NP-MRD: Showing NP-Card for 4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene (NP0247751)

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Record Information

Version

2.0

Created at

2022-09-07 09:42:55 UTC

Updated at

2022-09-07 09:42:56 UTC

NP-MRD ID

NP0247751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene

Description

4,6,8,10,12,14,16,18-Octamethoxy-19-methylpentacosa-1,19-diene belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups. 4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene is found in Stelletta clavosa. 4,6,8,10,12,14,16,18-Octamethoxy-19-methylpentacosa-1,19-diene is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171503522D          

 42 41  0  0  0  0            999 V2000
   14.2970  -15.9622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6346  -15.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.0667  -14.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   12.4989  -12.8479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5936  -12.0284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3507  -11.7005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.1741  -11.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 11 39  1  0  0  0  0
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  9 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END

     RDKit          3D

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  1 43  1  0
  1 44  1  0
 42106  1  0
 42107  1  0
 42108  1  0
 40103  1  0
 40104  1  0
 40105  1  0
 38100  1  0
 38101  1  0
 38102  1  0
 36 97  1  0
 36 98  1  0
 36 99  1  0
 34 94  1  0
 34 95  1  0
 34 96  1  0
 32 91  1  0
 32 92  1  0
 32 93  1  0
 30 88  1  0
 30 89  1  0
 30 90  1  0
 20 70  1  0
 20 71  1  0
 20 72  1  0
M  END


  Mrv1533004171503522D          

 42 41  0  0  0  0            999 V2000
   14.2970  -15.9622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6346  -15.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7292  -14.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0667  -14.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1614  -13.3396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4989  -12.8479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5936  -12.0284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3507  -11.7005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9311  -11.5366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1741  -11.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5116  -11.3727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7546  -11.7005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0921  -11.2088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3350  -11.5366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6726  -11.0449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9155  -11.3727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2531  -10.8810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4960  -11.2088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8336  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0765  -11.0449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4141  -10.5532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6570  -10.8810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9946  -10.3892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5751  -10.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1820  -10.5532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892   -9.5697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4268   -9.0780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5087   -9.7336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8463   -9.2419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9282   -9.8975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2658   -9.4058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3477  -10.0614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6853   -9.5697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7672  -10.2253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1048   -9.7336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1868  -10.3892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5243   -9.8975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6063  -10.5532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9438  -10.0614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0258  -10.7171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7828  -10.3892    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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  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  2  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  1  0  0  0  0
 19 31  1  0  0  0  0
 31 32  1  0  0  0  0
 17 33  1  0  0  0  0
 33 34  1  0  0  0  0
 15 35  1  0  0  0  0
 35 36  1  0  0  0  0
 13 37  1  0  0  0  0
 37 38  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  0  0  0  0
  9 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0247751

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC=C(C)C(CC(CC(CC(CC(CC(CC(CC(CC=C)OC)OC)OC)OC)OC)OC)OC)OC

> <INCHI_IDENTIFIER>
InChI=1S/C34H66O8/c1-12-14-15-16-18-26(3)34(42-11)25-33(41-10)24-32(40-9)23-31(39-8)22-30(38-7)21-29(37-6)20-28(36-5)19-27(35-4)17-13-2/h13,18,27-34H,2,12,14-17,19-25H2,1,3-11H3

> <INCHI_KEY>
YHNODRCOFQSLKV-UHFFFAOYSA-N

> <FORMULA>
C34H66O8

> <MOLECULAR_WEIGHT>
602.894

> <EXACT_MASS>
602.475769085

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
72.19001627858671

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene

> <ALOGPS_LOGP>
5.05

> <JCHEM_LOGP>
4.853007387666665

> <ALOGPS_LOGS>
-7.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.224530725175207

> <JCHEM_POLAR_SURFACE_AREA>
73.84000000000002

> <JCHEM_REFRACTIVITY>
173.1762999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
29

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.76e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      26.688 -29.796   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.451 -28.878   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      25.628 -27.348   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.391 -26.430   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      24.568 -24.901   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      23.331 -23.983   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.508 -22.453   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      24.921 -21.841   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.271 -21.535   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.858 -22.147   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      19.622 -21.229   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.209 -21.841   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.972 -20.923   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.559 -21.535   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.322 -20.617   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.909 -21.229   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.672 -20.311   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.259 -20.923   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.023 -20.005   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.610 -20.617   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.373 -19.699   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.960 -20.311   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.723 -19.393   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.310 -20.005   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.073 -19.087   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.340 -19.699   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.900 -17.863   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.663 -16.946   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.550 -18.169   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.313 -17.251   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       9.199 -18.475   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.963 -17.557   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      11.849 -18.781   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      10.613 -17.863   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      14.499 -19.087   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      13.262 -18.169   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      17.149 -19.393   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      15.912 -18.475   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      19.798 -19.699   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      18.562 -18.781   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      22.448 -20.005   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      23.861 -19.393   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    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   41                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   39                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   37                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   35                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   33                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   31                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   23   28                                                       
CONECT   28   27                                                            
CONECT   29   21   30                                                       
CONECT   30   29                                                            
CONECT   31   19   32                                                       
CONECT   32   31                                                            
CONECT   33   17   34                                                       
CONECT   34   33                                                            
CONECT   35   15   36                                                       
CONECT   36   35                                                            
CONECT   37   13   38                                                       
CONECT   38   37                                                            
CONECT   39   11   40                                                       
CONECT   40   39                                                            
CONECT   41    9   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₆₆O₈

Average Mass

602.8940 Da

Monoisotopic Mass

602.47577 Da

IUPAC Name

4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene

Traditional Name

4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene

CAS Registry Number

Not Available

SMILES

CCCCCC=C(C)C(CC(CC(CC(CC(CC(CC(CC(CC=C)OC)OC)OC)OC)OC)OC)OC)OC

InChI Identifier

InChI=1S/C34H66O8/c1-12-14-15-16-18-26(3)34(42-11)25-33(41-10)24-32(40-9)23-31(39-8)22-30(38-7)21-29(37-6)20-28(36-5)19-27(35-4)17-13-2/h13,18,27-34H,2,12,14-17,19-25H2,1,3-11H3

InChI Key

YHNODRCOFQSLKV-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
Stelletta clavosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Dialkyl ethers

Alternative Parents

Hydrocarbon derivatives

Substituents

Dialkyl ether
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	5.05	ALOGPS
logP	4.85	ChemAxon
logS	-7.1	ALOGPS
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	73.84 Å²	ChemAxon
Rotatable Bond Count	29	ChemAxon
Refractivity	173.18 m³·mol⁻¹	ChemAxon
Polarizability	72.19 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

85415366

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene (NP0247751)

MOL for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

3D MOL for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

3D SDF for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

3D-SDF for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

PDB for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

3D PDB for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

SMILES for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

INCHI for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

Structure for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)

3D Structure for NP0247751 (4,6,8,10,12,14,16,18-octamethoxy-19-methylpentacosa-1,19-diene)