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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 91 (1969), S. 97-103 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 60 (1996), S. 1845-1849 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The integrated molecular transform, FTm, is a unitary structure index that has been successfully used for the correlation of two- and three-dimensional structure representations with their physicochemical and pharmacological properties; it has also been shown to be a unique conformational descriptor. In the present instance correlation trials were undertaken by regressing reported molecular skin permeability values on their respective calculated three-dimensional FTm indices. The index functioned not only as a structure descriptor but as a natural delineator in the series, separating several outliers in the data set and showing that excellent correlations may be obtained within the classical divisions of chemical structure. These results not only provide a means of estimating skin permeability directly from structure but also may have theoretical implications for studies of the nature and mechanism of dermal transport. © 1996 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 70 (1998), S. 1185-1194 
    ISSN: 0020-7608
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The integrated molecular transform (FTm) is a unitary numerical index of structure that is capable of uniquely representing different molecular structure conformations with the exception of enantiomers. Other molecular indices have been derived from FTm as well as from the normalized molecular moment (Mn), for example, the analogous electronic and charge transforms (FTe and FTc) and moments (Me and Mc). In this study, each of these indices was calculated for up to 10 sampled conformations of each of the C1-C10 normal alkanes as they were subjected to a standard annealing process. Statistical analyses of the resulting data in the individual series and subsequent box plots, permitting facile examination of those results, indicated that the respective transform indices (FTm, FTe, FTc) are unique, that is, with no statistically significantly overlap across the series. For the Mn and Me indices, the numerical values for methane overlapped those of ethane in the first instance and both ethane and propane in the second. The Mc index values overlapped in several instances in the series. Inasmuch as the noted molecular indices are based only on parameters of structural origin, these results have profound implications for the correlation and estimation of properties derived not only from a general structure representation, but also for those properties which may be dependent on specific molecular conformations. This includes the potential for indices of molecular flexibility and conformationally dependent atomic electron densities.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 70: 1185-1194, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 56 (1995), S. 201-206 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The integrated molecular transform (FTm) is a unitary structure index that has been successfully used for the correlation of 2- and 3-dimensional structure representations with their physicochemical and pharmacological properties. In the present instance the reported pKa values in a series of 30 compounds consisting of five subseries were correlated with their FTm indices. The omission of four outliers gave a moderate correlation across the entire series; within the individual subseries the correlations were considerably improved even with inclusion of the outliers. In general, the logarithmic transform of the pKa did not improve the correlations. This method gives a relatively simple means of estimating pKa in several structure classes. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 64 (1997), S. 635-645 
    ISSN: 0020-7608
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The integrated molecular transform (FTm), a unitary structure index, has been successfully used for the correlation of 2- and 3-dimensional structure representations with their physicochemical and pharmacological properties and in structure-similarity studies. A recently introduced structure index, the normalized molecular moment (Mn), has been used in similarity and limited physicochemical studies. In the present instance, both indices were calculated after MM2 structure-optimization and used to correlate structure with organic diamagnetic susceptibility over a wide range of values. The FTm index also functioned as a data discriminator in this series of 72 compounds and excellent correlations were obtained both within principal data groups and within outlier groups; the Mn index was a somewhat less precise model in this case. The results suggest a study of correlations within classical chemical structure divisions.   © 1997 John Wiley & Sons, Inc. Int J Quant Chem 64: 635-645, 1997
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 65 (1997), S. 1047-1056 
    ISSN: 0020-7608
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The integrated molecular transform (FTm) has been used for the correlation of the structures of organic molecules with their physicochemical, thermodynamic, and pharmacological properties; it is also an excellent conformation index and functions as a discriminator of classical chemical structure types. In this study, it is used along with our recently introduced normalized molecular moment (Mn), and new structure indices, viz the integrated electronic transform (FTe), the integrated charge transform (FTc), and the electronic moment (Me), to establish appropriate models for the title subject. Initially, the principal absorption maxima in each of several series were regressed against the structural indices to determine which index best represented the structures in the context of the absorption data. The indices were then selectively regressed against the absorption data to generate absorbance estimation equations. In a series of multicyclic hydrocarbons, the FTm functioned as a topological structure discriminator as well as a structure surrogate. In the topological subsets, the FTe and FTc also were selectively useful. For a series of conjugated dienes, the FTm and the Mn were statistically appropriate. In a series of substituted benzenes, the discrimination of halobenzenes was apparent and could be represented by either the FTm, FTe, or Me indices. For other variously substituted benzenes, the FTm is the extant model and further work with larger, structurally delineated series is warranted. For a series of monoalkyl-substituted nitrobenzenes, the FTm and FTe parameters are appropriate variables. Satisfactory correlation of molar absorptivities was not possible in this study as it would require absorption curve integration in the range where the maxima occurs.   © 1997 John Wiley & Sons, Inc. Int J Quant Chem 65: 1047-1056, 1997
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 69 (1998), S. 49-56 
    ISSN: 0020-7608
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The unitary molecular structure indices, viz., the integrated molecular transform (FTm), the integrated electronic transform (FTe), the integrated charge transform (FTc), the normalized molecular moment (Mn), and the normalized electronic moment (Me) were used in separate trials to model the reported apparent distribution coefficients (log P′) of 25 dipeptides and 34 tripeptides. Linear regressions indicated that the two series should be considered separately as shown by the correlation coefficients and F statistics. In these cases, the former exceeded 0.75 generally and reached 0.795 for the FTe. The correlation coefficients for the FTc index were 0.692 and 0.380, respectively, for the two series and thus indicative of its inadequacy as a descriptor for this model. A bivariant regression of log P′ against Mn and Me did not improve on the monovariant models. The molecular weight as a structure surrogate gave adequate correlation coefficients but is not recommended as structure parameters are implicit rather than explicit. The Mn or Me correlations may be used to estimate log P′ for compounds similar to those in the dipeptide series, and FTe, likewise in the tripeptide series. The possible requirement for an amide group descriptor is discussed.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 69: 49-56, 1998
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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