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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:39:55 UTC

Update Date

2022-03-07 02:52:45 UTC

HMDB ID

HMDB0030933

Secondary Accession Numbers

HMDB30933

Metabolite Identification

Common Name

Avocadynofuran

Description

Avocadynofuran belongs to the class of organic compounds known as heteroaromatic compounds. Heteroaromatic compounds are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom. Avocadynofuran has been detected, but not quantified in, avocados (Persea americana) and fruits. This could make avocadynofuran a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Avocadynofuran.

Structure

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

HMDB0030933
     RDKit          3D
Avocadynofuran
 44 44  0  0  0  0  0  0  0  0999 V2000
    6.2507   -1.6964   -0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8628   -0.7531    0.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4044    0.4111    1.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5809    1.2732    0.4399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992    0.3930   -0.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6042    1.2614   -0.9446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4046    0.7263   -1.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2016    0.3072   -0.8854 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2293   -0.7529    0.1176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1187   -1.0759    0.6919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1857   -1.6369   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7740   -0.9780   -1.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3799    0.3808   -1.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4956    0.3693   -0.1112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4084    0.5682    1.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7111    0.4659    1.7223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4813    0.2106    0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7507    0.1557   -0.4624 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5812   -2.5200   -0.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2814    0.9630    1.7431 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7679    0.0825    2.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1523    1.5425   -0.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1624    2.1477    0.9601 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071   -0.3961   -0.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9351   -0.0406    0.8248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3453    2.2262   -0.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3644    1.6436   -1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7115   -0.0486   -2.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0629    1.5759   -2.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2657    1.2353   -0.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5813    0.0420   -1.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7975   -1.6663   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8543   -0.3521    0.9968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9023   -1.8525    1.5180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4412   -0.1969    1.3346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0377   -1.9029    0.5921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8345   -2.6636   -0.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7485   -1.6246   -1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2896   -1.1103   -2.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6344    1.1407   -0.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7650    0.7261   -2.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5407    0.7700    1.8431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9594    0.5790    2.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5554    0.0704    0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  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  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 14  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  1  0
M  END


  Mrv0541 05061305362D          

 18 18  0  0  0  0            999 V2000
    6.8531    3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5676    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2820    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9965    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7110    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4255    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1399    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8544    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5689    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2833    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9978    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7123    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4469    3.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4268    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8949    3.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0344    2.5803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1412    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2275    2.7519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  3  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 13  2  0  0  0  0
 17 14  1  0  0  0  0
 17 15  2  0  0  0  0
 18 16  1  0  0  0  0
 18 17  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0030933

> <DATABASE_NAME>
hmdb

> <SMILES>
C#CCCCCCCCCCCCC1=CC=CO1

> <INCHI_IDENTIFIER>
InChI=1S/C17H26O/c1-2-3-4-5-6-7-8-9-10-11-12-14-17-15-13-16-18-17/h1,13,15-16H,3-12,14H2

> <INCHI_KEY>
ONYOTXAYIZRIPJ-UHFFFAOYSA-N

> <FORMULA>
C17H26O

> <MOLECULAR_WEIGHT>
246.3877

> <EXACT_MASS>
246.198365454

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_AVERAGE_POLARIZABILITY>
32.4053659167233

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(tridec-12-yn-1-yl)furan

> <ALOGPS_LOGP>
6.61

> <JCHEM_LOGP>
5.9186756056666665

> <ALOGPS_LOGS>
-4.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.63862064474792

> <JCHEM_POLAR_SURFACE_AREA>
13.14

> <JCHEM_REFRACTIVITY>
77.3177

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.70e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(tridec-12-yn-1-yl)furan

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0030933
     RDKit          3D
Avocadynofuran
 44 44  0  0  0  0  0  0  0  0999 V2000
    6.2507   -1.6964   -0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8628   -0.7531    0.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4044    0.4111    1.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5809    1.2732    0.4399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992    0.3930   -0.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6042    1.2614   -0.9446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4046    0.7263   -1.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2016    0.3072   -0.8854 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2293   -0.7529    0.1176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1187   -1.0759    0.6919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1857   -1.6369   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7740   -0.9780   -1.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3799    0.3808   -1.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4956    0.3693   -0.1112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4084    0.5682    1.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7111    0.4659    1.7223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4813    0.2106    0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7507    0.1557   -0.4624 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5812   -2.5200   -0.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2814    0.9630    1.7431 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7679    0.0825    2.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1523    1.5425   -0.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1624    2.1477    0.9601 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071   -0.3961   -0.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9351   -0.0406    0.8248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3453    2.2262   -0.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3644    1.6436   -1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7115   -0.0486   -2.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0629    1.5759   -2.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2657    1.2353   -0.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5813    0.0420   -1.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7975   -1.6663   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8543   -0.3521    0.9968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9023   -1.8525    1.5180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4412   -0.1969    1.3346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0377   -1.9029    0.5921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8345   -2.6636   -0.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7485   -1.6246   -1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2896   -1.1103   -2.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6344    1.1407   -0.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7650    0.7261   -2.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5407    0.7700    1.8431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9594    0.5790    2.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5554    0.0704    0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  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  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 14  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  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      12.792   5.898   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.126   6.668   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.460   7.438   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.793   6.668   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.127   7.438   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.461   6.668   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.794   7.438   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.128   6.668   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      23.462   7.438   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.795   6.668   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      26.129   7.438   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      27.463   6.668   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      32.568   6.150   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      28.797   7.438   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      31.537   7.295   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      31.798   4.817   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      30.130   6.668   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      30.291   5.137   0.000  0.00  0.00           O+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   14                                                       
CONECT   13   15   16                                                       
CONECT   14   12   17                                                       
CONECT   15   13   17                                                       
CONECT   16   13   18                                                       
CONECT   17   14   15   18                                                  
CONECT   18   16   17                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

COMPND    HMDB0030933
HETATM    1  C1  UNL     1       6.251  -1.696  -0.075  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.863  -0.753   0.580  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.404   0.411   1.363  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.581   1.273   0.440  1.00  0.00           C  
HETATM    5  C5  UNL     1       3.399   0.393  -0.039  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.604   1.261  -0.945  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.405   0.726  -1.614  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.202   0.307  -0.885  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.229  -0.753   0.118  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.119  -1.076   0.692  1.00  0.00           C  
HETATM   11  C11 UNL     1      -2.186  -1.637  -0.114  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.774  -0.978  -1.283  1.00  0.00           C  
HETATM   13  C13 UNL     1      -3.380   0.381  -1.071  1.00  0.00           C  
HETATM   14  C14 UNL     1      -4.496   0.369  -0.111  1.00  0.00           C  
HETATM   15  C15 UNL     1      -4.408   0.568   1.231  1.00  0.00           C  
HETATM   16  C16 UNL     1      -5.711   0.466   1.722  1.00  0.00           C  
HETATM   17  C17 UNL     1      -6.481   0.211   0.617  1.00  0.00           C  
HETATM   18  O1  UNL     1      -5.751   0.156  -0.462  1.00  0.00           O  
HETATM   19  H1  UNL     1       6.581  -2.520  -0.666  1.00  0.00           H  
HETATM   20  H2  UNL     1       6.281   0.963   1.743  1.00  0.00           H  
HETATM   21  H3  UNL     1       4.768   0.083   2.199  1.00  0.00           H  
HETATM   22  H4  UNL     1       5.152   1.542  -0.453  1.00  0.00           H  
HETATM   23  H5  UNL     1       4.162   2.148   0.960  1.00  0.00           H  
HETATM   24  H6  UNL     1       3.907  -0.396  -0.676  1.00  0.00           H  
HETATM   25  H7  UNL     1       2.935  -0.041   0.825  1.00  0.00           H  
HETATM   26  H8  UNL     1       2.345   2.226  -0.390  1.00  0.00           H  
HETATM   27  H9  UNL     1       3.364   1.644  -1.721  1.00  0.00           H  
HETATM   28  H10 UNL     1       1.711  -0.049  -2.399  1.00  0.00           H  
HETATM   29  H11 UNL     1       1.063   1.576  -2.321  1.00  0.00           H  
HETATM   30  H12 UNL     1      -0.266   1.235  -0.388  1.00  0.00           H  
HETATM   31  H13 UNL     1      -0.581   0.042  -1.653  1.00  0.00           H  
HETATM   32  H14 UNL     1       0.798  -1.666  -0.172  1.00  0.00           H  
HETATM   33  H15 UNL     1       0.854  -0.352   0.997  1.00  0.00           H  
HETATM   34  H16 UNL     1      -0.902  -1.853   1.518  1.00  0.00           H  
HETATM   35  H17 UNL     1      -1.441  -0.197   1.335  1.00  0.00           H  
HETATM   36  H18 UNL     1      -3.038  -1.903   0.592  1.00  0.00           H  
HETATM   37  H19 UNL     1      -1.834  -2.664  -0.481  1.00  0.00           H  
HETATM   38  H20 UNL     1      -3.748  -1.625  -1.481  1.00  0.00           H  
HETATM   39  H21 UNL     1      -2.290  -1.110  -2.262  1.00  0.00           H  
HETATM   40  H22 UNL     1      -2.634   1.141  -0.762  1.00  0.00           H  
HETATM   41  H23 UNL     1      -3.765   0.726  -2.052  1.00  0.00           H  
HETATM   42  H24 UNL     1      -3.541   0.770   1.843  1.00  0.00           H  
HETATM   43  H25 UNL     1      -5.959   0.579   2.766  1.00  0.00           H  
HETATM   44  H26 UNL     1      -7.555   0.070   0.622  1.00  0.00           H  
CONECT    1    2    2    2   19
CONECT    2    3
CONECT    3    4   20   21
CONECT    4    5   22   23
CONECT    5    6   24   25
CONECT    6    7   26   27
CONECT    7    8   28   29
CONECT    8    9   30   31
CONECT    9   10   32   33
CONECT   10   11   34   35
CONECT   11   12   36   37
CONECT   12   13   38   39
CONECT   13   14   40   41
CONECT   14   15   15   18
CONECT   15   16   42
CONECT   16   17   17   43
CONECT   17   18   44
END

HMDB0030933
     RDKit          3D
Avocadynofuran
 44 44  0  0  0  0  0  0  0  0999 V2000
    6.2507   -1.6964   -0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8628   -0.7531    0.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4044    0.4111    1.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5809    1.2732    0.4399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992    0.3930   -0.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6042    1.2614   -0.9446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4046    0.7263   -1.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2016    0.3072   -0.8854 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2293   -0.7529    0.1176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1187   -1.0759    0.6919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1857   -1.6369   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7740   -0.9780   -1.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3799    0.3808   -1.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4956    0.3693   -0.1112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4084    0.5682    1.2311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7111    0.4659    1.7223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4813    0.2106    0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7507    0.1557   -0.4624 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5812   -2.5200   -0.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2814    0.9630    1.7431 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7679    0.0825    2.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1523    1.5425   -0.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1624    2.1477    0.9601 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071   -0.3961   -0.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9351   -0.0406    0.8248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3453    2.2262   -0.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3644    1.6436   -1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7115   -0.0486   -2.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0629    1.5759   -2.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2657    1.2353   -0.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5813    0.0420   -1.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7975   -1.6663   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8543   -0.3521    0.9968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9023   -1.8525    1.5180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4412   -0.1969    1.3346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0377   -1.9029    0.5921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8345   -2.6636   -0.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7485   -1.6246   -1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2896   -1.1103   -2.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6344    1.1407   -0.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7650    0.7261   -2.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5407    0.7700    1.8431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9594    0.5790    2.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5554    0.0704    0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  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  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 14  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-Dodecylfuran	HMDB
2-N-DODECYLFURAN	HMDB

Chemical Formula

C₁₇H₂₆O

Average Molecular Weight

246.3877

Monoisotopic Molecular Weight

246.198365454

IUPAC Name

2-(tridec-12-yn-1-yl)furan

Traditional Name

2-(tridec-12-yn-1-yl)furan

CAS Registry Number

24708-33-6

SMILES

C#CCCCCCCCCCCCC1=CC=CO1

InChI Identifier

InChI=1S/C17H26O/c1-2-3-4-5-6-7-8-9-10-11-12-14-17-15-13-16-18-17/h1,13,15-16H,3-12,14H2

InChI Key

ONYOTXAYIZRIPJ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as heteroaromatic compounds. Heteroaromatic compounds are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Heteroaromatic compounds

Sub Class

Not Available

Direct Parent

Heteroaromatic compounds

Alternative Parents

Substituents

Heteroaromatic compound
Furan
Acetylide
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0030933)
Cell membrane (HMDB: HMDB0030933)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0030933)

Source

Endogenous

Endogenous (HMDB: HMDB0030933)

Plant

Plant (HMDB: HMDB0030933)

Exogenous

Food

Food (HMDB: HMDB0030933)

Vegetable

Fruit vegetable

Avocado (FooDB: FOOD00130)

Fruit

Fruits (FooDB: FOOD00871)

Exogenous (HMDB: HMDB0030933)

Process

Not Available

Role

Not Available

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	0.024 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0067 g/L	ALOGPS
logP	6.61	ALOGPS
logP	5.92	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	13.14 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	77.32 m³·mol⁻¹	ChemAxon
Polarizability	32.41 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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	162.687	31661259
DarkChem	[M-H]-	163.899	31661259
DeepCCS	[M+H]+	164.773	30932474
DeepCCS	[M-H]-	160.978	30932474
DeepCCS	[M-2H]-	198.419	30932474
DeepCCS	[M+Na]+	174.083	30932474
AllCCS	[M+H]+	166.6	32859911
AllCCS	[M+H-H2O]+	163.1	32859911
AllCCS	[M+NH4]+	169.9	32859911
AllCCS	[M+Na]+	170.9	32859911
AllCCS	[M-H]-	171.5	32859911
AllCCS	[M+Na-2H]-	172.5	32859911
AllCCS	[M+HCOO]-	173.7	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	10.44 minutes	32390414
Predicted by Siyang on May 30, 2022	24.2462 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.82 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	39.4 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2708.1 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	835.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	302.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	508.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	539.8 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	986.2 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	1104.8 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	211.3 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	2243.9 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	638.3 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1950.3 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	812.2 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	548.7 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	783.9 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	691.0 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	7.9 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Avocadynofuran	C#CCCCCCCCCCCCC1=CC=CO1	2352.8	Standard polar	33892256
Avocadynofuran	C#CCCCCCCCCCCCC1=CC=CO1	1836.4	Standard non polar	33892256
Avocadynofuran	C#CCCCCCCCCCCCC1=CC=CO1	1835.8	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 - Avocadynofuran GC-MS (Non-derivatized) - 70eV, Positive	splash10-0ul9-6900000000-53df4323905a6f0bc243	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Avocadynofuran 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 - Avocadynofuran 10V, Positive-QTOF	splash10-0002-0190000000-4f8f7b958c7a57ea3db2	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 20V, Positive-QTOF	splash10-014j-4890000000-97e9139483cb6dee5dc6	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 40V, Positive-QTOF	splash10-0udl-9400000000-92884ba62382ca158463	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 10V, Negative-QTOF	splash10-0002-0090000000-1984c9236e50f0d69963	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 20V, Negative-QTOF	splash10-0002-3090000000-1ec23939f3ab9cd7389b	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 40V, Negative-QTOF	splash10-0i0a-9340000000-ecf7f4534a127ec14443	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 10V, Negative-QTOF	splash10-0002-0090000000-f57d5a2d63c28c67c24d	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 20V, Negative-QTOF	splash10-0002-1090000000-a6d0a61632ac8bb687a7	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 40V, Negative-QTOF	splash10-0159-9310000000-c6795858f7e02fbba4c2	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 10V, Positive-QTOF	splash10-0002-9440000000-32f1cdb8171e18e10c72	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 20V, Positive-QTOF	splash10-014l-9100000000-c37182e03da954a9fc0e	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Avocadynofuran 40V, Positive-QTOF	splash10-06a3-9000000000-4a765d8201102c612f40	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

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

FDB002902

KNApSAcK ID

C00054699

Chemspider ID

5257121

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6857797

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1823771

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 Avocadynofuran (HMDB0030933)

MOL for HMDB0030933 (Avocadynofuran)

3D MOL for HMDB0030933 (Avocadynofuran)

3D SDF for HMDB0030933 (Avocadynofuran)

3D-SDF for HMDB0030933 (Avocadynofuran)

PDB for HMDB0030933 (Avocadynofuran)

3D PDB for HMDB0030933 (Avocadynofuran)

SMILES for HMDB0030933 (Avocadynofuran)

INCHI for HMDB0030933 (Avocadynofuran)

Structure for HMDB0030933 (Avocadynofuran)

3D Structure for HMDB0030933 (Avocadynofuran)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra