NP-MRD: Showing NP-Card for methyl 8-(3-octyloxiran-2-yl)octanoate (NP0326818)

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Record Information

Version

1.0

Created at

2022-09-12 08:47:18 UTC

Updated at

2022-09-12 08:47:18 UTC

NP-MRD ID

NP0326818

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 8-(3-octyloxiran-2-yl)octanoate

Description

Methyl 8-(3-octyloxiran-2-yl)octanoate belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. methyl 8-(3-octyloxiran-2-yl)octanoate is found in Xeranthemum annuum. Methyl 8-(3-octyloxiran-2-yl)octanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 58 58  0  0  0  0  0  0  0  0999 V2000
   -7.7068   -3.4278    0.7231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1002   -1.9952    0.5611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9554   -1.0447    0.6982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8717   -1.2862   -0.3232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7610   -0.2505   -0.0761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6692   -0.4551   -1.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5340    0.5156   -0.9211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9008    0.3894    0.4293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7391    1.3450    0.6107 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9474    2.6976    0.5087 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3615    2.1244   -0.6142 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1282    2.2758   -0.8202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8090    2.9758    0.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2823    3.0987    0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9579    1.7488   -0.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4230    1.9699   -0.4184 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1577    0.6711   -0.6087 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0442   -0.1738    0.6137 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8068   -1.4362    0.3505 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4013   -1.6529   -0.7340 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8860   -2.4385    1.3208 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6153   -3.6419    1.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0697   -3.5415    1.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6486   -4.0062    0.9360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2817   -3.8884   -0.1897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8800   -1.7471    1.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5807   -1.8428   -0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3288   -0.0099    0.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5005   -1.1633    1.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4040   -2.2826   -0.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2263   -1.2047   -1.3700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4195   -0.3006    0.9662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2051    0.7631   -0.2110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2901   -1.5186   -1.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1068   -0.3880   -2.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7575    0.2018   -1.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8977    1.5438   -1.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4454   -0.6433    0.4711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6051    0.4313    1.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0414    1.0345    1.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9808    2.1054   -1.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2941    2.8069   -1.7579 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5205    1.2170   -0.8466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4162    4.0073    0.4638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7082    2.4655    1.2792 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8126    3.6923    0.7969 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4720    3.6527   -0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5102    1.2893   -1.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7360    1.1571    0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5802    2.6134   -1.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8700    2.4438    0.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6241    0.1296   -1.4323 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2192    0.8333   -0.8777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9630   -0.4228    0.7700 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4434    0.3613    1.4965 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2749   -3.7779    1.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8995   -4.4802    0.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2781   -3.5408    0.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  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  2  0
 19 21  1  0
 21 22  1  0
 11  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  1
 11 41  1  6
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 15 49  1  0
 16 50  1  0
 16 51  1  0
 17 52  1  0
 17 53  1  0
 18 54  1  0
 18 55  1  0
 22 56  1  0
 22 57  1  0
 22 58  1  0
M  END


  Mrv1533004161508052D          

 22 22  0  0  0  0            999 V2000
   -7.6677    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9533    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2388    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5243    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0954    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9520    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5395    2.6664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8743    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888    2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3033    1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0177    1.9520    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
  9 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  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326818

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCC1OC1CCCCCCCC(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C19H36O3/c1-3-4-5-6-8-11-14-17-18(22-17)15-12-9-7-10-13-16-19(20)21-2/h17-18H,3-16H2,1-2H3

> <INCHI_KEY>
CAMHHLOGFDZBBG-UHFFFAOYSA-N

> <FORMULA>
C19H36O3

> <MOLECULAR_WEIGHT>
312.494

> <EXACT_MASS>
312.266445019

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.669467943006595

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 8-(3-octyloxiran-2-yl)octanoate

> <ALOGPS_LOGP>
6.66

> <JCHEM_LOGP>
5.991695602

> <ALOGPS_LOGS>
-6.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.201905498818415

> <JCHEM_POLAR_SURFACE_AREA>
38.83

> <JCHEM_REFRACTIVITY>
90.57560000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.54e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 8-(3-octyloxiran-2-yl)octanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0     -14.313   3.644   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -12.979   2.874   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -11.646   3.644   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.312   2.874   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.978   3.644   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.645   2.874   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.311   3.644   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.977   2.874   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.644   3.644   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.874   4.977   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.104   3.644   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.770   2.874   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.564   3.644   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.897   2.874   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.231   3.644   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.565   2.874   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.898   3.644   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.232   2.874   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.566   3.644   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.566   5.184   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       9.899   2.874   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.233   3.644   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   11                                                  
CONECT   10    9   11                                                       
CONECT   11   10    9   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   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Value	Source
Methyl 8-(3-octyloxiran-2-yl)octanoic acid	Generator
Methyl 9,10-epoxystearate, carboxy 14C-labeled, (cis)-isomer	MeSH
Methyl cis-9,10-epoxystearate	MeSH
Methyl 9,10-epoxystearate, (2S-cis)-isomer	MeSH
trans-9,10-Epoxystearate methyl ester	MeSH
cis-9,10-Epoxystearate methyl ester	MeSH
Methyl 9,10-epoxystearate	MeSH
Methyl 9,10-epoxystearate, (2R-cis)-isomer	MeSH
Methyl 9,10-epoxystearate, (2R-trans)-isomer	MeSH
Methyl 9,10-epoxystearate, (cis)-isomer	MeSH
Methyl 9,10-epoxystearate, (trans)-isomer	MeSH
Methyl 9,10-epoxystearic acid	Generator

Chemical Formula

C₁₉H₃₆O₃

Average Mass

312.4940 Da

Monoisotopic Mass

312.26645 Da

IUPAC Name

methyl 8-(3-octyloxiran-2-yl)octanoate

Traditional Name

methyl 8-(3-octyloxiran-2-yl)octanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCC1OC1CCCCCCCC(=O)OC

InChI Identifier

InChI=1S/C19H36O3/c1-3-4-5-6-8-11-14-17-18(22-17)15-12-9-7-10-13-16-19(20)21-2/h17-18H,3-16H2,1-2H3

InChI Key

CAMHHLOGFDZBBG-UHFFFAOYSA-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
Xeranthemum annuum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Fatty acid ester
Fatty acid methyl ester
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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
logP	6.66	ALOGPS
logP	5.99	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	38.83 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	90.58 m³·mol⁻¹	ChemAxon
Polarizability	40.67 Å³	ChemAxon
Number of Rings	1	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 8-(3-octyloxiran-2-yl)octanoate (NP0326818)

MOL for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

3D MOL for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

3D SDF for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

3D-SDF for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

PDB for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

3D PDB for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

SMILES for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

INCHI for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

Structure for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)

3D Structure for NP0326818 (methyl 8-(3-octyloxiran-2-yl)octanoate)