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83-49-8 molecular structure
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(4R)-4-[(1S,2R,5R,7R,8S,10S,11S,14R,15R)-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid

ChemBase ID: 72951
Molecular Formular: C24H40O4
Molecular Mass: 392.572
Monoisotopic Mass: 392.29265976
SMILES and InChIs

SMILES:
C1[C@H](C[C@@H]2[C@](C1)([C@@H]1[C@@H](C[C@@H]2O)[C@H]2[C@](CC1)([C@H](CC2)[C@H](C)CCC(=O)O)C)C)O
Canonical SMILES:
O[C@@H]1CC[C@]2([C@@H](C1)[C@@H](O)C[C@@H]1[C@@H]2CC[C@]2([C@H]1CC[C@@H]2[C@@H](CCC(=O)O)C)C)C
InChI:
InChI=1S/C24H40O4/c1-14(4-7-22(27)28)17-5-6-18-16-13-21(26)20-12-15(25)8-10-24(20,3)19(16)9-11-23(17,18)2/h14-21,25-26H,4-13H2,1-3H3,(H,27,28)/t14-,15-,16+,17-,18+,19+,20+,21+,23-,24-/m1/s1
InChIKey:
DGABKXLVXPYZII-SIBKNCMHSA-N

Cite this record

CBID:72951 http://www.chembase.cn/molecule-72951.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(4R)-4-[(1S,2R,5R,7R,8S,10S,11S,14R,15R)-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid
(4R)-4-[(1S,2R,5R,7R,8S,10S,11S,14R,15R)-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-yl]pentanoic acid
(4R)-4-[(1S,2R,5R,7R,8S,10S,11S,14R,15R)-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0?,?.0??,??]heptadecan-14-yl]pentanoic acid
IUPAC Traditional name
hyodeoxycholic acid
Synonyms
HDCA
Hyodeoxycholic acid
6α-Dihydroxy-5β-cholan-24-oic acid
Hyodeoxycholic acid
3α,6α-Dihydroxy-5β-cholan-24-oic acid
HYODESOXY CHOLIC ACID
3α,6α-Dihydroxy-5 β-cholan-24-oic acid
5 β-Cholan-24-oic acid-3α,6α-diol
(3α,5β,6α)-3,6-Dihydroxycholan-24-oic Acid
3α,6α-Dihydroxy-5β-cholan-24-oate
6α-Hydroxylithocholic Acid
7-Deoxyhyocholic Acid
Hyodeoxycholic Acid
Hyodesoxycholic Acid
Iodeoxycholic Acid
NSC 60672
α-Hyodeoxycholic Acid
3α,6α-二羟基-5β-胆烷酸
猪去氧胆酸
CAS Number
83-49-8
EC Number
201-483-2
MDL Number
MFCD00003681
PubChem SID
162037871
24895601
PubChem CID
5283820
CHEMBL
272621
Chemspider ID
4446908
Wikipedia Title
Hyodeoxycholic_acid

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 4.791043  H Acceptors
H Donor LogD (pH = 5.5) 2.9274719 
LogD (pH = 7.4) 1.1525321  Log P 3.7133055 
Molar Refractivity 109.2738 cm3 Polarizability 43.768806 Å3
Polar Surface Area 77.76 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
DMSO expand Show data source
Ethanol expand Show data source
Methanol expand Show data source
Apperance
White Solid expand Show data source
Melting Point
195-197°C expand Show data source
200 - 201 °C expand Show data source
200-201 °C(lit.) expand Show data source
Density
? g/cm3 expand Show data source
Optical Rotation
[α]20/D +8.4°, c = 2 in ethanol expand Show data source
Storage Condition
-20°C expand Show data source
Refrigerator expand Show data source
Room Temperature (15-30°C) expand Show data source
RTECS
FZ2050000 expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
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German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Purity
≥98% expand Show data source
98% expand Show data source
Salt Data
Free Base expand Show data source
Certificate of Analysis
Download expand Show data source
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Empirical Formula (Hill Notation)
C24H40O4 expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Selleck Chemicals Selleck Chemicals Wikipedia Wikipedia TRC TRC
MP Biomedicals - 02157514 external link
Free Acid
Purity: 98%
MP Biomedicals - 05213756 external link
MP Biomedicals Rare Chemical collection
Selleck Chemicals - S2311 external link
Research Area: Metabolic Disease
Biological Activity:
Hyodeoxycholic(HDCA) acid is a secondary bile acid, one of the metabolic byproducts of intestinal bacteria. In rat intestinal microflora hyodeoxycholic acid is produced by a gram-positive rod—termed HDCA-1—from several isomers of hyocholic acid and muricholic acid. In pigs with a normal gastrointestinal flora the majority of hyodeoxycholic acid found in bile is of secondary nature, but a small amount was also found in germ free pigs, which supports the hypothesis that HDCA may be a primary bile acid in this species. In healthy humans only traces of HDCA have been found in urine, but in patients with cholestatic liver disease or intestinal malabsorption a significant amount has been found excreted. Hyodeoxycholic acid undergoes glucuronidation in human liver and kidneys. [1]
Toronto Research Chemicals - H998100 external link
It is isolated from pig bile. Antitumor agent.

REFERENCES

REFERENCES

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  • • http://en.wikipedia.org/wiki/Hyodeoxycholic_acid
  • • Abadie, C., et al.: Biochem. J., 299, 725 (1994)
  • • Taniguchi, T., et al.: J. Biol. Chem., 269, 10071 (1994)
  • • Davis, R., et al.: J. Lipid Res., 43, 533 (1994)
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PATENTS

PATENTS

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INTERNET

INTERNET

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