1995
DOI: 10.1002/jps.2600840225
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Rough Sets in the Analysis of the Structure–Activity Relationships of Antifungal Imidazolium Compounds

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Cited by 19 publications
(24 citation statements)
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“…Let us also remark that the interpretation of too many possible reducts by practitioners is often impossible. In medical applications, it is not however necessary to look for all reducts and one is often satisfied by computing a limited subset of reducts and/or choosing the most satisfactory subset according to some criteria (see, e.g., discussions in [19,20,28,24].…”
Section: Methodsmentioning
confidence: 99%
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“…Let us also remark that the interpretation of too many possible reducts by practitioners is often impossible. In medical applications, it is not however necessary to look for all reducts and one is often satisfied by computing a limited subset of reducts and/or choosing the most satisfactory subset according to some criteria (see, e.g., discussions in [19,20,28,24].…”
Section: Methodsmentioning
confidence: 99%
“…Similarly to previous medical applications [19,20,27,24,30,28,29] the following elements of the rough set theory are used:…”
Section: Methodsmentioning
confidence: 99%
See 2 more Smart Citations
“…The antimicrobial characteristics and bactericidal mechanism of various series of QACs (Csiba et al, 1987;Devinsky et al, 1991;Kourai et al, 1994b;Krysinski, 1990), including the derivatives of pyridinium salts (Devinsky et al, 1996;Kourai et al, 1994c;Krysinski, 1991;Okazaki et al, 1997aOkazaki et al, , 1997c, have been studied. The hydrophobicity of QACs (Kourai et al, 1995), the critical micelle concentration (Pavlikova-Moricka et al, 1994), and acidic dissociation constant (pKa) of the corresponding pyridines (Kourai et al, 1985) were measured to determine a quantitative structure-activity relationship.…”
Section: Introductionmentioning
confidence: 99%