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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:25:53 UTC

Update Date

2022-03-07 02:55:13 UTC

HMDB ID

HMDB0037190

Secondary Accession Numbers

HMDB37190

Metabolite Identification

Common Name

Rhodinyl isovalerate

Description

Rhodinyl isovalerate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. Based on a literature review a small amount of articles have been published on Rhodinyl isovalerate.

Structure

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

HMDB0037190
     RDKit          3D
Rhodinyl isovalerate
 45 44  0  0  0  0  0  0  0  0999 V2000
    6.4681    0.4421   -1.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5182    1.0322   -0.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8707    2.0837    0.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1058    0.6498   -0.9504 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    0.0959    0.2861 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191   -0.2606   -0.0786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2664   -0.8298    1.1015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9334   -2.0861    1.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1374   -1.2279    0.7228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9048   -0.0437    0.2222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2191   -0.5353   -0.1003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2110    0.2953   -0.5935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9009    1.5197   -0.7465 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5748   -0.1714   -0.9385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6187    0.2062    0.0597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9444   -0.3586   -0.4653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7344    1.7037    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4951    0.7117   -1.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2285   -0.3065   -2.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7422    3.0770   -0.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9401    1.9215    0.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1924    1.9854    1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4972    1.5371   -1.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0658   -0.1059   -1.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4410    0.9061    1.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0031   -0.7463    0.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5354    0.6897   -0.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9852   -0.9389   -0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2262   -0.1053    1.9230 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -1.8581    2.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2130   -2.5537    2.3354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1101   -2.8271    0.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1507   -2.0601   -0.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -1.6603    1.6480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4117    0.3332   -0.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9315    0.7936    0.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6081   -1.2692   -1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8434    0.3045   -1.9043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4475   -0.1768    1.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9023   -0.2852   -1.5743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9501   -1.4299   -0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7955    0.2198   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9313    2.0733   -0.8869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7840    2.1328    0.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5425    1.9357    0.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
M  END

  Mrv0541 05061309372D          

 17 16  0  0  0  0            999 V2000
   -4.8395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7342   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0197   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2671   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6961   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9816   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5526   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1618   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3052   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0197   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2671   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5908   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5908   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8763   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
 10  9  1  0  0  0  0
 12  1  2  0  0  0  0
 12  2  1  0  0  0  0
 12  7  1  0  0  0  0
 13  3  1  0  0  0  0
 13  4  1  0  0  0  0
 13 11  1  0  0  0  0
 14  5  1  0  0  0  0
 14  8  1  0  0  0  0
 14  9  1  0  0  0  0
 15 11  1  0  0  0  0
 16 15  2  0  0  0  0
 17 10  1  0  0  0  0
 17 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037190

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)CC(=O)OCCC(C)CCCC(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C15H28O2/c1-12(2)7-6-8-14(5)9-10-17-15(16)11-13(3)4/h13-14H,1,6-11H2,2-5H3

> <INCHI_KEY>
OZAWINZSOFVOBJ-UHFFFAOYSA-N

> <FORMULA>
C15H28O2

> <MOLECULAR_WEIGHT>
240.3816

> <EXACT_MASS>
240.20893014

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
30.36763817653543

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,7-dimethyloct-7-en-1-yl 3-methylbutanoate

> <ALOGPS_LOGP>
4.70

> <JCHEM_LOGP>
4.683238006333333

> <ALOGPS_LOGS>
-4.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.035596122808538

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
72.34159999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.55e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,7-dimethyloct-7-en-1-yl 3-methylbutanoate

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0037190
     RDKit          3D
Rhodinyl isovalerate
 45 44  0  0  0  0  0  0  0  0999 V2000
    6.4681    0.4421   -1.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5182    1.0322   -0.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8707    2.0837    0.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1058    0.6498   -0.9504 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    0.0959    0.2861 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191   -0.2606   -0.0786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2664   -0.8298    1.1015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9334   -2.0861    1.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1374   -1.2279    0.7228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9048   -0.0437    0.2222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2191   -0.5353   -0.1003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2110    0.2953   -0.5935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9009    1.5197   -0.7465 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5748   -0.1714   -0.9385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6187    0.2062    0.0597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9444   -0.3586   -0.4653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7344    1.7037    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4951    0.7117   -1.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2285   -0.3065   -2.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7422    3.0770   -0.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9401    1.9215    0.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1924    1.9854    1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4972    1.5371   -1.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0658   -0.1059   -1.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4410    0.9061    1.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0031   -0.7463    0.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5354    0.6897   -0.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9852   -0.9389   -0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2262   -0.1053    1.9230 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -1.8581    2.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2130   -2.5537    2.3354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1101   -2.8271    0.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1507   -2.0601   -0.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -1.6603    1.6480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4117    0.3332   -0.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9315    0.7936    0.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6081   -1.2692   -1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8434    0.3045   -1.9043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4475   -0.1768    1.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9023   -0.2852   -1.5743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9501   -1.4299   -0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7955    0.2198   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9313    2.0733   -0.8869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7840    2.1328    0.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5425    1.9357    0.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  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      -9.034  -4.565   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.700  -6.875   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.971  -4.565   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.637  -6.875   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.365  -6.875   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.033  -5.335   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.366  -4.565   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.699  -4.565   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.032  -4.565   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.302  -5.335   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.303  -4.565   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -7.700  -5.335   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.637  -5.335   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.365  -5.335   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.969  -5.335   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.969  -6.875   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       1.636  -4.565   0.000  0.00  0.00           O+0
CONECT    1   12                                                            
CONECT    2   12                                                            
CONECT    3   13                                                            
CONECT    4   13                                                            
CONECT    5   14                                                            
CONECT    6    7    8                                                       
CONECT    7    6   12                                                       
CONECT    8    6   14                                                       
CONECT    9   10   14                                                       
CONECT   10    9   17                                                       
CONECT   11   13   15                                                       
CONECT   12    1    2    7                                                  
CONECT   13    3    4   11                                                  
CONECT   14    5    8    9                                                  
CONECT   15   11   16   17                                                  
CONECT   16   15                                                            
CONECT   17   10   15                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   32    0
END

COMPND    HMDB0037190
HETATM    1  C1  UNL     1       6.468   0.442  -1.396  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.518   1.032  -0.707  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.871   2.084   0.316  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.106   0.650  -0.950  1.00  0.00           C  
HETATM    5  C5  UNL     1       3.444   0.096   0.286  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.019  -0.261  -0.079  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.266  -0.830   1.102  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.933  -2.086   1.630  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.137  -1.228   0.723  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.905  -0.044   0.222  1.00  0.00           C  
HETATM   11  O1  UNL     1      -2.219  -0.535  -0.100  1.00  0.00           O  
HETATM   12  C11 UNL     1      -3.211   0.295  -0.594  1.00  0.00           C  
HETATM   13  O2  UNL     1      -2.901   1.520  -0.746  1.00  0.00           O  
HETATM   14  C12 UNL     1      -4.575  -0.171  -0.938  1.00  0.00           C  
HETATM   15  C13 UNL     1      -5.619   0.206   0.060  1.00  0.00           C  
HETATM   16  C14 UNL     1      -6.944  -0.359  -0.465  1.00  0.00           C  
HETATM   17  C15 UNL     1      -5.734   1.704   0.140  1.00  0.00           C  
HETATM   18  H1  UNL     1       7.495   0.712  -1.228  1.00  0.00           H  
HETATM   19  H2  UNL     1       6.228  -0.307  -2.126  1.00  0.00           H  
HETATM   20  H3  UNL     1       5.742   3.077  -0.138  1.00  0.00           H  
HETATM   21  H4  UNL     1       6.940   1.921   0.595  1.00  0.00           H  
HETATM   22  H5  UNL     1       5.192   1.985   1.207  1.00  0.00           H  
HETATM   23  H6  UNL     1       3.497   1.537  -1.259  1.00  0.00           H  
HETATM   24  H7  UNL     1       4.066  -0.106  -1.753  1.00  0.00           H  
HETATM   25  H8  UNL     1       3.441   0.906   1.041  1.00  0.00           H  
HETATM   26  H9  UNL     1       4.003  -0.746   0.717  1.00  0.00           H  
HETATM   27  H10 UNL     1       1.535   0.690  -0.387  1.00  0.00           H  
HETATM   28  H11 UNL     1       1.985  -0.939  -0.953  1.00  0.00           H  
HETATM   29  H12 UNL     1       1.226  -0.105   1.923  1.00  0.00           H  
HETATM   30  H13 UNL     1       2.842  -1.858   2.214  1.00  0.00           H  
HETATM   31  H14 UNL     1       1.213  -2.554   2.335  1.00  0.00           H  
HETATM   32  H15 UNL     1       2.110  -2.827   0.826  1.00  0.00           H  
HETATM   33  H16 UNL     1      -0.151  -2.060  -0.016  1.00  0.00           H  
HETATM   34  H17 UNL     1      -0.598  -1.660   1.648  1.00  0.00           H  
HETATM   35  H18 UNL     1      -0.412   0.333  -0.710  1.00  0.00           H  
HETATM   36  H19 UNL     1      -0.931   0.794   0.921  1.00  0.00           H  
HETATM   37  H20 UNL     1      -4.608  -1.269  -1.105  1.00  0.00           H  
HETATM   38  H21 UNL     1      -4.843   0.304  -1.904  1.00  0.00           H  
HETATM   39  H22 UNL     1      -5.448  -0.177   1.070  1.00  0.00           H  
HETATM   40  H23 UNL     1      -6.902  -0.285  -1.574  1.00  0.00           H  
HETATM   41  H24 UNL     1      -6.950  -1.430  -0.212  1.00  0.00           H  
HETATM   42  H25 UNL     1      -7.796   0.220  -0.093  1.00  0.00           H  
HETATM   43  H26 UNL     1      -5.931   2.073  -0.887  1.00  0.00           H  
HETATM   44  H27 UNL     1      -4.784   2.133   0.498  1.00  0.00           H  
HETATM   45  H28 UNL     1      -6.543   1.936   0.847  1.00  0.00           H  
CONECT    1    2    2   18   19
CONECT    2    3    4
CONECT    3   20   21   22
CONECT    4    5   23   24
CONECT    5    6   25   26
CONECT    6    7   27   28
CONECT    7    8    9   29
CONECT    8   30   31   32
CONECT    9   10   33   34
CONECT   10   11   35   36
CONECT   11   12
CONECT   12   13   13   14
CONECT   14   15   37   38
CONECT   15   16   17   39
CONECT   16   40   41   42
CONECT   17   43   44   45
END

HMDB0037190
     RDKit          3D
Rhodinyl isovalerate
 45 44  0  0  0  0  0  0  0  0999 V2000
    6.4681    0.4421   -1.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5182    1.0322   -0.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8707    2.0837    0.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1058    0.6498   -0.9504 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    0.0959    0.2861 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191   -0.2606   -0.0786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2664   -0.8298    1.1015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9334   -2.0861    1.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1374   -1.2279    0.7228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9048   -0.0437    0.2222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2191   -0.5353   -0.1003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2110    0.2953   -0.5935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9009    1.5197   -0.7465 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5748   -0.1714   -0.9385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6187    0.2062    0.0597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9444   -0.3586   -0.4653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7344    1.7037    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4951    0.7117   -1.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2285   -0.3065   -2.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7422    3.0770   -0.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9401    1.9215    0.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1924    1.9854    1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4972    1.5371   -1.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0658   -0.1059   -1.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4410    0.9061    1.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0031   -0.7463    0.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5354    0.6897   -0.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9852   -0.9389   -0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2262   -0.1053    1.9230 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -1.8581    2.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2130   -2.5537    2.3354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1101   -2.8271    0.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1507   -2.0601   -0.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -1.6603    1.6480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4117    0.3332   -0.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9315    0.7936    0.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6081   -1.2692   -1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8434    0.3045   -1.9043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4475   -0.1768    1.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9023   -0.2852   -1.5743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9501   -1.4299   -0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7955    0.2198   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9313    2.0733   -0.8869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7840    2.1328    0.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5425    1.9357    0.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Rhodinyl isovaleric acid	Generator
(-)-3,7-Dimethyl-7-octen-1-yl isovalerate	HMDB
(S)-3,7,-Dimethyl-7-octenyl 3-methylbutanoate	HMDB
(S)-3,7-Dimethyloct-7-enyl isovalerate	HMDB
3,7-Dimethyl-7-octen-1-yl 3-methylbutanoate	HMDB
3,7-Dimethyl-7-octenyl ester(-)-isovaleric acid	HMDB
Butanoic acid, 3-methyl-, (3S)-3,7-dimethyl-7-octenyl ester	HMDB
FEMA 2987	HMDB

Chemical Formula

C₁₅H₂₈O₂

Average Molecular Weight

240.3816

Monoisotopic Molecular Weight

240.20893014

IUPAC Name

3,7-dimethyloct-7-en-1-yl 3-methylbutanoate

Traditional Name

3,7-dimethyloct-7-en-1-yl 3-methylbutanoate

CAS Registry Number

7778-96-3

SMILES

CC(C)CC(=O)OCCC(C)CCCC(C)=C

InChI Identifier

InChI=1S/C15H28O2/c1-12(2)7-6-8-14(5)9-10-17-15(16)11-13(3)4/h13-14H,1,6-11H2,2-5H3

InChI Key

OZAWINZSOFVOBJ-UHFFFAOYSA-N

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

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Bitter

Disposition

Biological location

Cellular substructure

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0037190)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037190)

Source

Endogenous

Endogenous (HMDB: HMDB0037190)

Animal

Animal (HMDB: HMDB0037190)

Exogenous

Food

Food (HMDB: HMDB0037190)

Exogenous (HMDB: HMDB0037190)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0037190)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0037190)

Lipid metabolism pathway (HMDB: HMDB0037190)

Cellular process

Cell signaling (HMDB: HMDB0037190)

Biochemical process

Lipid transport (HMDB: HMDB0037190)

Role

Biological role

Energy source (HMDB: HMDB0037190)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0037190)

Food and nutrition

Food additive

Flavoring agent

Flavoring Agent (HMDB: HMDB0037190)

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	0.0056 g/L	ALOGPS
logP	4.7	ALOGPS
logP	4.68	ChemAxon
logS	-4.6	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	10	ChemAxon
Refractivity	72.34 m³·mol⁻¹	ChemAxon
Polarizability	30.37 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]+	159.942	31661259
DarkChem	[M-H]-	156.908	31661259
DeepCCS	[M+H]+	165.333	30932474
DeepCCS	[M-H]-	162.367	30932474
DeepCCS	[M-2H]-	198.21	30932474
DeepCCS	[M+Na]+	174.121	30932474
AllCCS	[M+H]+	165.5	32859911
AllCCS	[M+H-H2O]+	162.2	32859911
AllCCS	[M+NH4]+	168.4	32859911
AllCCS	[M+Na]+	169.3	32859911
AllCCS	[M-H]-	164.7	32859911
AllCCS	[M+Na-2H]-	166.0	32859911
AllCCS	[M+HCOO]-	167.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Rhodinyl isovalerate	CC(C)CC(=O)OCCC(C)CCCC(C)=C	1819.4	Standard polar	33892256
Rhodinyl isovalerate	CC(C)CC(=O)OCCC(C)CCCC(C)=C	1476.1	Standard non polar	33892256
Rhodinyl isovalerate	CC(C)CC(=O)OCCC(C)CCCC(C)=C	1568.7	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 - Rhodinyl isovalerate GC-MS (Non-derivatized) - 70eV, Positive	splash10-0bti-9810000000-e81beb2542bd31deed0e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Rhodinyl isovalerate 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 - Rhodinyl isovalerate 10V, Positive-QTOF	splash10-000f-5690000000-22af5fcac1c8b0ebc42f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 20V, Positive-QTOF	splash10-000l-9400000000-19a523538818d455e9ce	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 40V, Positive-QTOF	splash10-066u-9100000000-789f37aec40989a24dcb	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 10V, Negative-QTOF	splash10-0019-7590000000-9e45d10a20bd27f5be45	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 20V, Negative-QTOF	splash10-0zgr-9810000000-54d7e612ac7ed44ba89d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 40V, Negative-QTOF	splash10-0a59-9400000000-3c90ef7765aa15862480	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 10V, Negative-QTOF	splash10-0a4r-0940000000-f923638b18adf7a62a37	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 20V, Negative-QTOF	splash10-0zg0-2910000000-09d43d2a220be2c74cbb	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 40V, Negative-QTOF	splash10-0f89-9500000000-80a351182bb3afa8aad2	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 10V, Positive-QTOF	splash10-001r-9410000000-d4ad9700f925df6b2bde	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 20V, Positive-QTOF	splash10-0012-9100000000-10cacee1b5c17976a072	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Rhodinyl isovalerate 40V, Positive-QTOF	splash10-0apl-9000000000-0b72536eb5a73f5ca56c	2021-09-25	Wishart 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

FDB016192

KNApSAcK ID

Not Available

Chemspider ID

17332816

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16204529

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Rhodinyl isovalerate (HMDB0037190)

MOL for HMDB0037190 (Rhodinyl isovalerate)

3D MOL for HMDB0037190 (Rhodinyl isovalerate)

3D SDF for HMDB0037190 (Rhodinyl isovalerate)

3D-SDF for HMDB0037190 (Rhodinyl isovalerate)

PDB for HMDB0037190 (Rhodinyl isovalerate)

3D PDB for HMDB0037190 (Rhodinyl isovalerate)

SMILES for HMDB0037190 (Rhodinyl isovalerate)

INCHI for HMDB0037190 (Rhodinyl isovalerate)

Structure for HMDB0037190 (Rhodinyl isovalerate)

3D Structure for HMDB0037190 (Rhodinyl isovalerate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra