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rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2004-5-4
pubmed:abstractText
A nonlinear regression analysis has been applied to develop a new method to predict the plasma protein-binding percent of structurally diverse pharmaceutical compounds. The analysis included over 300 launched drugs with experimental human plasma protein binding percent data. These drugs were classified according to protonation state and pharmacophore features. The correlation formula for each class is a simple sigmoidal function of variable LogP or LogD. A correlation formula of variable LogD at pH 7.4 with a good correlation coefficient (R-squared = 0.803) was obtained for neutral and basic drugs, with the exception of zwitterions. A correlation formula using LogP as variable for acidic drugs with one of the specific pharmacophore features gave a good correlation coefficient (R-squared = 0.786). The method was verified using the protein binding data of 20 compounds that had not been included in the data set to configure the formulas. The correlation coefficient (R-squared) between the experimental and predicted protein binding percent was 0.830. In conclusion, the method developed and described in this report can provide precise and useful prediction of plasma protein binding percent for new drug candidates.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-3549
pubmed:author
pubmed:copyrightInfo
Copyright 2004 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 93:1480-1494, 2004
pubmed:issnType
Print
pubmed:volume
93
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1480-94
pubmed:meshHeading
pubmed:year
2004
pubmed:articleTitle
Computational prediction of the plasma protein-binding percent of diverse pharmaceutical compounds.
pubmed:affiliation
Sumitomo Pharmaceuticals Co., Ltd., 1-98, Kasugade Naka 3-Chome, Konohana-ku, Osaka, 554-0022, Japan. kanaoka@sumitomopharm.co.jp
pubmed:publicationType
Journal Article