Semipreparative enantiomeric separation of a series of putative melatonin receptor agents using tri-acetylcellulose as chiral stationary phase

In order to obtain milligram amounts of the enantiomers of a series of compounds to be tested for binding to the melatonin binding site, a system for semipreparative enantiomeric separation was set up using tri‐acetylcellulose as the chiral stationary phase. Interactions of this class of compounds w...

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Veröffentlicht in:Chirality (New York, N.Y.) N.Y.), 1994, Vol.6 (7), p.596-604
Hauptverfasser: Jansen, Johanna M., Copinga, Swier, Gruppen, Gert, Isaksson, Roland, Witte, Dirk T., Grol, Cor J.
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Sprache:eng
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Zusammenfassung:In order to obtain milligram amounts of the enantiomers of a series of compounds to be tested for binding to the melatonin binding site, a system for semipreparative enantiomeric separation was set up using tri‐acetylcellulose as the chiral stationary phase. Interactions of this class of compounds with tri‐acetylcellulose were examined on an analytical scale with a series of 20 compounds. Apparently, both steric and electrostatic interactions determine retention behavior on tri‐acetylcellulose. Semipreparative separations were carried out for a subset of seven compounds. The purity of the first eluting enantiomer usually was around 99%, whereas the purity of the second eluting enantiomer was slightly less. The system described is easy to use and has the major advantage that a series of compounds can be separated with one technique. The purities obtained are sufficient for a first screen of their affinity. © 1994 Wiley‐Liss, Inc.
ISSN:0899-0042
1520-636X
DOI:10.1002/chir.530060714