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Identification of Novel Small‐molecule Inducers of Fetal Hemoglobin Using Pharmacophore and ‘PSEUDO’ Receptor Models
Author(s) -
Bohacek Regine,
Boosalis Michael S.,
McMartin Colin,
Faller Douglas V.,
Perrine Susan P.
Publication year - 2006
Publication title -
chemical biology and drug design
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 77
eISSN - 1747-0285
pISSN - 1747-0277
DOI - 10.1111/j.1747-0285.2006.00386.x
Subject(s) - pharmacophore , short chain fatty acid , inducer , fetal hemoglobin , biochemistry , gene , small molecule , chemistry , molecular model , fatty acid , biology , fetus , genetics , pregnancy , butyrate , fermentation
Pharmacologic reinduction of the developmentally silenced fetal ( γ ) globin genes has been achieved in hemoglobinopathy patients using short chain fatty acid derivatives, with therapeutic effects. However, higher‐potency inducers than are available in currently identified short chain fatty acid derivatives are desirable for long‐term use. Using several short‐chain fatty acids with established γ ‐globin induction activity, a pharmacophore template was constructed with the TFIT module of the flo software and used to select several new candidate compounds, three of which exhibited significant activity in a γ ‐globin gene reporter transcriptional assay which detects only strong inducers. The data were used to construct a new pharmacophore and a ‘pseudo’ receptor around it. Six hundred and thirty low‐molecular weight compounds were docked into this receptor model. Of 26 compounds selected and tested in functional assays, two compounds showed activity >500% over control levels and two had activity 200% over control range, significantly more active than previously identified short chain fatty acid derivative fetal globin gene inducers. Three compounds had less activity; the remainder showed moderate activity. These findings demonstrate the feasibility of using iterative construction of pharmacophores, pseudo‐binding site modeling, and virtual screening to identify small molecules with the ability to induce transcription of specific target genes, for potential therapeutics.