12-Ketodeoxycholic acid

Common Name

12-Ketodeoxycholic acid Description

12-Ketodeoxycholic acid is a bile acid. Bile acids are steroid acids found predominantly in bile of mammals. The distinction between different bile acids is minute, depends only on presence or absence of hydroxyl groups on positions 3, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic moleclies derived from the catabolism of cholesterol. They modliate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regliation of all the key enzymes involved in cholesterol homeostasis. Bile acids recircliate through the liver, bile ducts, small intestine and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH and, consequently, require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g., membrane disruption) and there are a plethora of mechanisms to limit their accumliation in blood and tissues. (PMID: 11316487 , 16037564 , 12576301 , 11907135 ). Structure

Synonyms

Value Source (3a,5b)-3-Hydroxy-12-oxo-cholan-24-OateHMDB (3a,5b)-3-Hydroxy-12-oxo-cholan-24-Oic acidHMDB (3alpha,5beta)-3-Hydroxy-12-oxo-cholan-24-OateHMDB (3alpha,5beta)-3-Hydroxy-12-oxo-cholan-24-Oic acidHMDB 12-DehydrodeoxycholateHMDB 12-Dehydrodeoxycholic acidHMDB 12-KetodeoxycholateHMDB 12-KetolithocholateHMDB 12-Ketolithocholic acidHMDB 12-oxo-3a-Hydroxy-5b-cholanateHMDB 12-oxo-3a-Hydroxy-5b-cholanic acidHMDB 12-OxolithocholateHMDB 12-Oxolithocholic acidHMDB 3a-Hydroxy-12-oxo-5b-cholan-24-OateHMDB 3a-Hydroxy-12-oxo-5b-cholan-24-Oic acidHMDB 3a-Hydroxy-12-oxo-5b-cholanateHMDB 3a-Hydroxy-12-oxo-5b-cholanic acidHMDB 3a-Hydroxy-12-oxo-5b-cholanoateHMDB 3a-Hydroxy-12-oxo-5b-cholanoic acidHMDB 3-Hydroxy-12-ketocholanoic acidMeSH 12-Ketolithocholic acid, (3beta,5beta)-isomerMeSH 3 alpha-Hydroxy-12-keto-5 beta-cholanoic acidMeSH

Chemical Formlia

C24H38O4 Average Molecliar Weight

390.5561 Monoisotopic Molecliar Weight

390.277009704 IUPAC Name

(4R)-4-[(1S,2S,5R,7R,10R,11S,14R,15R)-5-hydroxy-2,15-dimethyl-16-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid Traditional Name

12-ketolithocholic acid CAS Registry Number

5130-29-0 SMILES

[H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC(=O)[C@]12C)[C@H](C)CCC(O)=O

InChI Identifier

InChI=1S/C24H38O4/c1-14(4-9-22(27)28)18-7-8-19-17-6-5-15-12-16(25)10-11-23(15,2)20(17)13-21(26)24(18,19)3/h14-20,25H,4-13H2,1-3H3,(H,27,28)/t14-,15-,16-,17+,18-,19+,20+,23+,24-/m1/s1

InChI Key

CVNYHSDFZXHMMJ-VPUMZWJWSA-N Chemical Taxonomy Classification

Not classified Ontology Status

Expected but not Quantified Origin

  • Endogenous
  • Food
  • Biofunction

  • Cell signaling
  • Fat solubilization and Waste products
  • Fuel and energy storage
  • Fuel or energy source
  • Membrane integrity/stability
  • Application

  • Nutrients
  • Stabilizers
  • Surfactants and Emlisifiers
  • Cellliar locations

  • Extracellliar
  • Physical Properties State

    Solid Experimental Properties

    Property Value Reference Melting PointNot AvailableNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogPNot AvailableNot Available

    Predicted Properties

    Property Value Source Water Solubility0.013 mg/mLALOGPS logP3.78ALOGPS logP4.35ChemAxon logS-4.5ALOGPS pKa (Strongest Acidic)4.56ChemAxon pKa (Strongest Basic)-1.4ChemAxon Physiological Charge-1ChemAxon Hydrogen Acceptor Count4ChemAxon Hydrogen Donor Count2ChemAxon Polar Surface Area74.6 Å2ChemAxon Rotatable Bond Count4ChemAxon Refractivity108.37 m3·mol-1ChemAxon Polarizability45.52 Å3ChemAxon Number of Rings4ChemAxon Bioavailability1ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Spectrum Type Description Splash Key Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, Positivesplash10-00di-0009000000-8cbf377d4ac0ead7f478View in MoNA Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, Positivesplash10-05i0-0009000000-f445f21e6bb19a3e03e2View in MoNA Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, Positivesplash10-0400-3519000000-e95ed419ca30aa610aadView in MoNA Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, Negativesplash10-000i-0009000000-d2798e61ab8bdbb8b70cView in MoNA Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, Negativesplash10-00dr-1009000000-08abf1a9cb419252bf5aView in MoNA Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, Negativesplash10-0a4l-9006000000-1e75d302e82f8e8c004fView in MoNA

    Biological Properties Cellliar Locations

  • Extracellliar
  • Biofluid Locations

    Not Available Tissue Location

    Not Available Pathways

    Not Available Normal Concentrations Not Available Abnormal Concentrations

    Not Available Associated Disorders and Diseases Disease References

    None Associated OMIM IDs

    None External Links DrugBank ID

    Not Available DrugBank Metabolite ID

    Not Available Phenol Explorer Compound ID

    Not Available Phenol Explorer Metabolite ID

    Not Available FoodDB ID

    FDB021953 KNApSAcK ID

    Not Available Chemspider ID

    2338365 KEGG Compound ID

    Not Available BioCyc ID

    Not Available BiGG ID

    Not Available Wikipedia Link

    Not Available NuGOwiki Link

    HMDB00328 Metagene Link

    HMDB00328 METLIN ID

    5317 PubChem Compound

    3080612 PDB ID

    Not Available ChEBI ID

    803536

    Product: AS1842856

    References Synthesis Reference Suzuki, Yoshinori; Okamura, Akio; Shimomura, Kazuo; Suzuki, Tadayuki. Purification of bile acids. Jpn. Kokai Tokkyo Koho (1985), 6 pp. Material Safety Data Sheet (MSDS) Not Available General References
    1. Reddy B, Engle A, Katsifis S, Simi B, Bartram HP, Perrino P, Mahan C: Biochemical epidemiology of colon cancer: effect of types of dietary fiber on fecal mutagens, acid, and neutral sterols in healthy subjects. Cancer Res. 1989 Aug 15;49(16):4629-35. [PubMed:2545348 ]
    2. Barker GM, Radley S, Bain I, Davis A, Lawson AM, Keighley MR, Neoptolemos JP: Biliary bile acid profiles in patients with familial adenomatous polyposis before and after colectomy. Br J Surg. 1994 Mar;81(3):441-4. [PubMed:8173925 ]
    3. Andersen E, Karlaganis G, Sjovall J: Altered bile acid profiles in duodenal bile and urine in diabetic subjects. Eur J Clin Invest. 1988 Apr;18(2):166-72. [PubMed:3133222 ]
    4. St-Pierre MV, Kullak-Ublick GA, Hagenbuch B, Meier PJ: Transport of bile acids in hepatic and non-hepatic tissues. J Exp Biol. 2001 May;204(Pt 10):1673-86. [PubMed:11316487 ]
    5. Claudel T, Staels B, Kuipers F: The Farnesoid X receptor: a molecular link between bile acid and lipid and glucose metabolism. Arterioscler Thromb Vasc Biol. 2005 Oct;25(10):2020-30. Epub 2005 Jul 21. [PubMed:16037564 ]
    6. Chiang JY: Bile acid regulation of hepatic physiology: III. Bile acids and nuclear receptors. Am J Physiol Gastrointest Liver Physiol. 2003 Mar;284(3):G349-56. [PubMed:12576301 ]
    7. Davis RA, Miyake JH, Hui TY, Spann NJ: Regulation of cholesterol-7alpha-hydroxylase: BAREly missing a SHP. J Lipid Res. 2002 Apr;43(4):533-43. [PubMed:11907135 ]

    Enzymes

    General function:
    Involved in binding
    Specific function:
    Ileal protein which stimulates gastric acid and pepsinogen secretion. Seems to be able to bind to bile salts and bilirubins. Isoform 2 is essential for the survival of colon cancer cells to bile acid-induced apoptosis
    Gene Name:
    FABP6
    Uniprot ID:
    P51161
    Molecular weight:
    14371.2
    References
    1. Kurz M, Brachvogel V, Matter H, Stengelin S, Thuring H, Kramer W: Insights into the bile acid transportation system: the human ileal lipid-binding protein-cholyltaurine complex and its comparison with homologous structures. Proteins. 2003 Feb 1;50(2):312-28. [PubMed:12486725 ]

    Transporters

    General function:
    Involved in transporter activity
    Specific function:
    Mediates the Na(+)-independent transport of organic anions such as 17-beta-glucuronosyl estradiol, taurocholate, triiodothyronine (T3), leukotriene C4, dehydroepiandrosterone sulfate (DHEAS), methotrexate and sulfobromophthalein (BSP)
    Gene Name:
    SLCO1B3
    Uniprot ID:
    Q9NPD5
    Molecular weight:
    77402.2
    General function:
    Involved in transporter activity
    Specific function:
    Mediates the Na(+)-independent transport of organic anions such as pravastatin, taurocholate, methotrexate, dehydroepiandrosterone sulfate, 17-beta-glucuronosyl estradiol, estrone sulfate, prostaglandin E2, thromboxane B2, leukotriene C3, leukotriene E4, thyroxine and triiodothyronine. May play an important role in the clearance of bile acids and organic anions from the liver
    Gene Name:
    SLCO1B1
    Uniprot ID:
    Q9Y6L6
    Molecular weight:
    76448.0
    References
    1. Michalski C, Cui Y, Nies AT, Nuessler AK, Neuhaus P, Zanger UM, Klein K, Eichelbaum M, Keppler D, Konig J: A naturally occurring mutation in the SLC21A6 gene causing impaired membrane localization of the hepatocyte uptake transporter. J Biol Chem. 2002 Nov 8;277(45):43058-63. Epub 2002 Aug 23. [PubMed:12196548 ]
    General function:
    Involved in ATP binding
    Specific function:
    May act as an inducible transporter in the biliary and intestinal excretion of organic anions. Acts as an alternative route for the export of bile acids and glucuronides from cholestatic hepatocytes
    Gene Name:
    ABCC3
    Uniprot ID:
    O15438
    Molecular weight:
    169341.1
    General function:
    Involved in ATP binding
    Specific function:
    Involved in the ATP-dependent secretion of bile salts into the canaliculus of hepatocytes
    Gene Name:
    ABCB11
    Uniprot ID:
    O95342
    Molecular weight:
    146405.8
    General function:
    Involved in bile acid:sodium symporter activity
    Specific function:
    Plays a critical role in the sodium-dependent reabsorption of bile acids from the lumen of the small intestine. Plays a key role in cholesterol metabolism
    Gene Name:
    SLC10A2
    Uniprot ID:
    Q12908
    Molecular weight:
    37697.4
    References
    1. Kramer W, Girbig F, Glombik H, Corsiero D, Stengelin S, Weyland C: Identification of a ligand-binding site in the Na+/bile acid cotransporting protein from rabbit ileum. J Biol Chem. 2001 Sep 21;276(38):36020-7. Epub 2001 Jul 10. [PubMed:11447228 ]
    General function:
    Involved in bile acid:sodium symporter activity
    Specific function:
    The hepatic sodium/bile acid uptake system exhibits broad substrate specificity and transports various non-bile acid organic compounds as well. It is strictly dependent on the extracellular presence of sodium.
    Gene Name:
    SLC10A1
    Uniprot ID:
    Q14973
    Molecular weight:
    38118.64
    General function:
    Involved in transporter activity
    Specific function:
    Mediates the Na(+)-independent transport of organic anions such as sulfobromophthalein (BSP) and conjugated (taurocholate) and unconjugated (cholate) bile acids
    Gene Name:
    SLCO1A2
    Uniprot ID:
    P46721
    Molecular weight:
    74144.1
    General function:
    Involved in transporter activity
    Specific function:
    Mediates the Na(+)-independent transport of organic anions such as the thyroid hormones T3 (triiodo-L-thyronine), T4 (thyroxine) and rT3, and of estrone-3-sulfate and taurocholate
    Gene Name:
    SLCO4A1
    Uniprot ID:
    Q96BD0
    Molecular weight:
    77192.5

    PMID: 18096503