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COMMON NAME | : | b-hydroxyarchaeol(Ref. 0003) |
SYMBOL | : | b-OH-ArOH(Ref. 0003) |
FORMULA | : | C43H88O4 MOL.WT (average) : 669.156 |
BIOLOGICAL ACTIVITY |
PHYSICAL AND CHEMICAL PROPERTIES |
MELTING POINT | : | |
BOILING POINT | : | |
REFRACTIVE INDEX | : | |
OPTICAL ROTATION | : | [a]D=+5.65 degree |
DENSITY | : | |
SOLUBILITY | : |
SPECTRAL DATA |
UV SPECTRA | : | |
IR SPECTRA | : | |
NMR SPECTRA | : | 13C-NMR, 67.49 (C1 sn-2), 70.23 (C1 sn-3), 39.97 (C2 sn-2), 36.59 (C2 sn-3), 72.47 (C3 sn-2), 29.92 (C3 sn-3), 43.12 (C4 sn-2), 37.31-37.48 (C4 sn-3), 21.49 (C5 sn-2), 24.39 (C5 sn-3), 26.66 (C17 sn-2), 19.76-19.71 (C17 sn-3). Carbon numbers of the hydrocarbon chains are shown. |
MASS SPECTRA | : | positive FAB m/z 691 ([M+Na]); GC-MS of acetylated derivative m/z 397 (M-OC20H40OCOCH3), m/z 355 (OC20H40OCOCH3) |
OTHER SPECTRA | : | |
CHROMATOGRAM DATA |
SOURCE |
CHEMICAL SYNTHESIS |
METABOLISM |
GENETIC INFORMATION |
NOTE |
REFERENCES |
AUTHOR | : | Nishihara,M., and Koga,Y. |
TITLE | : | Hydroxyarchaetidylserine and Hydroxyarchaetidyl-myo-Inositol in Methanosarcina barkeri: Polar Lipids with a New Ether Core Portion. PubMed ID:1901027 |
JOURNAL | : | Biochim. Biophys. Acta |
VOL | : | 1082 PAGE : 211 -217 (1991) |
AUTHOR | : | Sprott, G. D., Ekiel, I., and Dicaire, C. |
TITLE | : | Novel, acid-labile, hydroxydiether lipid cores in methanogenic bacteria PubMed ID:2380184 |
JOURNAL | : | J Biol Chem. |
VOL | : | 265 PAGE : 13735-13740 (1990) |
AUTHOR | : | Koga,Y., Akagawa-Matsushita,M., Ohga,M., and Nishihara,M. |
TITLE | : | Taxonomic Significance of the Distribution of Component Parts of Polar Ether Lipids in Methanogens. |
JOURNAL | : | System. Appl. Microbiol. |
VOL | : | 16 PAGE : 342 -351 (1993) |