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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (1)transporters (8) Show 9 proteins XML

enzymes (1)transporters (8) Show 9 proteins

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2022-03-07 02:49:03 UTC

HMDB ID

HMDB0000506

Secondary Accession Numbers

HMDB00506

Metabolite Identification

Common Name

alpha-Muricholic acid

Description

alpha-Muricholic acid is a hydroxylated bile acid present in normal human urine (PMID: 1629271 ), and in free glycine-conjugated, taurine-conjugated, and sulfated forms in human feces (PMID: 3667743 ). 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 ).

Structure

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


  Mrv1652303062020102D          

 34 37  0  0  0  0            999 V2000
 9998.202110000.0028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.339910001.2523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.3399 9998.7683    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0607 9997.9350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2021 9997.5216    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9145 9997.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.3420 9997.9350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.627110000.0028    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9145 9998.7683    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.4890 9999.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7745 9999.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7745 9998.3496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.4890 9997.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2005 9999.1747    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.2005 9998.3496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.9150 9997.9372    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.6295 9998.3496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9999.627710000.8337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.913210000.4212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9132 9999.5961    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.6277 9999.1837    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.342210000.4212    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.3421 9999.5962    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10001.1268 9999.3413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.611610000.0087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.126810000.6762    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10001.126810001.5012    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10001.842410001.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.556110001.5012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.271810001.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.985410001.5012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.271810002.7387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.413210001.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.842410001.0887    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  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
 12  4  1  6  0  0  0
 17  7  1  6  0  0  0
 16  6  1  1  0  0  0
 13 15  1  0  0  0  0
 15  5  1  1  0  0  0
 10 14  1  0  0  0  0
 14  1  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 14  1  0  0  0  0
 20  9  1  6  0  0  0
 17 21  1  0  0  0  0
 21  8  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 27  1  0  0  0  0
 26 34  1  6  0  0  0
 27 28  1  0  0  0  0
 27 33  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 26 22  1  0  0  0  0
 26 25  1  0  0  0  0
 21 23  1  0  0  0  0
 23  3  1  6  0  0  0
 18 22  1  0  0  0  0
 22  2  1  1  0  0  0
M  END

HMDB0000506
     RDKit          3D
alpha-Muricholic acid
 69 72  0  0  0  0  0  0  0  0999 V2000
   -4.7297   -1.3866    0.3674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7933   -0.2522    0.7673 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4669    1.0624    0.6304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7087    1.2096    1.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8809    0.4289    1.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0936    0.0532   -0.0793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8543    0.0414    2.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5627   -0.4723   -0.0253 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7200   -0.4690   -1.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2827   -0.3202   -2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4727   -0.4153   -0.8203 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8903    0.0889   -0.8071 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7968   -0.5261   -1.8423 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9716   -1.8731   -1.7302 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0290    0.2988   -1.8556 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7263    1.4797   -2.5771 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373    0.5802   -0.5107 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1032    0.3728   -0.6305 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7451   -0.5951    0.2820 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8963   -1.0978   -0.3304 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8024   -1.7561    0.4458 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5103   -1.3820    1.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9574   -0.0440    0.6496 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2062    0.8770    1.8632 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4890   -0.1957    0.5507 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7161    0.7494    1.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7252    0.2862    1.4956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3730    0.3865    0.1619 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5852    1.7640   -0.3533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5021   -1.6117    1.0944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9859   -1.3438   -0.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0268   -2.3105    0.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5857   -0.4384    1.8705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7786    1.2206   -0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7664    1.9079    0.9224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4812    1.1394    2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0267    2.3024    1.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7043   -0.8493    2.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1752   -1.5508    0.1792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3011    0.3350   -1.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787   -1.4186   -1.8923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0882   -1.2285   -2.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1636    0.5972   -2.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5103   -1.4535   -0.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9667    1.1805   -0.9488 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2734   -0.3587   -2.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1851   -2.2696   -1.2918 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7585   -0.2341   -2.5391 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5549    2.1639   -1.8548 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5073    1.7025   -0.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3901    0.0534   -1.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7019    1.3330   -0.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0916   -0.1791    1.2458 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2350   -0.4361   -0.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3177   -2.5236    1.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6350   -2.1981   -0.5578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6565   -1.4577    2.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7847   -2.2158    0.8641 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2682    1.2327    1.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0607    0.3393    2.8109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6044    1.8023    1.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1058   -1.2056    0.8446 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    0.6808    2.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6993    1.7840    1.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7602   -0.7661    1.8256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528    0.9576    2.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7635    2.1149   -1.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5604    2.4731    0.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4859    1.8356   -0.9512 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
  2  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 28  8  1  0
 28 11  1  0
 25 12  1  0
 23 17  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  1
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  7 38  1  0
  8 39  1  1
  9 40  1  0
  9 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  1
 12 45  1  6
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 14 47  1  0
 15 48  1  6
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 17 50  1  1
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 18 52  1  0
 19 53  1  1
 20 54  1  0
 21 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 24 59  1  0
 24 60  1  0
 24 61  1  0
 25 62  1  1
 26 63  1  0
 26 64  1  0
 27 65  1  0
 27 66  1  0
 29 67  1  0
 29 68  1  0
 29 69  1  0
M  END


  Mrv1652303062020102D          

 34 37  0  0  0  0            999 V2000
 9998.202110000.0028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.339910001.2523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.3399 9998.7683    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0607 9997.9350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2021 9997.5216    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9145 9997.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.3420 9997.9350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.627110000.0028    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9145 9998.7683    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.4890 9999.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7745 9999.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7745 9998.3496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.4890 9997.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2005 9999.1747    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.2005 9998.3496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.9150 9997.9372    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.6295 9998.3496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9999.627710000.8337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.913210000.4212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9132 9999.5961    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.6277 9999.1837    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.342210000.4212    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.3421 9999.5962    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10001.1268 9999.3413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.611610000.0087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.126810000.6762    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10001.126810001.5012    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10001.842410001.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.556110001.5012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.271810001.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.985410001.5012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.271810002.7387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.413210001.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.842410001.0887    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  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
 12  4  1  6  0  0  0
 17  7  1  6  0  0  0
 16  6  1  1  0  0  0
 13 15  1  0  0  0  0
 15  5  1  1  0  0  0
 10 14  1  0  0  0  0
 14  1  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 14  1  0  0  0  0
 20  9  1  6  0  0  0
 17 21  1  0  0  0  0
 21  8  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 27  1  0  0  0  0
 26 34  1  6  0  0  0
 27 28  1  0  0  0  0
 27 33  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 26 22  1  0  0  0  0
 26 25  1  0  0  0  0
 21 23  1  0  0  0  0
 23  3  1  6  0  0  0
 18 22  1  0  0  0  0
 22  2  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0000506

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C24H40O5/c1-13(4-7-19(26)27)15-5-6-16-20-17(9-11-23(15,16)2)24(3)10-8-14(25)12-18(24)21(28)22(20)29/h13-18,20-22,25,28-29H,4-12H2,1-3H3,(H,26,27)/t13-,14-,15-,16+,17+,18+,20+,21+,22+,23-,24-/m1/s1

> <INCHI_KEY>
DKPMWHFRUGMUKF-GDYCBZMLSA-N

> <FORMULA>
C24H40O5

> <MOLECULAR_WEIGHT>
408.579

> <EXACT_MASS>
408.287574388

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
47.224097660836414

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R)-4-[(1S,2R,5R,7R,8S,9S,10S,11S,14R,15R)-5,8,9-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid

> <ALOGPS_LOGP>
2.16

> <JCHEM_LOGP>
2.716355646666667

> <ALOGPS_LOGS>
-3.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.6233491959118

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.595941876165357

> <JCHEM_PKA_STRONGEST_BASIC>
-2.69104497552095

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
110.55829999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.89e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R)-4-[(1S,2R,5R,7R,8S,9S,10S,11S,14R,15R)-5,8,9-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000506
     RDKit          3D
alpha-Muricholic acid
 69 72  0  0  0  0  0  0  0  0999 V2000
   -4.7297   -1.3866    0.3674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7933   -0.2522    0.7673 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4669    1.0624    0.6304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7087    1.2096    1.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8809    0.4289    1.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0936    0.0532   -0.0793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8543    0.0414    2.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5627   -0.4723   -0.0253 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7200   -0.4690   -1.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2827   -0.3202   -2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4727   -0.4153   -0.8203 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8903    0.0889   -0.8071 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7968   -0.5261   -1.8423 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9716   -1.8731   -1.7302 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0290    0.2988   -1.8556 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7263    1.4797   -2.5771 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373    0.5802   -0.5107 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1032    0.3728   -0.6305 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7451   -0.5951    0.2820 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8963   -1.0978   -0.3304 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8024   -1.7561    0.4458 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5103   -1.3820    1.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9574   -0.0440    0.6496 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2062    0.8770    1.8632 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4890   -0.1957    0.5507 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7161    0.7494    1.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7252    0.2862    1.4956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3730    0.3865    0.1619 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5852    1.7640   -0.3533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5021   -1.6117    1.0944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9859   -1.3438   -0.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0268   -2.3105    0.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5857   -0.4384    1.8705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7786    1.2206   -0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7664    1.9079    0.9224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4812    1.1394    2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0267    2.3024    1.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7043   -0.8493    2.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1752   -1.5508    0.1792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3011    0.3350   -1.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787   -1.4186   -1.8923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0882   -1.2285   -2.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1636    0.5972   -2.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5103   -1.4535   -0.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9667    1.1805   -0.9488 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2734   -0.3587   -2.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1851   -2.2696   -1.2918 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7585   -0.2341   -2.5391 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5549    2.1639   -1.8548 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5073    1.7025   -0.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3901    0.0534   -1.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7019    1.3330   -0.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0916   -0.1791    1.2458 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2350   -0.4361   -0.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3177   -2.5236    1.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6350   -2.1981   -0.5578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6565   -1.4577    2.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7847   -2.2158    0.8641 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2682    1.2327    1.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0607    0.3393    2.8109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6044    1.8023    1.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1058   -1.2056    0.8446 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    0.6808    2.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6993    1.7840    1.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7602   -0.7661    1.8256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528    0.9576    2.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7635    2.1149   -1.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5604    2.4731    0.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4859    1.8356   -0.9512 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
  2  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 28  8  1  0
 28 11  1  0
 25 12  1  0
 23 17  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  1
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  7 38  1  0
  8 39  1  1
  9 40  1  0
  9 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  1
 12 45  1  6
 13 46  1  6
 14 47  1  0
 15 48  1  6
 16 49  1  0
 17 50  1  1
 18 51  1  0
 18 52  1  0
 19 53  1  1
 20 54  1  0
 21 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 24 59  1  0
 24 60  1  0
 24 61  1  0
 25 62  1  1
 26 63  1  0
 26 64  1  0
 27 65  1  0
 27 66  1  0
 29 67  1  0
 29 68  1  0
 29 69  1  0
M  END

HEADER    PROTEIN                                 06-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAR-20         0                                  
HETATM    1  C   UNK     0    8663.3118666.672   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8667.3018669.004   0.000  0.00  0.00           C+0
HETATM    3  H   UNK     0    8667.3018664.367   0.000  0.00  0.00           H+0
HETATM    4  O   UNK     0    8659.3138662.812   0.000  0.00  0.00           O+0
HETATM    5  H   UNK     0    8663.3118662.040   0.000  0.00  0.00           H+0
HETATM    6  O   UNK     0    8664.6408661.264   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0    8667.3058662.812   0.000  0.00  0.00           O+0
HETATM    8  H   UNK     0    8665.9718666.672   0.000  0.00  0.00           H+0
HETATM    9  H   UNK     0    8664.6408664.367   0.000  0.00  0.00           H+0
HETATM   10  C   UNK     0    8661.9798665.896   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8660.6468665.126   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8660.6468663.586   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8661.9798662.816   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8663.3088665.126   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8663.3088663.586   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8664.6418662.816   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8665.9758663.586   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8665.9728668.223   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8664.6388667.453   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8664.6388665.913   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8665.9728665.143   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8667.3058667.453   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    8667.3058665.913   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0    8668.7708665.437   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    8669.6758666.683   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0    8668.7708667.929   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0    8668.7708669.469   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0    8670.1068670.239   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0    8671.4388669.469   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0    8672.7748670.239   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0    8674.1068669.469   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0    8672.7748671.779   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0    8667.4388670.239   0.000  0.00  0.00           C+0
HETATM   34  H   UNK     0    8670.1068668.699   0.000  0.00  0.00           H+0
CONECT    1   14                                                            
CONECT    2   22                                                            
CONECT    3   23                                                            
CONECT    4   12                                                            
CONECT    5   15                                                            
CONECT    6   16                                                            
CONECT    7   17                                                            
CONECT    8   21                                                            
CONECT    9   20                                                            
CONECT   10   11   14                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13    4                                                  
CONECT   13   12   15                                                       
CONECT   14   15   10    1   20                                             
CONECT   15   14   16   13    5                                             
CONECT   16   15   17    6                                                  
CONECT   17   16    7   21                                                  
CONECT   18   19   22                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   14    9                                             
CONECT   21   20   17    8   23                                             
CONECT   22   23   26   18    2                                             
CONECT   23   22   24   21    3                                             
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   27   34   22   25                                             
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   27                                                            
CONECT   34   26                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

COMPND    HMDB0000506
HETATM    1  C1  UNL     1      -4.730  -1.387   0.367  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.793  -0.252   0.767  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.467   1.062   0.630  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.709   1.210   1.447  1.00  0.00           C  
HETATM    5  C5  UNL     1      -6.881   0.429   1.092  1.00  0.00           C  
HETATM    6  O1  UNL     1      -7.094   0.053  -0.079  1.00  0.00           O  
HETATM    7  O2  UNL     1      -7.854   0.041   2.031  1.00  0.00           O  
HETATM    8  C6  UNL     1      -2.563  -0.472  -0.025  1.00  0.00           C  
HETATM    9  C7  UNL     1      -2.720  -0.469  -1.526  1.00  0.00           C  
HETATM   10  C8  UNL     1      -1.283  -0.320  -2.067  1.00  0.00           C  
HETATM   11  C9  UNL     1      -0.473  -0.415  -0.820  1.00  0.00           C  
HETATM   12  C10 UNL     1       0.890   0.089  -0.807  1.00  0.00           C  
HETATM   13  C11 UNL     1       1.797  -0.526  -1.842  1.00  0.00           C  
HETATM   14  O3  UNL     1       1.972  -1.873  -1.730  1.00  0.00           O  
HETATM   15  C12 UNL     1       3.029   0.299  -1.856  1.00  0.00           C  
HETATM   16  O4  UNL     1       2.726   1.480  -2.577  1.00  0.00           O  
HETATM   17  C13 UNL     1       3.637   0.580  -0.511  1.00  0.00           C  
HETATM   18  C14 UNL     1       5.103   0.373  -0.631  1.00  0.00           C  
HETATM   19  C15 UNL     1       5.745  -0.595   0.282  1.00  0.00           C  
HETATM   20  O5  UNL     1       6.896  -1.098  -0.330  1.00  0.00           O  
HETATM   21  C16 UNL     1       4.802  -1.756   0.446  1.00  0.00           C  
HETATM   22  C17 UNL     1       3.510  -1.382   1.078  1.00  0.00           C  
HETATM   23  C18 UNL     1       2.957  -0.044   0.650  1.00  0.00           C  
HETATM   24  C19 UNL     1       3.206   0.877   1.863  1.00  0.00           C  
HETATM   25  C20 UNL     1       1.489  -0.196   0.551  1.00  0.00           C  
HETATM   26  C21 UNL     1       0.716   0.749   1.487  1.00  0.00           C  
HETATM   27  C22 UNL     1      -0.725   0.286   1.496  1.00  0.00           C  
HETATM   28  C23 UNL     1      -1.373   0.387   0.162  1.00  0.00           C  
HETATM   29  C24 UNL     1      -1.585   1.764  -0.353  1.00  0.00           C  
HETATM   30  H1  UNL     1      -5.502  -1.612   1.094  1.00  0.00           H  
HETATM   31  H2  UNL     1      -4.986  -1.344  -0.690  1.00  0.00           H  
HETATM   32  H3  UNL     1      -4.027  -2.311   0.409  1.00  0.00           H  
HETATM   33  H4  UNL     1      -3.586  -0.438   1.870  1.00  0.00           H  
HETATM   34  H5  UNL     1      -4.779   1.221  -0.443  1.00  0.00           H  
HETATM   35  H6  UNL     1      -3.766   1.908   0.922  1.00  0.00           H  
HETATM   36  H7  UNL     1      -5.481   1.139   2.551  1.00  0.00           H  
HETATM   37  H8  UNL     1      -6.027   2.302   1.345  1.00  0.00           H  
HETATM   38  H9  UNL     1      -7.704  -0.849   2.500  1.00  0.00           H  
HETATM   39  H10 UNL     1      -2.175  -1.551   0.179  1.00  0.00           H  
HETATM   40  H11 UNL     1      -3.301   0.335  -1.950  1.00  0.00           H  
HETATM   41  H12 UNL     1      -3.179  -1.419  -1.892  1.00  0.00           H  
HETATM   42  H13 UNL     1      -1.088  -1.229  -2.672  1.00  0.00           H  
HETATM   43  H14 UNL     1      -1.164   0.597  -2.641  1.00  0.00           H  
HETATM   44  H15 UNL     1      -0.510  -1.454  -0.446  1.00  0.00           H  
HETATM   45  H16 UNL     1       0.967   1.181  -0.949  1.00  0.00           H  
HETATM   46  H17 UNL     1       1.273  -0.359  -2.831  1.00  0.00           H  
HETATM   47  H18 UNL     1       1.185  -2.270  -1.292  1.00  0.00           H  
HETATM   48  H19 UNL     1       3.758  -0.234  -2.539  1.00  0.00           H  
HETATM   49  H20 UNL     1       2.555   2.164  -1.855  1.00  0.00           H  
HETATM   50  H21 UNL     1       3.507   1.703  -0.375  1.00  0.00           H  
HETATM   51  H22 UNL     1       5.390   0.053  -1.681  1.00  0.00           H  
HETATM   52  H23 UNL     1       5.702   1.333  -0.531  1.00  0.00           H  
HETATM   53  H24 UNL     1       6.092  -0.179   1.246  1.00  0.00           H  
HETATM   54  H25 UNL     1       7.235  -0.436  -0.958  1.00  0.00           H  
HETATM   55  H26 UNL     1       5.318  -2.524   1.054  1.00  0.00           H  
HETATM   56  H27 UNL     1       4.635  -2.198  -0.558  1.00  0.00           H  
HETATM   57  H28 UNL     1       3.656  -1.458   2.193  1.00  0.00           H  
HETATM   58  H29 UNL     1       2.785  -2.216   0.864  1.00  0.00           H  
HETATM   59  H30 UNL     1       4.268   1.233   1.872  1.00  0.00           H  
HETATM   60  H31 UNL     1       3.061   0.339   2.811  1.00  0.00           H  
HETATM   61  H32 UNL     1       2.604   1.802   1.790  1.00  0.00           H  
HETATM   62  H33 UNL     1       1.106  -1.206   0.845  1.00  0.00           H  
HETATM   63  H34 UNL     1       1.073   0.681   2.523  1.00  0.00           H  
HETATM   64  H35 UNL     1       0.699   1.784   1.078  1.00  0.00           H  
HETATM   65  H36 UNL     1      -0.760  -0.766   1.826  1.00  0.00           H  
HETATM   66  H37 UNL     1      -1.253   0.958   2.232  1.00  0.00           H  
HETATM   67  H38 UNL     1      -0.764   2.115  -1.032  1.00  0.00           H  
HETATM   68  H39 UNL     1      -1.560   2.473   0.488  1.00  0.00           H  
HETATM   69  H40 UNL     1      -2.486   1.836  -0.951  1.00  0.00           H  
CONECT    1    2   30   31   32
CONECT    2    3    8   33
CONECT    3    4   34   35
CONECT    4    5   36   37
CONECT    5    6    6    7
CONECT    7   38
CONECT    8    9   28   39
CONECT    9   10   40   41
CONECT   10   11   42   43
CONECT   11   12   28   44
CONECT   12   13   25   45
CONECT   13   14   15   46
CONECT   14   47
CONECT   15   16   17   48
CONECT   16   49
CONECT   17   18   23   50
CONECT   18   19   51   52
CONECT   19   20   21   53
CONECT   20   54
CONECT   21   22   55   56
CONECT   22   23   57   58
CONECT   23   24   25
CONECT   24   59   60   61
CONECT   25   26   62
CONECT   26   27   63   64
CONECT   27   28   65   66
CONECT   28   29
CONECT   29   67   68   69
END

HMDB0000506
     RDKit          3D
alpha-Muricholic acid
 69 72  0  0  0  0  0  0  0  0999 V2000
   -4.7297   -1.3866    0.3674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7933   -0.2522    0.7673 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4669    1.0624    0.6304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7087    1.2096    1.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8809    0.4289    1.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0936    0.0532   -0.0793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8543    0.0414    2.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5627   -0.4723   -0.0253 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7200   -0.4690   -1.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2827   -0.3202   -2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4727   -0.4153   -0.8203 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8903    0.0889   -0.8071 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7968   -0.5261   -1.8423 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9716   -1.8731   -1.7302 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0290    0.2988   -1.8556 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7263    1.4797   -2.5771 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373    0.5802   -0.5107 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1032    0.3728   -0.6305 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7451   -0.5951    0.2820 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8963   -1.0978   -0.3304 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8024   -1.7561    0.4458 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5103   -1.3820    1.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9574   -0.0440    0.6496 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2062    0.8770    1.8632 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4890   -0.1957    0.5507 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7161    0.7494    1.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7252    0.2862    1.4956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3730    0.3865    0.1619 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5852    1.7640   -0.3533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5021   -1.6117    1.0944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9859   -1.3438   -0.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0268   -2.3105    0.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5857   -0.4384    1.8705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7786    1.2206   -0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7664    1.9079    0.9224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4812    1.1394    2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0267    2.3024    1.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7043   -0.8493    2.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1752   -1.5508    0.1792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3011    0.3350   -1.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787   -1.4186   -1.8923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0882   -1.2285   -2.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1636    0.5972   -2.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5103   -1.4535   -0.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9667    1.1805   -0.9488 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2734   -0.3587   -2.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1851   -2.2696   -1.2918 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7585   -0.2341   -2.5391 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5549    2.1639   -1.8548 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5073    1.7025   -0.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3901    0.0534   -1.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7019    1.3330   -0.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0916   -0.1791    1.2458 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2350   -0.4361   -0.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3177   -2.5236    1.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6350   -2.1981   -0.5578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6565   -1.4577    2.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7847   -2.2158    0.8641 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2682    1.2327    1.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0607    0.3393    2.8109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6044    1.8023    1.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1058   -1.2056    0.8446 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    0.6808    2.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6993    1.7840    1.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7602   -0.7661    1.8256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528    0.9576    2.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7635    2.1149   -1.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5604    2.4731    0.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4859    1.8356   -0.9512 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
  2  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 28  8  1  0
 28 11  1  0
 25 12  1  0
 23 17  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  1
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  7 38  1  0
  8 39  1  1
  9 40  1  0
  9 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  1
 12 45  1  6
 13 46  1  6
 14 47  1  0
 15 48  1  6
 16 49  1  0
 17 50  1  1
 18 51  1  0
 18 52  1  0
 19 53  1  1
 20 54  1  0
 21 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 24 59  1  0
 24 60  1  0
 24 61  1  0
 25 62  1  1
 26 63  1  0
 26 64  1  0
 27 65  1  0
 27 66  1  0
 29 67  1  0
 29 68  1  0
 29 69  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(3alpha,5beta,6beta,7alpha)-3,6,7-Trihydroxycholan-24-oic acid	ChEBI
5beta-Cholanic acid-3alpha,6beta,7alpha-triol	ChEBI
3alpha,6beta,7alpha-Trihydroxy-5beta-cholan-24-oic acid	KEGG
(3a,5b,6b,7a)-3,6,7-Trihydroxycholan-24-oate	Generator
(3a,5b,6b,7a)-3,6,7-Trihydroxycholan-24-oic acid	Generator
(3alpha,5beta,6beta,7alpha)-3,6,7-Trihydroxycholan-24-oate	Generator
(3α,5β,6β,7α)-3,6,7-Trihydroxycholan-24-oate	Generator
(3α,5β,6β,7α)-3,6,7-Trihydroxycholan-24-oic acid	Generator
5b-Cholanate-3a,6b,7a-triol	Generator
5b-Cholanic acid-3a,6b,7a-triol	Generator
5beta-Cholanate-3alpha,6beta,7alpha-triol	Generator
5β-Cholanate-3α,6β,7α-triol	Generator
5β-Cholanic acid-3α,6β,7α-triol	Generator
3a,6b,7a-Trihydroxy-5b-cholan-24-oate	Generator
3a,6b,7a-Trihydroxy-5b-cholan-24-oic acid	Generator
3alpha,6beta,7alpha-Trihydroxy-5beta-cholan-24-oate	Generator
3α,6β,7α-Trihydroxy-5β-cholan-24-oate	Generator
3α,6β,7α-Trihydroxy-5β-cholan-24-oic acid	Generator
a-Muricholate	Generator
a-Muricholic acid	Generator
alpha-Muricholate	Generator
α-Muricholate	Generator
α-Muricholic acid	Generator
Muricholic acid, (3alpha,5beta,6beta,7alpha)-isomer	MeSH
3,6,7-Trihydroxy-5-cholanoic acid	MeSH
Muricholic acid	MeSH
alpha-Muricholic acid	HMDB

Chemical Formula

C₂₄H₄₀O₅

Average Molecular Weight

408.579

Monoisotopic Molecular Weight

408.287574388

IUPAC Name

(4R)-4-[(1S,2R,5R,7R,8S,9S,10S,11S,14R,15R)-5,8,9-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid

Traditional Name

(4R)-4-[(1S,2R,5R,7R,8S,9S,10S,11S,14R,15R)-5,8,9-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid

CAS Registry Number

2393-58-0

SMILES

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

InChI Identifier

InChI=1S/C24H40O5/c1-13(4-7-19(26)27)15-5-6-16-20-17(9-11-23(15,16)2)24(3)10-8-14(25)12-18(24)21(28)22(20)29/h13-18,20-22,25,28-29H,4-12H2,1-3H3,(H,26,27)/t13-,14-,15-,16+,17+,18+,20+,21+,22+,23-,24-/m1/s1

InChI Key

DKPMWHFRUGMUKF-GDYCBZMLSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as trihydroxy bile acids, alcohols and derivatives. These are prenol lipids structurally characterized by a bile acid or alcohol which bears three hydroxyl groups.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Trihydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Trihydroxy bile acid, alcohol, or derivatives
3-hydroxysteroid
6-hydroxysteroid
7-hydroxysteroid
3-alpha-hydroxysteroid
Hydroxysteroid
Cyclic alcohol
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Polyol
Monocarboxylic acid or derivatives
Organic oxide
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

bile acid (CHEBI:81243 )
C24 bile acids, alcohols, and derivatives (LMST04010066 )

Ontology

Not Available

Cellular substructure

Extracellular (HMDB: HMDB0000506)

Biofluid or Excreta

Urine (HMDB: HMDB0000506)

Tissue substructure

Hepatic tissue (HMDB: HMDB0000506)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0000506)

Source

Endogenous

Endogenous (HMDB: HMDB0000506)

Animal

Animal (HMDB: HMDB0000506)

Exogenous

Food

Food (HMDB: HMDB0000506)

Animal origin

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Poultry

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

Lagomorph

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)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0000506)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0000506)

Cellular process

Cell signaling (HMDB: HMDB0000506)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0000506)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0000506)

Molecular messenger

Signaling molecule (HMDB: HMDB0000506)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0000506)

Emulsifier (HMDB: HMDB0000506)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	199 - 200 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.069 g/L	ALOGPS
logP	2.16	ALOGPS
logP	2.72	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	4.6	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	110.56 m³·mol⁻¹	ChemAxon
Polarizability	47.22 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	231.676	30932474
DeepCCS	[M+Na]+	205.693	30932474
AllCCS	[M+H]+	203.3	32859911
AllCCS	[M+H-H2O]+	201.3	32859911
AllCCS	[M+NH4]+	205.1	32859911
AllCCS	[M+Na]+	205.7	32859911
AllCCS	[M-H]-	201.0	32859911
AllCCS	[M+Na-2H]-	202.4	32859911
AllCCS	[M+HCOO]-	204.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
alpha-Muricholic acid	[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)[C@@H](O)[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(O)=O	3746.1	Standard polar	33892256
alpha-Muricholic acid	[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)[C@@H](O)[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(O)=O	3502.6	Standard non polar	33892256
alpha-Muricholic acid	[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)[C@@H](O)[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(O)=O	3627.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
alpha-Muricholic acid,1TMS,isomer #1	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3355.8	Semi standard non polar	33892256
alpha-Muricholic acid,1TMS,isomer #2	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3361.8	Semi standard non polar	33892256
alpha-Muricholic acid,1TMS,isomer #3	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3431.5	Semi standard non polar	33892256
alpha-Muricholic acid,1TMS,isomer #4	C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3405.9	Semi standard non polar	33892256
alpha-Muricholic acid,2TMS,isomer #1	C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3308.0	Semi standard non polar	33892256
alpha-Muricholic acid,2TMS,isomer #2	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3282.7	Semi standard non polar	33892256
alpha-Muricholic acid,2TMS,isomer #3	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3309.3	Semi standard non polar	33892256
alpha-Muricholic acid,2TMS,isomer #4	C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3310.4	Semi standard non polar	33892256
alpha-Muricholic acid,2TMS,isomer #5	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3319.8	Semi standard non polar	33892256
alpha-Muricholic acid,2TMS,isomer #6	C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3381.3	Semi standard non polar	33892256
alpha-Muricholic acid,3TMS,isomer #1	C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3275.9	Semi standard non polar	33892256
alpha-Muricholic acid,3TMS,isomer #2	C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3299.1	Semi standard non polar	33892256
alpha-Muricholic acid,3TMS,isomer #3	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3299.0	Semi standard non polar	33892256
alpha-Muricholic acid,3TMS,isomer #4	C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3304.1	Semi standard non polar	33892256
alpha-Muricholic acid,4TMS,isomer #1	C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3314.0	Semi standard non polar	33892256
alpha-Muricholic acid,1TBDMS,isomer #1	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3574.1	Semi standard non polar	33892256
alpha-Muricholic acid,1TBDMS,isomer #2	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3584.0	Semi standard non polar	33892256
alpha-Muricholic acid,1TBDMS,isomer #3	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3653.3	Semi standard non polar	33892256
alpha-Muricholic acid,1TBDMS,isomer #4	C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3673.9	Semi standard non polar	33892256
alpha-Muricholic acid,2TBDMS,isomer #1	C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3754.0	Semi standard non polar	33892256
alpha-Muricholic acid,2TBDMS,isomer #2	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3703.1	Semi standard non polar	33892256
alpha-Muricholic acid,2TBDMS,isomer #3	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3733.5	Semi standard non polar	33892256
alpha-Muricholic acid,2TBDMS,isomer #4	C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3773.1	Semi standard non polar	33892256
alpha-Muricholic acid,2TBDMS,isomer #5	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3758.7	Semi standard non polar	33892256
alpha-Muricholic acid,2TBDMS,isomer #6	C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3863.3	Semi standard non polar	33892256
alpha-Muricholic acid,3TBDMS,isomer #1	C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C	3895.8	Semi standard non polar	33892256
alpha-Muricholic acid,3TBDMS,isomer #2	C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3932.5	Semi standard non polar	33892256
alpha-Muricholic acid,3TBDMS,isomer #3	C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3911.7	Semi standard non polar	33892256
alpha-Muricholic acid,3TBDMS,isomer #4	C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	3949.2	Semi standard non polar	33892256
alpha-Muricholic acid,4TBDMS,isomer #1	C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21C	4116.0	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_3_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_3_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_3_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TMS_4_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Muricholic acid GC-MS (TBDMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Muricholic acid 10V, Negative-QTOF	splash10-0a4i-0001900000-3a052136aaad1f7a6938	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Muricholic acid 20V, Negative-QTOF	splash10-0a4r-0007900000-22aa0ad4e0928aedf2ca	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Muricholic acid 40V, Negative-QTOF	splash10-0a4i-1007900000-6419c8b1ffa27ffadfc8	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Muricholic acid 10V, Positive-QTOF	splash10-0a4i-0009500000-dcb14c8cf8d9d980be59	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Muricholic acid 20V, Positive-QTOF	splash10-000j-2389100000-31f9fcf2f00a46e40c20	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Muricholic acid 40V, Positive-QTOF	splash10-0002-9650000000-1b93af04c335777ff295	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Gall Bladder
Intestine
Kidney
Liver

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

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

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022082

KNApSAcK ID

Not Available

Chemspider ID

4446940

KEGG Compound ID

C17647

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5283852

PDB ID

Not Available

ChEBI ID

81243

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Hsia, S. L.; Elliott, Wm. H.; Matschiner, John T.; Doisy, E. A., Jr.; Thayer, Sidney A.; Doisy, Edward A. Bile acids. XIII. Further contributions to the constitution of muricholic acids. Journal of Biological Chemistry (1960), 235 1963-7.

Material Safety Data Sheet (MSDS)

Not Available

General References

Goto J, Hasegawa K, Nambara T, Iida T: Studies on steroids. CCLIV. Gas chromatographic-mass spectrometric determination of 4- and 6-hydroxylated bile acids in human urine with negative ion chemical ionization detection. J Chromatogr. 1992 Feb 7;574(1):1-7. [PubMed:1629271 ]
Ikawa S, Miyake M, Mura T, Ikeguchi M: High-performance liquid chromatographic-fluorescence determination of human faecal bile acids. J Chromatogr. 1987 Jul 29;400:149-61. [PubMed:3667743 ]
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 ]

Enzymes

Enzyme Details

1. Gastrotropin

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

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

Enzyme Details

1. Solute carrier organic anion transporter family member 1B3

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

Enzyme Details

2. Solute carrier organic anion transporter family member 1B1

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

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 ]

Enzyme Details

3. Canalicular multispecific organic anion transporter 2

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

Enzyme Details

4. Bile salt export pump

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

Enzyme Details

5. Ileal sodium/bile acid cotransporter

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

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 ]

Enzyme Details

6. Sodium/bile acid cotransporter

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

Enzyme Details

7. Solute carrier organic anion transporter family member 1A2

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

Enzyme Details

8. Solute carrier organic anion transporter family member 4A1

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

Showing metabocard for alpha-Muricholic acid (HMDB0000506)

MOL for HMDB0000506 (alpha-Muricholic acid)

3D MOL for HMDB0000506 (alpha-Muricholic acid)

3D SDF for HMDB0000506 (alpha-Muricholic acid)

3D-SDF for HMDB0000506 (alpha-Muricholic acid)

PDB for HMDB0000506 (alpha-Muricholic acid)

3D PDB for HMDB0000506 (alpha-Muricholic acid)

SMILES for HMDB0000506 (alpha-Muricholic acid)

INCHI for HMDB0000506 (alpha-Muricholic acid)

Structure for HMDB0000506 (alpha-Muricholic acid)

3D Structure for HMDB0000506 (alpha-Muricholic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

References

Transporters

References

References