Abstract
13-Demethyl-13-substituted-13,14-dihydroretinols were synthesized and their stability under various conditions was measured in order to evaluate whether they would be useful as affinity labels of retinol binding proteins and retinol metabolizing enzymes. The 13-chloro analog could not be isolated because it eliminated HCl under the Wittig reaction conditions of its preparation. The trans- and cis-13,14-epoxy analogs are stable in non-protic organic solvents, but undergo an elimination reaction under various chromatographic conditions and in mixtures of organic solvents with water or alcohol. The 13-hydroxy and 13-methoxy analogs are stable in aqueous solutions and are therefore suitable for biological studies.
Original language | English |
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Pages (from-to) | 38-50 |
Number of pages | 13 |
Journal | Bioorganic Chemistry |
Volume | 32 |
Issue number | 1 |
DOIs | |
State | Published - Feb 2004 |
Bibliographical note
Funding Information:This study was supported by a United States—Israel Binational Science Foundation Grant no. 2000390.
Funding
This study was supported by a United States—Israel Binational Science Foundation Grant no. 2000390.
Funders | Funder number |
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United States-Israel Binational Science Foundation | 2000390 |
Keywords
- Affinity label
- Epoxide
- Retinoids
- Stability