Literature DB >> 10441277

Combined molecular lipophilicity descriptors and their role in understanding intramolecular effects.

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Abstract

Traditional lipophilicity parameters (log P and log D) are well-known physico-chemical descriptors largely used in QSAR studies. Besides their numerical value, log P data contain a variety of information about inter- and intramolecular forces affecting partitioning and its related biological phenomena. The deconvolution of information from log P can be accessed only by adequate interpretative tools, such as new lipophilic-combined descriptors, of which features and some applications are presented in this review.

Year:  1999        PMID: 10441277     DOI: 10.1016/s1461-5347(99)00180-7

Source DB:  PubMed          Journal:  Pharm Sci Technolo Today        ISSN: 1461-5347


  8 in total

1.  Quantitative structure-permeation relationships (QSPeRs) to predict skin permeation: a critical evaluation.

Authors:  Sandrine Geinoz; Richard H Guy; Bernard Testa; Pierre-Alain Carrupt
Journal:  Pharm Res       Date:  2004-01       Impact factor: 4.200

2.  Theoretical and experimental exploration of the lipophilicity of zwitterionic drugs in the 1,2-dichloroethane/water system.

Authors:  Géraldine Bouchard; Alessandra Pagliara; Pierre-Alain Carrupt; Bernard Testa; Véronique Gobry; Hubert H Girault
Journal:  Pharm Res       Date:  2002-08       Impact factor: 4.200

3.  Design, Synthesis and Evaluation of Bifunctional Acridinine-Naphthalenediimide Redox-Active Conjugates as Antimalarials.

Authors:  Srikanta Dana; Sudhir Kumar Keshri; Jyoti Shukla; Kunwar Somesh Vikramdeo; Neelima Mondal; Pritam Mukhopadhyay; Suman Kumar Dhar
Journal:  ACS Omega       Date:  2016-09-01

4.  Lipophilicity behaviour of the Zwitterionic antihistamine cetirizine in phosphatidylcholine liposomes/water systems.

Authors:  G Plember van Balen; G Caron; G Ermondi; A Pagliara; T Grandi; G Bouchard; R Fruttero; P A Carrupt; B Testa
Journal:  Pharm Res       Date:  2001-05       Impact factor: 4.200

5.  High lipophilicity of perfluoroalkyl carboxylate and sulfonate: implications for their membrane permeability.

Authors:  Ping Jing; Patrick J Rodgers; Shigeru Amemiya
Journal:  J Am Chem Soc       Date:  2009-02-18       Impact factor: 15.419

Review 6.  High throughput methods to measure the propensity of compounds to form intramolecular hydrogen bonding.

Authors:  Giulia Caron; Maura Vallaro; Giuseppe Ermondi
Journal:  Medchemcomm       Date:  2017-04-27       Impact factor: 3.597

7.  Automated potentiometric titrations in KCl/water-saturated octanol: method for quantifying factors influencing ion-pair partitioning.

Authors:  Robert A Scherrer; Stephen F Donovan
Journal:  Anal Chem       Date:  2009-04-01       Impact factor: 6.986

8.  Construction of Quantitative Structure Activity Relationship (QSAR) Models to Predict Potency of Structurally Diversed Janus Kinase 2 Inhibitors.

Authors:  Saw Simeon; Nathjanan Jongkon
Journal:  Molecules       Date:  2019-12-01       Impact factor: 4.411

  8 in total

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