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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 21:39:30 UTC

Update Date

2021-09-26 22:52:17 UTC

HMDB ID

HMDB0244503

Secondary Accession Numbers

None

Metabolite Identification

Common Name

13-Azaprostanoic acid

Description

7-[2-(heptylamino)cyclopentyl]heptanoic 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 very few articles have been published on 7-[2-(heptylamino)cyclopentyl]heptanoic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). 13-azaprostanoic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 13-Azaprostanoic 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

HMDB0244503
     RDKit          3D
13-Azaprostanoic acid
 59 59  0  0  0  0  0  0  0  0999 V2000
    8.6525    0.3515   -1.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2281   -0.2076   -1.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3740    0.8508   -0.4620 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9172    0.4519   -0.3323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1928    1.5989    0.2968 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    1.3847    0.5018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4414    0.2101    1.4113 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0554   -0.0153    1.6191 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3417   -0.4773    0.4680 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7830   -1.8085   -0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1598   -2.7435    0.7283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4848   -1.9765    0.7257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620   -0.5182    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8627    0.2628   -0.3251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3200    0.4344   -0.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1230   -0.8024   -0.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6269   -0.5083   -0.3273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0710    0.2543    0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5716    0.4791    0.7524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8260    1.2313   -0.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0502    0.6491   -1.5716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8284    2.6316   -0.4966 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9302    0.7565   -0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6996    1.1813   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3108   -0.4567   -1.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8963   -0.4381   -2.1254 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1950   -1.1185   -0.4671 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7523    1.0740    0.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3880    1.7867   -1.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4740    0.2879   -1.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7941   -0.4830    0.2269 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6967    1.9409    1.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2987    2.4809   -0.3942 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3140    2.3208    0.9268 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2958    1.1592   -0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9326   -0.6793    0.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9252    0.3762    2.4045 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7741   -0.4487    2.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4854    0.2398   -0.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6448   -1.9405   -1.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7975   -2.1254    0.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1313   -2.9453    1.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2258   -3.6742    0.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9952   -2.3235   -0.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0699   -2.2323    1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3982   -0.0590    1.7141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3936    1.3082   -0.2862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5690   -0.0733   -1.3672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6548    1.0353    0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5958    1.0195   -1.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972   -1.4883    0.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8886   -1.3814   -1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2042   -1.4610   -0.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8362    0.0102   -1.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6343    1.2658    0.9622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8162   -0.2933    1.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1218   -0.4913    0.7742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8712    1.0964    1.6378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0906    3.0406   -1.0916 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  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  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 13  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 16 51  1  0
 16 52  1  0
 17 53  1  0
 17 54  1  0
 18 55  1  0
 18 56  1  0
 19 57  1  0
 19 58  1  0
 22 59  1  0
M  END


  Mrv1652309102123392D          

 22 22  0  0  0  0            999 V2000
   -3.1982   -3.7582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4136   -3.5033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2420   -2.6963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4574   -2.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2859   -1.6344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5013   -1.3794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3298   -0.5725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4549   -0.3175    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6264    0.4894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0744    1.1025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4869    1.8170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2938    1.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3801    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0945    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8090    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5235    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2380    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6669    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3814    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0958    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3814   -0.4125    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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 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  2  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0244503

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCNC1CCCC1CCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H37NO2/c1-2-3-4-7-10-16-20-18-14-11-13-17(18)12-8-5-6-9-15-19(21)22/h17-18,20H,2-16H2,1H3,(H,21,22)

> <INCHI_KEY>
RZZNGDIYQSCFGK-UHFFFAOYSA-N

> <FORMULA>
C19H37NO2

> <MOLECULAR_WEIGHT>
311.51

> <EXACT_MASS>
311.282429435

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
40.28212471422702

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-[2-(heptylamino)cyclopentyl]heptanoic acid

> <ALOGPS_LOGP>
4.24

> <JCHEM_LOGP>
3.0596626721660587

> <ALOGPS_LOGS>
-5.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.311031571569964

> <JCHEM_PKA_STRONGEST_BASIC>
11.029020066079644

> <JCHEM_POLAR_SURFACE_AREA>
49.33

> <JCHEM_REFRACTIVITY>
92.52619999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.55e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-[2-(heptylamino)cyclopentyl]heptanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0244503
     RDKit          3D
13-Azaprostanoic acid
 59 59  0  0  0  0  0  0  0  0999 V2000
    8.6525    0.3515   -1.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2281   -0.2076   -1.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3740    0.8508   -0.4620 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9172    0.4519   -0.3323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1928    1.5989    0.2968 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    1.3847    0.5018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4414    0.2101    1.4113 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0554   -0.0153    1.6191 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3417   -0.4773    0.4680 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7830   -1.8085   -0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1598   -2.7435    0.7283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4848   -1.9765    0.7257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620   -0.5182    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8627    0.2628   -0.3251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3200    0.4344   -0.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1230   -0.8024   -0.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6269   -0.5083   -0.3273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0710    0.2543    0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5716    0.4791    0.7524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8260    1.2313   -0.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0502    0.6491   -1.5716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8284    2.6316   -0.4966 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9302    0.7565   -0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6996    1.1813   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3108   -0.4567   -1.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8963   -0.4381   -2.1254 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1950   -1.1185   -0.4671 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7523    1.0740    0.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3880    1.7867   -1.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4740    0.2879   -1.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7941   -0.4830    0.2269 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6967    1.9409    1.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2987    2.4809   -0.3942 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3140    2.3208    0.9268 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2958    1.1592   -0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9326   -0.6793    0.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9252    0.3762    2.4045 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7741   -0.4487    2.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4854    0.2398   -0.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6448   -1.9405   -1.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7975   -2.1254    0.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1313   -2.9453    1.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2258   -3.6742    0.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9952   -2.3235   -0.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0699   -2.2323    1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3982   -0.0590    1.7141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3936    1.3082   -0.2862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5690   -0.0733   -1.3672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6548    1.0353    0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5958    1.0195   -1.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972   -1.4883    0.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8886   -1.3814   -1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2042   -1.4610   -0.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8362    0.0102   -1.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6343    1.2658    0.9622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8162   -0.2933    1.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1218   -0.4913    0.7742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8712    1.0964    1.6378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0906    3.0406   -1.0916 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  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  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 13  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 16 51  1  0
 16 52  1  0
 17 53  1  0
 17 54  1  0
 18 55  1  0
 18 56  1  0
 19 57  1  0
 19 58  1  0
 22 59  1  0
M  END

HEADER    PROTEIN                                 10-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-21         0                                  
HETATM    1  C   UNK     0      -5.970  -7.015   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.505  -6.539   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.185  -5.033   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.721  -4.557   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.400  -3.051   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.936  -2.575   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.616  -1.069   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       0.849  -0.593   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       1.169   0.914   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.139   2.058   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.909   3.392   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.415   3.072   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.576   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.910   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.243   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.577   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.911   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.245   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.578   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.912   0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      13.246   1.540   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      11.912  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

COMPND    HMDB0244503
HETATM    1  C1  UNL     1       8.652   0.351  -1.137  1.00  0.00           C  
HETATM    2  C2  UNL     1       7.228  -0.208  -1.085  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.374   0.851  -0.462  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.917   0.452  -0.332  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.193   1.599   0.297  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.726   1.385   0.502  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.441   0.210   1.411  1.00  0.00           C  
HETATM    8  N1  UNL     1       1.055  -0.015   1.619  1.00  0.00           N  
HETATM    9  C8  UNL     1       0.342  -0.477   0.468  1.00  0.00           C  
HETATM   10  C9  UNL     1       0.783  -1.809  -0.017  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.160  -2.743   0.728  1.00  0.00           C  
HETATM   12  C11 UNL     1      -1.485  -1.976   0.726  1.00  0.00           C  
HETATM   13  C12 UNL     1      -1.162  -0.518   0.720  1.00  0.00           C  
HETATM   14  C13 UNL     1      -1.863   0.263  -0.325  1.00  0.00           C  
HETATM   15  C14 UNL     1      -3.320   0.434  -0.280  1.00  0.00           C  
HETATM   16  C15 UNL     1      -4.123  -0.802  -0.322  1.00  0.00           C  
HETATM   17  C16 UNL     1      -5.627  -0.508  -0.327  1.00  0.00           C  
HETATM   18  C17 UNL     1      -6.071   0.254   0.867  1.00  0.00           C  
HETATM   19  C18 UNL     1      -7.572   0.479   0.752  1.00  0.00           C  
HETATM   20  C19 UNL     1      -7.826   1.231  -0.483  1.00  0.00           C  
HETATM   21  O1  UNL     1      -8.050   0.649  -1.572  1.00  0.00           O  
HETATM   22  O2  UNL     1      -7.828   2.632  -0.497  1.00  0.00           O  
HETATM   23  H1  UNL     1       8.930   0.757  -0.146  1.00  0.00           H  
HETATM   24  H2  UNL     1       8.700   1.181  -1.869  1.00  0.00           H  
HETATM   25  H3  UNL     1       9.311  -0.457  -1.498  1.00  0.00           H  
HETATM   26  H4  UNL     1       6.896  -0.438  -2.125  1.00  0.00           H  
HETATM   27  H5  UNL     1       7.195  -1.118  -0.467  1.00  0.00           H  
HETATM   28  H6  UNL     1       6.752   1.074   0.552  1.00  0.00           H  
HETATM   29  H7  UNL     1       6.388   1.787  -1.068  1.00  0.00           H  
HETATM   30  H8  UNL     1       4.474   0.288  -1.346  1.00  0.00           H  
HETATM   31  H9  UNL     1       4.794  -0.483   0.227  1.00  0.00           H  
HETATM   32  H10 UNL     1       4.697   1.941   1.237  1.00  0.00           H  
HETATM   33  H11 UNL     1       4.299   2.481  -0.394  1.00  0.00           H  
HETATM   34  H12 UNL     1       2.314   2.321   0.927  1.00  0.00           H  
HETATM   35  H13 UNL     1       2.296   1.159  -0.516  1.00  0.00           H  
HETATM   36  H14 UNL     1       2.933  -0.679   0.995  1.00  0.00           H  
HETATM   37  H15 UNL     1       2.925   0.376   2.404  1.00  0.00           H  
HETATM   38  H16 UNL     1       0.774  -0.449   2.502  1.00  0.00           H  
HETATM   39  H17 UNL     1       0.485   0.240  -0.393  1.00  0.00           H  
HETATM   40  H18 UNL     1       0.645  -1.940  -1.111  1.00  0.00           H  
HETATM   41  H19 UNL     1       1.797  -2.125   0.250  1.00  0.00           H  
HETATM   42  H20 UNL     1       0.131  -2.945   1.756  1.00  0.00           H  
HETATM   43  H21 UNL     1      -0.226  -3.674   0.142  1.00  0.00           H  
HETATM   44  H22 UNL     1      -1.995  -2.323  -0.199  1.00  0.00           H  
HETATM   45  H23 UNL     1      -2.070  -2.232   1.628  1.00  0.00           H  
HETATM   46  H24 UNL     1      -1.398  -0.059   1.714  1.00  0.00           H  
HETATM   47  H25 UNL     1      -1.394   1.308  -0.286  1.00  0.00           H  
HETATM   48  H26 UNL     1      -1.569  -0.073  -1.367  1.00  0.00           H  
HETATM   49  H27 UNL     1      -3.655   1.035   0.611  1.00  0.00           H  
HETATM   50  H28 UNL     1      -3.596   1.019  -1.223  1.00  0.00           H  
HETATM   51  H29 UNL     1      -3.997  -1.488   0.544  1.00  0.00           H  
HETATM   52  H30 UNL     1      -3.889  -1.381  -1.236  1.00  0.00           H  
HETATM   53  H31 UNL     1      -6.204  -1.461  -0.351  1.00  0.00           H  
HETATM   54  H32 UNL     1      -5.836   0.010  -1.283  1.00  0.00           H  
HETATM   55  H33 UNL     1      -5.634   1.266   0.962  1.00  0.00           H  
HETATM   56  H34 UNL     1      -5.816  -0.293   1.789  1.00  0.00           H  
HETATM   57  H35 UNL     1      -8.122  -0.491   0.774  1.00  0.00           H  
HETATM   58  H36 UNL     1      -7.871   1.096   1.638  1.00  0.00           H  
HETATM   59  H37 UNL     1      -7.091   3.041  -1.092  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3   26   27
CONECT    3    4   28   29
CONECT    4    5   30   31
CONECT    5    6   32   33
CONECT    6    7   34   35
CONECT    7    8   36   37
CONECT    8    9   38
CONECT    9   10   13   39
CONECT   10   11   40   41
CONECT   11   12   42   43
CONECT   12   13   44   45
CONECT   13   14   46
CONECT   14   15   47   48
CONECT   15   16   49   50
CONECT   16   17   51   52
CONECT   17   18   53   54
CONECT   18   19   55   56
CONECT   19   20   57   58
CONECT   20   21   21   22
CONECT   22   59
END

HMDB0244503
     RDKit          3D
13-Azaprostanoic acid
 59 59  0  0  0  0  0  0  0  0999 V2000
    8.6525    0.3515   -1.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2281   -0.2076   -1.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3740    0.8508   -0.4620 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9172    0.4519   -0.3323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1928    1.5989    0.2968 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    1.3847    0.5018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4414    0.2101    1.4113 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0554   -0.0153    1.6191 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3417   -0.4773    0.4680 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7830   -1.8085   -0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1598   -2.7435    0.7283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4848   -1.9765    0.7257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620   -0.5182    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8627    0.2628   -0.3251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3200    0.4344   -0.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1230   -0.8024   -0.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6269   -0.5083   -0.3273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0710    0.2543    0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5716    0.4791    0.7524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8260    1.2313   -0.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0502    0.6491   -1.5716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8284    2.6316   -0.4966 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9302    0.7565   -0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6996    1.1813   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3108   -0.4567   -1.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8963   -0.4381   -2.1254 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1950   -1.1185   -0.4671 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7523    1.0740    0.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3880    1.7867   -1.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4740    0.2879   -1.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7941   -0.4830    0.2269 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6967    1.9409    1.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2987    2.4809   -0.3942 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3140    2.3208    0.9268 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2958    1.1592   -0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9326   -0.6793    0.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9252    0.3762    2.4045 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7741   -0.4487    2.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4854    0.2398   -0.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6448   -1.9405   -1.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7975   -2.1254    0.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1313   -2.9453    1.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2258   -3.6742    0.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9952   -2.3235   -0.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0699   -2.2323    1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3982   -0.0590    1.7141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3936    1.3082   -0.2862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5690   -0.0733   -1.3672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6548    1.0353    0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5958    1.0195   -1.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972   -1.4883    0.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8886   -1.3814   -1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2042   -1.4610   -0.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8362    0.0102   -1.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6343    1.2658    0.9622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8162   -0.2933    1.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1218   -0.4913    0.7742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8712    1.0964    1.6378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0906    3.0406   -1.0916 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  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  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 13  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 16 51  1  0
 16 52  1  0
 17 53  1  0
 17 54  1  0
 18 55  1  0
 18 56  1  0
 19 57  1  0
 19 58  1  0
 22 59  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
7-[2-(Heptylamino)cyclopentyl]heptanoate	Generator
13-Azaprostanoate	Generator

Chemical Formula

C₁₉H₃₇NO₂

Average Molecular Weight

311.51

Monoisotopic Molecular Weight

311.282429435

IUPAC Name

7-[2-(heptylamino)cyclopentyl]heptanoic acid

Traditional Name

7-[2-(heptylamino)cyclopentyl]heptanoic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCNC1CCCC1CCCCCCC(O)=O

InChI Identifier

InChI=1S/C19H37NO2/c1-2-3-4-7-10-16-20-18-14-11-13-17(18)12-8-5-6-9-15-19(21)22/h17-18,20H,2-16H2,1H3,(H,21,22)

InChI Key

RZZNGDIYQSCFGK-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
Amino fatty acid
Amino acid or derivatives
Amino acid
Carboxylic acid derivative
Carboxylic acid
Secondary aliphatic amine
Secondary amine
Monocarboxylic acid or derivatives
Amine
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Non-excretory biofluid

Blood (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	4.24	ALOGPS
logP	3.06	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	4.31	ChemAxon
pKa (Strongest Basic)	11.03	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	49.33 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	92.53 m³·mol⁻¹	ChemAxon
Polarizability	40.28 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]+	182.82	30932474
DeepCCS	[M-H]-	178.801	30932474
DeepCCS	[M-2H]-	215.624	30932474
DeepCCS	[M+Na]+	191.672	30932474
AllCCS	[M+H]+	184.0	32859911
AllCCS	[M+H-H2O]+	181.5	32859911
AllCCS	[M+NH4]+	186.3	32859911
AllCCS	[M+Na]+	187.0	32859911
AllCCS	[M-H]-	184.4	32859911
AllCCS	[M+Na-2H]-	185.3	32859911
AllCCS	[M+HCOO]-	186.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
13-Azaprostanoic acid	CCCCCCCNC1CCCC1CCCCCCC(O)=O	3635.7	Standard polar	33892256
13-Azaprostanoic acid	CCCCCCCNC1CCCC1CCCCCCC(O)=O	2453.3	Standard non polar	33892256
13-Azaprostanoic acid	CCCCCCCNC1CCCC1CCCCCCC(O)=O	2389.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
13-Azaprostanoic acid,2TMS,isomer #1	CCCCCCCN(C1CCCC1CCCCCCC(=O)O[Si](C)(C)C)[Si](C)(C)C	2563.6	Semi standard non polar	33892256
13-Azaprostanoic acid,2TMS,isomer #1	CCCCCCCN(C1CCCC1CCCCCCC(=O)O[Si](C)(C)C)[Si](C)(C)C	2667.5	Standard non polar	33892256
13-Azaprostanoic acid,2TMS,isomer #1	CCCCCCCN(C1CCCC1CCCCCCC(=O)O[Si](C)(C)C)[Si](C)(C)C	2745.7	Standard polar	33892256
13-Azaprostanoic acid,2TBDMS,isomer #1	CCCCCCCN(C1CCCC1CCCCCCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3085.3	Semi standard non polar	33892256
13-Azaprostanoic acid,2TBDMS,isomer #1	CCCCCCCN(C1CCCC1CCCCCCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3036.3	Standard non polar	33892256
13-Azaprostanoic acid,2TBDMS,isomer #1	CCCCCCCN(C1CCCC1CCCCCCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2967.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 13-Azaprostanoic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-001m-5590000000-e0cb751dc8c762a6c771	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 13-Azaprostanoic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 13-Azaprostanoic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 13-Azaprostanoic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 13-Azaprostanoic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 13-Azaprostanoic acid GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	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 - 13-Azaprostanoic acid 10V, Positive-QTOF	splash10-01r6-0393000000-c2984c1b50b81785e978	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Azaprostanoic acid 20V, Positive-QTOF	splash10-01td-6931000000-863e46029b1f9e690331	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Azaprostanoic acid 40V, Positive-QTOF	splash10-05mo-9200000000-bb89582a9a8e690d57c5	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Azaprostanoic acid 10V, Negative-QTOF	splash10-03di-0019000000-2da4bb80733809e159f1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Azaprostanoic acid 20V, Negative-QTOF	splash10-03di-0179000000-e1ddec97ed7646c6eff2	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Azaprostanoic acid 40V, Negative-QTOF	splash10-000f-3910000000-74d6eea3ce2d239edecc	2021-10-12	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

1380

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

1423

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 13-Azaprostanoic acid (HMDB0244503)

MOL for HMDB0244503 (13-Azaprostanoic acid)

3D MOL for HMDB0244503 (13-Azaprostanoic acid)

3D SDF for HMDB0244503 (13-Azaprostanoic acid)

3D-SDF for HMDB0244503 (13-Azaprostanoic acid)

PDB for HMDB0244503 (13-Azaprostanoic acid)

3D PDB for HMDB0244503 (13-Azaprostanoic acid)

SMILES for HMDB0244503 (13-Azaprostanoic acid)

INCHI for HMDB0244503 (13-Azaprostanoic acid)

Structure for HMDB0244503 (13-Azaprostanoic acid)

3D Structure for HMDB0244503 (13-Azaprostanoic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra