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Bile acid


DATA No : BBA0313 INFORMANT : Mizuho Une

NAME : 5a-Cholestane-3b,7a,26-triol

COMMON NAME: 16-Deoxymyxinol
SYMBOL:
FORMULA: C27H48O3 MOL.WT (average) : 420.668


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BIOLOGICAL ACTIVITY

PHYSICAL AND CHEMICAL PROPERTIES
MELTING POINT:218-219(Ref. 0322) or 206-207(Ref. 0324)

BOILING POINT:

REFRACTIVE INDEX:

OPTICAL ROTATION:[a]D=+13pm3 (C=0.92, ethanol)(Ref. 0322)

DENSITY:

SOLUBILITY:
SPECTRAL DATA
UV SPECTRA:

IR SPECTRA:(Ref. 0322)

NMR SPECTRA:(Ref. 0323/0305)

MASS SPECTRA:(Ref. 0323/0324)

OTHER SPECTRA:
CHROMATOGRAM DATA

SOURCE
Bile from Eptatretus stoutii(Ref. 0322)Bile from Myxine glutinosa(Ref. 0322)Bile from Heptatretus burgeri(Ref. 0305)
CHEMICAL SYNTHESIS
(Ref. 0324)
METABOLISM

GENETIC INFORMATION

NOTE

REFERENCES
[0305]
AUTHOR:Une,M.,Kihira,K.,Kuramoto,T.,and Hoshita,T.
TITLE:Two new bile alcohols, 3-epimyxinol and 3-epi-16-deoxymyxinol, from the hagfish, Heptatretus burgeri.
JOURNAL:Tetrahedron Lett.
VOL: PAGE : 2527 -2530 (1978)
[TOP]

[0322]
AUTHOR:Anderson, I. G., and Haslewood, G. A.
TITLE:Comparative studies of bile salts. 16-Deoxymyxinol, a second bile alcohol from hagfish PubMed ID:5821731
JOURNAL:Biochem J.
VOL:112 PAGE : 763-765 (1969)
[TOP]

[0323]
AUTHOR:Tokes, L.
TITLE:Nuclear-magnetic-resonance and mass-spectral study of 16-deoxymyxinol PubMed ID:5821732
JOURNAL:Biochem J.
VOL:112 PAGE : 765-767 (1969)
[TOP]

[0324]
AUTHOR:Noll, B. W., Doisy, E. A., Jr., and Elliott, W. H.
TITLE:Bile acids. 39. Metabolism of 5 -cholestane-3,26-diol and 5 -cholestane-3,7,26-triol in the rat with a bile fistula PubMed ID:4715322
JOURNAL:J Lipid Res.
VOL:14 PAGE : 391-399 (1973)
[TOP]

Last updated June 19, 2007. Copyright © 1989-2007 Japanese Conference on the Biochemistry of Lipids (JCBL). All rights reserved.