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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 03:11:14 UTC

Update Date

2023-02-21 17:28:46 UTC

HMDB ID

HMDB0041497

Secondary Accession Numbers

HMDB41497

Metabolite Identification

Common Name

(S)-Neolyratyl acetate

Description

(S)-Neolyratyl acetate belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group). Based on a literature review a significant number of articles have been published on (S)-Neolyratyl acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0041497
     RDKit          3D
(S)-Neolyratyl acetate
 32 31  0  0  0  0  0  0  0  0999 V2000
   -0.6531   -0.6143   -3.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1681   -0.5692   -2.1649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7070   -0.2357   -0.8609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7246    0.5422   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5439    0.0241    0.8080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040    0.8844    1.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5637   -1.4451    1.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6195    0.2897   -0.5549 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4290    0.9202   -1.3838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0637    0.0326    0.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3179    0.4789    1.1901 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5404    0.0346    0.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8321    0.6459    1.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5103   -0.9152   -0.1192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2468   -0.9176   -4.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3631   -0.4113   -3.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2828   -0.8772   -2.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7369   -1.2793   -0.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7533    1.6184   -0.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3930    0.2865    1.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0700    1.2961    2.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8758    1.7068    0.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6012   -1.9903    0.1504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4915   -1.7127    1.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6404   -1.7578    1.6248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1570    1.1038   -2.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4126    1.2967   -1.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8863   -1.0514    1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3224    0.5628    1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6398   -0.0241    0.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    1.6784    0.8314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9122    0.6214    2.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  3
  5  6  1  0
  5  7  1  0
  3  8  1  0
  8  9  2  3
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  0
  6 21  1  0
  6 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
M  END

HMDB0041497
     RDKit          3D
(S)-Neolyratyl acetate
 32 31  0  0  0  0  0  0  0  0999 V2000
   -0.6531   -0.6143   -3.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1681   -0.5692   -2.1649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7070   -0.2357   -0.8609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7246    0.5422   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5439    0.0241    0.8080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040    0.8844    1.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5637   -1.4451    1.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6195    0.2897   -0.5549 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4290    0.9202   -1.3838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0637    0.0326    0.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3179    0.4789    1.1901 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5404    0.0346    0.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8321    0.6459    1.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5103   -0.9152   -0.1192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2468   -0.9176   -4.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3631   -0.4113   -3.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2828   -0.8772   -2.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7369   -1.2793   -0.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7533    1.6184   -0.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3930    0.2865    1.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0700    1.2961    2.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8758    1.7068    0.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6012   -1.9903    0.1504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4915   -1.7127    1.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6404   -1.7578    1.6248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1570    1.1038   -2.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4126    1.2967   -1.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8863   -1.0514    1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3224    0.5628    1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6398   -0.0241    0.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    1.6784    0.8314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9122    0.6214    2.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  3
  5  6  1  0
  5  7  1  0
  3  8  1  0
  8  9  2  3
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  0
  6 21  1  0
  6 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -4.414  -4.977   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.747   0.413   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.080   0.413   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.746  -0.357   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.588  -1.897   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.080  -4.207   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.414  -1.897   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.413  -2.667   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.414  -0.357   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.746  -1.897   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.255  -2.667   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.080  -2.667   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.255  -4.207   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       0.921  -1.897   0.000  0.00  0.00           O+0
CONECT    1    6                                                            
CONECT    2    9                                                            
CONECT    3    9                                                            
CONECT    4   10                                                            
CONECT    5   11                                                            
CONECT    6    1   12                                                       
CONECT    7    9   12                                                       
CONECT    8   10   14                                                       
CONECT    9    2    3    7                                                  
CONECT   10    4    8   12                                                  
CONECT   11    5   13   14                                                  
CONECT   12    6    7   10                                                  
CONECT   13   11                                                            
CONECT   14    8   11                                                       
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

COMPND    HMDB0041497
HETATM    1  C1  UNL     1      -0.653  -0.614  -3.340  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.168  -0.569  -2.165  1.00  0.00           C  
HETATM    3  C3  UNL     1      -0.707  -0.236  -0.861  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.725   0.542  -0.068  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.544   0.024   0.808  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.504   0.884   1.530  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.564  -1.445   1.132  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.620   0.290  -0.555  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.429   0.920  -1.384  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.064   0.033   0.874  1.00  0.00           C  
HETATM   11  O1  UNL     1       2.318   0.479   1.190  1.00  0.00           O  
HETATM   12  C11 UNL     1       3.540   0.035   0.712  1.00  0.00           C  
HETATM   13  C12 UNL     1       4.832   0.646   1.154  1.00  0.00           C  
HETATM   14  O2  UNL     1       3.510  -0.915  -0.119  1.00  0.00           O  
HETATM   15  H1  UNL     1      -1.247  -0.918  -4.247  1.00  0.00           H  
HETATM   16  H2  UNL     1       0.363  -0.411  -3.583  1.00  0.00           H  
HETATM   17  H3  UNL     1      -2.283  -0.877  -2.180  1.00  0.00           H  
HETATM   18  H4  UNL     1      -0.737  -1.279  -0.263  1.00  0.00           H  
HETATM   19  H5  UNL     1      -1.753   1.618  -0.265  1.00  0.00           H  
HETATM   20  H6  UNL     1      -4.393   0.286   1.837  1.00  0.00           H  
HETATM   21  H7  UNL     1      -3.070   1.296   2.456  1.00  0.00           H  
HETATM   22  H8  UNL     1      -3.876   1.707   0.888  1.00  0.00           H  
HETATM   23  H9  UNL     1      -2.601  -1.990   0.150  1.00  0.00           H  
HETATM   24  H10 UNL     1      -3.491  -1.713   1.652  1.00  0.00           H  
HETATM   25  H11 UNL     1      -1.640  -1.758   1.625  1.00  0.00           H  
HETATM   26  H12 UNL     1       1.157   1.104  -2.395  1.00  0.00           H  
HETATM   27  H13 UNL     1       2.413   1.297  -1.034  1.00  0.00           H  
HETATM   28  H14 UNL     1       0.886  -1.051   1.039  1.00  0.00           H  
HETATM   29  H15 UNL     1       0.322   0.563   1.507  1.00  0.00           H  
HETATM   30  H16 UNL     1       5.640  -0.024   0.795  1.00  0.00           H  
HETATM   31  H17 UNL     1       4.950   1.678   0.831  1.00  0.00           H  
HETATM   32  H18 UNL     1       4.912   0.621   2.278  1.00  0.00           H  
CONECT    1    2    2   15   16
CONECT    2    3   17
CONECT    3    4    8   18
CONECT    4    5    5   19
CONECT    5    6    7
CONECT    6   20   21   22
CONECT    7   23   24   25
CONECT    8    9    9   10
CONECT    9   26   27
CONECT   10   11   28   29
CONECT   11   12
CONECT   12   13   14   14
CONECT   13   30   31   32
END

HMDB0041497
     RDKit          3D
(S)-Neolyratyl acetate
 32 31  0  0  0  0  0  0  0  0999 V2000
   -0.6531   -0.6143   -3.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1681   -0.5692   -2.1649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7070   -0.2357   -0.8609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7246    0.5422   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5439    0.0241    0.8080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040    0.8844    1.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5637   -1.4451    1.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6195    0.2897   -0.5549 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4290    0.9202   -1.3838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0637    0.0326    0.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3179    0.4789    1.1901 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5404    0.0346    0.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8321    0.6459    1.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5103   -0.9152   -0.1192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2468   -0.9176   -4.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3631   -0.4113   -3.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2828   -0.8772   -2.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7369   -1.2793   -0.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7533    1.6184   -0.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3930    0.2865    1.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0700    1.2961    2.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8758    1.7068    0.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6012   -1.9903    0.1504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4915   -1.7127    1.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6404   -1.7578    1.6248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1570    1.1038   -2.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4126    1.2967   -1.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8863   -1.0514    1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3224    0.5628    1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6398   -0.0241    0.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    1.6784    0.8314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9122    0.6214    2.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  3
  5  6  1  0
  5  7  1  0
  3  8  1  0
  8  9  2  3
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  0
  6 21  1  0
  6 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(S)-Neolyratyl acetic acid	Generator
3-Ethenyl-5-methyl-2-methylidenehex-4-en-1-yl acetic acid	Generator

Chemical Formula

C₁₂H₁₈O₂

Average Molecular Weight

194.2701

Monoisotopic Molecular Weight

194.13067982

IUPAC Name

3-ethenyl-5-methyl-2-methylidenehex-4-en-1-yl acetate

Traditional Name

3-ethenyl-5-methyl-2-methylidenehex-4-en-1-yl acetate

CAS Registry Number

79507-87-2

SMILES

CC(C)=CC(C=C)C(=C)COC(C)=O

InChI Identifier

InChI=1S/C12H18O2/c1-6-12(7-9(2)3)10(4)8-14-11(5)13/h6-7,12H,1,4,8H2,2-3,5H3

InChI Key

OMXMXPLKVRQEIQ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acid derivatives

Direct Parent

Carboxylic acid esters

Alternative Parents

Substituents

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

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Source

Endogenous

Endogenous (HMDB: HMDB0041497)

Exogenous

Food

Food (HMDB: HMDB0041497)

Process

Naturally occurring process

Biological process

Cellular process

Cell signaling (HMDB: HMDB0041497)

Role

Biological role

Energy source (HMDB: HMDB0041497)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0041497)

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.12 g/L	ALOGPS
logP	3.35	ALOGPS
logP	2.54	ChemAxon
logS	-3.2	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	6	ChemAxon
Refractivity	59.25 m³·mol⁻¹	ChemAxon
Polarizability	22.42 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	146.87	31661259
DarkChem	[M-H]-	145.32	31661259
DeepCCS	[M+H]+	144.926	30932474
DeepCCS	[M-H]-	142.373	30932474
DeepCCS	[M-2H]-	177.774	30932474
DeepCCS	[M+Na]+	153.294	30932474
AllCCS	[M+H]+	146.1	32859911
AllCCS	[M+H-H2O]+	142.4	32859911
AllCCS	[M+NH4]+	149.6	32859911
AllCCS	[M+Na]+	150.6	32859911
AllCCS	[M-H]-	146.3	32859911
AllCCS	[M+Na-2H]-	147.5	32859911
AllCCS	[M+HCOO]-	148.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(S)-Neolyratyl acetate	CC(C)=CC(C=C)C(=C)COC(C)=O	1625.7	Standard polar	33892256
(S)-Neolyratyl acetate	CC(C)=CC(C=C)C(=C)COC(C)=O	1265.7	Standard non polar	33892256
(S)-Neolyratyl acetate	CC(C)=CC(C=C)C(=C)COC(C)=O	1291.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (S)-Neolyratyl acetate GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-9300000000-abba4c7dfa8ce6414c37	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (S)-Neolyratyl acetate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 10V, Positive-QTOF	splash10-000b-0900000000-7f0405a9535870196b44	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 20V, Positive-QTOF	splash10-000i-7900000000-5094e25b8486d672fe34	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 40V, Positive-QTOF	splash10-0ar9-9500000000-9ac67d2bc401ffc3a11d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 10V, Negative-QTOF	splash10-0006-3900000000-afc6585ddcc839dfe5f1	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 20V, Negative-QTOF	splash10-052f-9700000000-f8bf65fc828470c08823	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 40V, Negative-QTOF	splash10-0a4l-9500000000-6a2141d4125f58b7ed00	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 10V, Positive-QTOF	splash10-0a4i-4900000000-1c13f31e0f11f10c9440	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 20V, Positive-QTOF	splash10-0007-9000000000-c2ecde2087b79990bea4	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 40V, Positive-QTOF	splash10-0006-9000000000-e2bd29defa59ca0ad9fa	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 10V, Negative-QTOF	splash10-053r-2900000000-7d293a5159f041cf61ac	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 20V, Negative-QTOF	splash10-0a4i-9300000000-3188c927a1c58edd94f7	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (S)-Neolyratyl acetate 40V, Negative-QTOF	splash10-0a4l-9200000000-418a08581d6ddb1bfb80	2021-09-24	Wishart Lab	View Spectrum

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-04	FELIX lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB021467

KNApSAcK ID

Not Available

Chemspider ID

35015193

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101413630

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for (S)-Neolyratyl acetate (HMDB0041497)

MOL for HMDB0041497 ((S)-Neolyratyl acetate)

3D MOL for HMDB0041497 ((S)-Neolyratyl acetate)

3D SDF for HMDB0041497 ((S)-Neolyratyl acetate)

3D-SDF for HMDB0041497 ((S)-Neolyratyl acetate)

PDB for HMDB0041497 ((S)-Neolyratyl acetate)

3D PDB for HMDB0041497 ((S)-Neolyratyl acetate)

SMILES for HMDB0041497 ((S)-Neolyratyl acetate)

INCHI for HMDB0041497 ((S)-Neolyratyl acetate)

Structure for HMDB0041497 ((S)-Neolyratyl acetate)

3D Structure for HMDB0041497 ((S)-Neolyratyl acetate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra