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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-02-24 01:44:30 UTC

Update Date

2022-10-24 19:44:16 UTC

HMDB ID

HMDB0240758

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine

Description

(7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine is an acylcarnitine. More specifically, it is an (7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoic acid ester of carnitine. Acylcarnitines were first discovered more than 70 year ago (PMID: 13825279 ). It is believed that there are more than 1000 types of acylcarnitines in the human body. The general role of acylcarnitines is to transport acyl-groups (organic acids and fatty acids) from the cytoplasm into the mitochondria so that they can be broken down to produce energy. This process is known as beta-oxidation. According to a recent review (PMID: 35710135 ), acylcarnitines (ACs) can be classified into 9 different categories depending on the type and size of their acyl-group: 1) short-chain ACs; 2) medium-chain ACs; 3) long-chain ACs; 4) very long-chain ACs; 5) hydroxy ACs; 6) branched chain ACs; 7) unsaturated ACs; 8) dicarboxylic ACs and 9) miscellaneous ACs. Short-chain ACs have acyl-groups with two to five carbons (C2-C5), medium-chain ACs have acyl-groups with six to thirteen carbons (C6-C13), long-chain ACs have acyl-groups with fourteen to twenty once carbons (C14-C21) and very long-chain ACs have acyl groups with more than 22 carbons. (7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine is therefore classified as a very-long chain AC. As a very long-chain acylcarnitine (7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine is generally formed in the cytoplasm from very long acyl groups synthesized by fatty acid synthases or obtained from the diet. Very-long-chain fatty acids are generally too long to be involved in mitochondrial beta-oxidation. As a result peroxisomes are the main organelle where very-long-chain fatty acids are metabolized and their acylcarnitines synthesized (PMID: 18793625 ). Altered levels of very long-chain acylcarnitines can serve as useful markers for inherited disorders of peroxisomal metabolism. The study of acylcarnitines is an active area of research and it is likely that many novel acylcarnitines will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered. An excellent review of the current state of knowledge for acylcarnitines is available (PMID: 35710135 ).

Structure

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


  Mrv1652302242102442D          

 42 41  0  0  0  0            999 V2000
   -1.2375    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.7145    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.1434    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    3.7125    3.5724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    5.7158    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    4.2868    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    4.2868    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.8579    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    2.8579    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    1.4289    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  2  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  2  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  2  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  2  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  1  0  0  0  0
 27 25  1  0  0  0  0
 27 26  1  0  0  0  0
 28 25  1  0  0  0  0
 29 24  1  0  0  0  0
 30  2  1  0  0  0  0
 30  3  1  0  0  0  0
 30  4  1  0  0  0  0
 30 26  1  0  0  0  0
 31 28  2  0  0  0  0
 32 28  1  0  0  0  0
 33 29  2  0  0  0  0
 34 27  1  0  0  0  0
 34 29  1  0  0  0  0
 35  9  1  0  0  0  0
 36 10  1  0  0  0  0
 37 12  1  0  0  0  0
 38 13  1  0  0  0  0
 39 15  1  0  0  0  0
 40 16  1  0  0  0  0
 41 18  1  0  0  0  0
 42 19  1  0  0  0  0
M  CHG  2  30   1  32  -1
M  END

HMDB0240758
     RDKit          3D
(7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine
 83 82  0  0  0  0  0  0  0  0999 V2000
    9.4896    0.9670   -3.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9347   -0.0760   -2.0557 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6485    0.5844   -0.7189 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1032   -0.4777    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7867    0.1248    1.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2642   -0.9657    2.4045 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1247   -1.0327    2.9796 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0016   -0.1163    3.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0816    1.1835    2.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4215    1.7296    1.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3575    1.1972    0.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8212   -0.1158    0.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8685   -1.2131    0.1924 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5041   -1.2340   -1.1005 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7067   -1.5035   -2.2860 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4375   -1.6922   -2.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3826   -1.6809   -1.4429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6209   -0.5834   -1.8677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7070   -0.4992   -0.8552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4721   -1.7790   -0.7144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5956   -1.6711    0.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5894   -0.6593   -0.1114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5429   -0.0183   -1.1887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6870   -0.3418    0.7139 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6534    0.6259    0.3474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5237    1.7507    1.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7478    1.3741    2.7332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0050    0.1993    3.0387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6736    2.3262    3.7211 O   0  0  0  0  0  1  0  0  0  0  0  0
   -7.9659   -0.0454    0.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1066    0.7332   -0.0714 N   0  0  0  0  0  4  0  0  0  0  0  0
   -9.7349    1.1964    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1375   -0.1286   -0.6834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9047    1.8458   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9891    0.3984   -3.8320 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1745    1.6618   -2.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6202    1.5196   -3.4618 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6782   -0.8753   -1.9539 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0215   -0.5013   -2.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6213    0.9791   -0.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9650    1.4290   -0.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8594   -1.2819    0.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2024   -0.9159   -0.2500 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7868    0.4675    1.9789 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1687    0.9918    1.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9774   -1.8649    2.5405 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9649   -2.0066    3.5615 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8499    0.1243    4.1888 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0350   -0.6795    2.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8368    1.9121    2.9122 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7422    2.8048    1.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4843    1.9723    0.7176 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6450    1.3379   -0.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2271   -0.2425    1.8969 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4183   -2.1168    0.6565 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3514   -2.0471   -1.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0933   -0.2803   -1.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2941   -1.5651   -3.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0423   -1.8950   -3.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2160   -2.6477   -1.4850 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -1.4127   -0.4272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9551   -0.8842   -2.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0721    0.3861   -1.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1834   -0.3104    0.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3327    0.4071   -0.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7817   -2.5912   -0.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8501   -2.1639   -1.6777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0437   -2.6500    0.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1141   -1.3316    1.2465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3255    1.0131   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0895    2.6720    1.0415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4475    2.1074    1.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8761   -0.8349   -0.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1342   -0.6367    1.2017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5297    0.4893    1.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3934    2.1960    1.4747 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8476    1.2815    1.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4335   -0.8939    0.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6513   -0.5918   -1.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9528    0.5436   -0.9688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0329    2.7907   -0.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9703    1.8432   -1.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7183    1.8882   -1.6765 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  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 25 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 31 34  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  3 40  1  0
  3 41  1  0
  4 42  1  0
  4 43  1  0
  5 44  1  0
  5 45  1  0
  6 46  1  0
  7 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
 10 51  1  0
 11 52  1  0
 11 53  1  0
 12 54  1  0
 13 55  1  0
 14 56  1  0
 14 57  1  0
 15 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 18 62  1  0
 18 63  1  0
 19 64  1  0
 19 65  1  0
 20 66  1  0
 20 67  1  0
 21 68  1  0
 21 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 30 73  1  0
 30 74  1  0
 32 75  1  0
 32 76  1  0
 32 77  1  0
 33 78  1  0
 33 79  1  0
 33 80  1  0
 34 81  1  0
 34 82  1  0
 34 83  1  0
M  CHG  2  29  -1  31   1
M  END


  Mrv1652302242102442D          

 42 41  0  0  0  0            999 V2000
   -1.2375    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5  1  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  2  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  2  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  2  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  2  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  1  0  0  0  0
 27 25  1  0  0  0  0
 27 26  1  0  0  0  0
 28 25  1  0  0  0  0
 29 24  1  0  0  0  0
 30  2  1  0  0  0  0
 30  3  1  0  0  0  0
 30  4  1  0  0  0  0
 30 26  1  0  0  0  0
 31 28  2  0  0  0  0
 32 28  1  0  0  0  0
 33 29  2  0  0  0  0
 34 27  1  0  0  0  0
 34 29  1  0  0  0  0
 35  9  1  0  0  0  0
 36 10  1  0  0  0  0
 37 12  1  0  0  0  0
 38 13  1  0  0  0  0
 39 15  1  0  0  0  0
 40 16  1  0  0  0  0
 41 18  1  0  0  0  0
 42 19  1  0  0  0  0
M  CHG  2  30   1  32  -1
M  END
> <DATABASE_ID>
HMDB0240758

> <DATABASE_NAME>
hmdb

> <SMILES>
[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC(CC([O-])=O)C[N+](C)(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C29H49NO4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-29(33)34-27(25-28(31)32)26-30(2,3)4/h9-10,12-13,15-16,18-19,27H,5-8,11,14,17,20-26H2,1-4H3/b10-9-,13-12-,16-15-,19-18-

> <INCHI_KEY>
OLORTLVEDIELGC-SNPVRQPZSA-N

> <FORMULA>
C29H49NO4

> <MOLECULAR_WEIGHT>
475.714

> <EXACT_MASS>
475.366159062

$$$$

HMDB0240758
     RDKit          3D
(7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine
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  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 25 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 31 34  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  3 40  1  0
  3 41  1  0
  4 42  1  0
  4 43  1  0
  5 44  1  0
  5 45  1  0
  6 46  1  0
  7 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
 10 51  1  0
 11 52  1  0
 11 53  1  0
 12 54  1  0
 13 55  1  0
 14 56  1  0
 14 57  1  0
 15 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 18 62  1  0
 18 63  1  0
 19 64  1  0
 19 65  1  0
 20 66  1  0
 20 67  1  0
 21 68  1  0
 21 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 30 73  1  0
 30 74  1  0
 32 75  1  0
 32 76  1  0
 32 77  1  0
 33 78  1  0
 33 79  1  0
 33 80  1  0
 34 81  1  0
 34 82  1  0
 34 83  1  0
M  CHG  2  29  -1  31   1
M  END

HEADER    PROTEIN                                 24-FEB-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-21         0                                  
HETATM    1  C   UNK     0      -2.310  17.338   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.700   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.136   2.104   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.804   0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.080  16.004   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.310  14.670   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.080  13.337   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.310  12.003   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.080  10.669   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.310   9.336   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.770   9.336   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.000   8.002   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.770   6.668   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.310   6.668   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.080   5.335   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.310   4.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.770   4.001   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   2.667   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.540   2.667   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.310   4.001   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.540   5.335   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.310   6.668   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.850   6.668   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.620   5.335   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.240   2.667   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.470   4.001   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.780   5.335   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.160   5.335   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       8.470   1.334   0.000  0.00  0.00           N+1
HETATM   31  O   UNK     0      11.550   6.668   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      11.550   4.001   0.000  0.00  0.00           O-1
HETATM   33  O   UNK     0       6.930   6.668   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       6.930   4.001   0.000  0.00  0.00           O+0
HETATM   35  H   UNK     0      -4.620  10.669   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.080   8.002   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.540   8.002   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.000   5.335   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.620   5.335   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.080   2.667   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.770   1.334   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.310   1.334   0.000  0.00  0.00           H+0
CONECT    1    5                                                            
CONECT    2   30                                                            
CONECT    3   30                                                            
CONECT    4   30                                                            
CONECT    5    1    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   35                                                  
CONECT   10    9   11   36                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   37                                                  
CONECT   13   12   14   38                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   39                                                  
CONECT   16   15   17   40                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   41                                                  
CONECT   19   18   20   42                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   29                                                       
CONECT   25   27   28                                                       
CONECT   26   27   30                                                       
CONECT   27   25   26   34                                                  
CONECT   28   25   31   32                                                  
CONECT   29   24   33   34                                                  
CONECT   30    2    3    4   26                                             
CONECT   31   28                                                            
CONECT   32   28                                                            
CONECT   33   29                                                            
CONECT   34   27   29                                                       
CONECT   35    9                                                            
CONECT   36   10                                                            
CONECT   37   12                                                            
CONECT   38   13                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   18                                                            
CONECT   42   19                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   82    0
END

COMPND    HMDB0240758
HETATM    1  C1  UNL     1       9.490   0.967  -3.012  1.00  0.00           C  
HETATM    2  C2  UNL     1       8.935  -0.076  -2.056  1.00  0.00           C  
HETATM    3  C3  UNL     1       8.648   0.584  -0.719  1.00  0.00           C  
HETATM    4  C4  UNL     1       8.103  -0.478   0.194  1.00  0.00           C  
HETATM    5  C5  UNL     1       7.787   0.125   1.582  1.00  0.00           C  
HETATM    6  C6  UNL     1       7.264  -0.966   2.404  1.00  0.00           C  
HETATM    7  C7  UNL     1       6.125  -1.033   2.980  1.00  0.00           C  
HETATM    8  C8  UNL     1       5.002  -0.116   3.036  1.00  0.00           C  
HETATM    9  C9  UNL     1       5.082   1.183   2.424  1.00  0.00           C  
HETATM   10  C10 UNL     1       4.422   1.730   1.453  1.00  0.00           C  
HETATM   11  C11 UNL     1       3.358   1.197   0.647  1.00  0.00           C  
HETATM   12  C12 UNL     1       2.821  -0.116   0.946  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.868  -1.213   0.192  1.00  0.00           C  
HETATM   14  C14 UNL     1       3.504  -1.234  -1.101  1.00  0.00           C  
HETATM   15  C15 UNL     1       2.707  -1.504  -2.286  1.00  0.00           C  
HETATM   16  C16 UNL     1       1.438  -1.692  -2.456  1.00  0.00           C  
HETATM   17  C17 UNL     1       0.383  -1.681  -1.443  1.00  0.00           C  
HETATM   18  C18 UNL     1      -0.621  -0.583  -1.868  1.00  0.00           C  
HETATM   19  C19 UNL     1      -1.707  -0.499  -0.855  1.00  0.00           C  
HETATM   20  C20 UNL     1      -2.472  -1.779  -0.714  1.00  0.00           C  
HETATM   21  C21 UNL     1      -3.596  -1.671   0.296  1.00  0.00           C  
HETATM   22  C22 UNL     1      -4.589  -0.659  -0.111  1.00  0.00           C  
HETATM   23  O1  UNL     1      -4.543  -0.018  -1.189  1.00  0.00           O  
HETATM   24  O2  UNL     1      -5.687  -0.342   0.714  1.00  0.00           O  
HETATM   25  C23 UNL     1      -6.653   0.626   0.347  1.00  0.00           C  
HETATM   26  C24 UNL     1      -6.524   1.751   1.333  1.00  0.00           C  
HETATM   27  C25 UNL     1      -6.748   1.374   2.733  1.00  0.00           C  
HETATM   28  O3  UNL     1      -7.005   0.199   3.039  1.00  0.00           O  
HETATM   29  O4  UNL     1      -6.674   2.326   3.721  1.00  0.00           O1-
HETATM   30  C26 UNL     1      -7.966  -0.045   0.283  1.00  0.00           C  
HETATM   31  N1  UNL     1      -9.107   0.733  -0.071  1.00  0.00           N1+
HETATM   32  C27 UNL     1      -9.735   1.196   1.172  1.00  0.00           C  
HETATM   33  C28 UNL     1     -10.137  -0.129  -0.683  1.00  0.00           C  
HETATM   34  C29 UNL     1      -8.905   1.846  -0.914  1.00  0.00           C  
HETATM   35  H1  UNL     1       9.989   0.398  -3.832  1.00  0.00           H  
HETATM   36  H2  UNL     1      10.174   1.662  -2.510  1.00  0.00           H  
HETATM   37  H3  UNL     1       8.620   1.520  -3.462  1.00  0.00           H  
HETATM   38  H4  UNL     1       9.678  -0.875  -1.954  1.00  0.00           H  
HETATM   39  H5  UNL     1       8.021  -0.501  -2.488  1.00  0.00           H  
HETATM   40  H6  UNL     1       9.621   0.979  -0.344  1.00  0.00           H  
HETATM   41  H7  UNL     1       7.965   1.429  -0.808  1.00  0.00           H  
HETATM   42  H8  UNL     1       8.859  -1.282   0.303  1.00  0.00           H  
HETATM   43  H9  UNL     1       7.202  -0.916  -0.250  1.00  0.00           H  
HETATM   44  H10 UNL     1       8.787   0.467   1.979  1.00  0.00           H  
HETATM   45  H11 UNL     1       7.169   0.992   1.464  1.00  0.00           H  
HETATM   46  H12 UNL     1       7.977  -1.865   2.540  1.00  0.00           H  
HETATM   47  H13 UNL     1       5.965  -2.007   3.562  1.00  0.00           H  
HETATM   48  H14 UNL     1       4.850   0.124   4.189  1.00  0.00           H  
HETATM   49  H15 UNL     1       4.035  -0.680   2.877  1.00  0.00           H  
HETATM   50  H16 UNL     1       5.837   1.912   2.912  1.00  0.00           H  
HETATM   51  H17 UNL     1       4.742   2.805   1.201  1.00  0.00           H  
HETATM   52  H18 UNL     1       2.484   1.972   0.718  1.00  0.00           H  
HETATM   53  H19 UNL     1       3.645   1.338  -0.436  1.00  0.00           H  
HETATM   54  H20 UNL     1       2.227  -0.242   1.897  1.00  0.00           H  
HETATM   55  H21 UNL     1       2.418  -2.117   0.656  1.00  0.00           H  
HETATM   56  H22 UNL     1       4.351  -2.047  -1.100  1.00  0.00           H  
HETATM   57  H23 UNL     1       4.093  -0.280  -1.263  1.00  0.00           H  
HETATM   58  H24 UNL     1       3.294  -1.565  -3.269  1.00  0.00           H  
HETATM   59  H25 UNL     1       1.042  -1.895  -3.497  1.00  0.00           H  
HETATM   60  H26 UNL     1      -0.216  -2.648  -1.485  1.00  0.00           H  
HETATM   61  H27 UNL     1       0.635  -1.413  -0.427  1.00  0.00           H  
HETATM   62  H28 UNL     1      -0.955  -0.884  -2.874  1.00  0.00           H  
HETATM   63  H29 UNL     1      -0.072   0.386  -1.881  1.00  0.00           H  
HETATM   64  H30 UNL     1      -1.183  -0.310   0.139  1.00  0.00           H  
HETATM   65  H31 UNL     1      -2.333   0.407  -0.979  1.00  0.00           H  
HETATM   66  H32 UNL     1      -1.782  -2.591  -0.332  1.00  0.00           H  
HETATM   67  H33 UNL     1      -2.850  -2.164  -1.678  1.00  0.00           H  
HETATM   68  H34 UNL     1      -4.044  -2.650   0.525  1.00  0.00           H  
HETATM   69  H35 UNL     1      -3.114  -1.332   1.246  1.00  0.00           H  
HETATM   70  H36 UNL     1      -6.326   1.013  -0.657  1.00  0.00           H  
HETATM   71  H37 UNL     1      -7.089   2.672   1.042  1.00  0.00           H  
HETATM   72  H38 UNL     1      -5.447   2.107   1.294  1.00  0.00           H  
HETATM   73  H39 UNL     1      -7.876  -0.835  -0.526  1.00  0.00           H  
HETATM   74  H40 UNL     1      -8.134  -0.637   1.202  1.00  0.00           H  
HETATM   75  H41 UNL     1      -9.530   0.489   1.992  1.00  0.00           H  
HETATM   76  H42 UNL     1      -9.393   2.196   1.475  1.00  0.00           H  
HETATM   77  H43 UNL     1     -10.848   1.281   1.023  1.00  0.00           H  
HETATM   78  H44 UNL     1     -10.433  -0.894   0.057  1.00  0.00           H  
HETATM   79  H45 UNL     1      -9.651  -0.592  -1.566  1.00  0.00           H  
HETATM   80  H46 UNL     1     -10.953   0.544  -0.969  1.00  0.00           H  
HETATM   81  H47 UNL     1      -9.033   2.791  -0.337  1.00  0.00           H  
HETATM   82  H48 UNL     1      -7.970   1.843  -1.508  1.00  0.00           H  
HETATM   83  H49 UNL     1      -9.718   1.888  -1.677  1.00  0.00           H  
CONECT    1    2   35   36   37
CONECT    2    3   38   39
CONECT    3    4   40   41
CONECT    4    5   42   43
CONECT    5    6   44   45
CONECT    6    7    7   46
CONECT    7    8   47
CONECT    8    9   48   49
CONECT    9   10   10   50
CONECT   10   11   51
CONECT   11   12   52   53
CONECT   12   13   13   54
CONECT   13   14   55
CONECT   14   15   56   57
CONECT   15   16   16   58
CONECT   16   17   59
CONECT   17   18   60   61
CONECT   18   19   62   63
CONECT   19   20   64   65
CONECT   20   21   66   67
CONECT   21   22   68   69
CONECT   22   23   23   24
CONECT   24   25
CONECT   25   26   30   70
CONECT   26   27   71   72
CONECT   27   28   28   29
CONECT   30   31   73   74
CONECT   31   32   33   34
CONECT   32   75   76   77
CONECT   33   78   79   80
CONECT   34   81   82   83
END

HMDB0240758
     RDKit          3D
(7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine
 83 82  0  0  0  0  0  0  0  0999 V2000
    9.4896    0.9670   -3.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9347   -0.0760   -2.0557 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6485    0.5844   -0.7189 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1032   -0.4777    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7867    0.1248    1.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2642   -0.9657    2.4045 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1247   -1.0327    2.9796 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0016   -0.1163    3.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0816    1.1835    2.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4215    1.7296    1.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3575    1.1972    0.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8212   -0.1158    0.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8685   -1.2131    0.1924 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5041   -1.2340   -1.1005 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7067   -1.5035   -2.2860 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4375   -1.6922   -2.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3826   -1.6809   -1.4429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6209   -0.5834   -1.8677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7070   -0.4992   -0.8552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4721   -1.7790   -0.7144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5956   -1.6711    0.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5894   -0.6593   -0.1114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5429   -0.0183   -1.1887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6870   -0.3418    0.7139 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6534    0.6259    0.3474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5237    1.7507    1.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7478    1.3741    2.7332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0050    0.1993    3.0387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6736    2.3262    3.7211 O   0  0  0  0  0  1  0  0  0  0  0  0
   -7.9659   -0.0454    0.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1066    0.7332   -0.0714 N   0  0  0  0  0  4  0  0  0  0  0  0
   -9.7349    1.1964    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1375   -0.1286   -0.6834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9047    1.8458   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9891    0.3984   -3.8320 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1745    1.6618   -2.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6202    1.5196   -3.4618 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6782   -0.8753   -1.9539 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0215   -0.5013   -2.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6213    0.9791   -0.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9650    1.4290   -0.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8594   -1.2819    0.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2024   -0.9159   -0.2500 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7868    0.4675    1.9789 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1687    0.9918    1.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9774   -1.8649    2.5405 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9649   -2.0066    3.5615 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8499    0.1243    4.1888 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0350   -0.6795    2.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8368    1.9121    2.9122 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7422    2.8048    1.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4843    1.9723    0.7176 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6450    1.3379   -0.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2271   -0.2425    1.8969 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4183   -2.1168    0.6565 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3514   -2.0471   -1.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0933   -0.2803   -1.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2941   -1.5651   -3.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0423   -1.8950   -3.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2160   -2.6477   -1.4850 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -1.4127   -0.4272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9551   -0.8842   -2.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0721    0.3861   -1.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1834   -0.3104    0.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3327    0.4071   -0.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7817   -2.5912   -0.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8501   -2.1639   -1.6777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0437   -2.6500    0.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1141   -1.3316    1.2465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3255    1.0131   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0895    2.6720    1.0415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4475    2.1074    1.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8761   -0.8349   -0.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1342   -0.6367    1.2017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5297    0.4893    1.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3934    2.1960    1.4747 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8476    1.2815    1.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4335   -0.8939    0.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6513   -0.5918   -1.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9528    0.5436   -0.9688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0329    2.7907   -0.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9703    1.8432   -1.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7183    1.8882   -1.6765 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  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
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 13 14  1  0
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 17 18  1  0
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 24 25  1  0
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 31 33  1  0
 31 34  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  3 40  1  0
  3 41  1  0
  4 42  1  0
  4 43  1  0
  5 44  1  0
  5 45  1  0
  6 46  1  0
  7 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
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 33 78  1  0
 33 79  1  0
 33 80  1  0
 34 81  1  0
 34 82  1  0
 34 83  1  0
M  CHG  2  29  -1  31   1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3-[(7Z,10Z,13Z,16Z)-Docosa-7,10,13,16-tetraenoyloxy]-4-(trimethylammonio)butanoate	ChEBI
all-cis-7,10,13,16-Docosatetraenoylcarnitine	ChEBI
3-[(7Z,10Z,13Z,16Z)-Docosa-7,10,13,16-tetraenoyloxy]-4-(trimethylammonio)butanoic acid	Generator

Chemical Formula

C₂₉H₄₉NO₄

Average Molecular Weight

475.714

Monoisotopic Molecular Weight

475.366159062

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC(CC([O-])=O)C[N+](C)(C)C

InChI Identifier

InChI=1S/C29H49NO4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-29(33)34-27(25-28(31)32)26-30(2,3)4/h9-10,12-13,15-16,18-19,27H,5-8,11,14,17,20-26H2,1-4H3/b10-9-,13-12-,16-15-,19-18-

InChI Key

OLORTLVEDIELGC-SNPVRQPZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyl carnitines. These are organic compounds containing a fatty acid with the carboxylic acid attached to carnitine through an ester bond.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Acyl carnitines

Alternative Parents

Substituents

Acyl-carnitine
Dicarboxylic acid or derivatives
Tetraalkylammonium salt
Quaternary ammonium salt
Carboxylic acid ester
Carboxylic acid salt
Carboxylic acid derivative
Carboxylic acid
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic salt
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Amine
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

carboxylic ester (CHEBI:73122 )
O-acylcarnitine (CHEBI:73122 )
ammonium betaine (CHEBI:73122 )

Ontology

Physiological effect

Health effect

Cancer

Breast cancer (PMID: 35710135)

Diabetes mellitus type 2 (PMID: 35710135)
Celiac disease (PMID: 35710135)
Inflammatory bowel disease (PMID: 35710135)

Circulatory system disorder

Cardiac disorder

Cardiovascular disease (PMID: 35710135)
Heart failure (PMID: 35710135)

Renal system and urinary system

Renal disorder

Renal cell carcinoma (PMID: 35710135)

Disposition

Biological location

Cell

All cells and tissues (PMID: 35710135)

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 35710135)

Excreta

Biofluid or Excreta

Urine (PMID: 35710135)

Cellular substructure

cytoplasm (PMID: 35710135)
mitochondrion matrix (PMID: 35710135)

Organelle

peroxisome (PMID: 35710135)

Source

Endogenous

Endogenous (HMDB: HMDB0240758)

Process

Not Available

Role

Biological role

Energy source (PMID: 35710135)

Industrial application

Pharmaceutical industry

Biomarker

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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	238.51	30932474
DeepCCS	[M-H]-	236.685	30932474
DeepCCS	[M-2H]-	269.927	30932474
DeepCCS	[M+Na]+	244.116	30932474
AllCCS	[M+H]+	229.7	32859911
AllCCS	[M+H-H2O]+	228.1	32859911
AllCCS	[M+NH4]+	231.2	32859911
AllCCS	[M+Na]+	231.6	32859911
AllCCS	[M-H]-	222.5	32859911
AllCCS	[M+Na-2H]-	225.7	32859911
AllCCS	[M+HCOO]-	229.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC(CC([O-])=O)C[N+](C)(C)C	3972.8	Standard polar	33892256
(7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC(CC([O-])=O)C[N+](C)(C)C	2866.3	Standard non polar	33892256
(7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCCCC(=O)OC(CC([O-])=O)C[N+](C)(C)C	3320.4	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 - (7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - (7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine 10V, Positive-QTOF	splash10-004i-0000900000-a40408f47ae06d0c9f45	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine 20V, Positive-QTOF	splash10-002r-9000500000-9692ddb27b5859dca283	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine 40V, Positive-QTOF	splash10-000i-9000000000-e9262cbaff8cb4ad0ba6	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

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

28639213

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71464592

PDB ID

Not Available

ChEBI ID

73122

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

Sud M, Fahy E, Cotter D, Brown A, Dennis EA, Glass CK, Merrill AH Jr, Murphy RC, Raetz CR, Russell DW, Subramaniam S: LMSD: LIPID MAPS structure database. Nucleic Acids Res. 2007 Jan;35(Database issue):D527-32. doi: 10.1093/nar/gkl838. Epub 2006 Nov 10. [PubMed:17098933 ]
FRITZ IB: Action of carnitine on long chain fatty acid oxidation by liver. Am J Physiol. 1959 Aug;197:297-304. doi: 10.1152/ajplegacy.1959.197.2.297. [PubMed:13825279 ]
Duranti G, Boenzi S, Rizzo C, Rava L, Di Ciommo V, Carrozzo R, Meschini MC, Johnson DW, Dionisi-Vici C: Urine acylcarnitine analysis by ESI-MS/MS: a new tool for the diagnosis of peroxisomal biogenesis disorders. Clin Chim Acta. 2008 Dec;398(1-2):86-9. doi: 10.1016/j.cca.2008.08.018. Epub 2008 Aug 28. [PubMed:18793625 ]
Dambrova M, Makrecka-Kuka M, Kuka J, Vilskersts R, Nordberg D, Attwood MM, Smesny S, Sen ZD, Guo AC, Oler E, Tian S, Zheng J, Wishart DS, Liepinsh E, Schioth HB: Acylcarnitines: Nomenclature, Biomarkers, Therapeutic Potential, Drug Targets, and Clinical Trials. Pharmacol Rev. 2022 Jul;74(3):506-551. doi: 10.1124/pharmrev.121.000408. [PubMed:35710135 ]

Showing metabocard for (7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine (HMDB0240758)

MOL for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

3D MOL for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

3D SDF for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

3D-SDF for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

PDB for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

3D PDB for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

SMILES for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

INCHI for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

Structure for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

3D Structure for HMDB0240758 ((7Z,10Z,13Z,16Z)-Docosatetraenoylcarnitine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra