NP-MRD: Showing NP-Card for methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate (NP0258101)

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Record Information

Version

2.0

Created at

2022-09-07 23:24:41 UTC

Updated at

2022-09-07 23:24:41 UTC

NP-MRD ID

NP0258101

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate

Description

Methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate is found in Ononis speciosa. Methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241517422D          

 33 33  0  0  0  0            999 V2000
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    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  2  0  0  0  0
  8 10  1  0  0  0  0
 11  6  1  4  0  0  0
 11 12  2  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  2  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
 22 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

     RDKit          3D

 75 75  0  0  0  0  0  0  0  0999 V2000
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    7.4336   -2.9655   -0.0774 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9118    0.4225    1.3376 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0510    1.1110    2.3425 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1444    2.0215    2.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7635    2.5737    0.8006 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2672    2.3846    0.4968 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9856    0.9364    0.4835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4500    0.5678    0.2216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4091    1.1030    1.2128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8444    0.7473    0.9776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3892    1.2231   -0.3194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7850    0.9062   -0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7867    1.8678   -0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1194    1.6205   -0.6133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0838    2.6130   -0.3718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4562    2.3781   -0.6096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4646    0.3743   -1.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5141   -0.5968   -1.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8444   -1.8607   -1.8101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1949   -2.1427   -2.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1669   -0.3078   -1.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1951   -1.3451   -1.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6214   -1.4619   -2.4660 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7999   -2.3071   -0.4171 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5313   -1.1857   -0.8674 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8513    0.1508    1.9290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1875    0.8187    3.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6237    2.3967    3.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0248    3.6641    0.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2693    2.0313   -0.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7411    2.9591    1.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0752    2.8510   -0.4701 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5474    0.5201   -0.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3855    0.3920    1.3540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7140    0.9315   -0.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3627    2.2327    1.2236 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.9705   -0.3343    1.1496 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.0256    3.3180   -0.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4118    2.0844   -1.7974 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6639    3.3926   -0.6197 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 30  1  0
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 31 32  1  0
 31 33  2  0
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 29 70  1  0
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M  END


  Mrv1533004241517422D          

 33 33  0  0  0  0            999 V2000
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.0026   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1447   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    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  2  0  0  0  0
  8 10  1  0  0  0  0
 11  6  1  4  0  0  0
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 17 18  1  0  0  0  0
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 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258101

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC(OC(C)=O)C=CCCCCCCCC1=CC(OC)=CC(OC)=C1C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C27H42O6/c1-6-7-13-17-23(33-21(2)28)18-15-12-10-8-9-11-14-16-22-19-24(30-3)20-25(31-4)26(22)27(29)32-5/h15,18-20,23H,6-14,16-17H2,1-5H3

> <INCHI_KEY>
LYNBXJFKJLMEQJ-UHFFFAOYSA-N

> <FORMULA>
C27H42O6

> <MOLECULAR_WEIGHT>
462.627

> <EXACT_MASS>
462.298139072

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
54.25989748912799

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate

> <ALOGPS_LOGP>
7.15

> <JCHEM_LOGP>
7.247155634666667

> <ALOGPS_LOGS>
-6.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.5754242016703

> <JCHEM_POLAR_SURFACE_AREA>
71.06

> <JCHEM_REFRACTIVITY>
132.24849999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.01e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.334 -11.550   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.001 -11.550   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.670 -10.010   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      18.672  -9.240   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      18.672  -7.700   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      16.004 -13.860   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      14.670 -14.630   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.003 -11.550   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      13.337 -13.860   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      12.003 -14.630   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   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   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   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   20   30                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   66    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoic acid	Generator

Chemical Formula

C₂₇H₄₂O₆

Average Mass

462.6270 Da

Monoisotopic Mass

462.29814 Da

IUPAC Name

methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate

Traditional Name

methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate

CAS Registry Number

Not Available

SMILES

CCCCCC(OC(C)=O)C=CCCCCCCCC1=CC(OC)=CC(OC)=C1C(=O)OC

InChI Identifier

InChI=1S/C27H42O6/c1-6-7-13-17-23(33-21(2)28)18-15-12-10-8-9-11-14-16-22-19-24(30-3)20-25(31-4)26(22)27(29)32-5/h15,18-20,23H,6-14,16-17H2,1-5H3

InChI Key

LYNBXJFKJLMEQJ-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
Ononis speciosa	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
O-methoxybenzoic acid or derivatives
P-methoxybenzoic acid or derivatives
Benzoate ester
Dimethoxybenzene
M-dimethoxybenzene
Benzoic acid or derivatives
Anisole
Methoxybenzene
Phenol ether
Benzoyl
Phenoxy compound
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Ether
Carbonyl group
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	7.15	ALOGPS
logP	7.25	ChemAxon
logS	-6.9	ALOGPS
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	132.25 m³·mol⁻¹	ChemAxon
Polarizability	54.26 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 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate (NP0258101)

MOL for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

3D MOL for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

3D SDF for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

3D-SDF for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

PDB for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

3D PDB for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

SMILES for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

INCHI for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

Structure for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)

3D Structure for NP0258101 (methyl 2-[10-(acetyloxy)pentadec-8-en-1-yl]-4,6-dimethoxybenzoate)