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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 20:46:01 UTC

Update Date

2021-09-26 23:16:10 UTC

HMDB ID

HMDB0258926

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Tetranorprostanedioic acid

Description

Tetranorprostanedioic acid belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. Based on a literature review a small amount of articles have been published on Tetranorprostanedioic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). Tetranorprostanedioic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Tetranorprostanedioic acid is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0258926
     RDKit          3D
Tetranorprostanedioic acid
 48 48  0  0  0  0  0  0  0  0999 V2000
    7.2880   -2.2074   -0.2977 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8637   -1.0556   -0.4973 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7019   -0.0482   -0.9113 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4152   -0.7838   -0.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0787    0.6482   -0.5601 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6225    0.9372   -0.3586 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1644    0.6761    1.0502 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6880    1.0026    1.1981 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8145    0.1735    0.2832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6163    0.5951    0.5408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6122   -0.1421   -0.2971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6029   -1.6303   -0.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9716   -1.9906    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3129   -0.7003    1.2094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9956    0.3315    0.1768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9714    0.3656   -0.9624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2986    0.8312   -0.4597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3363    0.9095   -1.4812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3735    1.8743   -2.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2970   -0.0760   -1.5932 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3637    0.3260   -0.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8315   -1.4204   -0.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1247   -1.0456    0.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7095    1.3528    0.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2912    0.8313   -1.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4747    2.0140   -0.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0626    0.3041   -1.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3880   -0.3385    1.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7413    1.3732    1.7052 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5836    2.0784    0.9870 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4202    0.8652    2.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9083   -0.9061    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0791    0.3446   -0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6744    1.6717    0.2233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9018    0.5003    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5413    0.1292   -1.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8568   -1.9418    0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4742   -2.1819   -1.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8708   -2.8434    1.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7038   -2.2344   -0.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5513   -0.6178    2.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3167   -0.6878    1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9267    1.3395    0.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0248   -0.6133   -1.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5499    1.0921   -1.7163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6420    0.1418    0.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1111    1.8265    0.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0815   -1.0699   -1.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  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
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 15 11  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 20 48  1  0
M  END


  Mrv1652309112122462D          

 20 20  0  0  0  0            999 V2000
   -0.3369    4.8682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1608    4.2103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3112    3.5336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1006    3.7733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1165    4.5982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7585    3.2756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5185    3.5966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1765    3.0988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9365    3.4198    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0744    2.2802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0411    2.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5812    2.1304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3112    1.3509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4990    1.1949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0391    1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8492    1.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3893    2.2863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1994    2.1304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7395    2.7540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4695    1.3509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  3 11  1  0  0  0  0
 11 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  2  0  0  0  0
 18 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0258926

> <DATABASE_NAME>
hmdb

> <SMILES>
OC(=O)CCCCCCCC1CCCC1CCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H28O4/c17-15(18)10-5-3-1-2-4-7-13-8-6-9-14(13)11-12-16(19)20/h13-14H,1-12H2,(H,17,18)(H,19,20)

> <INCHI_KEY>
VDSTWEBFEFGHLI-UHFFFAOYSA-N

> <FORMULA>
C16H28O4

> <MOLECULAR_WEIGHT>
284.396

> <EXACT_MASS>
284.198759382

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
33.74524361153824

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-[2-(2-carboxyethyl)cyclopentyl]octanoic acid

> <ALOGPS_LOGP>
3.54

> <JCHEM_LOGP>
4.157515972666666

> <ALOGPS_LOGS>
-4.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.133229646675524

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.5087121705101465

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
76.84199999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.41e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-[2-(2-carboxyethyl)cyclopentyl]octanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0258926
     RDKit          3D
Tetranorprostanedioic acid
 48 48  0  0  0  0  0  0  0  0999 V2000
    7.2880   -2.2074   -0.2977 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8637   -1.0556   -0.4973 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7019   -0.0482   -0.9113 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4152   -0.7838   -0.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0787    0.6482   -0.5601 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6225    0.9372   -0.3586 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1644    0.6761    1.0502 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6880    1.0026    1.1981 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8145    0.1735    0.2832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6163    0.5951    0.5408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6122   -0.1421   -0.2971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6029   -1.6303   -0.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9716   -1.9906    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3129   -0.7003    1.2094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9956    0.3315    0.1768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9714    0.3656   -0.9624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2986    0.8312   -0.4597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3363    0.9095   -1.4812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3735    1.8743   -2.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2970   -0.0760   -1.5932 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3637    0.3260   -0.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8315   -1.4204   -0.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1247   -1.0456    0.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7095    1.3528    0.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2912    0.8313   -1.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4747    2.0140   -0.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0626    0.3041   -1.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3880   -0.3385    1.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7413    1.3732    1.7052 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5836    2.0784    0.9870 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4202    0.8652    2.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9083   -0.9061    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0791    0.3446   -0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6744    1.6717    0.2233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9018    0.5003    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5413    0.1292   -1.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8568   -1.9418    0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4742   -2.1819   -1.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8708   -2.8434    1.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7038   -2.2344   -0.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5513   -0.6178    2.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3167   -0.6878    1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9267    1.3395    0.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0248   -0.6133   -1.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5499    1.0921   -1.7163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6420    0.1418    0.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1111    1.8265    0.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0815   -1.0699   -1.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  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
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 15 11  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 20 48  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -0.629   9.087   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.300   7.859   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.581   6.596   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.054   7.044   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.084   8.583   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.283   6.114   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.701   6.714   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.929   5.784   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -7.348   6.384   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -5.739   4.256   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.077   5.141   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.085   3.977   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.581   2.522   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.931   2.231   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.940   3.395   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.452   3.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.460   4.268   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.972   3.977   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.980   5.141   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       6.476   2.522   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   11                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    3   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   40    0
END

COMPND    HMDB0258926
HETATM    1  O1  UNL     1       7.288  -2.207  -0.298  1.00  0.00           O  
HETATM    2  C1  UNL     1       6.864  -1.056  -0.497  1.00  0.00           C  
HETATM    3  O2  UNL     1       7.702  -0.048  -0.911  1.00  0.00           O  
HETATM    4  C2  UNL     1       5.415  -0.784  -0.278  1.00  0.00           C  
HETATM    5  C3  UNL     1       5.079   0.648  -0.560  1.00  0.00           C  
HETATM    6  C4  UNL     1       3.623   0.937  -0.359  1.00  0.00           C  
HETATM    7  C5  UNL     1       3.164   0.676   1.050  1.00  0.00           C  
HETATM    8  C6  UNL     1       1.688   1.003   1.198  1.00  0.00           C  
HETATM    9  C7  UNL     1       0.814   0.174   0.283  1.00  0.00           C  
HETATM   10  C8  UNL     1      -0.616   0.595   0.541  1.00  0.00           C  
HETATM   11  C9  UNL     1      -1.612  -0.142  -0.297  1.00  0.00           C  
HETATM   12  C10 UNL     1      -1.603  -1.630  -0.090  1.00  0.00           C  
HETATM   13  C11 UNL     1      -2.972  -1.991   0.471  1.00  0.00           C  
HETATM   14  C12 UNL     1      -3.313  -0.700   1.209  1.00  0.00           C  
HETATM   15  C13 UNL     1      -2.996   0.332   0.177  1.00  0.00           C  
HETATM   16  C14 UNL     1      -3.971   0.366  -0.962  1.00  0.00           C  
HETATM   17  C15 UNL     1      -5.299   0.831  -0.460  1.00  0.00           C  
HETATM   18  C16 UNL     1      -6.336   0.909  -1.481  1.00  0.00           C  
HETATM   19  O3  UNL     1      -6.373   1.874  -2.276  1.00  0.00           O  
HETATM   20  O4  UNL     1      -7.297  -0.076  -1.593  1.00  0.00           O  
HETATM   21  H1  UNL     1       8.364   0.326  -0.243  1.00  0.00           H  
HETATM   22  H2  UNL     1       4.832  -1.420  -0.972  1.00  0.00           H  
HETATM   23  H3  UNL     1       5.125  -1.046   0.776  1.00  0.00           H  
HETATM   24  H4  UNL     1       5.709   1.353   0.023  1.00  0.00           H  
HETATM   25  H5  UNL     1       5.291   0.831  -1.656  1.00  0.00           H  
HETATM   26  H6  UNL     1       3.475   2.014  -0.582  1.00  0.00           H  
HETATM   27  H7  UNL     1       3.063   0.304  -1.093  1.00  0.00           H  
HETATM   28  H8  UNL     1       3.388  -0.339   1.427  1.00  0.00           H  
HETATM   29  H9  UNL     1       3.741   1.373   1.705  1.00  0.00           H  
HETATM   30  H10 UNL     1       1.584   2.078   0.987  1.00  0.00           H  
HETATM   31  H11 UNL     1       1.420   0.865   2.262  1.00  0.00           H  
HETATM   32  H12 UNL     1       0.908  -0.906   0.489  1.00  0.00           H  
HETATM   33  H13 UNL     1       1.079   0.345  -0.768  1.00  0.00           H  
HETATM   34  H14 UNL     1      -0.674   1.672   0.223  1.00  0.00           H  
HETATM   35  H15 UNL     1      -0.902   0.500   1.598  1.00  0.00           H  
HETATM   36  H16 UNL     1      -1.541   0.129  -1.385  1.00  0.00           H  
HETATM   37  H17 UNL     1      -0.857  -1.942   0.673  1.00  0.00           H  
HETATM   38  H18 UNL     1      -1.474  -2.182  -1.054  1.00  0.00           H  
HETATM   39  H19 UNL     1      -2.871  -2.843   1.172  1.00  0.00           H  
HETATM   40  H20 UNL     1      -3.704  -2.234  -0.296  1.00  0.00           H  
HETATM   41  H21 UNL     1      -2.551  -0.618   2.022  1.00  0.00           H  
HETATM   42  H22 UNL     1      -4.317  -0.688   1.622  1.00  0.00           H  
HETATM   43  H23 UNL     1      -2.927   1.340   0.627  1.00  0.00           H  
HETATM   44  H24 UNL     1      -4.025  -0.613  -1.487  1.00  0.00           H  
HETATM   45  H25 UNL     1      -3.550   1.092  -1.716  1.00  0.00           H  
HETATM   46  H26 UNL     1      -5.642   0.142   0.338  1.00  0.00           H  
HETATM   47  H27 UNL     1      -5.111   1.826   0.040  1.00  0.00           H  
HETATM   48  H28 UNL     1      -7.081  -1.070  -1.620  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   21
CONECT    4    5   22   23
CONECT    5    6   24   25
CONECT    6    7   26   27
CONECT    7    8   28   29
CONECT    8    9   30   31
CONECT    9   10   32   33
CONECT   10   11   34   35
CONECT   11   12   15   36
CONECT   12   13   37   38
CONECT   13   14   39   40
CONECT   14   15   41   42
CONECT   15   16   43
CONECT   16   17   44   45
CONECT   17   18   46   47
CONECT   18   19   19   20
CONECT   20   48
END

HMDB0258926
     RDKit          3D
Tetranorprostanedioic acid
 48 48  0  0  0  0  0  0  0  0999 V2000
    7.2880   -2.2074   -0.2977 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8637   -1.0556   -0.4973 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7019   -0.0482   -0.9113 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4152   -0.7838   -0.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0787    0.6482   -0.5601 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6225    0.9372   -0.3586 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1644    0.6761    1.0502 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6880    1.0026    1.1981 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8145    0.1735    0.2832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6163    0.5951    0.5408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6122   -0.1421   -0.2971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6029   -1.6303   -0.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9716   -1.9906    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3129   -0.7003    1.2094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9956    0.3315    0.1768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9714    0.3656   -0.9624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2986    0.8312   -0.4597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3363    0.9095   -1.4812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3735    1.8743   -2.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2970   -0.0760   -1.5932 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3637    0.3260   -0.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8315   -1.4204   -0.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1247   -1.0456    0.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7095    1.3528    0.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2912    0.8313   -1.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4747    2.0140   -0.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0626    0.3041   -1.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3880   -0.3385    1.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7413    1.3732    1.7052 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5836    2.0784    0.9870 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4202    0.8652    2.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9083   -0.9061    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0791    0.3446   -0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6744    1.6717    0.2233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9018    0.5003    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5413    0.1292   -1.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8568   -1.9418    0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4742   -2.1819   -1.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8708   -2.8434    1.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7038   -2.2344   -0.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5513   -0.6178    2.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3167   -0.6878    1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9267    1.3395    0.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0248   -0.6133   -1.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5499    1.0921   -1.7163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6420    0.1418    0.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1111    1.8265    0.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0815   -1.0699   -1.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  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
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 15 11  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 20 48  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Tetranorprostanedioate	Generator
8-[2-(2-Carboxyethyl)cyclopentyl]octanoate	HMDB

Chemical Formula

C₁₆H₂₈O₄

Average Molecular Weight

284.396

Monoisotopic Molecular Weight

284.198759382

IUPAC Name

8-[2-(2-carboxyethyl)cyclopentyl]octanoic acid

Traditional Name

8-[2-(2-carboxyethyl)cyclopentyl]octanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CCCCCCCC1CCCC1CCC(O)=O

InChI Identifier

InChI=1S/C16H28O4/c17-15(18)10-5-3-1-2-4-7-13-8-6-9-14(13)11-12-16(19)20/h13-14H,1-12H2,(H,17,18)(H,19,20)

InChI Key

VDSTWEBFEFGHLI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
Dicarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

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	3.54	ALOGPS
logP	4.16	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	4.51	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	76.84 m³·mol⁻¹	ChemAxon
Polarizability	33.75 Å³	ChemAxon
Number of Rings	1	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+H]+	163.036	30932474
DeepCCS	[M-H]-	160.11	30932474
DeepCCS	[M-2H]-	196.796	30932474
DeepCCS	[M+Na]+	172.46	30932474
AllCCS	[M+H]+	170.9	32859911
AllCCS	[M+H-H2O]+	167.9	32859911
AllCCS	[M+NH4]+	173.7	32859911
AllCCS	[M+Na]+	174.5	32859911
AllCCS	[M-H]-	175.3	32859911
AllCCS	[M+Na-2H]-	176.1	32859911
AllCCS	[M+HCOO]-	177.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tetranorprostanedioic acid	OC(=O)CCCCCCCC1CCCC1CCC(O)=O	3530.5	Standard polar	33892256
Tetranorprostanedioic acid	OC(=O)CCCCCCCC1CCCC1CCC(O)=O	2172.1	Standard non polar	33892256
Tetranorprostanedioic acid	OC(=O)CCCCCCCC1CCCC1CCC(O)=O	2363.9	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 - Tetranorprostanedioic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-06vu-2980000000-5764ed9c702b39239c86	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetranorprostanedioic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetranorprostanedioic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetranorprostanedioic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetranorprostanedioic acid GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetranorprostanedioic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetranorprostanedioic acid GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetranorprostanedioic acid GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

28573220

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73753562

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Tetranorprostanedioic acid (HMDB0258926)

MOL for HMDB0258926 (Tetranorprostanedioic acid)

3D MOL for HMDB0258926 (Tetranorprostanedioic acid)

3D SDF for HMDB0258926 (Tetranorprostanedioic acid)

3D-SDF for HMDB0258926 (Tetranorprostanedioic acid)

PDB for HMDB0258926 (Tetranorprostanedioic acid)

3D PDB for HMDB0258926 (Tetranorprostanedioic acid)

SMILES for HMDB0258926 (Tetranorprostanedioic acid)

INCHI for HMDB0258926 (Tetranorprostanedioic acid)

Structure for HMDB0258926 (Tetranorprostanedioic acid)

3D Structure for HMDB0258926 (Tetranorprostanedioic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra