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Record Information

Version

5.0

Status

Predicted

Creation Date

2021-03-31 16:46:22 UTC

Update Date

2022-10-24 19:44:19 UTC

HMDB ID

HMDB0240794

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2,3-Dimethylideneoctanedioylcarnitine

Description

2,3-Dimethylideneoctanedioylcarnitine is an acylcarnitine. More specifically, it is an 2,3-dimethylideneoctanedioic 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. 2,3-Dimethylideneoctanedioylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine 2,3-Dimethylideneoctanedioylcarnitine is somewhat less abundant than short-chain acylcarnitines. These are formed either through esterification with L-carnitine or through the peroxisomal metabolism of longer chain acylcarnitines (PMID: 30540494 ). Many medium-chain acylcarnitines can serve as useful markers for inherited disorders of fatty acid metabolism. Carnitine octanoyltransferase (CrOT, EC:2.3.1.137) is responsible for the synthesis of all medium-chain (MCAC, C5-C12) and medium-length branched-chain acylcarnitines in peroxisomes (PMID: 10486279 ). 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

HMDB0240794
     RDKit          3D
2,3-Dimethylideneoctanedioylcarnitine
 51 50  0  0  0  0  0  0  0  0999 V2000
    1.6091    0.2128    3.0888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3266   -0.8892    2.4171 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2619   -2.0511    2.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3726   -1.9246    1.5940 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9587   -1.9052    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1391   -1.7556   -0.7629 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8003   -0.4551   -0.5531 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2745    0.3811    0.2235 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0105   -0.1450   -1.2134 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1526   -0.9949    1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1307   -2.1412    0.9237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036    0.0826    1.3494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2274    1.8403 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9230   -0.1098    0.5127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729    0.9474    0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1742    0.4503    0.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2768    1.4300    0.7957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0394    2.5331    0.2460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5337    1.0991    1.2880 O   0  0  0  0  0  1  0  0  0  0  0  0
   -2.9978    1.0483   -1.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7992    1.3575   -1.9052 N   0  0  0  0  0  4  0  0  0  0  0  0
   -2.2055    1.5657   -3.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7906    0.3518   -1.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2269    2.6441   -1.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4796    0.2339    3.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0266    1.0853    3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6954   -2.9828    2.5482 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6776   -2.0278    3.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0318   -2.8462    1.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0527   -1.0666    1.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2775   -1.0684   -0.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4549   -2.8650   -0.1424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7945   -1.9075   -1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8496   -2.5640   -0.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4409    0.7376   -0.9790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0295   -2.2008    0.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4730   -3.0207    1.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6258    1.8700    0.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0209    0.2806    2.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5243   -0.4912    0.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3901    0.0929   -1.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7547    1.8124   -1.5185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0985    2.2249   -3.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4259    0.5734   -3.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3731    1.9937   -3.9047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3518    0.2090   -2.9603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0719   -0.6425   -1.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0989    0.7104   -1.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2226    2.6749   -2.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0474    2.7288   -0.4283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7982    3.4959   -1.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  2 10  1  0
 10 11  2  3
 10 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  2  0
 17 19  1  0
 15 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 20 41  1  0
 20 42  1  0
 22 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  0
 23 47  1  0
 23 48  1  0
 24 49  1  0
 24 50  1  0
 24 51  1  0
M  CHG  2  19  -1  21   1
M  END


  Mrv1652303312118462D          

 24 23  0  0  0  0            999 V2000
    5.6645    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    1.6204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    1.6204    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    4.2355    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    4.5079    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    3.9336    5.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1086    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    4.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
M  CHG  2   8  -1  10   1
M  END
> <DATABASE_ID>
HMDB0240794

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H27NO6/c1-12(8-6-7-9-15(19)20)13(2)17(23)24-14(10-16(21)22)11-18(3,4)5/h14H,1-2,6-11H2,3-5H3,(H-,19,20,21,22)

> <INCHI_KEY>
YVJRBPYWDVJLNP-UHFFFAOYSA-N

> <FORMULA>
C17H27NO6

> <MOLECULAR_WEIGHT>
341.404

> <EXACT_MASS>
341.183837593

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
35.502003926447756

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(7-carboxy-2,3-dimethylideneheptanoyl)oxy]-4-(trimethylazaniumyl)butanoate

> <JCHEM_LOGP>
-2.219228962805078

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
4.604988397535921

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.000133772756527

> <JCHEM_PKA_STRONGEST_BASIC>
-6.939949048263247

> <JCHEM_POLAR_SURFACE_AREA>
103.73

> <JCHEM_REFRACTIVITY>
110.63809999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-[(7-carboxy-2,3-dimethylideneheptanoyl)oxy]-4-(trimethylammonio)butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0240794
     RDKit          3D
2,3-Dimethylideneoctanedioylcarnitine
 51 50  0  0  0  0  0  0  0  0999 V2000
    1.6091    0.2128    3.0888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3266   -0.8892    2.4171 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2619   -2.0511    2.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3726   -1.9246    1.5940 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9587   -1.9052    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1391   -1.7556   -0.7629 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8003   -0.4551   -0.5531 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2745    0.3811    0.2235 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0105   -0.1450   -1.2134 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1526   -0.9949    1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1307   -2.1412    0.9237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036    0.0826    1.3494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2274    1.8403 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9230   -0.1098    0.5127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729    0.9474    0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1742    0.4503    0.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2768    1.4300    0.7957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0394    2.5331    0.2460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5337    1.0991    1.2880 O   0  0  0  0  0  1  0  0  0  0  0  0
   -2.9978    1.0483   -1.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7992    1.3575   -1.9052 N   0  0  0  0  0  4  0  0  0  0  0  0
   -2.2055    1.5657   -3.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7906    0.3518   -1.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2269    2.6441   -1.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4796    0.2339    3.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0266    1.0853    3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6954   -2.9828    2.5482 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6776   -2.0278    3.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0318   -2.8462    1.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0527   -1.0666    1.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2775   -1.0684   -0.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4549   -2.8650   -0.1424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7945   -1.9075   -1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8496   -2.5640   -0.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4409    0.7376   -0.9790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0295   -2.2008    0.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4730   -3.0207    1.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6258    1.8700    0.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0209    0.2806    2.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5243   -0.4912    0.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3901    0.0929   -1.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7547    1.8124   -1.5185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0985    2.2249   -3.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4259    0.5734   -3.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3731    1.9937   -3.9047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3518    0.2090   -2.9603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0719   -0.6425   -1.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0989    0.7104   -1.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2226    2.6749   -2.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0474    2.7288   -0.4283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7982    3.4959   -1.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  2 10  1  0
 10 11  2  3
 10 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  2  0
 17 19  1  0
 15 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 20 41  1  0
 20 42  1  0
 22 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  0
 23 47  1  0
 23 48  1  0
 24 49  1  0
 24 50  1  0
 24 51  1  0
M  CHG  2  19  -1  21   1
M  END

HEADER    PROTEIN                                 31-MAR-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   31-MAR-21         0                                  
HETATM    1  O   UNK     0      10.574   7.645   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      10.574   6.105   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.240   5.335   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       7.906   6.105   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.573   5.335   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.573   3.795   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.239   3.025   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       7.906   3.025   0.000  0.00  0.00           O-1
HETATM    9  C   UNK     0       7.906   7.645   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       6.573   8.415   0.000  0.00  0.00           N+1
HETATM   11  C   UNK     0       7.343   9.748   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.803   7.081   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.239   9.185   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.907   5.335   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.907   3.795   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.241   6.105   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.241   7.645   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.575   5.335   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      15.908   6.105   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.242   5.335   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.576   6.105   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.909   5.335   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      21.243   6.105   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      19.909   3.795   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10                                                            
CONECT   14    2   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   46    0
END

COMPND    HMDB0240794
HETATM    1  C1  UNL     1       1.609   0.213   3.089  1.00  0.00           C  
HETATM    2  C2  UNL     1       1.327  -0.889   2.417  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.262  -2.051   2.599  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.373  -1.925   1.594  1.00  0.00           C  
HETATM    5  C5  UNL     1       2.959  -1.905   0.180  1.00  0.00           C  
HETATM    6  C6  UNL     1       4.139  -1.756  -0.763  1.00  0.00           C  
HETATM    7  C7  UNL     1       4.800  -0.455  -0.553  1.00  0.00           C  
HETATM    8  O1  UNL     1       4.274   0.381   0.224  1.00  0.00           O  
HETATM    9  O2  UNL     1       6.010  -0.145  -1.213  1.00  0.00           O  
HETATM   10  C8  UNL     1       0.153  -0.995   1.572  1.00  0.00           C  
HETATM   11  C9  UNL     1      -0.131  -2.141   0.924  1.00  0.00           C  
HETATM   12  C10 UNL     1      -0.804   0.083   1.349  1.00  0.00           C  
HETATM   13  O3  UNL     1      -0.750   1.227   1.840  1.00  0.00           O  
HETATM   14  O4  UNL     1      -1.923  -0.110   0.513  1.00  0.00           O  
HETATM   15  C11 UNL     1      -2.873   0.947   0.289  1.00  0.00           C  
HETATM   16  C12 UNL     1      -4.174   0.450   0.921  1.00  0.00           C  
HETATM   17  C13 UNL     1      -5.277   1.430   0.796  1.00  0.00           C  
HETATM   18  O5  UNL     1      -5.039   2.533   0.246  1.00  0.00           O  
HETATM   19  O6  UNL     1      -6.534   1.099   1.288  1.00  0.00           O1-
HETATM   20  C14 UNL     1      -2.998   1.048  -1.201  1.00  0.00           C  
HETATM   21  N1  UNL     1      -1.799   1.358  -1.905  1.00  0.00           N1+
HETATM   22  C15 UNL     1      -2.205   1.566  -3.310  1.00  0.00           C  
HETATM   23  C16 UNL     1      -0.791   0.352  -1.927  1.00  0.00           C  
HETATM   24  C17 UNL     1      -1.227   2.644  -1.513  1.00  0.00           C  
HETATM   25  H1  UNL     1       2.480   0.234   3.727  1.00  0.00           H  
HETATM   26  H2  UNL     1       1.027   1.085   3.038  1.00  0.00           H  
HETATM   27  H3  UNL     1       1.695  -2.983   2.548  1.00  0.00           H  
HETATM   28  H4  UNL     1       2.678  -2.028   3.652  1.00  0.00           H  
HETATM   29  H5  UNL     1       4.032  -2.846   1.811  1.00  0.00           H  
HETATM   30  H6  UNL     1       4.053  -1.067   1.861  1.00  0.00           H  
HETATM   31  H7  UNL     1       2.277  -1.068  -0.084  1.00  0.00           H  
HETATM   32  H8  UNL     1       2.455  -2.865  -0.142  1.00  0.00           H  
HETATM   33  H9  UNL     1       3.795  -1.907  -1.825  1.00  0.00           H  
HETATM   34  H10 UNL     1       4.850  -2.564  -0.471  1.00  0.00           H  
HETATM   35  H11 UNL     1       6.441   0.738  -0.979  1.00  0.00           H  
HETATM   36  H12 UNL     1      -1.029  -2.201   0.282  1.00  0.00           H  
HETATM   37  H13 UNL     1       0.473  -3.021   1.017  1.00  0.00           H  
HETATM   38  H14 UNL     1      -2.626   1.870   0.808  1.00  0.00           H  
HETATM   39  H15 UNL     1      -4.021   0.281   2.015  1.00  0.00           H  
HETATM   40  H16 UNL     1      -4.524  -0.491   0.455  1.00  0.00           H  
HETATM   41  H17 UNL     1      -3.390   0.093  -1.628  1.00  0.00           H  
HETATM   42  H18 UNL     1      -3.755   1.812  -1.519  1.00  0.00           H  
HETATM   43  H19 UNL     1      -3.099   2.225  -3.276  1.00  0.00           H  
HETATM   44  H20 UNL     1      -2.426   0.573  -3.760  1.00  0.00           H  
HETATM   45  H21 UNL     1      -1.373   1.994  -3.905  1.00  0.00           H  
HETATM   46  H22 UNL     1      -0.352   0.209  -2.960  1.00  0.00           H  
HETATM   47  H23 UNL     1      -1.072  -0.642  -1.589  1.00  0.00           H  
HETATM   48  H24 UNL     1       0.099   0.710  -1.328  1.00  0.00           H  
HETATM   49  H25 UNL     1      -0.223   2.675  -2.001  1.00  0.00           H  
HETATM   50  H26 UNL     1      -1.047   2.729  -0.428  1.00  0.00           H  
HETATM   51  H27 UNL     1      -1.798   3.496  -1.929  1.00  0.00           H  
CONECT    1    2    2   25   26
CONECT    2    3   10
CONECT    3    4   27   28
CONECT    4    5   29   30
CONECT    5    6   31   32
CONECT    6    7   33   34
CONECT    7    8    8    9
CONECT    9   35
CONECT   10   11   11   12
CONECT   11   36   37
CONECT   12   13   13   14
CONECT   14   15
CONECT   15   16   20   38
CONECT   16   17   39   40
CONECT   17   18   18   19
CONECT   20   21   41   42
CONECT   21   22   23   24
CONECT   22   43   44   45
CONECT   23   46   47   48
CONECT   24   49   50   51
END

HMDB0240794
     RDKit          3D
2,3-Dimethylideneoctanedioylcarnitine
 51 50  0  0  0  0  0  0  0  0999 V2000
    1.6091    0.2128    3.0888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3266   -0.8892    2.4171 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2619   -2.0511    2.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3726   -1.9246    1.5940 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9587   -1.9052    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1391   -1.7556   -0.7629 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8003   -0.4551   -0.5531 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2745    0.3811    0.2235 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0105   -0.1450   -1.2134 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1526   -0.9949    1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1307   -2.1412    0.9237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036    0.0826    1.3494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2274    1.8403 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9230   -0.1098    0.5127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729    0.9474    0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1742    0.4503    0.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2768    1.4300    0.7957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0394    2.5331    0.2460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5337    1.0991    1.2880 O   0  0  0  0  0  1  0  0  0  0  0  0
   -2.9978    1.0483   -1.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7992    1.3575   -1.9052 N   0  0  0  0  0  4  0  0  0  0  0  0
   -2.2055    1.5657   -3.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7906    0.3518   -1.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2269    2.6441   -1.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4796    0.2339    3.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0266    1.0853    3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6954   -2.9828    2.5482 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6776   -2.0278    3.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0318   -2.8462    1.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0527   -1.0666    1.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2775   -1.0684   -0.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4549   -2.8650   -0.1424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7945   -1.9075   -1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8496   -2.5640   -0.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4409    0.7376   -0.9790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0295   -2.2008    0.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4730   -3.0207    1.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6258    1.8700    0.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0209    0.2806    2.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5243   -0.4912    0.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3901    0.0929   -1.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7547    1.8124   -1.5185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0985    2.2249   -3.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4259    0.5734   -3.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3731    1.9937   -3.9047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3518    0.2090   -2.9603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0719   -0.6425   -1.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0989    0.7104   -1.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2226    2.6749   -2.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0474    2.7288   -0.4283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7982    3.4959   -1.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  2 10  1  0
 10 11  2  3
 10 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  2  0
 17 19  1  0
 15 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 20 41  1  0
 20 42  1  0
 22 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  0
 23 47  1  0
 23 48  1  0
 24 49  1  0
 24 50  1  0
 24 51  1  0
M  CHG  2  19  -1  21   1
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₇H₂₇NO₆

Average Molecular Weight

341.404

Monoisotopic Molecular Weight

341.183837593

IUPAC Name

3-[(7-carboxy-2,3-dimethylideneheptanoyl)oxy]-4-(trimethylazaniumyl)butanoate

Traditional Name

3-[(7-carboxy-2,3-dimethylideneheptanoyl)oxy]-4-(trimethylammonio)butanoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C17H27NO6/c1-12(8-6-7-9-15(19)20)13(2)17(23)24-14(10-16(21)22)11-18(3,4)5/h14H,1-2,6-11H2,3-5H3,(H-,19,20,21,22)

InChI Key

YVJRBPYWDVJLNP-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
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Quaternary ammonium salt
Carboxylic acid salt
Carboxylic acid ester
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic salt
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

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)

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
logP	-2.2	ChemAxon
pKa (Strongest Acidic)	4	ChemAxon
pKa (Strongest Basic)	-6.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	103.73 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	110.64 m³·mol⁻¹	ChemAxon
Polarizability	35.5 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	165.334	30932474
DeepCCS	[M-H]-	163.045	30932474
DeepCCS	[M-2H]-	196.069	30932474
DeepCCS	[M+Na]+	171.254	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2,3-Dimethylideneoctanedioylcarnitine	C[N+](C)(C)CC(CC([O-])=O)OC(=O)C(=C)C(=C)CCCCC(O)=O	3509.2	Standard polar	33892256
2,3-Dimethylideneoctanedioylcarnitine	C[N+](C)(C)CC(CC([O-])=O)OC(=O)C(=C)C(=C)CCCCC(O)=O	1788.4	Standard non polar	33892256
2,3-Dimethylideneoctanedioylcarnitine	C[N+](C)(C)CC(CC([O-])=O)OC(=O)C(=C)C(=C)CCCCC(O)=O	2234.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2,3-Dimethylideneoctanedioylcarnitine,1TMS,isomer #1	C=C(CCCCC(=O)O[Si](C)(C)C)C(=C)C(=O)OC(CC(=O)[O-])C[N+](C)(C)C	2239.7	Semi standard non polar	33892256
2,3-Dimethylideneoctanedioylcarnitine,1TBDMS,isomer #1	C=C(CCCCC(=O)O[Si](C)(C)C(C)(C)C)C(=C)C(=O)OC(CC(=O)[O-])C[N+](C)(C)C	2469.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2,3-Dimethylideneoctanedioylcarnitine 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 - 2,3-Dimethylideneoctanedioylcarnitine 10V, Positive-QTOF	Not Available	2021-04-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,3-Dimethylideneoctanedioylcarnitine 20V, Positive-QTOF	Not Available	2021-04-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,3-Dimethylideneoctanedioylcarnitine 40V, Positive-QTOF	Not Available	2021-04-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,3-Dimethylideneoctanedioylcarnitine 10V, Positive-QTOF	splash10-0006-0009000000-c19aa5e9614378d18364	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,3-Dimethylideneoctanedioylcarnitine 20V, Positive-QTOF	splash10-000l-9005000000-50849827df087c868911	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,3-Dimethylideneoctanedioylcarnitine 40V, Positive-QTOF	splash10-000i-9000000000-e9262cbaff8cb4ad0ba6	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
Acylcarnitine 2,3-Dimethylideneoctanedioylcarnitine		Not Available

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Ferdinandusse S, Mulders J, IJlst L, Denis S, Dacremont G, Waterham HR, Wanders RJ: Molecular cloning and expression of human carnitine octanoyltransferase: evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acids. Biochem Biophys Res Commun. 1999 Sep 16;263(1):213-8. [PubMed:10486279 ]
Blazenovic I, Kind T, Sa MR, Ji J, Vaniya A, Wancewicz B, Roberts BS, Torbasinovic H, Lee T, Mehta SS, Showalter MR, Song H, Kwok J, Jahn D, Kim J, Fiehn O: Structure Annotation of All Mass Spectra in Untargeted Metabolomics. Anal Chem. 2019 Feb 5;91(3):2155-2162. doi: 10.1021/acs.analchem.8b04698. Epub 2019 Jan 16. [PubMed:30608141 ]
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 ]
Violante S, Achetib N, van Roermund CWT, Hagen J, Dodatko T, Vaz FM, Waterham HR, Chen H, Baes M, Yu C, Argmann CA, Houten SM: Peroxisomes can oxidize medium- and long-chain fatty acids through a pathway involving ABCD3 and HSD17B4. FASEB J. 2019 Mar;33(3):4355-4364. doi: 10.1096/fj.201801498R. Epub 2018 Dec 12. [PubMed:30540494 ]
Yu D, Zhou L, Xuan Q, Wang L, Zhao X, Lu X, Xu G: Strategy for Comprehensive Identification of Acylcarnitines Based on Liquid Chromatography-High-Resolution Mass Spectrometry. Anal Chem. 2018 May 1;90(9):5712-5718. doi: 10.1021/acs.analchem.7b05471. Epub 2018 Apr 20. [PubMed:29651844 ]
Yan X, Markey SP, Marupaka R, Dong Q, Cooper BT, Mirokhin YA, Wallace WE, Stein SE: Mass Spectral Library of Acylcarnitines Derived from Human Urine. Anal Chem. 2020 May 5;92(9):6521-6528. doi: 10.1021/acs.analchem.0c00129. Epub 2020 Apr 23. [PubMed:32271007 ]
Zuniga A, Li L: Ultra-high performance liquid chromatography tandem mass spectrometry for comprehensive analysis of urinary acylcarnitines. Anal Chim Acta. 2011 Mar 9;689(1):77-84. doi: 10.1016/j.aca.2011.01.018. Epub 2011 Jan 18. [PubMed:21338760 ]
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 2,3-Dimethylideneoctanedioylcarnitine (HMDB0240794)

MOL for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

3D MOL for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

3D SDF for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

3D-SDF for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

PDB for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

3D PDB for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

SMILES for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

INCHI for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

Structure for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

3D Structure for HMDB0240794 (2,3-Dimethylideneoctanedioylcarnitine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra