NP-MRD: Showing NP-Card for (4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate (NP0328867)

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Record Information

Version

2.0

Created at

2022-09-12 12:43:04 UTC

Updated at

2022-09-12 12:43:04 UTC

NP-MRD ID

NP0328867

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate

Description

(4R)-5-[2-(5,8-dioxo-5,8-dihydronaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate belongs to the class of organic compounds known as wax monoesters. These are waxes bearing an ester group at exactly one position. (4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate is found in Cordia polycephala. Based on a literature review very few articles have been published on (4R)-5-[2-(5,8-dioxo-5,8-dihydronaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122214432D          

 51 52  0  0  1  0            999 V2000
  -24.2920   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -23.5775   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -22.8631   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -22.1486   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -21.4341   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -20.7197   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -20.0052   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -19.2907   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.5762   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.8618   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.1473   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.4328   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.7184   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4289   -1.6500    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
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0000   -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
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   -0.7145    1.2375    0.0000 O   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    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 37 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 40 47  1  0  0  0  0
 47 48  2  0  0  0  0
 34 49  2  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
M  END

     RDKit          3D

127128  0  0  0  0  0  0  0  0999 V2000
   14.0820   -3.1212    0.1409 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4252   -2.5137    1.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4768   -1.0617    1.4823 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.5482    2.2361   -0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5871   -0.0143   -0.6703 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3928    0.7089   -1.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2566    0.9722   -0.2491 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5025    1.6070    1.0518 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2846    2.1157    1.7197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8850    1.3416    2.0900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8072    0.1421    2.9351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2733   -1.1222    2.3657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1912   -1.6607    1.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5656   -1.9913    1.8421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5216   -2.4748    0.8171 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309122214432D          

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 26 27  2  0  0  0  0
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 29 30  1  0  0  0  0
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 40 47  1  0  0  0  0
 47 48  2  0  0  0  0
 34 49  2  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0328867

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCC[C@@H](C)C(CCC1=CC=C2C(=O)C=CC(=O)C2=C1)=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C47H76O4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-30-47(50)51-37-28-29-40(4)42(39(2)3)33-31-41-32-34-43-44(38-41)46(49)36-35-45(43)48/h32,34-36,38,40H,5-31,33,37H2,1-4H3/t40-/m1/s1

> <INCHI_KEY>
OVAKALBDGKRYHF-RRHRGVEJSA-N

> <FORMULA>
C47H76O4

> <MOLECULAR_WEIGHT>
705.121

> <EXACT_MASS>
704.574360927

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
127

> <JCHEM_AVERAGE_POLARIZABILITY>
92.83546755516461

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4R)-5-[2-(5,8-dioxo-5,8-dihydronaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate

> <JCHEM_LOGP>
15.461601913666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.44671815808816

> <JCHEM_PKA_STRONGEST_BASIC>
-6.7675399846423865

> <JCHEM_POLAR_SURFACE_AREA>
60.440000000000005

> <JCHEM_REFRACTIVITY>
219.19070000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
33

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4R)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0     -45.345  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -44.011  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -42.678  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -41.344  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -40.010  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -38.677  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -37.343  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -36.009  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -34.676  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -33.342  -5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -32.008  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -30.675  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -29.341  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -28.007  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -26.674  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -25.340  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -24.006  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -17.338  -5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0     -12.003  -6.930   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0     -10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   49                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   42                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   47                                                  
CONECT   41   40   42   43                                                  
CONECT   42   41   37                                                       
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   40   48                                                  
CONECT   48   47                                                            
CONECT   49   34   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  104    0
END

View in JSmol

Synonyms

Value	Source
(4R)-5-[2-(5,8-Dioxo-5,8-dihydronaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoic acid	Generator

Chemical Formula

C₄₇H₇₆O₄

Average Mass

705.1210 Da

Monoisotopic Mass

704.57436 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCC[C@@H](C)C(CCC1=CC=C2C(=O)C=CC(=O)C2=C1)=C(C)C

InChI Identifier

InChI=1S/C47H76O4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-30-47(50)51-37-28-29-40(4)42(39(2)3)33-31-41-32-34-43-44(38-41)46(49)36-35-45(43)48/h32,34-36,38,40H,5-31,33,37H2,1-4H3/t40-/m1/s1

InChI Key

OVAKALBDGKRYHF-RRHRGVEJSA-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
Cordia polycephala	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as wax monoesters. These are waxes bearing an ester group at exactly one position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Wax monoesters

Alternative Parents

Substituents

Wax monoester skeleton
Fatty alcohol ester
Naphthoquinone
Naphthalene
Aryl ketone
Quinone
Benzenoid
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

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

External Links

HMDB ID

Not Available

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

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162857656

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate (NP0328867)

MOL for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

3D MOL for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

3D SDF for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

3D-SDF for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

PDB for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

3D PDB for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

SMILES for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

INCHI for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

Structure for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)

3D Structure for NP0328867 ((4r)-5-[2-(5,8-dioxonaphthalen-2-yl)ethyl]-4,6-dimethylhept-5-en-1-yl hexacosanoate)