about
Conversion of 7-ketolithocholic acid to ursodeoxycholic acid by human intestinal anaerobic microorganisms: interchangeability of chenodeoxycholic acid and ursodeoxycholic acidImpaired oxidoreduction by 11β-hydroxysteroid dehydrogenase 1 results in the accumulation of 7-oxolithocholic acid.Reduction of 7-ketolithocholic acid by human liver enzyme preparations in vitro.Ursodeoxycholic acid, 7-ketolithocholic acid, and chenodeoxycholic acid are primary bile acids of the nutria (Myocastor coypus).Transformation of chenodeoxycholic acid to ursodeoxycholic acid in patients with Crohn's disease.Formation of ursodeoxycholic acid from chenodeoxycholic acid in the human colon: studies of the role of 7-ketolithocholic acid as an intermediate.Effect of 7-ketolithocholic acid on bile acid metabolism in humans.Metabolism in man of 7-ketolithocholic acid: precursor of cheno- and ursodeoxycholic acids.Hepatic reduction of the secondary bile acid 7-oxolithocholic acid is mediated by 11β-hydroxysteroid dehydrogenase 1.Oxidation of primary bile acids by a 7 alpha-hydroxysteroid dehydrogenase elaborating Clostridium bifermentans soil isolate.Ursodeoxycholic acid, chenodeoxycholic acid, and 7-ketolithocholic acid are primary bile acids of the guinea pig.Hepatic biotransformation and choleretic effect of 7-ketolithocholic acid in the ratHypercholeresis induced by ursodeoxycholic acid and 7-ketolithocholic acid in the rat: possible role of bicarbonate transportBile acids. VIII. Metabolism of 7-ketolithocholic acid-24-C14 in the ratReduction of 7-ketolithocholic acid to chenodeoxycholic acid by rat liver preparations in vitroMetabolism of two hydroxy-7-oxocholanic acids in isolated perfused rat liverAbsorption of 7-ketolithocholic acid in rat jejunum, ileum and colon
P921
Q28328780-8B62E732-0CC8-4935-BAA5-97C570BA1EE2Q37163081-10B76745-93C8-41B6-8127-5E82EC079BD0Q42202907-DE747FD5-6F74-4831-BF62-58477910905EQ42226527-CA31E730-3AE1-4144-A60E-901E89C9C23AQ42226530-ED7161BD-5DE5-42A7-85D4-5CB94C8FF97DQ42253517-2A645CC8-8920-4B6C-9835-621FC763FF0DQ42263942-476FF3EF-902B-4226-B582-31CE6631A6F7Q42273251-53D3C3C7-462A-4BEB-8795-8BBA63FD5347Q42744337-79F2F3D7-FE2B-4A43-9578-D2D320C92838Q45015111-193131C6-934B-415E-958E-1D8CEB9DE571Q46755501-4D4B3689-6526-48CC-9D5B-3BCF3C536FE6Q69791970-C03A56B6-CC36-41C0-BCD4-7E83E324B62CQ71211586-E108DEC3-FFE4-4A56-B295-BD8FC6714308Q77071649-A333394B-7D91-4396-B375-11F128E8A7A3Q93591665-0AD728F2-3133-4724-B320-F60846494B38Q93644275-8EE859D5-6290-4500-8170-1DFE049F5E7FQ93680577-6B9F3F6D-670C-40DC-8480-75A91946F642
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
nutriacholic acid
@en
type
label
nutriacholic acid
@en
altLabel
3-alpha-Hydroxy-7-oxo-5-beta-cholan-24-oic acid
@en
3alpha-Hydroxy-7-oxo-5beta-cholanic acid
@en
3alpha-hydroxy-7-oxo-5beta-cholan-24-oic acid
@en
7-Ketolithocholic acid
@en
7-oxo-3alpha-hydroxycholan-24-oic acid
@en
7-oxolithocholic acid
@en
Nutriacholic acid
@en
prefLabel
nutriacholic acid
@en
P6689
P486
P592
P661
P662
P683
P1579
P2017
C[C@H](CCC(=O)O)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C(=O)C[C@H]4[C@@]3(CC[C@H](C4)O)C)C
P2057
HMDB0000467
P2063
LMST04010150
P2067
P231
P232
P233
CC(CCC(=O)O)C1CCC2C1(CCC3C2C(=O)CC4C3(CCC(C4)O)C)C
P234
1S/C24H38O4/c1-14(4-7-21(27)28 ...... ,17-,18+,19+,22+,23+,24-/m1/s1
P235
DXOCDBGWDZAYRQ-AURDAFMXSA-N
P2566
100.022.803