13-Demethyl-13-substituted-13,14-dihydroretinols as potential affinity labels of retinol-binding proteins: Syntheses and stability studies

Revital Yefidoff, Limor Weiss, David Avisar, Amnon Albeck

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

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 languageEnglish
Pages (from-to)38-50
Number of pages13
JournalBioorganic Chemistry
Volume32
Issue number1
DOIs
StatePublished - 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.

FundersFunder number
United States-Israel Binational Science Foundation2000390

    Keywords

    • Affinity label
    • Epoxide
    • Retinoids
    • Stability

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