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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:56:19 UTC

Update Date

2022-03-07 02:53:38 UTC

HMDB ID

HMDB0033225

Secondary Accession Numbers

HMDB33225

Metabolite Identification

Common Name

(1R,4S,6R)-6-Hydroxyfenchone glucoside

Description

(1R,4S,6R)-6-Hydroxyfenchone glucoside belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. Based on a literature review a small amount of articles have been published on (1R,4S,6R)-6-Hydroxyfenchone glucoside.

Structure

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

HMDB0033225
     RDKit          3D
(1R,4S,6R)-6-Hydroxyfenchone glucoside
 49 51  0  0  0  0  0  0  0  0999 V2000
   -5.0572   -0.2538    0.5448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6945    0.3087    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7409    1.7963    0.0194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6613   -0.1231    1.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5766    0.2948    2.3099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7910   -1.1152    0.5475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2077   -2.1393    1.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7653   -1.6960   -0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1576   -0.3240   -1.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8130    0.2629   -1.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8099   -0.4720   -0.4348 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0586    0.3968    0.1451 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3832    0.1774   -0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9088    1.2269   -0.7851 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1980    1.0518   -1.1849 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0188    2.2456   -0.6844 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4949    3.3997   -1.2299 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8691   -0.1826   -0.6996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6408   -1.2820   -1.5593 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5801   -0.5374    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5612   -0.1241    1.6139 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2156    0.0044    1.1730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7291   -0.9282    2.0828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3714   -0.9116   -0.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0612   -0.8420    1.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8259    0.5627    0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8298    2.3003    0.4189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6452    2.2144    0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7868    2.0639   -1.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3428   -2.6172    0.9167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9613   -1.7236    2.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9588   -2.9448    1.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1926   -2.2658   -1.2281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6065   -2.2028   -0.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8460   -0.3781   -1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7725    1.3236   -1.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5564    0.1455   -2.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3856   -1.2891   -1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5043   -0.7459   -0.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3010    1.0663   -2.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0798    2.1122   -1.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0076    2.3168    0.4099 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7443    4.2211   -0.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9818   -0.0029   -0.7740 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074   -1.0471   -2.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5557   -1.6646    0.7738 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2503   -0.8376    1.6962 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4391    0.9805    1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9882   -1.8221    1.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  6  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  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
  9  2  1  0
 22 13  1  0
 11  6  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  7 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 13 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 18 44  1  0
 19 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
M  END


  Mrv0541 02241208202D          

 23 25  0  0  0  0            999 V2000
    0.6621    0.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6621   -0.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3756   -0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0877   -0.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0877    0.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3756    1.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0515    1.0332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3756    1.8582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8027    1.0332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5887    0.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7664    0.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4828    1.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1991    0.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1991   -0.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4828   -0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7664   -0.2028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4828    1.8582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9127    1.0332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9127   -0.6152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4828   -1.4457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1991   -1.8582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9127   -0.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5002   -0.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  1  7  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 10  1  0  0  0  0
  4  5  1  0  0  0  0
  4 22  1  0  0  0  0
  4 23  1  0  0  0  0
  5  6  1  0  0  0  0
  5  9  2  0  0  0  0
  6  8  1  0  0  0  0
  6 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 16  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 13 14  1  0  0  0  0
 13 18  1  0  0  0  0
 14 15  1  0  0  0  0
 14 19  1  0  0  0  0
 15 16  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0033225

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(C)C2CC(OC3OC(CO)C(O)C(O)C3O)C(C)(C2)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H26O7/c1-15(2)7-4-9(16(3,5-7)14(15)21)23-13-12(20)11(19)10(18)8(6-17)22-13/h7-13,17-20H,4-6H2,1-3H3

> <INCHI_KEY>
NSQBEKJIIBBOAS-UHFFFAOYSA-N

> <FORMULA>
C16H26O7

> <MOLECULAR_WEIGHT>
330.3734

> <EXACT_MASS>
330.167853186

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
34.15706093602991

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,3,3-trimethyl-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

> <ALOGPS_LOGP>
-0.16

> <JCHEM_LOGP>
0.06327324133333417

> <ALOGPS_LOGS>
-1.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.200078345309507

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210531199272449

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835454486346

> <JCHEM_POLAR_SURFACE_AREA>
116.45000000000002

> <JCHEM_REFRACTIVITY>
78.4726

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.18e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,3,3-trimethyl-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0033225
     RDKit          3D
(1R,4S,6R)-6-Hydroxyfenchone glucoside
 49 51  0  0  0  0  0  0  0  0999 V2000
   -5.0572   -0.2538    0.5448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6945    0.3087    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7409    1.7963    0.0194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6613   -0.1231    1.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5766    0.2948    2.3099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7910   -1.1152    0.5475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2077   -2.1393    1.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7653   -1.6960   -0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1576   -0.3240   -1.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8130    0.2629   -1.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8099   -0.4720   -0.4348 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0586    0.3968    0.1451 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3832    0.1774   -0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9088    1.2269   -0.7851 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1980    1.0518   -1.1849 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0188    2.2456   -0.6844 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4949    3.3997   -1.2299 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8691   -0.1826   -0.6996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6408   -1.2820   -1.5593 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5801   -0.5374    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5612   -0.1241    1.6139 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2156    0.0044    1.1730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7291   -0.9282    2.0828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3714   -0.9116   -0.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0612   -0.8420    1.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8259    0.5627    0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8298    2.3003    0.4189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6452    2.2144    0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7868    2.0639   -1.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3428   -2.6172    0.9167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9613   -1.7236    2.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9588   -2.9448    1.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1926   -2.2658   -1.2281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6065   -2.2028   -0.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8460   -0.3781   -1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7725    1.3236   -1.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5564    0.1455   -2.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3856   -1.2891   -1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5043   -0.7459   -0.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3010    1.0663   -2.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0798    2.1122   -1.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0076    2.3168    0.4099 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7443    4.2211   -0.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9818   -0.0029   -0.7740 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074   -1.0471   -2.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5557   -1.6646    0.7738 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2503   -0.8376    1.6962 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4391    0.9805    1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9882   -1.8221    1.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  6  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  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
  9  2  1  0
 22 13  1  0
 11  6  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  7 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 13 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 18 44  1  0
 19 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0       1.236   1.161   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.236  -0.379   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.568  -1.148   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.897  -0.379   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.897   1.161   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.568   1.929   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.096   1.929   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.568   3.469   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.232   1.929   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.966   0.440   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.431   1.161   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.768   1.929   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.105   1.161   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.105  -0.379   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.768  -1.148   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.431  -0.379   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -2.768   3.469   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -5.437   1.929   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -5.437  -1.148   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.768  -2.699   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.105  -3.469   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.437  -0.379   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.667  -1.713   0.000  0.00  0.00           C+0
CONECT    1    2    6    7                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5   22   23                                             
CONECT    5    4    6    9                                                  
CONECT    6    1    5    8   10                                             
CONECT    7    1   11                                                       
CONECT    8    6                                                            
CONECT    9    5                                                            
CONECT   10    3    6                                                       
CONECT   11    7   12   16                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16   20                                                  
CONECT   16   11   15                                                       
CONECT   17   12                                                            
CONECT   18   13                                                            
CONECT   19   14                                                            
CONECT   20   15   21                                                       
CONECT   21   20                                                            
CONECT   22    4                                                            
CONECT   23    4                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

COMPND    HMDB0033225
HETATM    1  C1  UNL     1      -5.057  -0.254   0.545  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.694   0.309   0.195  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.741   1.796   0.019  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.661  -0.123   1.178  1.00  0.00           C  
HETATM    5  O1  UNL     1      -2.577   0.295   2.310  1.00  0.00           O  
HETATM    6  C5  UNL     1      -1.791  -1.115   0.548  1.00  0.00           C  
HETATM    7  C6  UNL     1      -1.208  -2.139   1.412  1.00  0.00           C  
HETATM    8  C7  UNL     1      -2.765  -1.696  -0.500  1.00  0.00           C  
HETATM    9  C8  UNL     1      -3.158  -0.324  -1.075  1.00  0.00           C  
HETATM   10  C9  UNL     1      -1.813   0.263  -1.342  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.810  -0.472  -0.435  1.00  0.00           C  
HETATM   12  O2  UNL     1       0.059   0.397   0.145  1.00  0.00           O  
HETATM   13  C11 UNL     1       1.383   0.177  -0.040  1.00  0.00           C  
HETATM   14  O3  UNL     1       1.909   1.227  -0.785  1.00  0.00           O  
HETATM   15  C12 UNL     1       3.198   1.052  -1.185  1.00  0.00           C  
HETATM   16  C13 UNL     1       4.019   2.246  -0.684  1.00  0.00           C  
HETATM   17  O4  UNL     1       3.495   3.400  -1.230  1.00  0.00           O  
HETATM   18  C14 UNL     1       3.869  -0.183  -0.700  1.00  0.00           C  
HETATM   19  O5  UNL     1       3.641  -1.282  -1.559  1.00  0.00           O  
HETATM   20  C15 UNL     1       3.580  -0.537   0.720  1.00  0.00           C  
HETATM   21  O6  UNL     1       4.561  -0.124   1.614  1.00  0.00           O  
HETATM   22  C16 UNL     1       2.216   0.004   1.173  1.00  0.00           C  
HETATM   23  O7  UNL     1       1.729  -0.928   2.083  1.00  0.00           O  
HETATM   24  H1  UNL     1      -5.371  -0.912  -0.293  1.00  0.00           H  
HETATM   25  H2  UNL     1      -5.061  -0.842   1.468  1.00  0.00           H  
HETATM   26  H3  UNL     1      -5.826   0.563   0.654  1.00  0.00           H  
HETATM   27  H4  UNL     1      -2.830   2.300   0.419  1.00  0.00           H  
HETATM   28  H5  UNL     1      -4.645   2.214   0.493  1.00  0.00           H  
HETATM   29  H6  UNL     1      -3.787   2.064  -1.058  1.00  0.00           H  
HETATM   30  H7  UNL     1      -0.343  -2.617   0.917  1.00  0.00           H  
HETATM   31  H8  UNL     1      -0.961  -1.724   2.407  1.00  0.00           H  
HETATM   32  H9  UNL     1      -1.959  -2.945   1.598  1.00  0.00           H  
HETATM   33  H10 UNL     1      -2.193  -2.266  -1.228  1.00  0.00           H  
HETATM   34  H11 UNL     1      -3.607  -2.203  -0.035  1.00  0.00           H  
HETATM   35  H12 UNL     1      -3.846  -0.378  -1.891  1.00  0.00           H  
HETATM   36  H13 UNL     1      -1.773   1.324  -1.033  1.00  0.00           H  
HETATM   37  H14 UNL     1      -1.556   0.145  -2.401  1.00  0.00           H  
HETATM   38  H15 UNL     1      -0.386  -1.289  -1.010  1.00  0.00           H  
HETATM   39  H16 UNL     1       1.504  -0.746  -0.680  1.00  0.00           H  
HETATM   40  H17 UNL     1       3.301   1.066  -2.309  1.00  0.00           H  
HETATM   41  H18 UNL     1       5.080   2.112  -1.037  1.00  0.00           H  
HETATM   42  H19 UNL     1       4.008   2.317   0.410  1.00  0.00           H  
HETATM   43  H20 UNL     1       3.744   4.221  -0.765  1.00  0.00           H  
HETATM   44  H21 UNL     1       4.982  -0.003  -0.774  1.00  0.00           H  
HETATM   45  H22 UNL     1       3.907  -1.047  -2.470  1.00  0.00           H  
HETATM   46  H23 UNL     1       3.556  -1.665   0.774  1.00  0.00           H  
HETATM   47  H24 UNL     1       5.250  -0.838   1.696  1.00  0.00           H  
HETATM   48  H25 UNL     1       2.439   0.980   1.650  1.00  0.00           H  
HETATM   49  H26 UNL     1       1.988  -1.822   1.744  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3    4    9
CONECT    3   27   28   29
CONECT    4    5    5    6
CONECT    6    7    8   11
CONECT    7   30   31   32
CONECT    8    9   33   34
CONECT    9   10   35
CONECT   10   11   36   37
CONECT   11   12   38
CONECT   12   13
CONECT   13   14   22   39
CONECT   14   15
CONECT   15   16   18   40
CONECT   16   17   41   42
CONECT   17   43
CONECT   18   19   20   44
CONECT   19   45
CONECT   20   21   22   46
CONECT   21   47
CONECT   22   23   48
CONECT   23   49
END

HMDB0033225
     RDKit          3D
(1R,4S,6R)-6-Hydroxyfenchone glucoside
 49 51  0  0  0  0  0  0  0  0999 V2000
   -5.0572   -0.2538    0.5448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6945    0.3087    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7409    1.7963    0.0194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6613   -0.1231    1.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5766    0.2948    2.3099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7910   -1.1152    0.5475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2077   -2.1393    1.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7653   -1.6960   -0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1576   -0.3240   -1.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8130    0.2629   -1.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8099   -0.4720   -0.4348 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0586    0.3968    0.1451 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3832    0.1774   -0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9088    1.2269   -0.7851 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1980    1.0518   -1.1849 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0188    2.2456   -0.6844 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4949    3.3997   -1.2299 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8691   -0.1826   -0.6996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6408   -1.2820   -1.5593 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5801   -0.5374    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5612   -0.1241    1.6139 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2156    0.0044    1.1730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7291   -0.9282    2.0828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3714   -0.9116   -0.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0612   -0.8420    1.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8259    0.5627    0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8298    2.3003    0.4189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6452    2.2144    0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7868    2.0639   -1.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3428   -2.6172    0.9167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9613   -1.7236    2.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9588   -2.9448    1.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1926   -2.2658   -1.2281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6065   -2.2028   -0.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8460   -0.3781   -1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7725    1.3236   -1.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5564    0.1455   -2.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3856   -1.2891   -1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5043   -0.7459   -0.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3010    1.0663   -2.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0798    2.1122   -1.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0076    2.3168    0.4099 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7443    4.2211   -0.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9818   -0.0029   -0.7740 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074   -1.0471   -2.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5557   -1.6646    0.7738 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2503   -0.8376    1.6962 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4391    0.9805    1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9882   -1.8221    1.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  6  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  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
  9  2  1  0
 22 13  1  0
 11  6  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  7 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 13 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 18 44  1  0
 19 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₆H₂₆O₇

Average Molecular Weight

330.3734

Monoisotopic Molecular Weight

330.167853186

IUPAC Name

1,3,3-trimethyl-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

Traditional Name

1,3,3-trimethyl-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

CAS Registry Number

155960-76-2

SMILES

CC1(C)C2CC(OC3OC(CO)C(O)C(O)C3O)C(C)(C2)C1=O

InChI Identifier

InChI=1S/C16H26O7/c1-15(2)7-4-9(16(3,5-7)14(15)21)23-13-12(20)11(19)10(18)8(6-17)22-13/h7-13,17-20H,4-6H2,1-3H3

InChI Key

NSQBEKJIIBBOAS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Bicyclic monoterpenoid
Fenchane monoterpenoid
Norbornane monoterpenoid
Monoterpenoid
Monosaccharide
Oxane
Ketone
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Primary alcohol
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0033225)

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0033225)

Source

Endogenous

Endogenous (HMDB: HMDB0033225)

Plant

Plant (HMDB: HMDB0033225)

Animal

Animal (HMDB: HMDB0033225)

Exogenous

Food

Food (HMDB: HMDB0033225)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0033225)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0033225)

Cellular process

Cell signaling (HMDB: HMDB0033225)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0033225)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0033225)

Nutrient

Nutrient (HMDB: HMDB0033225)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0033225)

Emulsifier (HMDB: HMDB0033225)

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	21.8 g/L	ALOGPS
logP	-0.16	ALOGPS
logP	0.063	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	78.47 m³·mol⁻¹	ChemAxon
Polarizability	34.16 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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]+	175.976	31661259
DarkChem	[M-H]-	170.85	31661259
DeepCCS	[M+H]+	180.467	30932474
DeepCCS	[M-H]-	178.109	30932474
DeepCCS	[M-2H]-	211.045	30932474
DeepCCS	[M+Na]+	186.576	30932474
AllCCS	[M+H]+	178.4	32859911
AllCCS	[M+H-H2O]+	175.6	32859911
AllCCS	[M+NH4]+	181.0	32859911
AllCCS	[M+Na]+	181.7	32859911
AllCCS	[M-H]-	178.4	32859911
AllCCS	[M+Na-2H]-	178.6	32859911
AllCCS	[M+HCOO]-	179.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(1R,4S,6R)-6-Hydroxyfenchone glucoside	CC1(C)C2CC(OC3OC(CO)C(O)C(O)C3O)C(C)(C2)C1=O	3042.0	Standard polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside	CC1(C)C2CC(OC3OC(CO)C(O)C(O)C3O)C(C)(C2)C1=O	2483.4	Standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside	CC1(C)C2CC(OC3OC(CO)C(O)C(O)C3O)C(C)(C2)C1=O	2562.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(1R,4S,6R)-6-Hydroxyfenchone glucoside,1TMS,isomer #1	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C)C(O)C(O)C1O	2641.9	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,1TMS,isomer #2	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	2633.1	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,1TMS,isomer #3	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	2623.2	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,1TMS,isomer #4	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	2609.7	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TMS,isomer #1	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	2601.7	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TMS,isomer #2	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	2587.0	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TMS,isomer #3	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	2570.6	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TMS,isomer #4	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2584.5	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TMS,isomer #5	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2576.3	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TMS,isomer #6	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2588.1	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,3TMS,isomer #1	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2524.1	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,3TMS,isomer #2	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2523.8	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,3TMS,isomer #3	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2511.4	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,3TMS,isomer #4	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2519.8	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,4TMS,isomer #1	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2470.6	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,1TBDMS,isomer #1	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	2863.0	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,1TBDMS,isomer #2	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	2866.0	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,1TBDMS,isomer #3	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	2861.9	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,1TBDMS,isomer #4	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	2839.9	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TBDMS,isomer #1	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3039.8	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TBDMS,isomer #2	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3040.5	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TBDMS,isomer #3	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3011.7	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TBDMS,isomer #4	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3044.6	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TBDMS,isomer #5	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3040.3	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,2TBDMS,isomer #6	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3043.7	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,3TBDMS,isomer #1	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3244.3	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,3TBDMS,isomer #2	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3235.8	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,3TBDMS,isomer #3	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3238.5	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,3TBDMS,isomer #4	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3245.7	Semi standard non polar	33892256
(1R,4S,6R)-6-Hydroxyfenchone glucoside,4TBDMS,isomer #1	CC1(C)C(=O)C2(C)CC1CC2OC1OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3449.8	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 - (1R,4S,6R)-6-Hydroxyfenchone glucoside GC-MS (Non-derivatized) - 70eV, Positive	splash10-08mi-9474000000-da7fc4f4ed0541fa245e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside GC-MS (4 TMS) - 70eV, Positive	splash10-0udi-2211149000-f659ccfc74d90d1c2440	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 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 - (1R,4S,6R)-6-Hydroxyfenchone glucoside 10V, Positive-QTOF	splash10-0i0r-0905000000-6b57a42fc0ab5e59716f	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 20V, Positive-QTOF	splash10-0gba-3900000000-8154bc07ed21e483c3e9	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 40V, Positive-QTOF	splash10-0udi-3900000000-aeb01efa73dfec7b70ec	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 10V, Negative-QTOF	splash10-00or-1917000000-89441b654e7a79ec07cd	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 20V, Negative-QTOF	splash10-014i-1901000000-cd9e16de428cd6ea6fdd	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 40V, Negative-QTOF	splash10-014i-7900000000-9c23426e4567fd7c0628	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 10V, Negative-QTOF	splash10-004i-0009000000-1dbc4fa6bd9d0eda0450	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 20V, Negative-QTOF	splash10-004i-3609000000-2472941e9c36c6095fd7	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 40V, Negative-QTOF	splash10-0aou-9320000000-5733c032740f6903ca33	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 10V, Positive-QTOF	splash10-001i-0209000000-88acd2f0775d7f7b900a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 20V, Positive-QTOF	splash10-0uea-1923000000-c64def64df5cf680ad24	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4S,6R)-6-Hydroxyfenchone glucoside 40V, Positive-QTOF	splash10-08fs-8960000000-0efc27bf26e4fc44e481	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
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

FDB011240

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

73815122

PDB ID

Not Available

ChEBI ID

175226

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 (1R,4S,6R)-6-Hydroxyfenchone glucoside (HMDB0033225)

MOL for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

3D MOL for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

3D SDF for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

3D-SDF for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

PDB for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

3D PDB for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

SMILES for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

INCHI for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

Structure for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

3D Structure for HMDB0033225 ((1R,4S,6R)-6-Hydroxyfenchone glucoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra