NP-MRD: Showing NP-Card for 6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate (NP0252069)

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Record Information

Version

2.0

Created at

2022-09-07 15:27:59 UTC

Updated at

2022-09-07 15:28:00 UTC

NP-MRD ID

NP0252069

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate

Description

6,6,9-Trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]Tetradecan-12-yl octadecanoate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate is found in Lactarius vellereus. 6,6,9-Trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]Tetradecan-12-yl octadecanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251514582D          

 37 41  0  0  0  0            999 V2000
   12.2921   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0066   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7210   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4355   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1500   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8645   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5789   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2934   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.0079   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.7223   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4368   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.1513   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   24.4381   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   25.1526   -3.9130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   26.6207   -3.8361    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
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  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 21 37  1  0  0  0  0
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 34 37  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004251514582D          

 37 41  0  0  0  0            999 V2000
   12.2921   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0066   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   15.1500   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   16.5789   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   18.0079   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   20.8658   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5802   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2947   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0092   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7236   -3.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.4381   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.4381   -2.6755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.1526   -3.9130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.8671   -3.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9533   -2.6801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.7603   -2.5085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1728   -3.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.7248   -2.6099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.9797   -3.3945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.2347   -4.1792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9883   -4.5147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9021   -5.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.7271   -5.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9883   -6.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.0951   -5.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.6826   -4.7923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.8757   -4.6207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.7041   -5.4277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.0687   -4.4492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.6207   -3.8361    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  2  0  0  0  0
 18 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
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 27 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 21 37  1  0  0  0  0
 24 37  1  0  0  0  0
 34 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252069

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCC(=O)OC1OCC23OC2C2CC(C)(C)CC2C2(C)CC132

> <INCHI_IDENTIFIER>
InChI=1S/C33H56O4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-27(34)36-29-32-23-31(32,4)26-22-30(2,3)21-25(26)28-33(32,37-28)24-35-29/h25-26,28-29H,5-24H2,1-4H3

> <INCHI_KEY>
VRKPUGRREPONNX-UHFFFAOYSA-N

> <FORMULA>
C33H56O4

> <MOLECULAR_WEIGHT>
516.807

> <EXACT_MASS>
516.417860283

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
65.50509943015257

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate

> <ALOGPS_LOGP>
8.45

> <JCHEM_LOGP>
9.569706062666668

> <ALOGPS_LOGS>
-7.55

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9949951527714433

> <JCHEM_POLAR_SURFACE_AREA>
48.06

> <JCHEM_REFRACTIVITY>
147.72959999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.45e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      22.945  -7.304   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      24.279  -6.534   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      25.613  -7.304   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      26.946  -6.534   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      28.280  -7.304   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      29.614  -6.534   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      30.947  -7.304   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      32.281  -6.534   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      33.615  -7.304   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      34.948  -6.534   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      36.282  -7.304   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      37.616  -6.534   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      38.949  -7.304   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      40.283  -6.534   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      41.617  -7.304   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      42.950  -6.534   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      44.284  -7.304   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      45.618  -6.534   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      45.618  -4.994   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      46.951  -7.304   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      48.285  -6.534   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      48.446  -5.003   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      49.952  -4.683   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      50.722  -6.016   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      51.753  -4.872   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      52.229  -6.336   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      52.705  -7.801   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      54.112  -8.427   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      53.951  -9.959   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      55.491  -9.959   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      54.112 -11.491   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      52.444 -10.279   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      51.674  -8.946   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      50.168  -8.625   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      49.848 -10.132   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      48.662  -8.305   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      49.692  -7.161   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   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   37                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   37                                             
CONECT   25   24   26                                                       
CONECT   26   25   24   27                                                  
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   29   33                                                       
CONECT   33   32   27   34                                                  
CONECT   34   33   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   21   24   34                                             
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Value	Source
6,6,9-Trimethyl-2,13-dioxapentacyclo[9.3.0.0,.0,.0,]tetradecan-12-yl octadecanoic acid	Generator
6,6,9-Trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoic acid	Generator

Chemical Formula

C₃₃H₅₆O₄

Average Mass

516.8070 Da

Monoisotopic Mass

516.41786 Da

IUPAC Name

6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate

Traditional Name

6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCC(=O)OC1OCC23OC2C2CC(C)(C)CC2C2(C)CC132

InChI Identifier

InChI=1S/C33H56O4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-27(34)36-29-32-23-31(32,4)26-22-30(2,3)21-25(26)28-33(32,37-28)24-35-29/h25-26,28-29H,5-24H2,1-4H3

InChI Key

VRKPUGRREPONNX-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
Lactarius vellereus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Fatty acid ester
Oxepane
Fatty acyl
Oxolane
Carboxylic acid ester
Acetal
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	8.45	ALOGPS
logP	9.57	ChemAxon
logS	-7.6	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	48.06 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	147.73 m³·mol⁻¹	ChemAxon
Polarizability	65.51 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

14866388

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate (NP0252069)

MOL for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

3D MOL for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

3D SDF for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

3D-SDF for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

PDB for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

3D PDB for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

SMILES for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

INCHI for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

Structure for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)

3D Structure for NP0252069 (6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl octadecanoate)