In Silico and RP HPLC Studies of Biologically Active 1,3,4-Thiadiazol-2-yl)-benzene-1,3-diols

Biologically active compounds from the 1,3,4-thiadiazol-2-yl)-benzene-1,3-diols group described earlier have been studied. Various approaches were used to determine their lipophilicity and predict pharmacokinetic properties. The lipophilicity parameters log k<sub>w</sub> were determined using isocratic column chromatography and various stationary phases. Based on the standard curve and retention measurements by using an octadecyl column, the log D<sub>7.4</sub> distribution coefficient was determined. A weak correlation was found between the experimentally determined log k<sub>w</sub> parameters and the in silico calculated log P descriptors. It was shown that the compounds partially exist in an ionized anionic form at physiological pH. The determined log D<sub>7.4</sub> parameter indicates that most of them have lipophilic character at the level recommended for potential drugs.

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Publication Details

Journal
Molecules
Published
2025-09-28
DOI
https://doi.org/10.3390/molecules30193913
Primary Topic
Synthesis and biological activity
Type
article
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article

In Silico and RP HPLC Studies of Biologically Active 1,3,4-Thiadiazol-2-yl)-benzene-1,3-diols

Tadeusz Paszko, Beata Paw, Bogusław Senczyna, Marek Studziński et al.
Molecules
Synthesis and biological activity
article

In Silico and RP HPLC Studies of Biologically Active 1,3,4-Thiadiazol-2-yl)-benzene-1,3-diols

Tadeusz Paszko, Beata Paw, Bogusław Senczyna, Marek Studziński, Joanna Matysiak, Katarzyna Barańska
article en

Abstract

Biologically active compounds from the 1,3,4-thiadiazol-2-yl)-benzene-1,3-diols group described earlier have been studied. Various approaches were used to determine their lipophilicity and predict pharmacokinetic properties. The lipophilicity parameters log k<sub>w</sub> were determined using isocratic column chromatography and various stationary phases. Based on the standard curve and retention measurements by using an octadecyl column, the log D<sub>7.4</sub> distribution coefficient was determined. A weak correlation was found between the experimentally determined log k<sub>w</sub> parameters and the in silico calculated log P descriptors. It was shown that the compounds partially exist in an ionized anionic form at physiological pH. The determined log D<sub>7.4</sub> parameter indicates that most of them have lipophilic character at the level recommended for potential drugs.

MoleculesVol. 30(19)
Medical University of Lublin (PL), University of Life Sciences in Lublin (PL), Maria Curie-Skłodowska University (PL)
Openalex Percentile: Top 80%
Synthesis and biological activity
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