Literature DB >> 11510839

High-throughput liquid chromatography/mass spectrometry method for the determination of the chromatographic hydrophobicity index.

G Camurri1, A Zaramella.   

Abstract

A fast gradient reversed-phase liquid chromatography (LC) method, using an acetonitrile gradient was developed to determine the chromatographic hydrophobicity index (CHI), as reported by Valco et al. (Anal. Chem. 1997, 69, 2022-2029). The analytical method provides retention times, based on UV detection at two different wavelengths, which then are converted into CHI values after calibration with a set of test compounds. The CHI of each compound is measured at three different pH values, 2.0, 7.4, and 10.5; so using an 8-min gradient at each pH value one compound can be analyzed in approximately 24 min. The aim of this work is to improve the throughput of the CHI screening using a LC/MS approach, so the application of the LC/MS technique is an extension of the LC/UV approach previously reported by Valco et al. This approach allows contemporary injection of N compounds into the LC/MS system, the retention time of each compound can be then extracted from the selected ion recording chromatograms. The throughput of the existing screening method could be increased by N times, where N is the number of compounds injected, so only three runs are needed to determine the CHI at three different pH values for a set of N compounds. The highest value of N depends on the total number of channels that can be monitored simultaneously; in the present work, 32 channels were used. This LC/MS method has been tested for a number of commercial products analyzed as mixtures, and data obtained were compared with those coming from the classical LC/UV approach. In the same way, the method was tested for a number of compounds associated with two GlaxoWellcome projects in the antibacterial area. Data reported show that the LC/MS method can be successfully applied for analyzing compounds in mixtures and for compounds with poor UW absorption, which cannot be analyzed with the standard LC/UV method.

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Year:  2001        PMID: 11510839     DOI: 10.1021/ac001388j

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  6 in total

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Journal:  Nat Commun       Date:  2016-11-04       Impact factor: 14.919

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Journal:  ACS Infect Dis       Date:  2018-03-26       Impact factor: 5.084

3.  Discovery and Optimization of 5-Amino-1,2,3-triazole-4-carboxamide Series against Trypanosoma cruzi.

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Journal:  J Med Chem       Date:  2017-08-27       Impact factor: 7.446

4.  Optimization of TAM16, a Benzofuran That Inhibits the Thioesterase Activity of Pks13; Evaluation toward a Preclinical Candidate for a Novel Antituberculosis Clinical Target.

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Journal:  J Med Chem       Date:  2021-12-15       Impact factor: 8.039

5.  Group-Based Optimization of Potent and Cell-Active Inhibitors of the von Hippel-Lindau (VHL) E3 Ubiquitin Ligase: Structure-Activity Relationships Leading to the Chemical Probe (2S,4R)-1-((S)-2-(1-Cyanocyclopropanecarboxamido)-3,3-dimethylbutanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide (VH298).

Authors:  Pedro Soares; Morgan S Gadd; Julianty Frost; Carles Galdeano; Lucy Ellis; Ola Epemolu; Sonia Rocha; Kevin D Read; Alessio Ciulli
Journal:  J Med Chem       Date:  2017-09-18       Impact factor: 7.446

6.  Using LC Retention Times in Organic Structure Determination: Drug Metabolite Identification.

Authors:  William L Fitch; Cyrus Khojasteh; Ignacio Aliagas; Kevin Johnson
Journal:  Drug Metab Lett       Date:  2018
  6 in total

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