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Molecular shape descriptors
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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/jps.2600631207openalex-snapshot
Solubility of Nonelectrolytes in Polar Solvents II: Solubility of Aliphatic Alcohols in Water
inferredcites →https://doi.org/10.1002/jps.2600641215openalex-snapshot
Molecular Connectivity II: Relationship to Water Solubility and Boiling Point
inferredcites →https://doi.org/10.1002/jps.2600641216openalex-snapshot
Molecular Connectivity III: Relationship to Partition Coefficients
inferredcites →https://doi.org/10.1002/jps.2600650603openalex-snapshot
Comparison of several molecular topological indexes with molecular surface area in aqueous solubility estimation
inferredcites →https://doi.org/10.1002/qua.560160309openalex-snapshot
Possible connection between lipophilicity and steric substituent constants
inferredcites →https://doi.org/10.1007/978-3-662-30502-7openalex-snapshot
Die herzwirksamen Glykoside
inferredcites →https://doi.org/10.1016/0022-5193(77)90298-3openalex-snapshot
Mapping of dihydrofolate-reductase receptor site by correlation with minimal topological (steric) differences
inferredcites →https://doi.org/10.1016/b978-0-08-021308-8.50906-6openalex-snapshot
INHIBITION OF EXCITATORY EVENTS IN CARDIAC TISSUES BY THE OPTICAL ISOMERS OF VERAPAMIL AND D 600
inferredcites →https://doi.org/10.1021/j100640a027openalex-snapshot
Thermodynamic group contributions from ion pair extraction equilibriums for use in the prediction of partition coefficients. Correlation of surface area with group contributions
inferredcites →https://doi.org/10.1021/j100663a023openalex-snapshot
Theory of hydrophobic bonding. II. Correlation of hydrocarbon solubility in water with solvent cavity surface area
inferredcites →https://doi.org/10.1021/ja00544a005openalex-snapshot
A QSAR investigation of dihydrofolate reductase inhibition by Baker triazines based upon molecular shape analysis
inferredcites →https://doi.org/10.1021/ja01077a028openalex-snapshot
A New Substituent Constant, π, Derived from Partition Coefficients
inferredcites →https://doi.org/10.1021/jm00227a007openalex-snapshot
Dependence of hydrophobicity of apolar molecules on their molecular volume
inferredcites →https://doi.org/10.1021/jm00290a004openalex-snapshot
Interdependence between physical parameters and selection of substituent groups for correlation studies
inferredcites →https://doi.org/10.1038/2141095a0openalex-snapshot
Specific Anosmia: a Clue to the Olfactory Code
inferredcites →https://doi.org/10.1038/2161084a0openalex-snapshot
Molecular Shape and Odour : Pattern Analysis by PAPA
inferredcites →https://doi.org/10.1073/pnas.71.8.2925openalex-snapshot
Empirical Correlation Between Hydrophobic Free Energy and Aqueous Cavity Surface Area
inferredcites →https://doi.org/10.1080/01621459.1949.10483310openalex-snapshot
The Monte Carlo Method
inferredcites →https://doi.org/10.1093/carcin/2.4.269openalex-snapshot
A quantitative structure-activity analysis of the mutagenic and carcinogenic action of 43 structurally related heterocyclic compounds
inferredcites →https://doi.org/10.1098/rspb.1976.0034openalex-snapshot
Kinetic aspects of structure─activity relations: the binding of sulphonamides by carbonic anhydrase
inferredcites →https://doi.org/10.1098/rstb.1981.0124openalex-snapshot
Lead optimization: quantitative structure-activity relations
inferredcites →https://doi.org/10.1111/j.1749-6632.1964.tb45075.xopenalex-snapshot
CURRENT STATUS OF THE STERIC THEORY OF ODOR
inferredcites →https://doi.org/10.1126/science.165.3899.1266openalex-snapshot
Ant Alarm Pheromone Activity: Correlation with Molecular Shape by Scanning Computer
inferredcites →https://doi.org/10.1507/endocrine1927.39.6_511openalex-snapshot
Biological Activity and Chemical Structure
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470125786.ch6openalex-snapshot
Searching Databases of Three‐Dimensional Structures
inferred← citeshttps://doi.org/10.1002/cem.1180070603openalex-snapshot
Statistical thinking and technique for QSAR and related studies. Part I: General theory
inferred← citeshttps://doi.org/10.1002/chin.200127266openalex-snapshot
ChemInform Abstract: TI‐MTD Model: Applications in Molecular Design
inferred← citeshttps://doi.org/10.1002/qsar.19840030202openalex-snapshot
Biological Receptor Maps. 1 Steric Maps. The SIBIS Method
inferred← citeshttps://doi.org/10.1007/978-94-007-1733-6_15openalex-snapshot
Molecular Shape Descriptors: Applications to Structure-Activity Studies
inferred← citeshttps://doi.org/10.1007/bf00134182openalex-snapshot
Modelling steric effects in DNA-binding platinum(II)-am(m)ine complexes
inferred← citeshttps://doi.org/10.1016/0166-1280(89)85013-4openalex-snapshot
The limits of applicability of topological indices
inferred← citeshttps://doi.org/10.1016/0895-7177(88)90569-9openalex-snapshot
A characterization of molecular similarity methods for property prediction
inferred← citeshttps://doi.org/10.1016/b0-08-045044-x/00242-xopenalex-snapshot
Quantitative Structure–Activity Relationship – A Historical Perspective and the Future
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.10.014openalex-snapshot
3D QSAR study of hypolipidemic asarones by comparative molecular surface analysis
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