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Record Information

Version

5.0

Status

Predicted

Creation Date

2021-08-30 20:16:38 UTC

Update Date

2022-11-15 17:47:03 UTC

HMDB ID

HMDB0242422

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Deoxycholyllysine

Description

Deoxycholyllysine belongs to a class of molecules known as bile acid-amino acid conjugates. These are bile acid conjugates that consist of a primary bile acid such as cholic acid, doxycholic acid and chenodeoxycholic acid, conjugated to an amino acid. Deoxycholyllysine consists of the bile acid deoxycholic acid conjugated to the amino acid Lysine conjugated at the C24 acyl site.Bile acids play an important role in regulating various physiological systems, such as fat digestion, cholesterol metabolism, vitamin absorption, liver function, and enterohepatic circulation through their combined signaling, detergent, and antimicrobial mechanisms (PMID: 34127070 ). Bile acids also act as detergents in the gut and support the absorption of fats through the intestinal membrane. These same properties allow for the disruption of bacterial membranes, thereby allowing them to serve a bacteriocidal or bacteriostatic function. In humans (and other mammals) bile acids are normally conjugated with the amino acids glycine and taurine by the liver. This conjugation catalyzed by two liver enzymes, bile acid CoA ligase (BAL) and bile acid CoA: amino acid N-acyltransferase (BAT). Glycine and taurine bound BAs are also referred to as bile salts due to their decreased pKa and complete ionization resulting in these compounds being present as anions in vivo. Unlike glycine and taurine-conjugated bile acids, these recently discovered bile acids, such as Deoxycholyllysine, are produced by the gut microbiota, making them secondary bile acids (PMID: 32103176 ) or microbially conjugated bile acids (MCBAs) (PMID: 34127070 ). Evidence suggests that these bile acid-amino acid conjugates are produced by microbes belonging to Clostridia species (PMID: 32103176 ). These unusual bile acid-amino acid conjugates are found in higher frequency in patients with inflammatory bowel disease (IBD), cystic fibrosis (CF) and in infants (PMID: 32103176 ). Deoxycholyllysine appears to act as an agonist for the farnesoid X receptor (FXR) and it can also lead to reduced expression of bile acid synthesis genes (PMID: 32103176 ). It currently appears that microbially conjugated bile acids (MCBAs) or amino acid-bile acid conjugates are only conjugated to cholic acid, deoxycholic acid and chenodeoxycholic acid (PMID: 34127070 ). It has been estimated that if microbial conjugation of bile acids is very promiscuous and occurs for all potential oxidized, epimerized, and dehydroxylated states of each hydroxyl group present on cholic acid (C3, C7, C12) in addition to ring orientation, the total number of potential human bile acid conjugates could be over 2800 (PMID: 34127070 ).

Structure

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


  Mrv1652308302122262D          

 37 40  0  0  0  0            999 V2000
    9.1168   -3.4686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4023   -3.0561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6879   -3.4686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4023   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6879   -1.8186    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9734   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9734   -3.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2589   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5445   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8300   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8300   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1155   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0293   -3.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2223   -3.2231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8098   -2.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0028   -2.3371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4508   -2.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6438   -2.7787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3889   -1.9941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4181   -1.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6730   -1.0379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4800   -0.8664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1210   -0.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2999   -0.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9749   -1.3435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1168   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8313   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5458   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2602   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9747   -1.8186    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
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 19 25  1  0  0  0  0
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 16 27  1  0  0  0  0
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 29 31  1  0  0  0  0
 12 31  1  0  0  0  0
 15 31  1  0  0  0  0
 31 32  1  0  0  0  0
  4 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
M  END

HMDB0242422
     RDKit          3D
Deoxycholyllysine
 89 92  0  0  0  0  0  0  0  0999 V2000
    2.1139    0.0394   -1.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2538   -0.4385   -0.5937 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5845   -1.9187   -0.5478 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0891   -2.0142   -0.3306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4687   -1.3733    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5197   -1.3206    1.7893 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7387   -0.9556    1.1247 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0734   -0.5164    1.2552 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4479    0.2680    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7276    0.9430   -0.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0107    0.2164   -0.0093 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1884    1.1936   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1973    2.2941    0.6124 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9099   -1.7952    1.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6568   -2.7442    0.5232 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9287   -1.8671    2.2205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1360   -0.1108   -1.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0854    1.7940    1.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4287   -1.5040   -0.3302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9474   -1.5600    0.0193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4165   -2.5546   -0.7919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2444   -0.2532   -0.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925    0.1927    1.3458 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3294   -0.7822   -2.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1036    0.4246   -1.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6472    0.8656   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6561    0.1435    0.2536 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1176   -2.4710    0.2570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4198   -2.2944   -1.5760 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6087   -1.4630   -1.1157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3521   -3.0874   -0.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4880    2.8246    1.7734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0256    1.6996   -0.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5867    0.0916    2.1143 H   0  0  0  0  0  0  0  0  0  0  0  0
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 37 89  1  0
M  END


  Mrv1652308302122262D          

 37 40  0  0  0  0            999 V2000
    9.1168   -3.4686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4023   -3.0561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6879   -3.4686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4023   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6879   -1.8186    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9734   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9734   -3.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2589   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5445   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8300   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8300   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1155   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0293   -3.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2223   -3.2231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8098   -2.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0028   -2.3371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4508   -2.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6438   -2.7787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3889   -1.9941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4181   -1.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6730   -1.0379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4800   -0.8664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1210   -0.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6860   -0.5963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9409   -1.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4930   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7479   -1.5525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2999   -0.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1069   -1.1109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6589   -0.4978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3618   -1.8955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9749   -1.3435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1168   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8313   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5458   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2602   -2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9747   -1.8186    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 16 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 12 31  1  0  0  0  0
 15 31  1  0  0  0  0
 31 32  1  0  0  0  0
  4 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242422

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(CCC(=O)NC(CCCCN)C(O)=O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H52N2O5/c1-18(7-12-27(35)32-25(28(36)37)6-4-5-15-31)22-10-11-23-21-9-8-19-16-20(33)13-14-29(19,2)24(21)17-26(34)30(22,23)3/h18-26,33-34H,4-17,31H2,1-3H3,(H,32,35)(H,36,37)

> <INCHI_KEY>
NQGPNQJTMGFHLB-UHFFFAOYSA-N

> <FORMULA>
C30H52N2O5

> <MOLECULAR_WEIGHT>
520.755

> <EXACT_MASS>
520.387622782

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
61.41723230272345

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-amino-2-(4-{5,16-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl}pentanamido)hexanoic acid

> <ALOGPS_LOGP>
0.34

> <JCHEM_LOGP>
0.8598488255908988

> <ALOGPS_LOGS>
-5.23

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.555596302569263

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.683568826461423

> <JCHEM_PKA_STRONGEST_BASIC>
10.20544725276104

> <JCHEM_POLAR_SURFACE_AREA>
132.88000000000002

> <JCHEM_REFRACTIVITY>
143.8064

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.04e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-amino-2-(4-{5,16-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl}pentanamido)hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0242422
     RDKit          3D
Deoxycholyllysine
 89 92  0  0  0  0  0  0  0  0999 V2000
    2.1139    0.0394   -1.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2538   -0.4385   -0.5937 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5845   -1.9187   -0.5478 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0891   -2.0142   -0.3306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4687   -1.3733    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5197   -1.3206    1.7893 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7387   -0.9556    1.1247 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0734   -0.5164    1.2552 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4479    0.2680    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7276    0.9430   -0.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0107    0.2164   -0.0093 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1884    1.1936   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1973    2.2941    0.6124 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9099   -1.7952    1.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6568   -2.7442    0.5232 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9287   -1.8671    2.2205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1360   -0.1108   -1.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0953    1.4235   -1.2655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3771    1.9866   -0.7236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2140    0.7413   -0.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5354    0.8822   -0.0753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7222    1.9490    0.9603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0854    1.7940    1.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9782    1.0830    0.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4374    1.0178    1.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2071    0.6264   -0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2799   -0.2298    0.1784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3877    0.1443   -1.2489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1962   -0.6979   -0.8963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5733   -0.3573    0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1140   -1.2557    1.4975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0803   -0.4143    0.4599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4287   -1.5040   -0.3302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9474   -1.5600    0.0193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4165   -2.5546   -0.7919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2444   -0.2532   -0.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925    0.1927    1.3458 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3294   -0.7822   -2.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1036    0.4246   -1.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6472    0.8656   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6561    0.1435    0.2536 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1176   -2.4710    0.2570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4198   -2.2944   -1.5760 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6087   -1.4630   -1.1157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3521   -3.0874   -0.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5067   -0.5754    2.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3137    0.0650    2.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3931   -0.4959   -0.8432 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5777    0.9516   -0.2644 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7683    1.5355   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7384    1.8106    0.6317 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1790    0.0213    1.0939 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1681   -0.6438   -0.6329 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0918    0.5767   -0.1007 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1664    1.4574   -1.3553 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5704    2.1871    1.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1489    3.2262    0.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2487   -2.7375    2.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3713   -0.6337   -1.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1549    1.5616   -2.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7816    1.8943   -0.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8893    2.6503   -1.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3063    2.5592    0.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3101    0.3863   -1.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2446    1.1575   -0.9203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6793    2.9291    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9819    1.9946    1.7483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0121    1.3301    2.6401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4880    2.8246    1.7734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0256    1.6996   -0.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6458    0.2791    1.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7432    2.0160    1.5208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7161    1.5798   -0.4662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6483   -0.5843   -0.6430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0462   -0.4852   -1.8956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0993    1.0081   -1.9303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4140   -0.5181   -1.6851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4386   -1.7820   -0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0133   -0.7599    2.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4706   -2.1528    1.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1427   -1.6215    1.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8013   -0.5757    1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8584   -2.4869   -0.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5943   -1.3885   -1.4123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9465   -1.8997    1.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5102   -3.4134   -0.2662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4121    1.2049    1.3690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0035   -0.4935    1.6921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5867    0.0916    2.1143 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  1  0
 11 12  1  0
 12 13  1  0
  8 14  1  0
 14 15  2  0
 14 16  1  0
  2 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
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 22 23  1  0
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 32 33  1  0
 33 34  1  0
 34 35  1  0
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 36 37  1  0
 36 17  1  0
 36 20  1  0
 32 21  1  0
 30 24  1  0
  1 38  1  0
  1 39  1  0
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  3 42  1  0
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  4 44  1  0
  4 45  1  0
  7 46  1  0
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 10 50  1  0
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 11 52  1  0
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 34 85  1  0
 35 86  1  0
 37 87  1  0
 37 88  1  0
 37 89  1  0
M  END

HEADER    PROTEIN                                 30-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-AUG-21         0                                  
HETATM    1  O   UNK     0      17.018  -6.475   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      15.684  -5.705   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      14.351  -6.475   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      15.684  -4.165   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      14.351  -3.395   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      13.017  -4.165   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      13.017  -5.705   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      11.683  -3.395   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.350  -4.165   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.016  -3.395   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.016  -1.855   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.682  -4.165   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.521  -5.696   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.015  -6.016   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.245  -4.683   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.739  -4.363   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.708  -5.507   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.202  -5.187   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.726  -3.722   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.780  -3.402   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.256  -1.937   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.763  -1.617   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.226  -0.793   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.281  -1.113   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.756  -2.578   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.787  -1.433   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.263  -2.898   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.293  -1.754   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.800  -2.074   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.830  -0.929   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.275  -3.538   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.420  -2.508   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      17.018  -3.395   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      18.352  -4.165   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      19.685  -3.395   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      21.019  -4.165   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0      22.353  -3.395   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   33                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   31                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   31                                                  
CONECT   16   15   17   27                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   19   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   16   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   12   15   32                                             
CONECT   32   31                                                            
CONECT   33    4   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

COMPND    HMDB0242422
HETATM    1  C1  UNL     1       2.114   0.039  -1.795  1.00  0.00           C  
HETATM    2  C2  UNL     1       1.254  -0.438  -0.594  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.585  -1.919  -0.548  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.089  -2.014  -0.331  1.00  0.00           C  
HETATM    5  C5  UNL     1       3.469  -1.373   1.001  1.00  0.00           C  
HETATM    6  O1  UNL     1       2.520  -1.321   1.789  1.00  0.00           O  
HETATM    7  N1  UNL     1       4.739  -0.956   1.125  1.00  0.00           N  
HETATM    8  C6  UNL     1       6.073  -0.516   1.255  1.00  0.00           C  
HETATM    9  C7  UNL     1       6.448   0.268   0.010  1.00  0.00           C  
HETATM   10  C8  UNL     1       7.728   0.943  -0.114  1.00  0.00           C  
HETATM   11  C9  UNL     1       9.011   0.216  -0.009  1.00  0.00           C  
HETATM   12  C10 UNL     1      10.188   1.194  -0.297  1.00  0.00           C  
HETATM   13  N2  UNL     1      10.197   2.294   0.612  1.00  0.00           N  
HETATM   14  C11 UNL     1       6.910  -1.795   1.302  1.00  0.00           C  
HETATM   15  O2  UNL     1       6.657  -2.744   0.523  1.00  0.00           O  
HETATM   16  O3  UNL     1       7.929  -1.867   2.220  1.00  0.00           O  
HETATM   17  C12 UNL     1      -0.136  -0.111  -1.016  1.00  0.00           C  
HETATM   18  C13 UNL     1      -0.095   1.424  -1.266  1.00  0.00           C  
HETATM   19  C14 UNL     1      -1.377   1.987  -0.724  1.00  0.00           C  
HETATM   20  C15 UNL     1      -2.214   0.741  -0.649  1.00  0.00           C  
HETATM   21  C16 UNL     1      -3.535   0.882  -0.075  1.00  0.00           C  
HETATM   22  C17 UNL     1      -3.722   1.949   0.960  1.00  0.00           C  
HETATM   23  C18 UNL     1      -5.085   1.794   1.633  1.00  0.00           C  
HETATM   24  C19 UNL     1      -5.978   1.083   0.694  1.00  0.00           C  
HETATM   25  C20 UNL     1      -7.437   1.018   1.109  1.00  0.00           C  
HETATM   26  C21 UNL     1      -8.207   0.626  -0.119  1.00  0.00           C  
HETATM   27  O4  UNL     1      -9.280  -0.230   0.178  1.00  0.00           O  
HETATM   28  C22 UNL     1      -7.388   0.144  -1.249  1.00  0.00           C  
HETATM   29  C23 UNL     1      -6.196  -0.698  -0.896  1.00  0.00           C  
HETATM   30  C24 UNL     1      -5.573  -0.357   0.412  1.00  0.00           C  
HETATM   31  C25 UNL     1      -6.114  -1.256   1.498  1.00  0.00           C  
HETATM   32  C26 UNL     1      -4.080  -0.414   0.460  1.00  0.00           C  
HETATM   33  C27 UNL     1      -3.429  -1.504  -0.330  1.00  0.00           C  
HETATM   34  C28 UNL     1      -1.947  -1.560   0.019  1.00  0.00           C  
HETATM   35  O5  UNL     1      -1.417  -2.555  -0.792  1.00  0.00           O  
HETATM   36  C29 UNL     1      -1.244  -0.253  -0.020  1.00  0.00           C  
HETATM   37  C30 UNL     1      -0.793   0.193   1.346  1.00  0.00           C  
HETATM   38  H1  UNL     1       2.329  -0.782  -2.488  1.00  0.00           H  
HETATM   39  H2  UNL     1       3.104   0.425  -1.441  1.00  0.00           H  
HETATM   40  H3  UNL     1       1.647   0.866  -2.331  1.00  0.00           H  
HETATM   41  H4  UNL     1       1.656   0.143   0.254  1.00  0.00           H  
HETATM   42  H5  UNL     1       1.118  -2.471   0.257  1.00  0.00           H  
HETATM   43  H6  UNL     1       1.420  -2.294  -1.576  1.00  0.00           H  
HETATM   44  H7  UNL     1       3.609  -1.463  -1.116  1.00  0.00           H  
HETATM   45  H8  UNL     1       3.352  -3.087  -0.331  1.00  0.00           H  
HETATM   46  H9  UNL     1       4.507  -0.575   2.407  1.00  0.00           H  
HETATM   47  H10 UNL     1       6.314   0.065   2.128  1.00  0.00           H  
HETATM   48  H11 UNL     1       6.393  -0.496  -0.843  1.00  0.00           H  
HETATM   49  H12 UNL     1       5.578   0.952  -0.264  1.00  0.00           H  
HETATM   50  H13 UNL     1       7.768   1.536  -1.093  1.00  0.00           H  
HETATM   51  H14 UNL     1       7.738   1.811   0.632  1.00  0.00           H  
HETATM   52  H15 UNL     1       9.179   0.021   1.094  1.00  0.00           H  
HETATM   53  H16 UNL     1       9.168  -0.644  -0.633  1.00  0.00           H  
HETATM   54  H17 UNL     1      11.092   0.577  -0.101  1.00  0.00           H  
HETATM   55  H18 UNL     1      10.166   1.457  -1.355  1.00  0.00           H  
HETATM   56  H19 UNL     1       9.570   2.187   1.421  1.00  0.00           H  
HETATM   57  H20 UNL     1      10.149   3.226   0.139  1.00  0.00           H  
HETATM   58  H21 UNL     1       8.249  -2.737   2.670  1.00  0.00           H  
HETATM   59  H22 UNL     1      -0.371  -0.634  -1.932  1.00  0.00           H  
HETATM   60  H23 UNL     1      -0.155   1.562  -2.396  1.00  0.00           H  
HETATM   61  H24 UNL     1       0.782   1.894  -0.833  1.00  0.00           H  
HETATM   62  H25 UNL     1      -1.889   2.650  -1.487  1.00  0.00           H  
HETATM   63  H26 UNL     1      -1.306   2.559   0.187  1.00  0.00           H  
HETATM   64  H27 UNL     1      -2.310   0.386  -1.715  1.00  0.00           H  
HETATM   65  H28 UNL     1      -4.245   1.158  -0.920  1.00  0.00           H  
HETATM   66  H29 UNL     1      -3.679   2.929   0.420  1.00  0.00           H  
HETATM   67  H30 UNL     1      -2.982   1.995   1.748  1.00  0.00           H  
HETATM   68  H31 UNL     1      -5.012   1.330   2.640  1.00  0.00           H  
HETATM   69  H32 UNL     1      -5.488   2.825   1.773  1.00  0.00           H  
HETATM   70  H33 UNL     1      -6.026   1.700  -0.249  1.00  0.00           H  
HETATM   71  H34 UNL     1      -7.646   0.279   1.899  1.00  0.00           H  
HETATM   72  H35 UNL     1      -7.743   2.016   1.521  1.00  0.00           H  
HETATM   73  H36 UNL     1      -8.716   1.580  -0.466  1.00  0.00           H  
HETATM   74  H37 UNL     1      -9.648  -0.584  -0.643  1.00  0.00           H  
HETATM   75  H38 UNL     1      -8.046  -0.485  -1.896  1.00  0.00           H  
HETATM   76  H39 UNL     1      -7.099   1.008  -1.930  1.00  0.00           H  
HETATM   77  H40 UNL     1      -5.414  -0.518  -1.685  1.00  0.00           H  
HETATM   78  H41 UNL     1      -6.439  -1.782  -0.973  1.00  0.00           H  
HETATM   79  H42 UNL     1      -6.013  -0.760   2.478  1.00  0.00           H  
HETATM   80  H43 UNL     1      -5.471  -2.153   1.514  1.00  0.00           H  
HETATM   81  H44 UNL     1      -7.143  -1.622   1.298  1.00  0.00           H  
HETATM   82  H45 UNL     1      -3.801  -0.576   1.526  1.00  0.00           H  
HETATM   83  H46 UNL     1      -3.858  -2.487  -0.026  1.00  0.00           H  
HETATM   84  H47 UNL     1      -3.594  -1.388  -1.412  1.00  0.00           H  
HETATM   85  H48 UNL     1      -1.946  -1.900   1.106  1.00  0.00           H  
HETATM   86  H49 UNL     1      -1.510  -3.413  -0.266  1.00  0.00           H  
HETATM   87  H50 UNL     1      -0.412   1.205   1.369  1.00  0.00           H  
HETATM   88  H51 UNL     1       0.003  -0.494   1.692  1.00  0.00           H  
HETATM   89  H52 UNL     1      -1.587   0.092   2.114  1.00  0.00           H  
CONECT    1    2   38   39   40
CONECT    2    3   17   41
CONECT    3    4   42   43
CONECT    4    5   44   45
CONECT    5    6    6    7
CONECT    7    8   46
CONECT    8    9   14   47
CONECT    9   10   48   49
CONECT   10   11   50   51
CONECT   11   12   52   53
CONECT   12   13   54   55
CONECT   13   56   57
CONECT   14   15   15   16
CONECT   16   58
CONECT   17   18   36   59
CONECT   18   19   60   61
CONECT   19   20   62   63
CONECT   20   21   36   64
CONECT   21   22   32   65
CONECT   22   23   66   67
CONECT   23   24   68   69
CONECT   24   25   30   70
CONECT   25   26   71   72
CONECT   26   27   28   73
CONECT   27   74
CONECT   28   29   75   76
CONECT   29   30   77   78
CONECT   30   31   32
CONECT   31   79   80   81
CONECT   32   33   82
CONECT   33   34   83   84
CONECT   34   35   36   85
CONECT   35   86
CONECT   36   37
CONECT   37   87   88   89
END

HMDB0242422
     RDKit          3D
Deoxycholyllysine
 89 92  0  0  0  0  0  0  0  0999 V2000
    2.1139    0.0394   -1.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2538   -0.4385   -0.5937 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5845   -1.9187   -0.5478 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0891   -2.0142   -0.3306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4687   -1.3733    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5197   -1.3206    1.7893 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7387   -0.9556    1.1247 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0734   -0.5164    1.2552 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4479    0.2680    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7276    0.9430   -0.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0107    0.2164   -0.0093 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1884    1.1936   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1973    2.2941    0.6124 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9099   -1.7952    1.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6568   -2.7442    0.5232 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9287   -1.8671    2.2205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1360   -0.1108   -1.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0953    1.4235   -1.2655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3771    1.9866   -0.7236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2140    0.7413   -0.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5354    0.8822   -0.0753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7222    1.9490    0.9603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0854    1.7940    1.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9782    1.0830    0.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4374    1.0178    1.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2071    0.6264   -0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2799   -0.2298    0.1784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3877    0.1443   -1.2489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1962   -0.6979   -0.8963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5733   -0.3573    0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1140   -1.2557    1.4975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0803   -0.4143    0.4599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4287   -1.5040   -0.3302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9474   -1.5600    0.0193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4165   -2.5546   -0.7919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2444   -0.2532   -0.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925    0.1927    1.3458 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3294   -0.7822   -2.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1036    0.4246   -1.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6472    0.8656   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6561    0.1435    0.2536 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1176   -2.4710    0.2570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4198   -2.2944   -1.5760 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6087   -1.4630   -1.1157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3521   -3.0874   -0.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5067   -0.5754    2.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3137    0.0650    2.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3931   -0.4959   -0.8432 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5777    0.9516   -0.2644 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7683    1.5355   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7384    1.8106    0.6317 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1790    0.0213    1.0939 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1681   -0.6438   -0.6329 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0918    0.5767   -0.1007 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1664    1.4574   -1.3553 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5704    2.1871    1.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1489    3.2262    0.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2487   -2.7375    2.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3713   -0.6337   -1.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1549    1.5616   -2.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7816    1.8943   -0.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8893    2.6503   -1.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3063    2.5592    0.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3101    0.3863   -1.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2446    1.1575   -0.9203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6793    2.9291    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9819    1.9946    1.7483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0121    1.3301    2.6401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4880    2.8246    1.7734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0256    1.6996   -0.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6458    0.2791    1.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7432    2.0160    1.5208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7161    1.5798   -0.4662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6483   -0.5843   -0.6430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0462   -0.4852   -1.8956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0993    1.0081   -1.9303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4140   -0.5181   -1.6851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4386   -1.7820   -0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0133   -0.7599    2.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4706   -2.1528    1.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1427   -1.6215    1.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8013   -0.5757    1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8584   -2.4869   -0.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5943   -1.3885   -1.4123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9465   -1.8997    1.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5102   -3.4134   -0.2662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4121    1.2049    1.3690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0035   -0.4935    1.6921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5867    0.0916    2.1143 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  1  0
 11 12  1  0
 12 13  1  0
  8 14  1  0
 14 15  2  0
 14 16  1  0
  2 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  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 17  1  0
 36 20  1  0
 32 21  1  0
 30 24  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  2 41  1  0
  3 42  1  0
  3 43  1  0
  4 44  1  0
  4 45  1  0
  7 46  1  0
  8 47  1  0
  9 48  1  0
  9 49  1  0
 10 50  1  0
 10 51  1  0
 11 52  1  0
 11 53  1  0
 12 54  1  0
 12 55  1  0
 13 56  1  0
 13 57  1  0
 16 58  1  0
 17 59  1  0
 18 60  1  0
 18 61  1  0
 19 62  1  0
 19 63  1  0
 20 64  1  0
 21 65  1  0
 22 66  1  0
 22 67  1  0
 23 68  1  0
 23 69  1  0
 24 70  1  0
 25 71  1  0
 25 72  1  0
 26 73  1  0
 27 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  1  0
 32 82  1  0
 33 83  1  0
 33 84  1  0
 34 85  1  0
 35 86  1  0
 37 87  1  0
 37 88  1  0
 37 89  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
6-Amino-2-[(4-{5,16-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0,.0,]heptadecan-14-yl}-1-hydroxypentylidene)amino]hexanoate	HMDB

Chemical Formula

C₃₀H₅₂N₂O₅

Average Molecular Weight

520.755

Monoisotopic Molecular Weight

520.387622782

IUPAC Name

6-amino-2-(4-{5,16-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl}pentanamido)hexanoic acid

Traditional Name

6-amino-2-(4-{5,16-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl}pentanamido)hexanoic acid

CAS Registry Number

Not Available

SMILES

CC(CCC(=O)NC(CCCCN)C(O)=O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C

InChI Identifier

InChI=1S/C30H52N2O5/c1-18(7-12-27(35)32-25(28(36)37)6-4-5-15-31)22-10-11-23-21-9-8-19-16-20(33)13-14-29(19,2)24(21)17-26(34)30(22,23)3/h18-26,33-34H,4-17,31H2,1-3H3,(H,32,35)(H,36,37)

InChI Key

NQGPNQJTMGFHLB-UHFFFAOYSA-N

Chemical Taxonomy

Classification

Not classified

Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

State

Not Available

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

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	0.34	ALOGPS
logP	0.86	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	3.68	ChemAxon
pKa (Strongest Basic)	10.21	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	132.88 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	143.81 m³·mol⁻¹	ChemAxon
Polarizability	61.42 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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
DeepCCS	[M-2H]-	250.364	30932474
DeepCCS	[M+Na]+	225.592	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Deoxycholyllysine	CC(CCC(=O)NC(CCCCN)C(O)=O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C	3291.9	Standard polar	33892256
Deoxycholyllysine	CC(CCC(=O)NC(CCCCN)C(O)=O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C	3377.6	Standard non polar	33892256
Deoxycholyllysine	CC(CCC(=O)NC(CCCCN)C(O)=O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C	4456.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Deoxycholyllysine,4TMS,isomer #1	CC(CCC(=O)NC(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4268.5	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #1	CC(CCC(=O)NC(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4251.3	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #1	CC(CCC(=O)NC(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4724.1	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #10	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4643.4	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #10	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4451.9	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #10	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	5054.3	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #11	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4579.5	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #11	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4432.4	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #11	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4947.3	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #2	CC(CCC(=O)N(C(CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4191.8	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #2	CC(CCC(=O)N(C(CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4208.7	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #2	CC(CCC(=O)N(C(CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4929.9	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #3	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4376.9	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #3	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4374.5	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #3	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4914.1	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #4	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4608.8	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #4	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4434.2	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #4	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4960.0	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #5	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4326.6	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #5	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4358.7	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #5	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4797.6	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #6	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4539.8	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #6	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4415.7	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #6	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4845.3	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #7	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C	4645.4	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #7	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C	4541.9	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #7	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C	5035.4	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #8	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4297.6	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #8	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4267.2	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #8	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4823.4	Standard polar	33892256
Deoxycholyllysine,4TMS,isomer #9	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4576.4	Semi standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #9	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4319.4	Standard non polar	33892256
Deoxycholyllysine,4TMS,isomer #9	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4883.3	Standard polar	33892256
Deoxycholyllysine,5TMS,isomer #1	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4209.8	Semi standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #1	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4296.2	Standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #1	CC(CCC(=O)N(C(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4614.4	Standard polar	33892256
Deoxycholyllysine,5TMS,isomer #2	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4428.5	Semi standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #2	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4356.8	Standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #2	CC(CCC(=O)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4651.5	Standard polar	33892256
Deoxycholyllysine,5TMS,isomer #3	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4552.9	Semi standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #3	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4482.4	Standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #3	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C	4847.8	Standard polar	33892256
Deoxycholyllysine,5TMS,isomer #4	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4515.1	Semi standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #4	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4476.4	Standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #4	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4732.4	Standard polar	33892256
Deoxycholyllysine,5TMS,isomer #5	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4474.1	Semi standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #5	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4370.1	Standard non polar	33892256
Deoxycholyllysine,5TMS,isomer #5	CC(CCC(=O)N(C(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C	4759.9	Standard polar	33892256

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Deoxycholyllysine 10V, Positive-QTOF	splash10-0fk9-0000490000-071017fb41801241f665	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Deoxycholyllysine 20V, Positive-QTOF	splash10-001i-5905850000-d5017095b896d6c02a47	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Deoxycholyllysine 40V, Positive-QTOF	splash10-0532-9401000000-8afa7287a9fdafefcf70	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Deoxycholyllysine 10V, Negative-QTOF	splash10-014i-0000090000-afc030cd5304f761b25f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Deoxycholyllysine 20V, Negative-QTOF	splash10-014i-2201090000-372677ab317bae27b125	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Deoxycholyllysine 40V, Negative-QTOF	splash10-00kf-8406940000-aed5eed5b6614bb85413	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Intestine

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

85794040

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Guzior DV, Quinn RA: Review: microbial transformations of human bile acids. Microbiome. 2021 Jun 14;9(1):140. doi: 10.1186/s40168-021-01101-1. [PubMed:34127070 ]
Quinn RA, Melnik AV, Vrbanac A, Fu T, Patras KA, Christy MP, Bodai Z, Belda-Ferre P, Tripathi A, Chung LK, Downes M, Welch RD, Quinn M, Humphrey G, Panitchpakdi M, Weldon KC, Aksenov A, da Silva R, Avila-Pacheco J, Clish C, Bae S, Mallick H, Franzosa EA, Lloyd-Price J, Bussell R, Thron T, Nelson AT, Wang M, Leszczynski E, Vargas F, Gauglitz JM, Meehan MJ, Gentry E, Arthur TD, Komor AC, Poulsen O, Boland BS, Chang JT, Sandborn WJ, Lim M, Garg N, Lumeng JC, Xavier RJ, Kazmierczak BI, Jain R, Egan M, Rhee KE, Ferguson D, Raffatellu M, Vlamakis H, Haddad GG, Siegel D, Huttenhower C, Mazmanian SK, Evans RM, Nizet V, Knight R, Dorrestein PC: Global chemical effects of the microbiome include new bile-acid conjugations. Nature. 2020 Mar;579(7797):123-129. doi: 10.1038/s41586-020-2047-9. Epub 2020 Feb 26. [PubMed:32103176 ]

Showing metabocard for Deoxycholyllysine (HMDB0242422)

MOL for HMDB0242422 (Deoxycholyllysine)

3D MOL for HMDB0242422 (Deoxycholyllysine)

3D SDF for HMDB0242422 (Deoxycholyllysine)

3D-SDF for HMDB0242422 (Deoxycholyllysine)

PDB for HMDB0242422 (Deoxycholyllysine)

3D PDB for HMDB0242422 (Deoxycholyllysine)

SMILES for HMDB0242422 (Deoxycholyllysine)

INCHI for HMDB0242422 (Deoxycholyllysine)

Structure for HMDB0242422 (Deoxycholyllysine)

3D Structure for HMDB0242422 (Deoxycholyllysine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

MS/MS Spectra