Further validation of a pharmacophore model for α1-adrenoceptor antagonists
inferredcites →https://doi.org/10.1016/s0968-0896(99)00194-7openalex-snapshot
Relevance of theoretical molecular descriptors in quantitative structure–activity relationship analysis of α1-adrenergic receptor antagonists
inferredcites →https://doi.org/10.1016/s0968-0896(99)00263-1openalex-snapshot
Ligand design for α1 adrenoceptor subtype selective antagonists
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α1 Adrenoceptor subtype selectivity
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Advances in biomolecular simulations: methodology and recent applications
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The Solute−Solvent System: Solvent Constraints on the Conformational Dynamics of Acetylcholine
inferredcites →https://doi.org/10.1021/jm010934dopenalex-snapshot
Development of a Virtual Screening Method for Identification of “Frequent Hitters” in Compound Libraries
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α 1 -Adrenoceptor Antagonists. 4. Pharmacophore-Based Design, Synthesis, and Biological Evaluation of New Imidazo-, Benzimidazo-, and Indoloarylpiperazine Derivatives
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Molecular Properties That Influence the Oral Bioavailability of Drug Candidates
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Synthesis, Pharmacological Evaluation, and Structure−Activity Relationship and Quantitative Structure−Activity Relationship Studies on Novel Derivatives of 2,4-Diamino-6,7-dimethoxyquinazoline α1-Adrenoceptor Antagonists
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Lipophilicity in Molecular Modeling
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9783527621286.ch1openalex-snapshot
A Fresh Look at Molecular Structure and Properties
inferred← citeshttps://doi.org/10.1002/9783527621460.ch8openalex-snapshot
Computational Modeling of Selective Pharmacophores at the α 1 ‐Adrenergic Receptors
inferred← citeshttps://doi.org/10.1002/cbdv.200900072openalex-snapshot
Partition Coefficient and Molecular Flexibility: The Concept of Lipophilicity Space
inferred← citeshttps://doi.org/10.1002/cbdv.201400177openalex-snapshot
Small Molecules as Exemplars of Emergent Properties and Diversification into the ‘Adjacent Possible’
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Approaching Pharmacological Space: Events and Components
inferred← citeshttps://doi.org/10.1007/978-1-4939-7899-1_12openalex-snapshot
Approaching Pharmacological Space: Events and Components
inferred← citeshttps://doi.org/10.1016/b0-08-045044-x/00142-5openalex-snapshot
Molecular Fields to Assess Recognition Forces and Property Spaces
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12659-9openalex-snapshot
Molecular Fields to Assess Recognition Forces and Property Spaces☆
inferred← citeshttps://doi.org/10.1016/j.drudis.2007.11.007openalex-snapshot
Assessing drug-likeness – what are we missing?
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.097openalex-snapshot
On the choice of optimal conformation in linear free-energy relationships. Reactivity of 2-[(carboxymethyl)sulfanyl]-4-oxo-4-arylbutanoic acids with diphenyldiazomethane
inferred← citeshttps://doi.org/10.1021/tx300247ropenalex-snapshot
Quantitative Prediction of Antitarget Interaction Profiles for Chemical Compounds
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A Cu2+ Probe over Nizatidine and Ranitidine, or In Silico Vs. Experimentally Obtained Complexation of Drugs
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