Abstract
Several 8,16-Ethanoretinals 3 were synthesized from cyclohexanones. From the binding experiments of these analogs with apoprotein of phoborhodopsin, it was found that retinal was incorporated as 6s-trans conformation in the protein and the fine structure in absorption spectra of pigments were dependent on the coplanarity of the conjugated polyene structure in the chromophore.
Keywords: ethanoretinal, retinal analog, phoborhodopsin, chromophore, s-trans conformation
Letters in Organic Chemistry
Title: Synthesis of 8,16-Ethanoretinals and Their Interactions with Apoprotein of Phoborhodopsin from Natronobacterium pharaonis
Volume: 1 Issue: 1
Author(s): Akimori Wada, Yoshimi Takakura, Kenta Yamazaki, Tetsuo Takahashi and Masayoshi Ito
Affiliation:
Keywords: ethanoretinal, retinal analog, phoborhodopsin, chromophore, s-trans conformation
Abstract: Several 8,16-Ethanoretinals 3 were synthesized from cyclohexanones. From the binding experiments of these analogs with apoprotein of phoborhodopsin, it was found that retinal was incorporated as 6s-trans conformation in the protein and the fine structure in absorption spectra of pigments were dependent on the coplanarity of the conjugated polyene structure in the chromophore.
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Cite this article as:
Wada Akimori, Takakura Yoshimi, Yamazaki Kenta, Takahashi Tetsuo and Ito Masayoshi, Synthesis of 8,16-Ethanoretinals and Their Interactions with Apoprotein of Phoborhodopsin from Natronobacterium pharaonis, Letters in Organic Chemistry 2004; 1 (1) . https://dx.doi.org/10.2174/1570178043488789
DOI https://dx.doi.org/10.2174/1570178043488789 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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