Uses
ChemicalBook > CAS DataBase List > Chenodeoxycholic acid

Chenodeoxycholic acid

Uses
Product Name
Chenodeoxycholic acid
CAS No.
474-25-9
Chemical Name
Chenodeoxycholic acid
Synonyms
CDCA;CHENODIOL;CHENODEOXYCHOLATE;3ALPHA,7ALPHA-DIHYDROXY-5BETA-CHOLANIC ACID;Chenix;ChenodeoxychoL;3a,7a-Dihydroxy-5b-cholanoic acid;Fluibil;Kebilis;chendol
CBNumber
CB4285737
Molecular Formula
C24H40O4
Formula Weight
392.57
MOL File
474-25-9.mol
More
Less

Chenodeoxycholic acid Property

Melting point:
165-167 °C (lit.)
alpha 
12 º (c=1, CHCl3)
Boiling point:
437.26°C (rough estimate)
Density 
0.9985 (rough estimate)
refractive index 
1.4460 (estimate)
Flash point:
9℃
storage temp. 
room temp
solubility 
PRACTICALLY INSOLUBLE
form 
Powder
pka
pKa 4.34 (Uncertain)
color 
White to off-white
Water Solubility 
PRACTICALLY INSOLUBLE
Merck 
13,2062
BRN 
3219887
InChIKey
RUDATBOHQWOJDD-BSWAIDMHSA-N
LogP
3.05 at 20℃
CAS DataBase Reference
474-25-9(CAS DataBase Reference)
EPA Substance Registry System
Chenodiol (474-25-9)
More
Less

Safety

Hazard Codes 
Xn
Risk Statements 
63
Safety Statements 
22-24/25-45-36/37
RIDADR 
UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany 
2
RTECS 
FZ1980000
HS Code 
29181990
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C9377
Product name
Chenodeoxycholic acid
Purity
≥97%
Packaging
5g
Price
$184
Updated
2024/03/01
Sigma-Aldrich
Product number
C9377
Product name
Chenodeoxycholic acid
Purity
≥97%
Packaging
25g
Price
$414
Updated
2024/03/01
Alfa Aesar
Product number
J60364
Product name
Chenodeoxycholic acid
Packaging
5g
Price
$83.9
Updated
2023/06/20
Alfa Aesar
Product number
J60364
Product name
Chenodeoxycholic acid
Packaging
25g
Price
$252
Updated
2023/06/20
Cayman Chemical
Product number
10011286
Product name
Chenodeoxycholic Acid
Purity
≥95%
Packaging
1g
Price
$32
Updated
2024/03/01
More
Less

Chenodeoxycholic acid Chemical Properties,Usage,Production

Uses

Chenodeoxycholic acid is a bile acid synthesized in the liver from cholesterol. henodeoxycholic acid has been used in a study to assess its effects as a long-term replacement therapy for cerebrotendinous xanthomatosis (CTX). It has also been used in a study to investigate its effects on the small-intestinal absorption of bile acids in patients with ileostomies.

Description

Chenodeoxycholic acid is the first agent to be introduced into the US market for the treatment of radiolucent gallstones. Large scale clinical trials have demonstrated the safety and efficacy of this agent. Chenodeoxycholic acid reduces the biliary concentration of cholesterol relative to that of bile acids and phospholipid, reducing the saturation and thus the lithogenicity of the bile. Success rates in dissolving gallstones are in the range of 50-70% within 4-24 months of treatment. Continuation of the drug after stone dissolution may be required to prevent reoccurrence. Chenodeoxycholic acid is the 7α-isomer of ursodeoxycholic acid which was introduced into the European market in 1978.

chenodeoxycholic acid structure

Chemical Properties

Off-White Solid

Originator

Rowell (USA)

History

Chenodeoxycholic acid was isolated in 1924 from goose gall by Adolf Windaus and human gall by Heinrich Wieland.Its complete structural configuation was elucidated by Hans Lettre at the University of Gottingen.
In 1968, William Admirand and Donald Small at Boston University Medical School established that in patients with gallstones their bile was saturated with cholesterol, sometimes even exhibiting microcrystals, whereas this was not the case in normal people.It was then found that biliary levels of cholic acid and chenodeoxycholic acid were lower in patients with cholesterol gallstones than in normal people. Leslie Thistle and John Schoenfield at the Mayo Clinic in Rochester, Minnesota, then administered individual bile salts by mouth for four months and found that chenodeoxycholic acid reduced the amount of cholesterol in the bile.This led to a national collaborative study in the United States, which confirmed the effectiveness of chenodeoxycholic acid in bringing about dissolution of gallstones in selected patients. However, recent developments such as laparoscopic cholecystectomy and endoscopic biliary techniques have curtailed the role of chenodeoxycholic acid and ursodeoxycholic acid in the treatment of cholelithiasis.

Uses

anticholithogenic, antilipemic agent

Uses

An apoptosis inducer via PKC-dependent signalling pathway.

Uses

A major bile acid in many vertebrates, occurring as the N-glycine and/or N-taurine conjugate. With other bile acids, forms mixed micelles with lecithin in bile which solubilize cholesterol and thus fa cilitates its excretion. Fcilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol.

Uses

Chenodeoxycholic acid is a bile acid that induces apoptosis through protein kinase C signaling pathways.It is a major bile acid in many vertebrates, occurring as the N-glycine and/or N-taurine conjugate. With other bile acids, forms mixed micelles with lecithin in bile which solubilize cholesterol and thus facilitates its excretion.Bile acids are essential for solubilization and transport of dietary lipids, are the major products of cholesterol catabolism, and are physiological ligands for farnesoid X receptor (FXR), a nuclear receptor that regulates genes involved in lipid metabolism.They are also inherently cytotoxic, as physiological imbalance contributes to increased oxidative stress. Bile acid-controlled signaling pathways are promising novel targets to treat such metabolic diseases as obesity, type II diabetes, hyperlipidemia, and atherosclerosis.

  1. Chenodeoxycholic acid is widely utilized in therapeutic applications. It is applied in medical therapy to dissolve gallstones. It is employed in the treatment of cerebrotendineous xanthomatosis. It is used to treat constipation and cerebrotendineous xanthomatosis. It acts as a urea receptor in supramolecular chemistry which can contain anions. It is a staining additive commonly used with ruthenium or organic photo-sensitizers in the preparation of staining solutions for dye solar cells.
  2. Chenodeoxycholic Acid is a staining additive commonly used with ruthenium or organic photo-sensitizers in the preparation of staining solutions for Dye Solar Cells. This co-adsorbent will prevent dye aggregation on the semiconductor surface, reducing losses in the solar cell's operation.
  3. Chenodeoxycholic Acid is a white solid added with the dye powder to the solvent while preparing staining solutions. The concentration of co-adsorbent is typically 10 fold the dye concentration.
  4. Chenodeoxycholic acid has been used in a study to assess its effects as a long-term replacement therapy for cerebrotendinous xanthomatosis (CTX).
  5. It has also been used in a study to investigate its effects on the small-intestinal absorption of bile acids in patients with ileostomies.
  6. Chenodeoxycholic acid (CDCA) is a hydrophobic primary bile acid that activates nuclear receptors involved in cholesterol metabolism.EC50 concentrations for activation of FXR range from 13-34 μM.In cells, CDCA also binds to bile acid binding proteins (BABP) with a reported stoichiometry of 1:2.CDCA toxicity is linked to increased cellular glutathione levels and increased oxidative stress. Exposure of cells to excess CDCA contributes to liver and intestinal cancers.

Definition

ChEBI: Chenodeoxycholic acid is a dihydroxy-5beta-cholanic acid that is (5beta)-cholan-24-oic acid substituted by hydroxy groups at positions 3 and 7 respectively. It has a role as a human metabolite and a mouse metabolite. It is a bile acid, a dihydroxy-5beta-cholanic acid and a C24-steroid. It is a conjugate acid of a chenodeoxycholate.

Manufacturing Process

To 1,400 ml of an approximately 50% water/triglycol solution of the potassium salt of chenodeoxycholic acid, obtained by the Wolff-Kishner reduction (using hydrazine hydrate and potassium hydroxide) from 50 g of 7- acetyl-12-ketochenodeoxycholic acid, 220 ml of dilute hydrochloric acid is added to bring the pH to 2. The solution is stirred and the crude chenodeoxycholic acid precipitates. The precipitate is recovered and dried to constant weight at about 60°C. About 36 g of the crude chenodeoxycholic acid, melting in the range of 126°-129°C, is obtained.
25 g of crude chenodeoxycholic acid so obtained is dissolved in 750 ml of acetonitrile while stirring and heating. 3 g of activated charcoal is added and then removed by suction filtering. The resulting liquid filtrate is cooled, the pure chenodeoxycholic acid crystallizing out. The crystals are recovered by suction filtering and the recovered crystals dried under vacuum. The yield is 19 g of pure chenodeoxycholic acid with a melting range of 168°-171°C.

brand name

CHEWM

Therapeutic Function

Gallostone dissolving agent

World Health Organization (WHO)

Chenodeoxycholic acid was introduced in 1975 for the treatment of cholelithiasis. It is available in several countries and the World Health Organization is not aware that registration has been refused in any other country.

General Description

Chenodeoxycholic acid is a bile acid synthesized in the liver from cholesterol.

Flammability and Explosibility

Non flammable

Purification Methods

This major bile acid in vertebrates (~80mg) is chromatographed on silica gel (5g) and eluted with CHCl3/EtOAc (3:2) and crystallised from EtOAc/hexane. It has IR: max 1705 cm-1(CHCl3). It also crystallises from EtOAc, EtOAc/heptane after purifying via the poorly soluble Na and K salt if necessary. [Kametani et al. J Org Chem 4 7 2331 1982, Beilstein 10 IV 1604.]

Chenodeoxycholic acid Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Chenodeoxycholic acid Suppliers

Shandong JunRui Pharmaceutical Co., Ltd.
Tel
0539-5636807 15318528770
Fax
0539-5636807
Email
ffeng813@qq.com
Country
China
ProdList
247
Advantage
58
Shaanxi Pioneer Biotech Co.,Ltd
Tel
029-86107037-8021 15353537425
Email
sales@pioneerbiotech.com
Country
China
ProdList
249
Advantage
58
Taizhou Hoyoo Chemical Co.,Ltd
Tel
0576-0576-88666163 15057600339
Fax
0576-88666163
Email
hoyoochem@yahoo.com
Country
China
ProdList
111
Advantage
58
Wuhan Feiyue Biotechnology Co., LTD
Tel
027-87002654 18062720658
Email
andydeng@feiyuebio.com
Country
China
ProdList
805
Advantage
58
Tianyuan Natural Product Co.,Ltd.
Tel
028-85012281 13808177790
Fax
86-28-85121102
Email
xianlihong8888@163.com
Country
China
ProdList
50
Advantage
62
Shanghai Boyle Chemical Co., Ltd.
Tel
Fax
86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2923
Advantage
55
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
future industrial shanghai co., ltd
Tel
400-0066400 13621662912
Fax
021-55660885
Email
sales@jonln.com
Country
China
ProdList
1998
Advantage
65
TAIYUAN RHF CO.,LTD.
Tel
+86 351 7031519
Fax
+86 351 7031519
Email
sales@RHFChem.com
Country
China
ProdList
2341
Advantage
56
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18501085097
Fax
010-89508210
Email
sales3.gd@hwrkchemical.com
Country
China
ProdList
7583
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Shijiazhuang Sdyano Fine Chemical Co., Ltd.
Tel
0311-89250318 031166536426
Fax
4000311741
Email
master@sjzsdyn.com
Country
China
ProdList
2882
Advantage
65
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9984
Advantage
60
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9552
Advantage
66
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
zhangsn@titansci.com
Country
China
ProdList
14113
Advantage
59
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Fax
021-50795055
Email
sales@accelachem.com
Country
China
ProdList
11660
Advantage
64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32344
Advantage
50
China DongFan Chemical Co.,LTD
Tel
86-0571-85151182
Fax
86-0571-85151182
Country
China
ProdList
5700
Advantage
66
XiaoGan ShenYuan ChemPharm co,ltd
Tel
0712-0712-2580635 15527768850
Email
1791901229@qq.com
Country
China
ProdList
8849
Advantage
52
Shandong Xiya Chemical Co., Ltd
Tel
13355009207 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18739
Advantage
57
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14443
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
Aktin Chemicals, Inc.
Tel
86-28-85159085
Fax
86-28-85152372
Email
info@aktinchem.com
Country
China
ProdList
297
Advantage
62
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9664
Advantage
60
Wuhan Fortuna Chemical Co., Ltd
Tel
027-027-59207852 13308628970
Fax
QQ3130921841
Email
buy@fortunachem.com
Country
China
ProdList
2894
Advantage
58
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4647
Advantage
58
BioBioPha Co., Ltd.
Tel
0871-65217109 13211707573;
Fax
0871-65215563
Email
y.liu@mail.biobiopha.com
Country
China
ProdList
5654
Advantage
65
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Fax
021-55068248
Email
shyysw007@163.com
Country
China
ProdList
4941
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9872
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17779
Advantage
75
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6139
Advantage
55
Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
Country
China
ProdList
9442
Advantage
58
Shanghai Topbiochem Technology Co., Ltd
Tel
+86-21-60341587
Fax
+86-21-61294319
Email
sales@topbiochem.com
Country
China
ProdList
6181
Advantage
58
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9901
Advantage
58
Shanghai Jian Chao Chemical Technology Co., Ltd.
Tel
021-50430803 18017383231
Fax
qq:2817624287
Email
983544897@qq.com
Country
China
ProdList
9352
Advantage
55
Haoyuan Chemexpress Co., Ltd.
Tel
021-58950125
Fax
(86) 21-58955996
Email
info@chemexpress.com
Country
China
ProdList
7553
Advantage
61
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25004
Advantage
65
The future of Shanghai Industrial Co., Ltd.
Tel
021-61552785
Fax
021-55660885
Email
sales@shshiji.com
Country
China
ProdList
9552
Advantage
55
Shanghai Ruji Biology Technology Co., Ltd.
Tel
+86-21-65211385-8001 36031160
Fax
+86-21-65211385-8004
Email
sales@shruji.com
Country
China
ProdList
3224
Advantage
55
Cantotech Chemicals, Ltd.
Tel
86-0755-86635001
Fax
86-0755-22642228
Email
cantotech@126.com
Country
China
ProdList
4576
Advantage
55
Shanghai Tauto Biotech Co., Ltd.
Tel
021-51320588
Fax
0086-21-51320502
Email
tauto@tautobiotech.com
Country
China
ProdList
3989
Advantage
66
Hunan Furui Biopharma Technology Co., Ltd.
Tel
15902102743
Fax
0731-57805668
Email
shelley@furuipharma.com
Country
China
ProdList
425
Advantage
55
Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4428
Advantage
55
More
Less

View Lastest Price from Chenodeoxycholic acid manufacturers

Hebei Dangtong Import and export Co LTD
Product
Chenodeoxycholic acid 474-25-9
Price
US $98.00-90.00/kilograms
Min. Order
1kilograms
Purity
99%
Supply Ability
200tons
Release date
2023-02-14
Sinoway Industrial co., ltd.
Product
Chenodeoxycholic Acid 474-25-9
Price
US $85.00-45.00/Kg/Bag
Min. Order
1Kg/Bag
Purity
0.90
Supply Ability
20 tons
Release date
2024-01-02
airuikechemical co., ltd.
Product
chenodeoxycholic acid 474-25-9
Price
US $0.00-0.00/Kg
Min. Order
1Kg
Purity
99.9%
Supply Ability
200tons
Release date
2024-04-09

474-25-9, Chenodeoxycholic acidRelated Search:


  • (R)-4-((3R,7R,8R,9S,10S,13R,14S,17R)-3,7-dihydroxy-10,13-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid
  • (R)-4-((3R,5S,7R,10S,13R)-3,7-dihydroxy-10,13-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid
  • URSODEOXYCHOLOC ACID,3,7-dihydroxy-,(3-alpha,5-beta,7-alpha)-cholan-24-oicaci
  • 5β-Cholanic acid-3α,7α-diol Chenodiol
  • CDCA
  • CHENODEOXYCHOLIC ACID
  • CHENODESOXYCHOLIC ACID
  • CHENODIOL
  • CHOLAN-24-OIC ACID, 3,7-DIHYDROXY-, (3A,5B,7A)-
  • DEOXYCHENOCHOLIC ACID
  • 3 α ,7 α -Dihydroxy-5β-cholan-24-oic acid.
  • 5β-Cholanic acid-3α,7α-diol
  • CHENODEOXYCHOLIC ACID BP/USP/EP
  • CHENODEOXYCHOLIC ACID(RG)
  • 17β-(1-Methyl-3-carboxypropyl)etiocholane-3α,7α-diol
  • 3α,7α-Dihydroxy-5β-cholanoic acid
  • 3α,7α-Dihydroxycholanic acid
  • 5β-Cholan-24-oic acid, 3α,7α-dihydroxy- (8CI)
  • 5β-Cholanic acid, 3α,7α-dihydroxy- (7CI)
  • Chenix
  • Chenocedon
  • Chenocol
  • Chenodex
  • Chenofalk
  • Chenossil
  • Cholan-24-oic acid, 3,7-dihydroxy-, (3α,5β,7α)-
  • Cholanorm
  • Fluibil
  • Hekbilin
  • Kebilis
  • Ulmenide
  • 5-BETA-CHOLAN-24-OICACID,3-ALPHA,7-ALPHA-DIHYDROXY-
  • CHENODEOXYCHOLATE
  • 3a,7a-Dihydroxy-5β-cholanic acid
  • 5β-Cholanic acid-3a,7a-diol
  • Chenodoxycholic acid
  • CHENODEOXYCHOLIC ACID CRYSTALLINE
  • CHENODEOXYCHOLIC ACID :CHOLAN-24-OICACID, 3,7-DIHYDROXY-, (3A,5B,7A)-,
  • ChenodeoxycholicAcidCp9598%Min
  • CHENODEXOXYCHOLICACID
  • (4R)-4-[(3R,5S,7R,8S,9S,10R,13R,14S,17R)-3,7-dihydroxy-10,13-dimethyl-2,3,4]
  • 3ALPHA,7ALPHA-DIHYDROXY-5BETA-CHOLANIC ACID
  • 5BETA-CHOLANIC ACID-3ALPHA,7ALPHA-DIOL
  • 5BETA-CHOLANIC ACID-3,7-DIOL
  • 5B-CHOLANIC ACID-3A,7A-DIOL
  • (3a,5,7a)-3,7-Dihydroxycholan-24-oic Acid
  • 17-(1-Methyl-3-carboxypropyl)etiocholane-3a,7a-diol
  • URSODEOXYCHOLOC ACID
  • 3,7-dihydroxy-,(3-alpha,5-beta,7-alpha)-cholan-24-oicaci
  • 3,7-dihydroxy-,(3alpha,5beta,7alpha)-cholan-24-oicaci
  • 3,7-Dihydroxy-5-Cholanicacid
  • 3-alpha,7-alpha-dihydroxy-5-beta-cholan-24-oicaci
  • 3-alpha,7-alpha-dihydroxy-5-beta-cholan-24-oicacid
  • 3-alpha,7-alpha-dihydroxycholanicacid
  • 3-alpha,7-alpha-dihydroxycholansaeure
  • 7-alpha-hydroxylithocholicacid
  • anthropodeoxycholicacid
  • anthropodesoxycholicacid