NP-MRD: Showing NP-Card for oleyl acetate (NP0266805)

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Record Information

Version

2.0

Created at

2022-09-08 11:22:38 UTC

Updated at

2022-09-08 11:22:38 UTC

NP-MRD ID

NP0266805

Secondary Accession Numbers

None

Natural Product Identification

Common Name

oleyl acetate

Description

Oleyl acetate, also known as oleyl acetic acid, belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. oleyl acetate is found in Bombus muscorum. oleyl acetate was first documented in 1988 (PMID: 3143910). Oleyl acetate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 60 59  0  0  0  0  0  0  0  0999 V2000
   -5.9868    2.6982    0.9609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6859    1.6980    0.0848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7562    0.6205   -0.4178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1323   -0.1606    0.7196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2312   -1.1992    0.0868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5311   -2.0637    1.0533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6349   -1.4547    2.0437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4390   -0.7134    1.4909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6455   -1.6631    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2980   -1.5620   -0.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6810   -0.4343   -1.3573 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3714    0.4235   -1.9648 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3174   -0.1022   -2.9499 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2327   -1.1970   -2.5361 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0545   -0.7837   -1.3283 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9001    0.4177   -1.6164 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6942    0.8062   -0.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6135   -0.3058    0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3494    0.1059    1.1460 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2141    1.1640    1.0797 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9721    1.5761    2.2881 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3968    1.8105    0.0270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2029    3.2507    0.3989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7417    3.4600    1.2533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5595    2.2679    1.8719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5110    1.2385    0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1276    2.2439   -0.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3909   -0.1062   -0.9841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0052    0.9905   -1.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5029    0.5672    1.2856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9436   -0.5847    1.3139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6064   -0.6944   -0.6591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9434   -1.8389   -0.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2879   -2.7330    1.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9321   -2.8093    0.4400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2067   -2.2904    2.6817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1403   -0.7901    2.7815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8260    0.1661    0.9895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8383   -0.4190    2.3967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3071   -2.5621    1.2934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2792   -2.4096   -0.9142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2273   -0.8940   -2.2611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5055    0.1899   -0.9225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9751    0.9597   -1.1544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1632    1.2949   -2.4762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7562   -0.4760   -3.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9938    0.7200   -3.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0511   -1.2860   -3.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7891   -2.1765   -2.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4232   -0.6231   -0.4284 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6843   -1.6781   -1.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6424    0.1409   -2.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3118    1.2719   -2.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1963    1.7828   -0.5210 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9338    0.9321    0.4327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3407   -0.5052   -0.7931 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0290   -1.2372    0.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7943    2.6378    2.4784 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0392    1.3152    2.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6354    1.0028    3.1748 H   0  0  0  0  0  0  0  0  0  0  0  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
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 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
 20 22  2  0
  9 40  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
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 13 47  1  0
 14 48  1  0
 14 49  1  0
 15 50  1  0
 15 51  1  0
 16 52  1  0
 16 53  1  0
 17 54  1  0
 17 55  1  0
 18 56  1  0
 18 57  1  0
 21 58  1  0
 21 59  1  0
 21 60  1  0
M  END

  Mrv1572004251600462D          

 24 23  0  0  0  0            999 V2000
   -9.1263    2.5046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3052   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4118    2.0921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4118    1.2671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6974    0.8546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6974    0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9829   -0.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9829   -1.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2684   -1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2684   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5539   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6961   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9816   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2671   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5526   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1618   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5908   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5908   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8763   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9829   -2.8579    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5539   -3.6829    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  2  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20  2  1  0  0  0  0
 21 20  2  0  0  0  0
 22 19  1  0  0  0  0
 22 20  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266805

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(CCCCCCCC)=C(/[H])CCCCCCCCOC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20(2)21/h10-11H,3-9,12-19H2,1-2H3/b11-10-

> <INCHI_KEY>
GYGAZRPDUOHMAF-KHPPLWFESA-N

> <FORMULA>
C20H38O2

> <MOLECULAR_WEIGHT>
310.522

> <EXACT_MASS>
310.287180464

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
41.35948190170423

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9Z)-octadec-9-en-1-yl acetate

> <ALOGPS_LOGP>
8.31

> <JCHEM_LOGP>
7.108487009666667

> <ALOGPS_LOGS>
-7.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.993812176968582

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
96.81699999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.84e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(9Z)-octadec-9-en-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-16   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-16         0                                  
HETATM    1  C   UNK     0     -17.036   4.675   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.303  -4.565   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -15.702   3.905   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -15.702   2.365   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -14.368   1.595   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -14.368   0.055   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -13.035  -0.715   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -13.035  -2.255   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -11.701  -3.025   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -11.701  -4.565   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -10.367  -5.335   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -9.034  -4.565   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -7.700  -5.335   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.366  -4.565   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.033  -5.335   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.699  -4.565   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.365  -5.335   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.032  -4.565   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.302  -5.335   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.969  -5.335   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.969  -6.875   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       1.636  -4.565   0.000  0.00  0.00           O+0
HETATM   23  H   UNK     0     -13.035  -5.335   0.000  0.00  0.00           H+0
HETATM   24  H   UNK     0     -10.367  -6.875   0.000  0.00  0.00           H+0
CONECT    1    3                                                            
CONECT    2   20                                                            
CONECT    3    1    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   23                                                  
CONECT   11   10   12   24                                                  
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   22                                                       
CONECT   20    2   21   22                                                  
CONECT   21   20                                                            
CONECT   22   19   20                                                       
CONECT   23   10                                                            
CONECT   24   11                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   46    0
END

View in JSmol

Synonyms

Value	Source
(Z)-Octadec-9-en-1-yl acetate	ChEBI
9-Octadecen-1-yl acetate	ChEBI
9Z-Octadecenyl acetate	ChEBI
Acetic acid oleyl ester	ChEBI
Acetic acid, 9-octadecenyl ester	ChEBI
Z-9-Octadecen-1-ol acetate	ChEBI
(Z)-Octadec-9-en-1-yl acetic acid	Generator
9-Octadecen-1-yl acetic acid	Generator
9Z-Octadecenyl acetic acid	Generator
Acetate oleyl ester	Generator
Acetate, 9-octadecenyl ester	Generator
Z-9-Octadecen-1-ol acetic acid	Generator
Oleyl acetic acid	Generator

Chemical Formula

C₂₀H₃₈O₂

Average Mass

310.5220 Da

Monoisotopic Mass

310.28718 Da

IUPAC Name

(9Z)-octadec-9-en-1-yl acetate

Traditional Name

(9Z)-octadec-9-en-1-yl acetate

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCCCCC)=C(/[H])CCCCCCCCOC(C)=O

InChI Identifier

InChI=1S/C20H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20(2)21/h10-11H,3-9,12-19H2,1-2H3/b11-10-

InChI Key

GYGAZRPDUOHMAF-KHPPLWFESA-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
Bombus muscorum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohol esters

Direct Parent

Fatty alcohol esters

Alternative Parents

Substituents

Fatty alcohol ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Wax monoesters (LMFA07010389 )

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	8.31	ALOGPS
logP	7.11	ChemAxon
logS	-7.2	ALOGPS
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	96.82 m³·mol⁻¹	ChemAxon
Polarizability	41.36 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

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

5363289

PDB ID

Not Available

ChEBI ID

134476

Good Scents ID

Not Available

References

General References

Tsirka SA, Kyriakidis DA: In vitro alterations of L-asparaginase activity of Tetrahymena pyriformis by lipids. Mol Cell Biochem. 1988 Oct;83(2):147-55. doi: 10.1007/BF00226142. [PubMed:3143910 ]
LOTUS database [Link]

Showing NP-Card for oleyl acetate (NP0266805)

MOL for NP0266805 (oleyl acetate)

3D MOL for NP0266805 (oleyl acetate)

3D SDF for NP0266805 (oleyl acetate)

3D-SDF for NP0266805 (oleyl acetate)

PDB for NP0266805 (oleyl acetate)

3D PDB for NP0266805 (oleyl acetate)

SMILES for NP0266805 (oleyl acetate)

INCHI for NP0266805 (oleyl acetate)

Structure for NP0266805 (oleyl acetate)

3D Structure for NP0266805 (oleyl acetate)