|
Journal of Lipid Research, Vol 33, 599-604, Copyright © 1992 by Lipid Research, Inc.
A proposed nomenclature for bile acids
AF Hofmann, J Sjovall, G Kurz, A Radominska, CD Schteingart, GS Tint, ZR Vlahcevic and KD Setchell
Department of Medicine, University of California-San Diego, La Jolla 92093.
A proposal is made for a system of nomenclature of the more common
unconjugated and conjugated bile acids. Acceptable trivial names for bile
acids are tabulated, and guidelines are proposed for using these existing
trivial names as roots to create acceptable semi-systematic names for other
bile acids, as well as for new natural bile acids that will be discovered
in the future. The term alpha-hyocholic is recommended to replace
hyocholic, and beta-hyocholic to replace omega- muricholic. The term
murideoxycholic acid is recommended for 3 alpha,6 beta-dihydroxy-5
beta-cholan-24-oic acid. Proposals are also made for bile acids with
epimeric hydroxy groups, for unsaturated bile acids, and for bile acids
with oxo- and/or hydroxy-oxo- substituents on the nucleus and/or on the
side chain. For conjugated bile acids, the term "aminoacyl amidates" is
recommended to replace "amidates" for bile acids conjugated in N-acyl
linkage with amino acids. Nomenclature for other types of conjugates
(sulfates, glucuronides, glucosides) is included as well as abbreviations.
It is recommended that the historic tradition of naming a newly discovered
bile acid after the species from which it was isolated be abandoned, and
that in the future such a bile acid should be named using the principles
contained in this paper.

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
A. K. Deo and S. M. Bandiera
Biotransformation of Lithocholic Acid by Rat Hepatic Microsomes: Metabolite Analysis by Liquid Chromatography/Mass Spectrometry
Drug Metab. Dispos.,
February 1, 2008;
36(2):
442 - 451.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Kakiyama, T. Iida, T. Goto, N. Mano, J. Goto, T. Nambara, L. R. Hagey, C. D. Schteingart, and A. F. Hofmann
Identification of a novel bile acid in swans, tree ducks, and geese: 3{alpha},7{alpha},15{alpha}-trihydroxy-5{beta}-cholan-24-oic acid
J. Lipid Res.,
July 1, 2006;
47(7):
1551 - 1558.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. M. Ridlon, D.-J. Kang, and P. B. Hylemon
Bile salt biotransformations by human intestinal bacteria
J. Lipid Res.,
February 1, 2006;
47(2):
241 - 259.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. V. Venkatachalam, D. E. Llanos, K. J. Karami, and V. A. Malinovskii
Isolation, partial purification, and characterization of a novel petromyzonol sulfotransferase from Petromyzon marinus (lamprey) larval liver
J. Lipid Res.,
March 1, 2004;
45(3):
486 - 495.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. G. Schuetz, S. Strom, K. Yasuda, V. Lecureur, M. Assem, C. Brimer, J. Lamba, R. B. Kim, V. Ramachandran, B. J. Komoroski, et al.
Disrupted Bile Acid Homeostasis Reveals an Unexpected Interaction among Nuclear Hormone Receptors, Transporters, and Cytochrome P450
J. Biol. Chem.,
October 12, 2001;
276(42):
39411 - 39418.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J.-P. Raufman, P. Zimniak, and A. Bartoszko-Malik
Lithocholyltaurine interacts with cholinergic receptors on dispersed chief cells from guinea pig stomach
Am J Physiol Gastrointest Liver Physiol,
June 1, 1998;
274(6):
G997 - G1004.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 1992 by the American Society for Biochemistry and Molecular Biology.
|
Advertisement
Advertisement
|