NP-MRD: Showing NP-Card for decanoyllevocarnitine (NP0150518)

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Record Information

Version

2.0

Created at

2022-09-02 06:38:52 UTC

Updated at

2022-09-02 06:38:52 UTC

NP-MRD ID

NP0150518

Secondary Accession Numbers

None

Natural Product Identification

Common Name

decanoyllevocarnitine

Description

O-decanoyl-L-carnitine 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. Thus, O-decanoyl-L-carnitine is considered to be a fatty ester lipid molecule. decanoyllevocarnitine is found in Apis cerana. decanoyllevocarnitine was first documented in 2001 (PMID: 11420183). O-decanoyl-L-carnitine is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 54  0  0  0  0  0  0  0  0999 V2000
    7.1612   -1.0773   -0.6943 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8891   -1.7790   -1.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9344   -1.8842    0.0514 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5561   -0.5321    0.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8830    0.3017   -0.4699 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5072    1.6405    0.0998 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5738    1.4620    1.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3310    0.7064    0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6088    1.4444   -0.2028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6518    0.7070   -0.6016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5090   -0.3113   -1.2782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8739    1.1733   -0.2148 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1129    0.5268   -0.5652 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9510    1.5055   -1.2579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3098    1.9439   -2.5210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2112    1.5543   -2.9612 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9648    2.8926   -3.3425 O   0  0  0  0  0  1  0  0  0  0  0  0
   -3.6404   -0.0071    0.7291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8510   -0.7103    0.7420 N   0  0  0  0  0  4  0  0  0  0  0  0
   -4.6450   -1.9329    1.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8656    0.0065    1.5463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4034   -1.1617   -0.4902 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3200   -1.2669    0.3914 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1515   -0.0018   -0.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0057   -1.5927   -1.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1362   -2.8284   -1.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4330   -1.2477   -1.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0010   -2.3646   -0.3420 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3501   -2.4862    0.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4727   -0.0505    0.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8459   -0.6192    1.4410 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5696    0.4280   -1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9533   -0.1871   -0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0441    2.3286   -0.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4500    2.1496    0.4384 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2813    2.5222    1.5725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0910    1.0528    2.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7156    0.6253    1.8117 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6004   -0.3312    0.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3058    2.4321    0.1930 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2703    1.5539   -1.0839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8241   -0.3053   -1.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9674    1.1652   -1.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1347    2.4488   -0.6930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8063   -0.6220    1.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7145    0.8539    1.4571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9454   -1.7080    2.3914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2132   -2.6789    0.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6179   -2.3055    1.9058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9711    1.0502    1.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5026   -0.0420    2.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8454   -0.4786    1.4895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7392   -1.2013   -1.3497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8311   -2.2111   -0.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3394   -0.5509   -0.6684 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0
 14 15  1  0
 15 17  1  0
 15 16  2  0
 13 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
 13 42  1  6
 14 43  1  0
 14 44  1  0
 18 45  1  0
 18 46  1  0
 20 47  1  0
 20 48  1  0
 20 49  1  0
 21 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  0
 22 54  1  0
 22 55  1  0
  9 40  1  0
  9 41  1  0
  8 38  1  0
  8 39  1  0
  7 36  1  0
  7 37  1  0
  6 34  1  0
  6 35  1  0
  5 32  1  0
  5 33  1  0
  4 30  1  0
  4 31  1  0
  3 28  1  0
  3 29  1  0
  2 26  1  0
  2 27  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
M  CHG  2  17  -1  19   1
M  END


  Mrv1652303231705542D          

 23 22  0  0  1  0            999 V2000
    2.8066    2.4454    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    2.8579    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8066    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    4.5079    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    3.5211    4.5079    0.0000 O   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 N   0  3  0  0  0  0  0  0  0  0  0  0
    2.3941    2.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2191    0.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    1.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    3.2704    0.0000 O   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    2.0329    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
    6.3789    2.8579    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
    7.8079    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 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
  2 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  CHG  2   5  -1   8   1
M  END
> <DATABASE_ID>
NP0150518

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@](CC([O-])=O)(C[N+](C)(C)C)OC(=O)CCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C17H33NO4/c1-5-6-7-8-9-10-11-12-17(21)22-15(13-16(19)20)14-18(2,3)4/h15H,5-14H2,1-4H3/t15-/m1/s1

> <INCHI_KEY>
LZOSYCMHQXPBFU-OAHLLOKOSA-N

> <FORMULA>
C17H33NO4

> <MOLECULAR_WEIGHT>
315.454

> <EXACT_MASS>
315.240958547

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
37.297431178372086

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R)-3-(decanoyloxy)-4-(trimethylazaniumyl)butanoate

> <ALOGPS_LOGP>
-0.85

> <JCHEM_LOGP>
-0.633864135805079

> <ALOGPS_LOGS>
-6.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.216763902737658

> <JCHEM_PKA_STRONGEST_BASIC>
-7.057186892022333

> <JCHEM_POLAR_SURFACE_AREA>
66.43

> <JCHEM_REFRACTIVITY>
109.4707

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.35e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
O-decanoyl-L-carnitine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-MAR-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-MAR-17         0                                  
HETATM    1  H   UNK     0       5.239   4.565   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       6.573   5.335   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.239   6.105   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.239   7.645   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.905   8.415   0.000  0.00  0.00           O-1
HETATM    6  O   UNK     0       6.573   8.415   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.573   3.795   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       5.239   3.025   0.000  0.00  0.00           N+1
HETATM    9  C   UNK     0       4.469   4.358   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.009   1.691   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.905   2.255   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.906   6.105   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.240   3.795   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.574   6.105   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.907   5.335   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.241   6.105   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  C   UNK     0      21.243   6.105   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7   12                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4                                                            
CONECT    7    2    8                                                       
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8                                                            
CONECT   12    2   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   44    0
END

View in JSmol

Synonyms

Value	Source
L-Decanoylcarnitine	ChEBI
O-Decanoyl-(R)-carnitine	ChEBI
O-Decanoyl-R-carnitine	ChEBI

Chemical Formula

C₁₇H₃₃NO₄

Average Mass

315.4540 Da

Monoisotopic Mass

315.24096 Da

IUPAC Name

(3R)-3-(decanoyloxy)-4-(trimethylazaniumyl)butanoate

Traditional Name

O-decanoyl-L-carnitine

CAS Registry Number

Not Available

SMILES

[H][C@@](CC([O-])=O)(C[N+](C)(C)C)OC(=O)CCCCCCCCC

InChI Identifier

InChI=1S/C17H33NO4/c1-5-6-7-8-9-10-11-12-17(21)22-15(13-16(19)20)14-18(2,3)4/h15H,5-14H2,1-4H3/t15-/m1/s1

InChI Key

LZOSYCMHQXPBFU-OAHLLOKOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Apis cerana	LOTUS Database	35616633

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

O-acyl-L-carnitine (CHEBI:28717 )
O-decanoylcarnitine (CHEBI:28717 )
Fatty acyl carnitines (C03299 )
Fatty acyl carnitines (LMFA07070006 )

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	-0.85	ALOGPS
logP	-0.63	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	4.22	ChemAxon
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	66.43 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	109.47 m³·mol⁻¹	ChemAxon
Polarizability	37.3 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

External Links

HMDB ID

HMDB0062631

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C03299

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11953821

PDB ID

Not Available

ChEBI ID

28717

Good Scents ID

Not Available

References

General References

Tran TN, Retterstol K, Christophersen BO: Differences in the conversion of the polyunsaturated fatty acids [1-(14)C]22:4(n-6) and [1-(14)C]22:5(n-3) to [(14)C]22:5(n-6) and [(14)C]22:6(n-3) in isolated rat hepatocytes. Biochim Biophys Acta. 2001 May 31;1532(1-2):137-47. doi: 10.1016/s1388-1981(01)00127-5. [PubMed:11420183 ]
LOTUS database [Link]

Showing NP-Card for decanoyllevocarnitine (NP0150518)

MOL for NP0150518 (decanoyllevocarnitine)

3D MOL for NP0150518 (decanoyllevocarnitine)

3D SDF for NP0150518 (decanoyllevocarnitine)

3D-SDF for NP0150518 (decanoyllevocarnitine)

PDB for NP0150518 (decanoyllevocarnitine)

3D PDB for NP0150518 (decanoyllevocarnitine)

SMILES for NP0150518 (decanoyllevocarnitine)

INCHI for NP0150518 (decanoyllevocarnitine)

Structure for NP0150518 (decanoyllevocarnitine)

3D Structure for NP0150518 (decanoyllevocarnitine)