Literature DB >> 11375745

Estimation of aqueous solubility in drug design.

J Huuskonen1.   

Abstract

The solubility of drugs in water is of central importance in the process of drug discovery and development from molecular design to pharmaceutical formulation and biopharmacy. The ability to estimate the aqueous solubility and other properties of a promising lead compound affecting its pharmacokinetics is a prerequisite to rational drug design, although it has received much less attention than the prediction of drug-receptor interactions. In this review, methods for the estimation of aqueous solubility of organic compounds are described and limited to approaches, which might be used in the early stage of drug design and development.

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Year:  2001        PMID: 11375745     DOI: 10.2174/1386207013331147

Source DB:  PubMed          Journal:  Comb Chem High Throughput Screen        ISSN: 1386-2073            Impact factor:   1.339


  2 in total

1.  In silico prediction of aqueous solubility, human plasma protein binding and volume of distribution of compounds from calculated pKa and AlogP98 values.

Authors:  Mario Lobell; Vinothini Sivarajah
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

2.  Rapid experimental measurements of physicochemical properties to inform models and testing.

Authors:  Chantel I Nicolas; Kamel Mansouri; Katherine A Phillips; Christopher M Grulke; Ann M Richard; Antony J Williams; James Rabinowitz; Kristin K Isaacs; Alice Yau; John F Wambaugh
Journal:  Sci Total Environ       Date:  2018-05-02       Impact factor: 7.963

  2 in total

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