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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (2) Show 2 proteins XML

Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2022-03-07 02:49:07 UTC

HMDB ID

HMDB0000951

Secondary Accession Numbers

HMDB00951

Metabolite Identification

Common Name

Taurochenodesoxycholic acid

Description

Taurochenodesoxycholic acid is a bile acid formed in the liver by conjugation of chenodeoxycholate with taurine, usually as the sodium salt. Bile acids are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, depending only on the 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 molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate 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 accumulation in blood and tissues (PMID: 11316487 , 16037564 , 12576301 , 11907135 ). Taurochenodesoxycholic acid has been found to be a microbial metabolite.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652309201916022D          

 39 42  0  0  0  0            999 V2000
 9998.933710001.0346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7957 9999.7851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9358 9997.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9994.6538 9997.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7957 9997.3033    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5083 9998.5503    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2209 9999.7851    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9337 9998.5503    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5078 9999.3714    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.5078 9997.7214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2223 9998.1338    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.2223 9998.9589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9996.0810 9999.3700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.3665 9998.9575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.3665 9998.1324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.0810 9997.7200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7955 9998.1324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.7955 9998.9575    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.220310000.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.505810000.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.934810000.2053    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.9348 9999.3803    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.7194 9999.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.2043 9999.7928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.719610001.2909    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.434010001.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.150010001.2909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.863910001.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.579810001.2909    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10003.293710001.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.009710001.2909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.725710001.7035    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
10005.138310002.4195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.313010002.4195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10005.441710001.2909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.863910002.5288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.004710001.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.434010000.8782    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9999.719410000.4603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  9 12  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 14  1  0  0  0  0
 13 18  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 20  1  0  0  0  0
 11  3  1  6  0  0  0
 20  9  1  0  0  0  0
  9  6  1  6  0  0  0
 12  7  1  1  0  0  0
 15  4  1  6  0  0  0
  9 18  1  0  0  0  0
 18  2  1  1  0  0  0
 17 10  1  0  0  0  0
 17  5  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 26  1  0  0  0  0
 25 37  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 36  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  2  0  0  0  0
 32 35  1  0  0  0  0
 39 25  1  0  0  0  0
 39 38  1  6  0  0  0
 39 21  1  0  0  0  0
 39 24  1  0  0  0  0
 22  8  1  6  0  0  0
 12 22  1  0  0  0  0
 19 21  1  0  0  0  0
 21  1  1  1  0  0  0
M  END

HMDB0000951
     RDKit          3D
Taurochenodesoxycholic acid
 79 82  0  0  0  0  0  0  0  0999 V2000
    2.7209    1.6752   -0.8381 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4520    1.1563    0.5225 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2064   -0.0116    1.0270 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6810    0.1133    1.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4857    0.2465   -0.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0450   -0.0656   -1.1831 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8352    0.7483   -0.0076 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6182    0.8765   -1.1897 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8473   -0.4260   -1.9282 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6871   -1.6096   -0.9201 S   0  0  0  0  0  6  0  0  0  0  0  0
    7.8112   -1.8471    0.2995 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8533   -2.8642   -1.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1796   -1.0539   -0.4298 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0029    1.1553    0.9221 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5176    2.5908    0.8538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6776    2.5278   -0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1759    1.1798    0.2733 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3247    0.6033   -0.4127 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8277   -0.5302    0.4822 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6827   -1.5062    0.6240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4225   -0.8963    1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0476    0.2760    0.2678 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2970   -0.1711   -1.1181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0932   -1.1264    0.0639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7973   -2.4125   -0.7237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8293   -1.6137    1.3207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1586   -2.2299    0.9581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0969   -1.1978    0.3751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.1066   -0.8418    1.2701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2937    0.0365    0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0389   -0.3192   -0.7278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5266    0.9804   -1.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4671    1.6148   -0.4143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9187    1.8944    0.8658 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9983    2.5060   -1.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6775    0.8818   -1.6032 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7053    2.1928   -0.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8442    2.0155    1.2103 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8457   -0.2917    2.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0309   -0.9413    0.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8484    1.0874    1.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1067   -0.6554    1.8529 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2294    1.0166    0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6161    1.3146   -1.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1306    1.5574   -1.9393 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9212   -0.8438   -2.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5099   -0.2093   -2.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1807   -0.0697   -0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120    0.8907    2.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1061    2.9391    1.8468 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2605    3.3216    0.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4031    3.2894    0.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3859    2.6490   -1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4352    1.2733    1.3736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2182    0.2632   -1.4403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9329   -0.0489    1.5013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -2.1639   -0.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0232   -2.2168    1.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3377   -1.6813    1.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6294   -0.4640    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5713   -0.8330   -1.4238 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1619   -0.8587   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3166    0.6308   -1.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7750   -2.6892   -1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5101   -3.2389   -0.0775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1083   -2.2155   -1.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0378   -0.7716    2.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2214   -2.3433    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6163   -2.5715    1.9094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0590   -3.1313    0.3238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5802   -1.5207   -0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2975    0.1227    1.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0594    0.6468    0.9589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9043    0.6696   -0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4464   -0.8812   -1.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1123    0.8602   -2.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3521    1.7434   -1.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1032    2.5220   -0.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3567    2.5093    1.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
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 14 15  1  0
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 17 18  1  0
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 27 28  1  0
 28 29  1  0
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 22 14  1  0
 31 24  1  0
 22 17  1  0
 33 18  1  0
  1 35  1  0
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  2 38  1  1
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  7 43  1  0
  8 44  1  0
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  9 46  1  0
  9 47  1  0
 13 48  1  0
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 18 55  1  6
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 26 67  1  0
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 27 70  1  0
 28 71  1  6
 29 72  1  0
 30 73  1  0
 30 74  1  0
 31 75  1  6
 32 76  1  0
 32 77  1  0
 33 78  1  6
 34 79  1  0
M  END


  Mrv1652309201916022D          

 39 42  0  0  0  0            999 V2000
 9998.933710001.0346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7957 9999.7851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9358 9997.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9994.6538 9997.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7957 9997.3033    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5083 9998.5503    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2209 9999.7851    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9337 9998.5503    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5078 9999.3714    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.5078 9997.7214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2223 9998.1338    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.2223 9998.9589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9996.0810 9999.3700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.3665 9998.9575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.3665 9998.1324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.0810 9997.7200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7955 9998.1324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.7955 9998.9575    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.220310000.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.505810000.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.934810000.2053    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.9348 9999.3803    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.7194 9999.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.2043 9999.7928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.719610001.2909    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.434010001.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.150010001.2909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.863910001.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.579810001.2909    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10003.293710001.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.009710001.2909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.725710001.7035    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
10005.138310002.4195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.313010002.4195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10005.441710001.2909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.863910002.5288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.004710001.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.434010000.8782    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9999.719410000.4603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  9 12  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 14  1  0  0  0  0
 13 18  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 20  1  0  0  0  0
 11  3  1  6  0  0  0
 20  9  1  0  0  0  0
  9  6  1  6  0  0  0
 12  7  1  1  0  0  0
 15  4  1  6  0  0  0
  9 18  1  0  0  0  0
 18  2  1  1  0  0  0
 17 10  1  0  0  0  0
 17  5  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 26  1  0  0  0  0
 25 37  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 36  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  2  0  0  0  0
 32 35  1  0  0  0  0
 39 25  1  0  0  0  0
 39 38  1  6  0  0  0
 39 21  1  0  0  0  0
 39 24  1  0  0  0  0
 22  8  1  6  0  0  0
 12 22  1  0  0  0  0
 19 21  1  0  0  0  0
 21  1  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0000951

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C26H45NO6S/c1-16(4-7-23(30)27-12-13-34(31,32)33)19-5-6-20-24-21(9-11-26(19,20)3)25(2)10-8-18(28)14-17(25)15-22(24)29/h16-22,24,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33)/t16-,17+,18-,19-,20+,21+,22-,24+,25+,26-/m1/s1

> <INCHI_KEY>
BHTRKEVKTKCXOH-BJLOMENOSA-N

> <FORMULA>
C26H45NO6S

> <MOLECULAR_WEIGHT>
499.704

> <EXACT_MASS>
499.296758867

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
56.655747046215936

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R)-5,9-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanamido]ethane-1-sulfonic acid

> <ALOGPS_LOGP>
1.38

> <JCHEM_LOGP>
1.0968020386753499

> <ALOGPS_LOGS>
-4.82

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.47697536728532

> <JCHEM_PKA_STRONGEST_ACIDIC>
-0.8004715356003853

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3160397423134701

> <JCHEM_POLAR_SURFACE_AREA>
123.92999999999999

> <JCHEM_REFRACTIVITY>
130.67899999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.48e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R)-5,9-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanamido]ethanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000951
     RDKit          3D
Taurochenodesoxycholic acid
 79 82  0  0  0  0  0  0  0  0999 V2000
    2.7209    1.6752   -0.8381 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4520    1.1563    0.5225 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2064   -0.0116    1.0270 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6810    0.1133    1.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4857    0.2465   -0.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0450   -0.0656   -1.1831 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8352    0.7483   -0.0076 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6182    0.8765   -1.1897 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8473   -0.4260   -1.9282 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6871   -1.6096   -0.9201 S   0  0  0  0  0  6  0  0  0  0  0  0
    7.8112   -1.8471    0.2995 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8533   -2.8642   -1.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1796   -1.0539   -0.4298 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0029    1.1553    0.9221 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5176    2.5908    0.8538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6776    2.5278   -0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1759    1.1798    0.2733 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3247    0.6033   -0.4127 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8277   -0.5302    0.4822 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6827   -1.5062    0.6240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4225   -0.8963    1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0476    0.2760    0.2678 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2970   -0.1711   -1.1181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0932   -1.1264    0.0639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7973   -2.4125   -0.7237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8293   -1.6137    1.3207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1586   -2.2299    0.9581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0969   -1.1978    0.3751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.1066   -0.8418    1.2701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2937    0.0365    0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0389   -0.3192   -0.7278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5266    0.9804   -1.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4671    1.6148   -0.4143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9187    1.8944    0.8658 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9983    2.5060   -1.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6775    0.8818   -1.6032 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7053    2.1928   -0.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8442    2.0155    1.2103 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8457   -0.2917    2.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0309   -0.9413    0.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8484    1.0874    1.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1067   -0.6554    1.8529 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2294    1.0166    0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6161    1.3146   -1.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1306    1.5574   -1.9393 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9212   -0.8438   -2.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5099   -0.2093   -2.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1807   -0.0697   -0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120    0.8907    2.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1061    2.9391    1.8468 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2605    3.3216    0.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4031    3.2894    0.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3859    2.6490   -1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4352    1.2733    1.3736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2182    0.2632   -1.4403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9329   -0.0489    1.5013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -2.1639   -0.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0232   -2.2168    1.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3377   -1.6813    1.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6294   -0.4640    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5713   -0.8330   -1.4238 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1619   -0.8587   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3166    0.6308   -1.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7750   -2.6892   -1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5101   -3.2389   -0.0775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1083   -2.2155   -1.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0378   -0.7716    2.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2214   -2.3433    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6163   -2.5715    1.9094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0590   -3.1313    0.3238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5802   -1.5207   -0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2975    0.1227    1.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0594    0.6468    0.9589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9043    0.6696   -0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4464   -0.8812   -1.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1123    0.8602   -2.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3521    1.7434   -1.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1032    2.5220   -0.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3567    2.5093    1.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  2  0
 10 13  1  0
  2 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 19 24  1  0
 24 25  1  6
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 22 14  1  0
 31 24  1  0
 22 17  1  0
 33 18  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  1
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 13 48  1  0
 14 49  1  1
 15 50  1  0
 15 51  1  0
 16 52  1  0
 16 53  1  0
 17 54  1  1
 18 55  1  6
 19 56  1  1
 20 57  1  0
 20 58  1  0
 21 59  1  0
 21 60  1  0
 23 61  1  0
 23 62  1  0
 23 63  1  0
 25 64  1  0
 25 65  1  0
 25 66  1  0
 26 67  1  0
 26 68  1  0
 27 69  1  0
 27 70  1  0
 28 71  1  6
 29 72  1  0
 30 73  1  0
 30 74  1  0
 31 75  1  6
 32 76  1  0
 32 77  1  0
 33 78  1  6
 34 79  1  0
M  END

HEADER    PROTEIN                                 20-SEP-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-SEP-19         0                                  
HETATM    1  C   UNK     0    8664.6768668.598   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8660.6858666.266   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0    8664.6808662.405   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0    8656.6878662.405   0.000  0.00  0.00           O+0
HETATM    5  H   UNK     0    8660.6858661.633   0.000  0.00  0.00           H+0
HETATM    6  H   UNK     0    8662.0158663.961   0.000  0.00  0.00           H+0
HETATM    7  H   UNK     0    8663.3468666.266   0.000  0.00  0.00           H+0
HETATM    8  H   UNK     0    8664.6768663.961   0.000  0.00  0.00           H+0
HETATM    9  C   UNK     0    8662.0158665.493   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8662.0158662.413   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8663.3488663.183   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8663.3488664.723   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8659.3518665.491   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8658.0178664.721   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8658.0178663.180   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8659.3518662.411   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8660.6858663.180   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8660.6858664.721   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8663.3458667.820   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8662.0118667.050   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8664.6788667.050   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8664.6788665.510   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    8666.1438665.034   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0    8667.0488666.280   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    8666.1438669.076   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0    8667.4778669.847   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0    8668.8138669.076   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0    8670.1468669.847   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0    8671.4828669.076   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0    8672.8158669.847   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0    8674.1518669.076   0.000  0.00  0.00           C+0
HETATM   32  S   UNK     0    8675.4888669.847   0.000  0.00  0.00           S+0
HETATM   33  O   UNK     0    8676.2588671.183   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0    8674.7188671.183   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0    8676.8258669.076   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0    8670.1468671.387   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0    8664.8098669.847   0.000  0.00  0.00           C+0
HETATM   38  H   UNK     0    8667.4778668.306   0.000  0.00  0.00           H+0
HETATM   39  C   UNK     0    8666.1438667.526   0.000  0.00  0.00           C+0
CONECT    1   21                                                            
CONECT    2   18                                                            
CONECT    3   11                                                            
CONECT    4   15                                                            
CONECT    5   17                                                            
CONECT    6    9                                                            
CONECT    7   12                                                            
CONECT    8   22                                                            
CONECT    9   12   20    6   18                                             
CONECT   10   11   17                                                       
CONECT   11   10   12    3                                                  
CONECT   12    9   11    7   22                                             
CONECT   13   14   18                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16    4                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   10    5                                             
CONECT   18   13   17    9    2                                             
CONECT   19   20   21                                                       
CONECT   20   19    9                                                       
CONECT   21   22   39   19    1                                             
CONECT   22   21   23    8   12                                             
CONECT   23   22   24                                                       
CONECT   24   23   39                                                       
CONECT   25   26   37   39                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   36                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   35                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   32                                                            
CONECT   36   28                                                            
CONECT   37   25                                                            
CONECT   38   39                                                            
CONECT   39   25   38   21   24                                             
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

COMPND    HMDB0000951
HETATM    1  C1  UNL     1       2.721   1.675  -0.838  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.452   1.156   0.522  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.206  -0.012   1.027  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.681   0.113   1.142  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.486   0.246  -0.060  1.00  0.00           C  
HETATM    6  O1  UNL     1       5.045  -0.066  -1.183  1.00  0.00           O  
HETATM    7  N1  UNL     1       6.835   0.748  -0.008  1.00  0.00           N  
HETATM    8  C6  UNL     1       7.618   0.877  -1.190  1.00  0.00           C  
HETATM    9  C7  UNL     1       7.847  -0.426  -1.928  1.00  0.00           C  
HETATM   10  S1  UNL     1       8.687  -1.610  -0.920  1.00  0.00           S  
HETATM   11  O2  UNL     1       7.811  -1.847   0.299  1.00  0.00           O  
HETATM   12  O3  UNL     1       8.853  -2.864  -1.712  1.00  0.00           O  
HETATM   13  O4  UNL     1      10.180  -1.054  -0.430  1.00  0.00           O  
HETATM   14  C8  UNL     1       1.003   1.155   0.922  1.00  0.00           C  
HETATM   15  C9  UNL     1       0.518   2.591   0.854  1.00  0.00           C  
HETATM   16  C10 UNL     1      -0.678   2.528  -0.123  1.00  0.00           C  
HETATM   17  C11 UNL     1      -1.176   1.180   0.273  1.00  0.00           C  
HETATM   18  C12 UNL     1      -2.325   0.603  -0.413  1.00  0.00           C  
HETATM   19  C13 UNL     1      -2.828  -0.530   0.482  1.00  0.00           C  
HETATM   20  C14 UNL     1      -1.683  -1.506   0.624  1.00  0.00           C  
HETATM   21  C15 UNL     1      -0.423  -0.896   1.155  1.00  0.00           C  
HETATM   22  C16 UNL     1       0.048   0.276   0.268  1.00  0.00           C  
HETATM   23  C17 UNL     1       0.297  -0.171  -1.118  1.00  0.00           C  
HETATM   24  C18 UNL     1      -4.093  -1.126   0.064  1.00  0.00           C  
HETATM   25  C19 UNL     1      -3.797  -2.413  -0.724  1.00  0.00           C  
HETATM   26  C20 UNL     1      -4.829  -1.614   1.321  1.00  0.00           C  
HETATM   27  C21 UNL     1      -6.159  -2.230   0.958  1.00  0.00           C  
HETATM   28  C22 UNL     1      -7.097  -1.198   0.375  1.00  0.00           C  
HETATM   29  O5  UNL     1      -8.107  -0.842   1.270  1.00  0.00           O  
HETATM   30  C23 UNL     1      -6.294   0.037   0.088  1.00  0.00           C  
HETATM   31  C24 UNL     1      -5.039  -0.319  -0.728  1.00  0.00           C  
HETATM   32  C25 UNL     1      -4.527   0.980  -1.259  1.00  0.00           C  
HETATM   33  C26 UNL     1      -3.467   1.615  -0.414  1.00  0.00           C  
HETATM   34  O6  UNL     1      -3.919   1.894   0.866  1.00  0.00           O  
HETATM   35  H1  UNL     1       1.998   2.506  -1.115  1.00  0.00           H  
HETATM   36  H2  UNL     1       2.677   0.882  -1.603  1.00  0.00           H  
HETATM   37  H3  UNL     1       3.705   2.193  -0.961  1.00  0.00           H  
HETATM   38  H4  UNL     1       2.844   2.016   1.210  1.00  0.00           H  
HETATM   39  H5  UNL     1       2.846  -0.292   2.057  1.00  0.00           H  
HETATM   40  H6  UNL     1       3.031  -0.941   0.414  1.00  0.00           H  
HETATM   41  H7  UNL     1       4.848   1.087   1.727  1.00  0.00           H  
HETATM   42  H8  UNL     1       5.107  -0.655   1.853  1.00  0.00           H  
HETATM   43  H9  UNL     1       7.229   1.017   0.913  1.00  0.00           H  
HETATM   44  H10 UNL     1       8.616   1.315  -1.009  1.00  0.00           H  
HETATM   45  H11 UNL     1       7.131   1.557  -1.939  1.00  0.00           H  
HETATM   46  H12 UNL     1       6.921  -0.844  -2.319  1.00  0.00           H  
HETATM   47  H13 UNL     1       8.510  -0.209  -2.793  1.00  0.00           H  
HETATM   48  H14 UNL     1      10.181  -0.070  -0.352  1.00  0.00           H  
HETATM   49  H15 UNL     1       1.012   0.891   2.026  1.00  0.00           H  
HETATM   50  H16 UNL     1       0.106   2.939   1.847  1.00  0.00           H  
HETATM   51  H17 UNL     1       1.260   3.322   0.567  1.00  0.00           H  
HETATM   52  H18 UNL     1      -1.403   3.289   0.206  1.00  0.00           H  
HETATM   53  H19 UNL     1      -0.386   2.649  -1.158  1.00  0.00           H  
HETATM   54  H20 UNL     1      -1.435   1.273   1.374  1.00  0.00           H  
HETATM   55  H21 UNL     1      -2.218   0.263  -1.440  1.00  0.00           H  
HETATM   56  H22 UNL     1      -2.933  -0.049   1.501  1.00  0.00           H  
HETATM   57  H23 UNL     1      -1.551  -2.164  -0.253  1.00  0.00           H  
HETATM   58  H24 UNL     1      -2.023  -2.217   1.439  1.00  0.00           H  
HETATM   59  H25 UNL     1       0.338  -1.681   1.209  1.00  0.00           H  
HETATM   60  H26 UNL     1      -0.629  -0.464   2.139  1.00  0.00           H  
HETATM   61  H27 UNL     1      -0.571  -0.833  -1.424  1.00  0.00           H  
HETATM   62  H28 UNL     1       1.162  -0.859  -1.233  1.00  0.00           H  
HETATM   63  H29 UNL     1       0.317   0.631  -1.876  1.00  0.00           H  
HETATM   64  H30 UNL     1      -4.775  -2.689  -1.198  1.00  0.00           H  
HETATM   65  H31 UNL     1      -3.510  -3.239  -0.077  1.00  0.00           H  
HETATM   66  H32 UNL     1      -3.108  -2.216  -1.568  1.00  0.00           H  
HETATM   67  H33 UNL     1      -5.038  -0.772   2.012  1.00  0.00           H  
HETATM   68  H34 UNL     1      -4.221  -2.343   1.868  1.00  0.00           H  
HETATM   69  H35 UNL     1      -6.616  -2.571   1.909  1.00  0.00           H  
HETATM   70  H36 UNL     1      -6.059  -3.131   0.324  1.00  0.00           H  
HETATM   71  H37 UNL     1      -7.580  -1.521  -0.553  1.00  0.00           H  
HETATM   72  H38 UNL     1      -8.297   0.123   1.257  1.00  0.00           H  
HETATM   73  H39 UNL     1      -6.059   0.647   0.959  1.00  0.00           H  
HETATM   74  H40 UNL     1      -6.904   0.670  -0.606  1.00  0.00           H  
HETATM   75  H41 UNL     1      -5.446  -0.881  -1.611  1.00  0.00           H  
HETATM   76  H42 UNL     1      -4.112   0.860  -2.288  1.00  0.00           H  
HETATM   77  H43 UNL     1      -5.352   1.743  -1.362  1.00  0.00           H  
HETATM   78  H44 UNL     1      -3.103   2.522  -0.895  1.00  0.00           H  
HETATM   79  H45 UNL     1      -3.357   2.509   1.360  1.00  0.00           H  
CONECT    1    2   35   36   37
CONECT    2    3   14   38
CONECT    3    4   39   40
CONECT    4    5   41   42
CONECT    5    6    6    7
CONECT    7    8   43
CONECT    8    9   44   45
CONECT    9   10   46   47
CONECT   10   11   11   12   12
CONECT   10   13
CONECT   13   48
CONECT   14   15   22   49
CONECT   15   16   50   51
CONECT   16   17   52   53
CONECT   17   18   22   54
CONECT   18   19   33   55
CONECT   19   20   24   56
CONECT   20   21   57   58
CONECT   21   22   59   60
CONECT   22   23
CONECT   23   61   62   63
CONECT   24   25   26   31
CONECT   25   64   65   66
CONECT   26   27   67   68
CONECT   27   28   69   70
CONECT   28   29   30   71
CONECT   29   72
CONECT   30   31   73   74
CONECT   31   32   75
CONECT   32   33   76   77
CONECT   33   34   78
CONECT   34   79
END

HMDB0000951
     RDKit          3D
Taurochenodesoxycholic acid
 79 82  0  0  0  0  0  0  0  0999 V2000
    2.7209    1.6752   -0.8381 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4520    1.1563    0.5225 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2064   -0.0116    1.0270 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6810    0.1133    1.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4857    0.2465   -0.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0450   -0.0656   -1.1831 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8352    0.7483   -0.0076 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6182    0.8765   -1.1897 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8473   -0.4260   -1.9282 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6871   -1.6096   -0.9201 S   0  0  0  0  0  6  0  0  0  0  0  0
    7.8112   -1.8471    0.2995 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8533   -2.8642   -1.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1796   -1.0539   -0.4298 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0029    1.1553    0.9221 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5176    2.5908    0.8538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6776    2.5278   -0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1759    1.1798    0.2733 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3247    0.6033   -0.4127 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8277   -0.5302    0.4822 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6827   -1.5062    0.6240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4225   -0.8963    1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0476    0.2760    0.2678 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2970   -0.1711   -1.1181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0932   -1.1264    0.0639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7973   -2.4125   -0.7237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8293   -1.6137    1.3207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1586   -2.2299    0.9581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0969   -1.1978    0.3751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.1066   -0.8418    1.2701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2937    0.0365    0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0389   -0.3192   -0.7278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5266    0.9804   -1.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4671    1.6148   -0.4143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9187    1.8944    0.8658 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9983    2.5060   -1.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6775    0.8818   -1.6032 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7053    2.1928   -0.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8442    2.0155    1.2103 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8457   -0.2917    2.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0309   -0.9413    0.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8484    1.0874    1.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1067   -0.6554    1.8529 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2294    1.0166    0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6161    1.3146   -1.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1306    1.5574   -1.9393 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9212   -0.8438   -2.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5099   -0.2093   -2.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1807   -0.0697   -0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120    0.8907    2.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1061    2.9391    1.8468 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2605    3.3216    0.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4031    3.2894    0.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3859    2.6490   -1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4352    1.2733    1.3736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2182    0.2632   -1.4403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9329   -0.0489    1.5013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -2.1639   -0.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0232   -2.2168    1.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3377   -1.6813    1.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6294   -0.4640    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5713   -0.8330   -1.4238 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1619   -0.8587   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3166    0.6308   -1.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7750   -2.6892   -1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5101   -3.2389   -0.0775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1083   -2.2155   -1.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0378   -0.7716    2.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2214   -2.3433    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6163   -2.5715    1.9094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0590   -3.1313    0.3238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5802   -1.5207   -0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2975    0.1227    1.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0594    0.6468    0.9589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9043    0.6696   -0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4464   -0.8812   -1.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1123    0.8602   -2.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3521    1.7434   -1.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1032    2.5220   -0.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3567    2.5093    1.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  2  0
 10 13  1  0
  2 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 19 24  1  0
 24 25  1  6
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 22 14  1  0
 31 24  1  0
 22 17  1  0
 33 18  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  1
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 13 48  1  0
 14 49  1  1
 15 50  1  0
 15 51  1  0
 16 52  1  0
 16 53  1  0
 17 54  1  1
 18 55  1  6
 19 56  1  1
 20 57  1  0
 20 58  1  0
 21 59  1  0
 21 60  1  0
 23 61  1  0
 23 62  1  0
 23 63  1  0
 25 64  1  0
 25 65  1  0
 25 66  1  0
 26 67  1  0
 26 68  1  0
 27 69  1  0
 27 70  1  0
 28 71  1  6
 29 72  1  0
 30 73  1  0
 30 74  1  0
 31 75  1  6
 32 76  1  0
 32 77  1  0
 33 78  1  6
 34 79  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Chenodeoxycholoyltaurine	ChEBI
Taurine chenodeoxycholate	ChEBI
Taurochenodeoxycholate	ChEBI
Taurochenodeoxycholic acid	Kegg
Taurine chenodeoxycholic acid	Generator
Taurochenodesoxycholate	Generator
12-Deoxycholyltaurine	HMDB
12-Desoxycholyltaurine	HMDB
3a,7a-Dihydroxy-N-(2-sulfoethyl)-5b-cholan-24-amide	HMDB
Chenodeoxycholyltaurine	HMDB
Chenyltaurine	HMDB
N-(3a,7a-Dihydroxy-5b-cholan-24-oyl)-taurine	HMDB
Acid, taurochenodeoxycholic	HMDB
Chenodeoxycholate, taurine	HMDB

Chemical Formula

C₂₆H₄₅NO₆S

Average Molecular Weight

499.704

Monoisotopic Molecular Weight

499.296758867

IUPAC Name

2-[(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R)-5,9-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanamido]ethane-1-sulfonic acid

Traditional Name

2-[(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R)-5,9-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanamido]ethanesulfonic acid

CAS Registry Number

516-35-8

SMILES

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

InChI Identifier

InChI=1S/C26H45NO6S/c1-16(4-7-23(30)27-12-13-34(31,32)33)19-5-6-20-24-21(9-11-26(19,20)3)25(2)10-8-18(28)14-17(25)15-22(24)29/h16-22,24,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33)/t16-,17+,18-,19-,20+,21+,22-,24+,25+,26-/m1/s1

InChI Key

BHTRKEVKTKCXOH-BJLOMENOSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as taurinated bile acids and derivatives. These are bile acid derivatives containing a taurine conjugated to the bile acid moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Taurinated bile acids and derivatives

Alternative Parents

Substituents

Taurinated bile acid
Dihydroxy bile acid, alcohol, or derivatives
Hydroxy bile acid, alcohol, or derivatives
3-hydroxysteroid
Hydroxysteroid
3-alpha-hydroxysteroid
7-hydroxysteroid
Fatty acyl
Fatty amide
N-acyl-amine
Alkanesulfonic acid
Cyclic alcohol
Organic sulfonic acid or derivatives
Organosulfonic acid or derivatives
Organosulfonic acid
Sulfonyl
Secondary alcohol
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid derivative
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Alcohol
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

bile acid taurine conjugate (CHEBI:16525 )
C26 bile acids, alcohols, and derivatives (C05465 )
Taurine conjugates (C05465 )
Taurine conjugates (LMST05040005 )

Ontology

Physiological effect

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 27163928)
Bile (PMID: 659989)

Organ

Excreta

Biofluid or Excreta

Urine (PMID: 3944741)
Feces (PMID: 22664055)

Cellular substructure

Tissue

Nervous tissue

Hepatic tissue (HMDB: HMDB0000951)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0000951)

Source

Exogenous

Exogenous (HMDB: HMDB0000951)

Food

Food (HMDB: HMDB0000951)

Animal origin

Poultry

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Endogenous

Endogenous (HMDB: HMDB0000951)

Microbe

Microbe (HMDB: HMDB0000951)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0000951)

Biochemical pathway

Disease pathway

Congenital Bile Acid Synthesis Defect Type II (HMDB: HMDB0000951)
27-Hydroxylase Deficiency (PathBank: SMP0120652)
Cerebrotendinous Xanthomatosis (CTX) (PathBank: SMP0120683)
Familial Hypercholanemia (FHCA) (PathBank: SMP0120697)
Zellweger Syndrome (PathBank: SMP0120715)
Congenital Bile Acid Synthesis Defect Type II (PathBank: SMP0120687)
Congenital Bile Acid Synthesis Defect Type III (PathBank: SMP0120688)

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0000951)
Bile Acid Biosynthesis (PathBank: SMP0087329)

Lipid metabolism pathway (HMDB: HMDB0000951)

Cellular process

Cell signaling (HMDB: HMDB0000951)

Biochemical process

Lipid transport (HMDB: HMDB0000951)

Role

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct Type	Data Source	CCS Value (Å²)	Reference
[M-H]-	Not Available	205.394	http://allccs.zhulab.cn/database/detail?ID=AllCCS00000231

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0075 g/L	ALOGPS
logP	1.38	ALOGPS
logP	1.1	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	-0.8	ChemAxon
pKa (Strongest Basic)	-0.32	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	123.93 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	130.68 m³·mol⁻¹	ChemAxon
Polarizability	56.66 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	218.698	32859911
AllCCS	[M-H]-	209.892	32859911
DeepCCS	[M-2H]-	253.427	30932474
DeepCCS	[M+Na]+	227.443	30932474
AllCCS	[M+H]+	218.7	32859911
AllCCS	[M+H-H2O]+	217.3	32859911
AllCCS	[M+NH4]+	219.9	32859911
AllCCS	[M+Na]+	220.3	32859911
AllCCS	[M-H]-	209.9	32859911
AllCCS	[M+Na-2H]-	212.4	32859911
AllCCS	[M+HCOO]-	215.3	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	7.11 minutes	32390414
Predicted by Siyang on May 30, 2022	13.5293 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	3.97 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	119.2 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2925.9 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	165.4 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	211.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	167.9 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	505.8 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	522.5 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	569.6 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	438.3 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1050.7 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	509.0 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1577.3 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	329.2 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	407.6 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	280.0 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	221.5 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	68.0 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Taurochenodesoxycholic acid	[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(=O)NCCS(O)(=O)=O	4944.0	Standard polar	33892256
Taurochenodesoxycholic acid	[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(=O)NCCS(O)(=O)=O	4091.6	Standard non polar	33892256
Taurochenodesoxycholic acid	[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(=O)NCCS(O)(=O)=O	4583.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Taurochenodesoxycholic acid,1TMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C	4160.5	Semi standard non polar	33892256
Taurochenodesoxycholic acid,1TMS,isomer #2	C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O	4274.3	Semi standard non polar	33892256
Taurochenodesoxycholic acid,1TMS,isomer #3	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O	4333.3	Semi standard non polar	33892256
Taurochenodesoxycholic acid,1TMS,isomer #4	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O	4263.8	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4115.9	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TMS,isomer #2	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C	4193.1	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TMS,isomer #3	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C	4085.7	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TMS,isomer #4	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O	4329.0	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TMS,isomer #5	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O	4246.2	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TMS,isomer #6	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O	4329.4	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4162.4	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4441.4	Standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4880.2	Standard polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #2	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4045.1	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #2	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4510.2	Standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #2	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4945.1	Standard polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #3	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C	4142.7	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #3	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C	4519.4	Standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #3	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C	4852.8	Standard polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #4	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O	4279.2	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #4	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O	4507.0	Standard non polar	33892256
Taurochenodesoxycholic acid,3TMS,isomer #4	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O	4830.4	Standard polar	33892256
Taurochenodesoxycholic acid,4TMS,isomer #1	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4130.5	Semi standard non polar	33892256
Taurochenodesoxycholic acid,4TMS,isomer #1	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4653.8	Standard non polar	33892256
Taurochenodesoxycholic acid,4TMS,isomer #1	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C	4702.8	Standard polar	33892256
Taurochenodesoxycholic acid,1TBDMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4355.7	Semi standard non polar	33892256
Taurochenodesoxycholic acid,1TBDMS,isomer #2	C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O	4473.3	Semi standard non polar	33892256
Taurochenodesoxycholic acid,1TBDMS,isomer #3	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O	4519.7	Semi standard non polar	33892256
Taurochenodesoxycholic acid,1TBDMS,isomer #4	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O	4520.9	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TBDMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4506.3	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TBDMS,isomer #2	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4578.1	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TBDMS,isomer #3	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4544.2	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TBDMS,isomer #4	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O	4738.6	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TBDMS,isomer #5	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O	4695.3	Semi standard non polar	33892256
Taurochenodesoxycholic acid,2TBDMS,isomer #6	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O	4779.1	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4745.4	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	5223.1	Standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #1	C[C@H](CCC(=O)NCCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4964.3	Standard polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #2	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4705.6	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #2	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	5232.2	Standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #2	C[C@H](CCC(=O)N(CCS(=O)(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	5033.0	Standard polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #3	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4781.2	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #3	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	5301.6	Standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #3	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C	4952.0	Standard polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #4	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O	4925.9	Semi standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #4	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O	5282.2	Standard non polar	33892256
Taurochenodesoxycholic acid,3TBDMS,isomer #4	C[C@H](CCC(=O)N(CCS(=O)(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O	4925.1	Standard polar	33892256

Spectra

Biological Properties

Cellular Locations

Extracellular

Biospecimen Locations

Bile
Blood
Feces
Urine

Tissue Locations

Placenta

Pathways

Name	SMPDB/PathBank	KEGG
Primary bile acid biosynthesis	Not Available
Congenital Bile Acid Synthesis Defect Type II		Not Available
Congenital Bile Acid Synthesis Defect Type III		Not Available
Familial Hypercholanemia (FHCA)		Not Available
Zellweger Syndrome		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Bile	Detected and Quantified	>0.01 uM	Adult (>18 years old)	Both	Normal	659989	details
Blood	Detected and Quantified	0.30 +/- 0.08 uM	Adult (>18 years old)	Both	Normal	Geigy Scientific ...	details
Blood	Detected and Quantified	0.3(0.1-0.3) uM	Infant (0-1 year old)	Both	Normal	27163928	details
Blood	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details
Feces	Detected and Quantified	6.03 +/- 5.00 nmol/g dry feces	Not Specified	Not Specified	Normal	22664055	details
Feces	Detected but not Quantified	Not Quantified	Children (6 - 18 years old)	Not Specified	Normal	27609529	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	27543620	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	29808030	details
Urine	Detected and Quantified	0.00065 +/- 0.0019 umol/mmol creatinine	Children (1-13 years old)	Both	Normal	3944741	details
Urine	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	0.4(0.3-1.2) uM	Infant (0-1 year old)	Both	Severe acute malnutrition	27163928	details
Feces	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Recurrent Clostridium difficile infection	24284963	details
Feces	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Recurrent Clostridium difficile infection	24284963	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Clostridium difficile infection	24284963	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal Cancer	27275383	details
Feces	Detected but not Quantified	Not Quantified	Children (6 - 18 years old)	Not Specified	Crohns disease	27609529	details
Feces	Detected but not Quantified	Not Quantified	Children (6 - 18 years old)	Not Specified	Ulcerative colitis	27609529	details
Feces	Detected but not Quantified	Not Quantified	Children (6 - 18 years old)	Not Specified	Unclassified IBD	27609529	details
Urine	Detected and Quantified	0.013 +/- 0.021 umol/mmol creatinine	Adult (>18 years old)	Both	Biliary atresia	3944741	details

Associated Disorders and Diseases

Disease References

Colorectal cancer
Brown DG, Rao S, Weir TL, O'Malia J, Bazan M, Brown RJ, Ryan EP: Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer Metab. 2016 Jun 6;4:11. doi: 10.1186/s40170-016-0151-y. eCollection 2016. [PubMed:27275383 ]
Crohn's disease
Kolho KL, Pessia A, Jaakkola T, de Vos WM, Velagapudi V: Faecal and Serum Metabolomics in Paediatric Inflammatory Bowel Disease. J Crohns Colitis. 2017 Mar 1;11(3):321-334. doi: 10.1093/ecco-jcc/jjw158. [PubMed:27609529 ]
Ulcerative colitis
Kolho KL, Pessia A, Jaakkola T, de Vos WM, Velagapudi V: Faecal and Serum Metabolomics in Paediatric Inflammatory Bowel Disease. J Crohns Colitis. 2017 Mar 1;11(3):321-334. doi: 10.1093/ecco-jcc/jjw158. [PubMed:27609529 ]
Biliary atresia
Nittono H, Obinata K, Nakatsu N, Watanabe T, Niijima S, Sasaki H, Arisaka O, Kato H, Yabuta K, Miyano T: Sulfated and nonsulfated bile acids in urine of patients with biliary atresia: analysis of bile acids by high-performance liquid chromatography. J Pediatr Gastroenterol Nutr. 1986 Jan;5(1):23-9. [PubMed:3944741 ]

Associated OMIM IDs

114500 (Colorectal cancer)
266600 (Crohn's disease)
210500 (Biliary atresia)

External Links

DrugBank ID

DB08833

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022335

KNApSAcK ID

Not Available

Chemspider ID

343282

KEGG Compound ID

C05465

BioCyc ID

CHENODEOXYCHOLOYLTAURINE

BiGG ID

45864

Wikipedia Link

Not Available

METLIN ID

5897

PubChem Compound

387316

PDB ID

Not Available

ChEBI ID

16525

Food Biomarker Ontology

Not Available

VMH ID

TDCHOLA

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Karbach Ia I; Rybak P G Synthesis of conjugated bile acids. Ukrainskii biokhimicheskii zhurnal (1979), 51(1), 76-9.

Material Safety Data Sheet (MSDS)

Download (PDF)

General References

Bloch CA, Watkins JB: Determination of conjugated bile acids in human bile and duodenal fluid by reverse-phase high-performance liquid chromatography. J Lipid Res. 1978 May;19(4):510-3. [PubMed:659989 ]
Makino I, Shinozaki K, Nakagawa S, Mashimo K: Measurement of sulfated and nonsulfated bile acids in human serum and urine. J Lipid Res. 1974 Mar;15(2):132-8. [PubMed:4832755 ]
Pouwels MJ, Tack CJ, Span PN, Olthaar AJ, Sweep CG, Huvers FC, Lutterman JA, Hermus AR: Role of hexosamines in insulin resistance and nutrient sensing in human adipose and muscle tissue. J Clin Endocrinol Metab. 2004 Oct;89(10):5132-7. [PubMed:15472217 ]
Ijare OB, Somashekar BS, Jadegoud Y, Nagana Gowda GA: 1H and 13C NMR characterization and stereochemical assignments of bile acids in aqueous media. Lipids. 2005 Oct;40(10):1031-41. [PubMed:16382575 ]
Schwenk M, Hofmann AF, Carlson GL, Carter JA, Coulston F, Greim H: Bile acid conjugation in the chimpanzee: effective sulfation of lithocholic acid. Arch Toxicol. 1978 Apr 27;40(2):109-18. [PubMed:580732 ]
Bolhuis PA, Sinaasappel M: Bile acid clearance and biocompatibility of XAD-4 haemoperfusion. Int J Artif Organs. 1978 May;1(3):135-41. [PubMed:689756 ]
Roda A, Pellicciari R, Polimeni C, Cerre C, Forti GC, Sadeghpour B, Sapigni E, Gioacchini AM, Natalini B: Metabolism, pharmacokinetics, and activity of a new 6-fluoro analogue of ursodeoxycholic acid in rats and hamsters. Gastroenterology. 1995 Apr;108(4):1204-14. [PubMed:7698590 ]
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 ]
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 ]
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 ]
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 ]
Elshenawy S, Pinney SE, Stuart T, Doulias PT, Zura G, Parry S, Elovitz MA, Bennett MJ, Bansal A, Strauss JF 3rd, Ischiropoulos H, Simmons RA: The Metabolomic Signature of the Placenta in Spontaneous Preterm Birth. Int J Mol Sci. 2020 Feb 4;21(3). pii: ijms21031043. doi: 10.3390/ijms21031043. [PubMed:32033212 ]

Enzymes

Enzyme Details

1. Bile acid-CoA:amino acid N-acyltransferase

General function:: Involved in thiolester hydrolase activity
Specific function:: Involved in bile acid metabolism. In liver hepatocytes catalyzes the second step in the conjugation of C24 bile acids (choloneates) to glycine and taurine before excretion into bile canaliculi. The major components of bile are cholic acid and chenodeoxycholic acid. In a first step the bile acids are converted to an acyl-CoA thioester, either in peroxisomes (primary bile acids deriving from the cholesterol pathway), or cytoplasmic at the endoplasmic reticulum (secondary bile acids). May catalyze the conjugation of primary or secondary bile acids, or both. The conjugation increases the detergent properties of bile acids in the intestine, which facilitates lipid and fat-soluble vitamin absorption. In turn, bile acids are deconjugated by bacteria in the intestine and are recycled back to the liver for reconjugation (secondary bile acids). May also act as an acyl-CoA thioesterase that regulates intracellular levels of free fatty acids. In vitro, catalyzes the hydrolysis of long- and very long-chain saturated acyl-CoAs to the free fatty acid and coenzyme A (CoASH), and conjugates glycine to these acyl-CoAs.
Gene Name:: BAAT
Uniprot ID:: Q14032
Molecular weight:: 46298.865

Reactions

Chenodeoxycholoyl-CoA + Taurine → Taurochenodesoxycholic acid + Coenzyme A	details

Enzyme Details

2. Cytochrome P450 3A4

General function:: Involved in monooxygenase activity
Specific function:: Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It performs a variety of oxidation reactions (e.g. caffeine 8-oxidation, omeprazole sulphoxidation, midazolam 1'-hydroxylation and midazolam 4-hydroxylation) of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. Acts as a 1,8-cineole 2-exo-monooxygenase. The enzyme also hydroxylates etoposide.
Gene Name:: CYP3A4
Uniprot ID:: P08684
Molecular weight:: 57255.585

Reactions

Taurochenodesoxycholic acid + NADPH + Oxygen → Taurohyocholate + NADP + Water	details

Showing metabocard for Taurochenodesoxycholic acid (HMDB0000951)

MOL for HMDB0000951 (Taurochenodesoxycholic acid)

3D MOL for HMDB0000951 (Taurochenodesoxycholic acid)

3D SDF for HMDB0000951 (Taurochenodesoxycholic acid)

3D-SDF for HMDB0000951 (Taurochenodesoxycholic acid)

PDB for HMDB0000951 (Taurochenodesoxycholic acid)

3D PDB for HMDB0000951 (Taurochenodesoxycholic acid)

SMILES for HMDB0000951 (Taurochenodesoxycholic acid)

INCHI for HMDB0000951 (Taurochenodesoxycholic acid)

Structure for HMDB0000951 (Taurochenodesoxycholic acid)

3D Structure for HMDB0000951 (Taurochenodesoxycholic acid)

Experimental Collision Cross Sections

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

Enzymes

Reactions

Reactions