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 |
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creator | Jansen, Johanna M. Copinga, Swier Gruppen, Gert Isaksson, Roland Witte, Dirk T. Grol, Cor J. |
description | 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. |
doi_str_mv | 10.1002/chir.530060714 |
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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.</description><identifier>ISSN: 0899-0042</identifier><identifier>EISSN: 1520-636X</identifier><identifier>DOI: 10.1002/chir.530060714</identifier><identifier>PMID: 7986673</identifier><language>eng</language><publisher>New York: Alan R. Liss, Inc</publisher><subject>2-amidotetralins ; Binding Sites ; Cellulose - analogs & derivatives ; chromatography ; Chromatography, High Pressure Liquid - methods ; enantiomers ; Indicators and Reagents ; melatonin ; Melatonin - analogs & derivatives ; Melatonin - isolation & purification ; Melatonin - metabolism ; Receptors, Cell Surface - metabolism ; Receptors, Melatonin ; semipreparative separation ; Stereoisomerism ; Structure-Activity Relationship ; tri-acetylcellulose</subject><ispartof>Chirality (New York, N.Y.), 1994, Vol.6 (7), p.596-604</ispartof><rights>Copyright © 1994 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3784-a5666cc75e732f4d5bf44acee31c79e2afa0e23583f64105b93eafc5bf5b78613</citedby><cites>FETCH-LOGICAL-c3784-a5666cc75e732f4d5bf44acee31c79e2afa0e23583f64105b93eafc5bf5b78613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchir.530060714$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchir.530060714$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,4024,27923,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7986673$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jansen, Johanna M.</creatorcontrib><creatorcontrib>Copinga, Swier</creatorcontrib><creatorcontrib>Gruppen, Gert</creatorcontrib><creatorcontrib>Isaksson, Roland</creatorcontrib><creatorcontrib>Witte, Dirk T.</creatorcontrib><creatorcontrib>Grol, Cor J.</creatorcontrib><title>Semipreparative enantiomeric separation of a series of putative melatonin receptor agents using tri-acetylcellulose as chiral stationary phase</title><title>Chirality (New York, N.Y.)</title><addtitle>Chirality</addtitle><description>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.</description><subject>2-amidotetralins</subject><subject>Binding Sites</subject><subject>Cellulose - analogs & derivatives</subject><subject>chromatography</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>enantiomers</subject><subject>Indicators and Reagents</subject><subject>melatonin</subject><subject>Melatonin - analogs & derivatives</subject><subject>Melatonin - isolation & purification</subject><subject>Melatonin - metabolism</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Receptors, Melatonin</subject><subject>semipreparative separation</subject><subject>Stereoisomerism</subject><subject>Structure-Activity Relationship</subject><subject>tri-acetylcellulose</subject><issn>0899-0042</issn><issn>1520-636X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS0EaqeFLTskr9hl6sSvZIkGaCuNCmpBIDbWHfemdUniYDu08yf6m5s0oxE7Vn7cc7577EvI25wtc8aKE3vrwlJyxhTTuXhBFrksWKa4-vmSLFhZVRljojgkRzHeMcYqxcUBOdBVqZTmC_J4ha3rA_YQILm_SLGDLjnfYnCWxt2976ivKYzn4DBO-35Is77FBpLvXEcDWuyTDxRusEuRDtF1NzQFl4HFtG0sNs3Q-IgUIp1iQ0NjeqZD2NL-FiK-Jq9qaCK-2a3H5PvnT99WZ9n6y-n56sM6s1yXIgOplLJWS9S8qMW13NRCjF2Q51ZXWEANDAsuS14rkTO5qThCbUeZ3OhS5fyYvJ-5ffB_BozJtC5OAaFDP0SjValKocUoXM5CG3yMAWvTB9eOeU3OzDQAM73E7AcwGt7tyMOmxeu9fPfjY72a6_euwe1_aGZ1dn75LzubvS4mfNh7Ifw2I1pL8-Pi1BRXvy7414_arPkThYmmqg</recordid><startdate>1994</startdate><enddate>1994</enddate><creator>Jansen, Johanna M.</creator><creator>Copinga, Swier</creator><creator>Gruppen, Gert</creator><creator>Isaksson, Roland</creator><creator>Witte, Dirk T.</creator><creator>Grol, Cor J.</creator><general>Alan R. 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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.</abstract><cop>New York</cop><pub>Alan R. Liss, Inc</pub><pmid>7986673</pmid><doi>10.1002/chir.530060714</doi><tpages>9</tpages></addata></record> |
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subjects | 2-amidotetralins Binding Sites Cellulose - analogs & derivatives chromatography Chromatography, High Pressure Liquid - methods enantiomers Indicators and Reagents melatonin Melatonin - analogs & derivatives Melatonin - isolation & purification Melatonin - metabolism Receptors, Cell Surface - metabolism Receptors, Melatonin semipreparative separation Stereoisomerism Structure-Activity Relationship tri-acetylcellulose |
title | Semipreparative enantiomeric separation of a series of putative melatonin receptor agents using tri-acetylcellulose as chiral stationary phase |
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