Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-02-24 01:47:43 UTC

Update Date

2022-10-24 19:44:17 UTC

HMDB ID

HMDB0240776

Secondary Accession Numbers

None

Metabolite Identification

Common Name

O-(13-Carboxytridecanoyl)carnitine

Description

O-(13-Carboxytridecanoyl)carnitine is an acylcarnitine. More specifically, it is an tetradecanedioic 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. O-(13-Carboxytridecanoyl)carnitine is therefore classified as a long chain AC. As a long-chain acylcarnitine O-(13-Carboxytridecanoyl)carnitine is generally formed through esterification with long-chain fatty acids obtained from the diet. The main function of most long-chain acylcarnitines is to ensure long chain fatty acid transport into the mitochondria (PMID: 22804748 ). Altered levels of long-chain acylcarnitines can serve as useful markers for inherited disorders of long-chain fatty acid metabolism. Carnitine palmitoyltransferase I (CPT I, EC:2.3.1.21) is involved in the synthesis of long-chain acylcarnitines (more than C12) on the mitochondrial outer membrane. Elevated serum/plasma levels of long-chain acylcarnitines are not only markers for incomplete FA oxidation but also are indicators of altered carbohydrate and lipid metabolism. High serum concentrations of long-chain acylcarnitines in the postprandial or fed state are markers of insulin resistance and arise from insulin's inability to inhibit CPT-1-dependent fatty acid metabolism in muscles and the heart (PMID: 19073774 ). Increased intracellular content of long-chain acylcarnitines is thought to serve as a feedback inhibition mechanism of insulin action (PMID: 23258903 ). In healthy subjects, increased concentrations of insulin effectively inhibits long-chain acylcarnitine production. Several studies have also found increased levels of circulating long-chain acylcarnitines in chronic heart failure patients (PMID: 26796394 ). 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

  Mrv1652302242102472D          

 28 27  0  0  0  0            999 V2000
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2539   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   10.7171    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 18 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 14  1  0  0  0  0
 20 16  1  0  0  0  0
 21 15  1  0  0  0  0
 22  1  1  0  0  0  0
 22  2  1  0  0  0  0
 22  3  1  0  0  0  0
 22 17  1  0  0  0  0
 23 19  2  0  0  0  0
 24 19  1  0  0  0  0
 25 20  2  0  0  0  0
 26 20  1  0  0  0  0
 27 21  2  0  0  0  0
 28 18  1  0  0  0  0
 28 21  1  0  0  0  0
M  CHG  2  22   1  26  -1
M  END

HMDB0240776
     RDKit          3D
O-(13-Carboxytridecanoyl)carnitine
 67 66  0  0  0  0  0  0  0  0999 V2000
   -7.3683   -1.6728   -0.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1046   -1.1663   -0.1676 N   0  0  0  0  0  4  0  0  0  0  0  0
   -5.6077   -2.2967    0.6228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4773   -0.1158    0.7197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2283   -0.8500   -1.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4442    0.4098   -1.1445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1485    1.6832   -1.4214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6860    1.7104   -2.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5346    0.7973   -3.6450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4233    2.8278   -3.2351 O   0  0  0  0  0  1  0  0  0  0  0  0
   -3.6553    0.3779    0.0188 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2936    0.2773    0.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6503    0.2055   -1.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6026    0.2550    1.3665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0899    0.1448    1.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5007    0.1285    2.5723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9992    0.0211    2.6000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6228    1.2114    1.8741 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1214    1.0362    1.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7975    2.1868    1.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3962    2.2876   -0.1724 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7418    1.0183   -0.9032 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2282    0.7692   -0.8204 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6367   -0.4872   -1.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9715   -1.7312   -1.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4421   -2.8936   -1.8135 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9555   -3.1127   -2.9392 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4161   -3.7315   -1.3030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8564   -2.3530   -0.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1984   -2.2141   -1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0756   -0.8408   -0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8842   -1.8647    1.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4277   -2.7579    1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1631   -3.0753   -0.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8706   -0.6396    1.6566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3771    0.3987    0.3115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6892    0.5321    1.0896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7815   -0.9544   -2.2026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4765   -1.7068   -1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6581    0.3279   -1.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9803    1.9517   -0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3430    2.4938   -1.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8996   -0.6427    1.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7893    1.1728    1.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2810    1.0129    0.6180 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1797   -0.8069    0.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2531    1.0993    3.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1094   -0.7348    3.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3070    0.0971    3.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3845   -0.9011    2.1643 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2867    1.2258    0.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3465    2.1747    2.3224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4517    0.0771    1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4242    0.9686    3.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4385    3.1421    1.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9013    2.1129    1.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3061    2.5325   -0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9853    3.1421   -0.6547 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2111    0.1432   -0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4511    1.1604   -1.9961 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7583    1.6379   -1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4899    0.5889    0.2531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2868   -0.3267   -2.6252 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7271   -0.5567   -1.5762 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2597   -1.8850    0.0289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8677   -1.6428   -1.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2489   -3.3800   -0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
  6 11  1  0
 11 12  1  0
 12 13  2  0
 12 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  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 23 62  1  0
 24 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 28 67  1  0
M  CHG  2   2   1  10  -1
M  END

  Mrv1652302242102472D          

 28 27  0  0  0  0            999 V2000
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2539   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   10.7171    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 18 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 14  1  0  0  0  0
 20 16  1  0  0  0  0
 21 15  1  0  0  0  0
 22  1  1  0  0  0  0
 22  2  1  0  0  0  0
 22  3  1  0  0  0  0
 22 17  1  0  0  0  0
 23 19  2  0  0  0  0
 24 19  1  0  0  0  0
 25 20  2  0  0  0  0
 26 20  1  0  0  0  0
 27 21  2  0  0  0  0
 28 18  1  0  0  0  0
 28 21  1  0  0  0  0
M  CHG  2  22   1  26  -1
M  END
> <DATABASE_ID>
HMDB0240776

> <DATABASE_NAME>
hmdb

> <SMILES>
C[N+](C)(C)CC(CC([O-])=O)OC(=O)CCCCCCCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H39NO6/c1-22(2,3)17-18(16-20(25)26)28-21(27)15-13-11-9-7-5-4-6-8-10-12-14-19(23)24/h18H,4-17H2,1-3H3,(H-,23,24,25,26)

> <INCHI_KEY>
AHBCTRVDGQMKHC-UHFFFAOYSA-N

> <FORMULA>
C21H39NO6

> <MOLECULAR_WEIGHT>
401.544

> <EXACT_MASS>
401.27773798

$$$$

HMDB0240776
     RDKit          3D
O-(13-Carboxytridecanoyl)carnitine
 67 66  0  0  0  0  0  0  0  0999 V2000
   -7.3683   -1.6728   -0.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1046   -1.1663   -0.1676 N   0  0  0  0  0  4  0  0  0  0  0  0
   -5.6077   -2.2967    0.6228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4773   -0.1158    0.7197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2283   -0.8500   -1.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4442    0.4098   -1.1445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1485    1.6832   -1.4214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6860    1.7104   -2.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5346    0.7973   -3.6450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4233    2.8278   -3.2351 O   0  0  0  0  0  1  0  0  0  0  0  0
   -3.6553    0.3779    0.0188 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2936    0.2773    0.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6503    0.2055   -1.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6026    0.2550    1.3665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0899    0.1448    1.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5007    0.1285    2.5723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9992    0.0211    2.6000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6228    1.2114    1.8741 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1214    1.0362    1.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7975    2.1868    1.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3962    2.2876   -0.1724 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7418    1.0183   -0.9032 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2282    0.7692   -0.8204 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6367   -0.4872   -1.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9715   -1.7312   -1.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4421   -2.8936   -1.8135 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9555   -3.1127   -2.9392 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4161   -3.7315   -1.3030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8564   -2.3530   -0.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1984   -2.2141   -1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0756   -0.8408   -0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8842   -1.8647    1.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4277   -2.7579    1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1631   -3.0753   -0.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8706   -0.6396    1.6566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3771    0.3987    0.3115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6892    0.5321    1.0896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7815   -0.9544   -2.2026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4765   -1.7068   -1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6581    0.3279   -1.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9803    1.9517   -0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3430    2.4938   -1.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8996   -0.6427    1.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7893    1.1728    1.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2810    1.0129    0.6180 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1797   -0.8069    0.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2531    1.0993    3.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1094   -0.7348    3.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3070    0.0971    3.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3845   -0.9011    2.1643 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2867    1.2258    0.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3465    2.1747    2.3224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4517    0.0771    1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4242    0.9686    3.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4385    3.1421    1.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9013    2.1129    1.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3061    2.5325   -0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9853    3.1421   -0.6547 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2111    0.1432   -0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4511    1.1604   -1.9961 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7583    1.6379   -1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4899    0.5889    0.2531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2868   -0.3267   -2.6252 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7271   -0.5567   -1.5762 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2597   -1.8850    0.0289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8677   -1.6428   -1.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2489   -3.3800   -0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
  6 11  1  0
 11 12  1  0
 12 13  2  0
 12 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  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 23 62  1  0
 24 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 28 67  1  0
M  CHG  2   2   1  10  -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      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.127  -1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.207  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.003   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.670   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.004   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.338   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      18.672   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      -2.667  -1.540   0.000  0.00  0.00           N+1
HETATM   23  O   UNK     0      20.005   0.770   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      18.672  -1.540   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O-1
HETATM   27  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
CONECT    1   22                                                            
CONECT    2   22                                                            
CONECT    3   22                                                            
CONECT    4    5    6                                                       
CONECT    5    4    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   14                                                       
CONECT   13   11   15                                                       
CONECT   14   12   19                                                       
CONECT   15   13   21                                                       
CONECT   16   18   20                                                       
CONECT   17   18   22                                                       
CONECT   18   16   17   28                                                  
CONECT   19   14   23   24                                                  
CONECT   20   16   25   26                                                  
CONECT   21   15   27   28                                                  
CONECT   22    1    2    3   17                                             
CONECT   23   19                                                            
CONECT   24   19                                                            
CONECT   25   20                                                            
CONECT   26   20                                                            
CONECT   27   21                                                            
CONECT   28   18   21                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   54    0
END

COMPND    HMDB0240776
HETATM    1  C1  UNL     1      -7.368  -1.673  -0.747  1.00  0.00           C  
HETATM    2  N1  UNL     1      -6.105  -1.166  -0.168  1.00  0.00           N1+
HETATM    3  C2  UNL     1      -5.608  -2.297   0.623  1.00  0.00           C  
HETATM    4  C3  UNL     1      -6.477  -0.116   0.720  1.00  0.00           C  
HETATM    5  C4  UNL     1      -5.228  -0.850  -1.241  1.00  0.00           C  
HETATM    6  C5  UNL     1      -4.444   0.410  -1.144  1.00  0.00           C  
HETATM    7  C6  UNL     1      -5.149   1.683  -1.421  1.00  0.00           C  
HETATM    8  C7  UNL     1      -5.686   1.710  -2.805  1.00  0.00           C  
HETATM    9  O1  UNL     1      -5.535   0.797  -3.645  1.00  0.00           O  
HETATM   10  O2  UNL     1      -6.423   2.828  -3.235  1.00  0.00           O1-
HETATM   11  O3  UNL     1      -3.655   0.378   0.019  1.00  0.00           O  
HETATM   12  C8  UNL     1      -2.294   0.277   0.060  1.00  0.00           C  
HETATM   13  O4  UNL     1      -1.650   0.206  -1.002  1.00  0.00           O  
HETATM   14  C9  UNL     1      -1.603   0.255   1.366  1.00  0.00           C  
HETATM   15  C10 UNL     1      -0.090   0.145   1.190  1.00  0.00           C  
HETATM   16  C11 UNL     1       0.501   0.129   2.572  1.00  0.00           C  
HETATM   17  C12 UNL     1       1.999   0.021   2.600  1.00  0.00           C  
HETATM   18  C13 UNL     1       2.623   1.211   1.874  1.00  0.00           C  
HETATM   19  C14 UNL     1       4.121   1.036   1.946  1.00  0.00           C  
HETATM   20  C15 UNL     1       4.797   2.187   1.266  1.00  0.00           C  
HETATM   21  C16 UNL     1       4.396   2.288  -0.172  1.00  0.00           C  
HETATM   22  C17 UNL     1       4.742   1.018  -0.903  1.00  0.00           C  
HETATM   23  C18 UNL     1       6.228   0.769  -0.820  1.00  0.00           C  
HETATM   24  C19 UNL     1       6.637  -0.487  -1.564  1.00  0.00           C  
HETATM   25  C20 UNL     1       5.972  -1.731  -1.026  1.00  0.00           C  
HETATM   26  C21 UNL     1       6.442  -2.894  -1.814  1.00  0.00           C  
HETATM   27  O5  UNL     1       5.955  -3.113  -2.939  1.00  0.00           O  
HETATM   28  O6  UNL     1       7.416  -3.731  -1.303  1.00  0.00           O  
HETATM   29  H1  UNL     1      -7.856  -2.353  -0.026  1.00  0.00           H  
HETATM   30  H2  UNL     1      -7.198  -2.214  -1.679  1.00  0.00           H  
HETATM   31  H3  UNL     1      -8.076  -0.841  -0.929  1.00  0.00           H  
HETATM   32  H4  UNL     1      -4.884  -1.865   1.349  1.00  0.00           H  
HETATM   33  H5  UNL     1      -6.428  -2.758   1.210  1.00  0.00           H  
HETATM   34  H6  UNL     1      -5.163  -3.075  -0.015  1.00  0.00           H  
HETATM   35  H7  UNL     1      -6.871  -0.640   1.657  1.00  0.00           H  
HETATM   36  H8  UNL     1      -7.377   0.399   0.312  1.00  0.00           H  
HETATM   37  H9  UNL     1      -5.689   0.532   1.090  1.00  0.00           H  
HETATM   38  H10 UNL     1      -5.781  -0.954  -2.203  1.00  0.00           H  
HETATM   39  H11 UNL     1      -4.477  -1.707  -1.289  1.00  0.00           H  
HETATM   40  H12 UNL     1      -3.658   0.328  -1.993  1.00  0.00           H  
HETATM   41  H13 UNL     1      -5.980   1.952  -0.764  1.00  0.00           H  
HETATM   42  H14 UNL     1      -4.343   2.494  -1.373  1.00  0.00           H  
HETATM   43  H15 UNL     1      -1.900  -0.643   1.961  1.00  0.00           H  
HETATM   44  H16 UNL     1      -1.789   1.173   1.965  1.00  0.00           H  
HETATM   45  H17 UNL     1       0.281   1.013   0.618  1.00  0.00           H  
HETATM   46  H18 UNL     1       0.180  -0.807   0.679  1.00  0.00           H  
HETATM   47  H19 UNL     1       0.253   1.099   3.095  1.00  0.00           H  
HETATM   48  H20 UNL     1       0.109  -0.735   3.164  1.00  0.00           H  
HETATM   49  H21 UNL     1       2.307   0.097   3.664  1.00  0.00           H  
HETATM   50  H22 UNL     1       2.384  -0.901   2.164  1.00  0.00           H  
HETATM   51  H23 UNL     1       2.287   1.226   0.811  1.00  0.00           H  
HETATM   52  H24 UNL     1       2.346   2.175   2.322  1.00  0.00           H  
HETATM   53  H25 UNL     1       4.452   0.077   1.485  1.00  0.00           H  
HETATM   54  H26 UNL     1       4.424   0.969   3.024  1.00  0.00           H  
HETATM   55  H27 UNL     1       4.439   3.142   1.773  1.00  0.00           H  
HETATM   56  H28 UNL     1       5.901   2.113   1.377  1.00  0.00           H  
HETATM   57  H29 UNL     1       3.306   2.533  -0.279  1.00  0.00           H  
HETATM   58  H30 UNL     1       4.985   3.142  -0.655  1.00  0.00           H  
HETATM   59  H31 UNL     1       4.211   0.143  -0.489  1.00  0.00           H  
HETATM   60  H32 UNL     1       4.451   1.160  -1.996  1.00  0.00           H  
HETATM   61  H33 UNL     1       6.758   1.638  -1.256  1.00  0.00           H  
HETATM   62  H34 UNL     1       6.490   0.589   0.253  1.00  0.00           H  
HETATM   63  H35 UNL     1       6.287  -0.327  -2.625  1.00  0.00           H  
HETATM   64  H36 UNL     1       7.727  -0.557  -1.576  1.00  0.00           H  
HETATM   65  H37 UNL     1       6.260  -1.885   0.029  1.00  0.00           H  
HETATM   66  H38 UNL     1       4.868  -1.643  -1.150  1.00  0.00           H  
HETATM   67  H39 UNL     1       8.249  -3.380  -0.809  1.00  0.00           H  
CONECT    1    2   29   30   31
CONECT    2    3    4    5
CONECT    3   32   33   34
CONECT    4   35   36   37
CONECT    5    6   38   39
CONECT    6    7   11   40
CONECT    7    8   41   42
CONECT    8    9    9   10
CONECT   11   12
CONECT   12   13   13   14
CONECT   14   15   43   44
CONECT   15   16   45   46
CONECT   16   17   47   48
CONECT   17   18   49   50
CONECT   18   19   51   52
CONECT   19   20   53   54
CONECT   20   21   55   56
CONECT   21   22   57   58
CONECT   22   23   59   60
CONECT   23   24   61   62
CONECT   24   25   63   64
CONECT   25   26   65   66
CONECT   26   27   27   28
CONECT   28   67
END

HMDB0240776
     RDKit          3D
O-(13-Carboxytridecanoyl)carnitine
 67 66  0  0  0  0  0  0  0  0999 V2000
   -7.3683   -1.6728   -0.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1046   -1.1663   -0.1676 N   0  0  0  0  0  4  0  0  0  0  0  0
   -5.6077   -2.2967    0.6228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4773   -0.1158    0.7197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2283   -0.8500   -1.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4442    0.4098   -1.1445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1485    1.6832   -1.4214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6860    1.7104   -2.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5346    0.7973   -3.6450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4233    2.8278   -3.2351 O   0  0  0  0  0  1  0  0  0  0  0  0
   -3.6553    0.3779    0.0188 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2936    0.2773    0.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6503    0.2055   -1.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6026    0.2550    1.3665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0899    0.1448    1.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5007    0.1285    2.5723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9992    0.0211    2.6000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6228    1.2114    1.8741 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1214    1.0362    1.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7975    2.1868    1.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3962    2.2876   -0.1724 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7418    1.0183   -0.9032 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2282    0.7692   -0.8204 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6367   -0.4872   -1.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9715   -1.7312   -1.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4421   -2.8936   -1.8135 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9555   -3.1127   -2.9392 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4161   -3.7315   -1.3030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8564   -2.3530   -0.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1984   -2.2141   -1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0756   -0.8408   -0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8842   -1.8647    1.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4277   -2.7579    1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1631   -3.0753   -0.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8706   -0.6396    1.6566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3771    0.3987    0.3115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6892    0.5321    1.0896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7815   -0.9544   -2.2026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4765   -1.7068   -1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6581    0.3279   -1.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9803    1.9517   -0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3430    2.4938   -1.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8996   -0.6427    1.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7893    1.1728    1.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2810    1.0129    0.6180 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1797   -0.8069    0.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2531    1.0993    3.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1094   -0.7348    3.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3070    0.0971    3.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3845   -0.9011    2.1643 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2867    1.2258    0.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3465    2.1747    2.3224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4517    0.0771    1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4242    0.9686    3.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4385    3.1421    1.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9013    2.1129    1.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3061    2.5325   -0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9853    3.1421   -0.6547 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2111    0.1432   -0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4511    1.1604   -1.9961 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7583    1.6379   -1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4899    0.5889    0.2531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2868   -0.3267   -2.6252 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7271   -0.5567   -1.5762 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2597   -1.8850    0.0289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8677   -1.6428   -1.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2489   -3.3800   -0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
  6 11  1  0
 11 12  1  0
 12 13  2  0
 12 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  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 23 62  1  0
 24 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 28 67  1  0
M  CHG  2   2   1  10  -1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
13-Carboxytridecanoylcarnitine	ChEBI
3-[(13-Carboxytridecanoyl)oxy]-4-(trimethylammonio)butanoate	ChEBI
3-[(13-Carboxytridecanoyl)oxy]-4-(trimethylammonio)butanoic acid	Generator

Chemical Formula

C₂₁H₃₉NO₆

Average Molecular Weight

401.544

Monoisotopic Molecular Weight

401.27773798

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[N+](C)(C)CC(CC([O-])=O)OC(=O)CCCCCCCCCCCCC(O)=O

InChI Identifier

InChI=1S/C21H39NO6/c1-22(2,3)17-18(16-20(25)26)28-21(27)15-13-11-9-7-5-4-6-8-10-12-14-19(23)24/h18H,4-17H2,1-3H3,(H-,23,24,25,26)

InChI Key

AHBCTRVDGQMKHC-UHFFFAOYSA-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
Tricarboxylic acid or derivatives
Tetraalkylammonium salt
Quaternary ammonium salt
Carboxylic acid ester
Carboxylic acid salt
Carboxylic acid derivative
Carboxylic acid
Organic nitrogen compound
Organic salt
Organooxygen compound
Organonitrogen compound
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:73071 )
O-acylcarnitine (CHEBI:73071 )
ammonium betaine (CHEBI:73071 )

Ontology

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

Exogenous

Exogenous (HMDB: HMDB0240776)

Endogenous

Endogenous (HMDB: HMDB0240776)

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]+	177.971	30932474
DeepCCS	[M-H]-	175.622	30932474
DeepCCS	[M-2H]-	208.505	30932474
DeepCCS	[M+Na]+	183.892	30932474
AllCCS	[M+H]+	209.6	32859911
AllCCS	[M+H-H2O]+	207.6	32859911
AllCCS	[M+NH4]+	211.4	32859911
AllCCS	[M+Na]+	211.9	32859911
AllCCS	[M-H]-	206.3	32859911
AllCCS	[M+Na-2H]-	207.7	32859911
AllCCS	[M+HCOO]-	209.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
O-(13-Carboxytridecanoyl)carnitine	C[N+](C)(C)CC(CC([O-])=O)OC(=O)CCCCCCCCCCCCC(O)=O	4075.0	Standard polar	33892256
O-(13-Carboxytridecanoyl)carnitine	C[N+](C)(C)CC(CC([O-])=O)OC(=O)CCCCCCCCCCCCC(O)=O	2407.2	Standard non polar	33892256
O-(13-Carboxytridecanoyl)carnitine	C[N+](C)(C)CC(CC([O-])=O)OC(=O)CCCCCCCCCCCCC(O)=O	2780.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
O-(13-Carboxytridecanoyl)carnitine,1TMS,isomer #1	C[N+](C)(C)CC(CC(=O)[O-])OC(=O)CCCCCCCCCCCCC(=O)O[Si](C)(C)C	2851.0	Semi standard non polar	33892256
O-(13-Carboxytridecanoyl)carnitine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCCCCCCCCCCCC(=O)OC(CC(=O)[O-])C[N+](C)(C)C	3098.2	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 - O-(13-Carboxytridecanoyl)carnitine 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 - O-(13-Carboxytridecanoyl)carnitine 10V, Positive-QTOF	splash10-0udi-0000900000-23222690e793ea8d985d	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - O-(13-Carboxytridecanoyl)carnitine 20V, Positive-QTOF	splash10-0f79-9000500000-4658bc89c72261b465f9	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - O-(13-Carboxytridecanoyl)carnitine 40V, Positive-QTOF	splash10-000i-9000000000-e9262cbaff8cb4ad0ba6	2021-09-21	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

28639187

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71464554

PDB ID

Not Available

ChEBI ID

73071

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 ]
Reuter SE, Evans AM: Carnitine and acylcarnitines: pharmacokinetic, pharmacological and clinical aspects. Clin Pharmacokinet. 2012 Sep 1;51(9):553-72. doi: 10.1007/BF03261931. [PubMed:22804748 ]
Bruce CR, Hoy AJ, Turner N, Watt MJ, Allen TL, Carpenter K, Cooney GJ, Febbraio MA, Kraegen EW: Overexpression of carnitine palmitoyltransferase-1 in skeletal muscle is sufficient to enhance fatty acid oxidation and improve high-fat diet-induced insulin resistance. Diabetes. 2009 Mar;58(3):550-8. doi: 10.2337/db08-1078. Epub 2008 Dec 10. [PubMed:19073774 ]
Schooneman MG, Vaz FM, Houten SM, Soeters MR: Acylcarnitines: reflecting or inflicting insulin resistance? Diabetes. 2013 Jan;62(1):1-8. doi: 10.2337/db12-0466. [PubMed:23258903 ]
Ahmad T, Kelly JP, McGarrah RW, Hellkamp AS, Fiuzat M, Testani JM, Wang TS, Verma A, Samsky MD, Donahue MP, Ilkayeva OR, Bowles DE, Patel CB, Milano CA, Rogers JG, Felker GM, O'Connor CM, Shah SH, Kraus WE: Prognostic Implications of Long-Chain Acylcarnitines in Heart Failure and Reversibility With Mechanical Circulatory Support. J Am Coll Cardiol. 2016 Jan 26;67(3):291-9. doi: 10.1016/j.jacc.2015.10.079. [PubMed:26796394 ]
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 O-(13-Carboxytridecanoyl)carnitine (HMDB0240776)

MOL for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

3D MOL for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

3D SDF for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

3D-SDF for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

PDB for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

3D PDB for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

SMILES for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

INCHI for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

Structure for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

3D Structure for HMDB0240776 (O-(13-Carboxytridecanoyl)carnitine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra