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Coenzyme Q


DATA No : VCQ0017 INFORMANT : Tetsuya Nakamura

NAME : 2,3-Dimethoxy-5-methyl-6-[10-(2,2,5,5-tetramethyl-3-pyrrolin-1-oxyl-3-carboxy)decyl ]-1,4-benzoquinone

COMMON NAME:
SYMBOL: Q0C10TMOPOC
FORMULA: C28H41O7N1 MOL.WT (average) : 503.628


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BIOLOGICAL ACTIVITY

PHYSICAL AND CHEMICAL PROPERTIES
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SPECTRAL DATA
UV SPECTRA:
[Spectrum 0001] (Ref. 0038)

IR SPECTRA:

NMR SPECTRA:

MASS SPECTRA:

OTHER SPECTRA:EPR spectrum
[Spectrum 0002] (Ref. 0038)
CHROMATOGRAM DATA

SOURCE

CHEMICAL SYNTHESIS
The spin labeled Q derivative, 2,3-Dimethoxy-5-methyl-6-[10-(2,2,5,5-tetramethyl-3-pyrrolin-1-oxyl-3-carboxy)decyl ]-1,4-benzoquinone (Q0C10TMOPOC), was prepared by the esterification of 2,3-Dimethoxy-5-methyl-6-(10-hydroxydecyl )-1,4-benzoquinone and 2,2,5,5-tetramethyl-3-pyrrolin-1-oxyl-3-carboxylic acid (TMPOC).(Ref. 0038)
METABOLISM

GENETIC INFORMATION

NOTE

REFERENCES
[0038]
AUTHOR:Yu, C. A., and Yu, L.
TITLE:Study of ubiquinone binding in ubiquinol-cytochrome c reductase by spin labeled ubiquinone derivative PubMed ID:6261756
JOURNAL:Biochem Biophys Res Commun.
VOL:98 PAGE : 1063-1069 (1981)
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Last updated June 19, 2007. Copyright © 1989-2007 Japanese Conference on the Biochemistry of Lipids (JCBL). All rights reserved.