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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:42:39 UTC

Update Date

2022-03-07 02:52:56 UTC

HMDB ID

HMDB0031367

Secondary Accession Numbers

HMDB31367

Metabolite Identification

Common Name

Linalool oxide D 3-[apiosyl-(1->6)-glucoside]

Description

Linalool oxide D 3-[apiosyl-(1->6)-glucoside] belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Based on a literature review very few articles have been published on Linalool oxide D 3-[apiosyl-(1->6)-glucoside].

Structure

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

  Mrv0541 05061305542D          

 32 34  0  0  0  0            999 V2000
   -4.9785  -10.1186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3627   -7.7918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4736   -8.8466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1526   -9.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2945   -9.6573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2027   -7.4132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6876   -8.0806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5986   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5887   -0.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0835   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3822   -7.4994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9040   -4.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3889   -5.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0533   -5.9921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2329   -6.0783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0467   -8.2531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3521   -8.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3957   -0.8575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2395   -3.8173    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2094   -5.1522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5383   -6.6595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4888   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847   -0.6860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9341   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -2.5687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7479   -5.4109    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8973   -6.8320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5316   -8.9205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  2  0  0  0  0
  7  6  1  0  0  0  0
 11  8  1  0  0  0  0
 12  6  1  0  0  0  0
 13 11  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19  2  1  0  0  0  0
 19  3  1  0  0  0  0
 19 12  1  0  0  0  0
 20  4  1  0  0  0  0
 20  5  1  0  0  0  0
 20  7  1  0  0  0  0
 21  9  1  0  0  0  0
 21 10  1  0  0  0  0
 21 16  1  0  0  0  0
 22  9  1  0  0  0  0
 23 13  1  0  0  0  0
 24 14  1  0  0  0  0
 25 15  1  0  0  0  0
 26 16  1  0  0  0  0
 27 21  1  0  0  0  0
 28  8  1  0  0  0  0
 28 18  1  0  0  0  0
 29 10  1  0  0  0  0
 29 18  1  0  0  0  0
 30 11  1  0  0  0  0
 30 17  1  0  0  0  0
 31 12  1  0  0  0  0
 31 17  1  0  0  0  0
 32 19  1  0  0  0  0
 32 20  1  0  0  0  0
M  END

HMDB0031367
     RDKit          3D
Linalool oxide D 3-[apiosyl-(1->6)-glucoside]
 68 70  0  0  0  0  0  0  0  0999 V2000
   -7.1886    1.1243   -0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7906   -0.0688    0.3330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4879   -0.2350    1.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9067   -0.1372    2.5640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8830   -1.5485    0.7965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4769   -1.5772    0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7484   -0.2643    0.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6619   -0.1659   -0.3866 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4902    0.2392    0.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0475    1.2878   -0.4545 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4088    1.5361   -0.1966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2082    1.4905   -1.4552 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127    1.6939   -1.4774 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4587    0.9215   -0.9423 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2789    1.6033    0.0016 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1843    0.5586    0.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6147    0.0016   -1.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8920    0.4327   -1.3680 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5445   -1.5090   -1.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3119   -2.0105   -0.6624 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5747    0.5645   -1.9509 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0185    1.7149   -2.5462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8967    0.8307    1.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2716    1.4274    2.1580 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6348   -0.6474    1.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3526   -1.0756    2.3174 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4476   -0.9473    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2013   -2.0729    0.6991 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7571    0.7730   -0.1007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9997    2.0899   -0.1410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1975    0.4507   -1.4888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7397    0.8699    0.8283 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1155    1.2327   -0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5861    2.0084    0.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3771   -0.9437    0.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6631    0.6701    2.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9966    0.2240    3.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2460   -1.1111    2.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5006   -2.0667    0.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0371   -2.2147    1.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9254   -2.3555    0.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3716   -1.9279   -0.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5817   -0.0140    1.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6324    0.4220    1.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3970    2.6461    0.0911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419    2.3273   -2.1030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8688    0.5808   -2.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1591   -0.0123   -0.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0455    0.9342    0.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6132   -0.1703    0.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1872   -0.1189   -2.1357 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7748   -1.9070   -2.0377 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3403   -1.9490   -0.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2957   -2.5757    0.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2654   -0.2334   -2.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4905    2.4911   -2.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9471    1.0051    1.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4655    0.7621    2.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -1.2606    0.6736 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0497   -2.0309    2.2407 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6766   -1.1341   -0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5609   -2.6255   -0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7447    2.9211   -0.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2965    2.1415    0.7015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5026    2.1378   -1.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6088    1.3383   -1.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9053   -0.3683   -1.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2827    0.1416   -2.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  3  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  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 17 21  1  0
 21 22  1  0
 11 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
  7 29  1  0
 29 30  1  0
 29 31  1  0
 29 32  1  0
 32  3  1  0
 27  9  1  0
 21 14  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  4 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  9 44  1  0
 11 45  1  0
 12 46  1  0
 12 47  1  0
 14 48  1  0
 16 49  1  0
 16 50  1  0
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 21 55  1  0
 22 56  1  0
 23 57  1  0
 24 58  1  0
 25 59  1  0
 26 60  1  0
 27 61  1  0
 28 62  1  0
 30 63  1  0
 30 64  1  0
 30 65  1  0
 31 66  1  0
 31 67  1  0
 31 68  1  0
M  END

  Mrv0541 05061305542D          

 32 34  0  0  0  0            999 V2000
   -4.9785  -10.1186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3627   -7.7918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4736   -8.8466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1526   -9.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2945   -9.6573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2027   -7.4132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6876   -8.0806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5986   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5887   -0.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0835   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3822   -7.4994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9040   -4.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3889   -5.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0533   -5.9921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2329   -6.0783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0467   -8.2531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3521   -8.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3957   -0.8575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2395   -3.8173    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2094   -5.1522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5383   -6.6595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4888   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847   -0.6860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9341   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -2.5687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7479   -5.4109    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8973   -6.8320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5316   -8.9205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  2  0  0  0  0
  7  6  1  0  0  0  0
 11  8  1  0  0  0  0
 12  6  1  0  0  0  0
 13 11  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19  2  1  0  0  0  0
 19  3  1  0  0  0  0
 19 12  1  0  0  0  0
 20  4  1  0  0  0  0
 20  5  1  0  0  0  0
 20  7  1  0  0  0  0
 21  9  1  0  0  0  0
 21 10  1  0  0  0  0
 21 16  1  0  0  0  0
 22  9  1  0  0  0  0
 23 13  1  0  0  0  0
 24 14  1  0  0  0  0
 25 15  1  0  0  0  0
 26 16  1  0  0  0  0
 27 21  1  0  0  0  0
 28  8  1  0  0  0  0
 28 18  1  0  0  0  0
 29 10  1  0  0  0  0
 29 18  1  0  0  0  0
 30 11  1  0  0  0  0
 30 17  1  0  0  0  0
 31 12  1  0  0  0  0
 31 17  1  0  0  0  0
 32 19  1  0  0  0  0
 32 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0031367

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(C)OC(C)(CCC1OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C21H36O11/c1-5-20(4)7-6-12(19(2,3)32-20)31-17-15(25)14(24)13(23)11(30-17)8-28-18-16(26)21(27,9-22)10-29-18/h5,11-18,22-27H,1,6-10H2,2-4H3

> <INCHI_KEY>
AINNVCLTLJOODL-UHFFFAOYSA-N

> <FORMULA>
C21H36O11

> <MOLECULAR_WEIGHT>
464.5039

> <EXACT_MASS>
464.225761994

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_AVERAGE_POLARIZABILITY>
47.28547883827528

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(6-ethenyl-2,2,6-trimethyloxan-3-yl)oxy]oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.50

> <JCHEM_LOGP>
-1.378577491333333

> <ALOGPS_LOGS>
-1.61

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.31814832203954

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.704980744413382

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1423790163389214

> <JCHEM_POLAR_SURFACE_AREA>
167.52999999999997

> <JCHEM_REFRACTIVITY>
108.1276

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.13e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(6-ethenyl-2,2,6-trimethyloxan-3-yl)oxy]oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0031367
     RDKit          3D
Linalool oxide D 3-[apiosyl-(1->6)-glucoside]
 68 70  0  0  0  0  0  0  0  0999 V2000
   -7.1886    1.1243   -0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7906   -0.0688    0.3330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4879   -0.2350    1.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9067   -0.1372    2.5640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8830   -1.5485    0.7965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4769   -1.5772    0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7484   -0.2643    0.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6619   -0.1659   -0.3866 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4902    0.2392    0.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0475    1.2878   -0.4545 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4088    1.5361   -0.1966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2082    1.4905   -1.4552 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127    1.6939   -1.4774 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4587    0.9215   -0.9423 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2789    1.6033    0.0016 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1843    0.5586    0.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6147    0.0016   -1.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8920    0.4327   -1.3680 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5445   -1.5090   -1.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3119   -2.0105   -0.6624 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5747    0.5645   -1.9509 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0185    1.7149   -2.5462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8967    0.8307    1.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2716    1.4274    2.1580 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6348   -0.6474    1.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3526   -1.0756    2.3174 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4476   -0.9473    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2013   -2.0729    0.6991 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7571    0.7730   -0.1007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9997    2.0899   -0.1410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1975    0.4507   -1.4888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7397    0.8699    0.8283 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1155    1.2327   -0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5861    2.0084    0.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3771   -0.9437    0.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6631    0.6701    2.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9966    0.2240    3.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2460   -1.1111    2.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5006   -2.0667    0.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0371   -2.2147    1.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9254   -2.3555    0.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3716   -1.9279   -0.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5817   -0.0140    1.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6324    0.4220    1.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3970    2.6461    0.0911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419    2.3273   -2.1030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8688    0.5808   -2.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1591   -0.0123   -0.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0455    0.9342    0.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6132   -0.1703    0.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1872   -0.1189   -2.1357 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7748   -1.9070   -2.0377 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3403   -1.9490   -0.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2957   -2.5757    0.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2654   -0.2334   -2.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4905    2.4911   -2.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9471    1.0051    1.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4655    0.7621    2.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -1.2606    0.6736 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0497   -2.0309    2.2407 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6766   -1.1341   -0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5609   -2.6255   -0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7447    2.9211   -0.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2965    2.1415    0.7015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5026    2.1378   -1.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6088    1.3383   -1.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9053   -0.3683   -1.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2827    0.1416   -2.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  3  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  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 17 21  1  0
 21 22  1  0
 11 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
  7 29  1  0
 29 30  1  0
 29 31  1  0
 29 32  1  0
 32  3  1  0
 27  9  1  0
 21 14  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  4 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  9 44  1  0
 11 45  1  0
 12 46  1  0
 12 47  1  0
 14 48  1  0
 16 49  1  0
 16 50  1  0
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 21 55  1  0
 22 56  1  0
 23 57  1  0
 24 58  1  0
 25 59  1  0
 26 60  1  0
 27 61  1  0
 28 62  1  0
 30 63  1  0
 30 64  1  0
 30 65  1  0
 31 66  1  0
 31 67  1  0
 31 68  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      -9.293 -18.888   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.410 -14.545   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.617 -16.514   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.618 -16.863   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.016 -18.027   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.845 -13.838   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.750 -15.084   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.851  -7.448   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.832  -1.281   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.556  -3.330   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.756  -8.693   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.313 -13.999   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -7.287  -8.533   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -8.193  -9.778   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -7.566 -11.185   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.048  -3.330   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.035 -11.346   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.572  -4.795   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.687 -15.406   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.124 -16.491   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.802  -2.425   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -6.339  -1.601   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -7.914  -7.126   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -9.724  -9.617   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -8.471 -12.431   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -6.512  -2.854   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -2.771  -1.281   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -5.477  -6.041   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -3.032  -4.795   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -5.129 -10.100   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -5.408 -12.753   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -6.592 -16.652   0.000  0.00  0.00           O+0
CONECT    1    5                                                            
CONECT    2   19                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5    1   20                                                       
CONECT    6    7   12                                                       
CONECT    7    6   20                                                       
CONECT    8   11   28                                                       
CONECT    9   21   22                                                       
CONECT   10   21   29                                                       
CONECT   11    8   13   30                                                  
CONECT   12    6   19   31                                                  
CONECT   13   11   14   23                                                  
CONECT   14   13   15   24                                                  
CONECT   15   14   17   25                                                  
CONECT   16   18   21   26                                                  
CONECT   17   15   30   31                                                  
CONECT   18   16   28   29                                                  
CONECT   19    2    3   12   32                                             
CONECT   20    4    5    7   32                                             
CONECT   21    9   10   16   27                                             
CONECT   22    9                                                            
CONECT   23   13                                                            
CONECT   24   14                                                            
CONECT   25   15                                                            
CONECT   26   16                                                            
CONECT   27   21                                                            
CONECT   28    8   18                                                       
CONECT   29   10   18                                                       
CONECT   30   11   17                                                       
CONECT   31   12   17                                                       
CONECT   32   19   20                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

COMPND    HMDB0031367
HETATM    1  C1  UNL     1      -7.189   1.124  -0.065  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.791  -0.069   0.333  1.00  0.00           C  
HETATM    3  C3  UNL     1      -5.488  -0.235   1.084  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.907  -0.137   2.564  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.883  -1.549   0.797  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.477  -1.577   0.349  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.748  -0.264   0.422  1.00  0.00           C  
HETATM    8  O1  UNL     1      -1.662  -0.166  -0.387  1.00  0.00           O  
HETATM    9  C8  UNL     1      -0.490   0.239   0.236  1.00  0.00           C  
HETATM   10  O2  UNL     1       0.048   1.288  -0.454  1.00  0.00           O  
HETATM   11  C9  UNL     1       1.409   1.536  -0.197  1.00  0.00           C  
HETATM   12  C10 UNL     1       2.208   1.490  -1.455  1.00  0.00           C  
HETATM   13  O3  UNL     1       3.513   1.694  -1.477  1.00  0.00           O  
HETATM   14  C11 UNL     1       4.459   0.921  -0.942  1.00  0.00           C  
HETATM   15  O4  UNL     1       5.279   1.603   0.002  1.00  0.00           O  
HETATM   16  C12 UNL     1       6.184   0.559   0.321  1.00  0.00           C  
HETATM   17  C13 UNL     1       6.615   0.002  -1.012  1.00  0.00           C  
HETATM   18  O5  UNL     1       7.892   0.433  -1.368  1.00  0.00           O  
HETATM   19  C14 UNL     1       6.544  -1.509  -1.007  1.00  0.00           C  
HETATM   20  O6  UNL     1       5.312  -2.011  -0.662  1.00  0.00           O  
HETATM   21  C15 UNL     1       5.575   0.565  -1.951  1.00  0.00           C  
HETATM   22  O7  UNL     1       6.019   1.715  -2.546  1.00  0.00           O  
HETATM   23  C16 UNL     1       1.897   0.831   1.003  1.00  0.00           C  
HETATM   24  O8  UNL     1       1.272   1.427   2.158  1.00  0.00           O  
HETATM   25  C17 UNL     1       1.635  -0.647   1.010  1.00  0.00           C  
HETATM   26  O9  UNL     1       1.353  -1.076   2.317  1.00  0.00           O  
HETATM   27  C18 UNL     1       0.448  -0.947   0.135  1.00  0.00           C  
HETATM   28  O10 UNL     1      -0.201  -2.073   0.699  1.00  0.00           O  
HETATM   29  C19 UNL     1      -3.757   0.773  -0.101  1.00  0.00           C  
HETATM   30  C20 UNL     1      -3.000   2.090  -0.141  1.00  0.00           C  
HETATM   31  C21 UNL     1      -4.197   0.451  -1.489  1.00  0.00           C  
HETATM   32  O11 UNL     1      -4.740   0.870   0.828  1.00  0.00           O  
HETATM   33  H1  UNL     1      -8.116   1.233  -0.599  1.00  0.00           H  
HETATM   34  H2  UNL     1      -6.586   2.008   0.140  1.00  0.00           H  
HETATM   35  H3  UNL     1      -7.377  -0.944   0.135  1.00  0.00           H  
HETATM   36  H4  UNL     1      -6.663   0.670   2.677  1.00  0.00           H  
HETATM   37  H5  UNL     1      -4.997   0.224   3.099  1.00  0.00           H  
HETATM   38  H6  UNL     1      -6.246  -1.111   2.936  1.00  0.00           H  
HETATM   39  H7  UNL     1      -5.501  -2.067   0.002  1.00  0.00           H  
HETATM   40  H8  UNL     1      -5.037  -2.215   1.698  1.00  0.00           H  
HETATM   41  H9  UNL     1      -2.925  -2.355   0.938  1.00  0.00           H  
HETATM   42  H10 UNL     1      -3.372  -1.928  -0.721  1.00  0.00           H  
HETATM   43  H11 UNL     1      -2.582  -0.014   1.475  1.00  0.00           H  
HETATM   44  H12 UNL     1      -0.632   0.422   1.321  1.00  0.00           H  
HETATM   45  H13 UNL     1       1.397   2.646   0.091  1.00  0.00           H  
HETATM   46  H14 UNL     1       1.742   2.327  -2.103  1.00  0.00           H  
HETATM   47  H15 UNL     1       1.869   0.581  -2.047  1.00  0.00           H  
HETATM   48  H16 UNL     1       4.159  -0.012  -0.430  1.00  0.00           H  
HETATM   49  H17 UNL     1       7.045   0.934   0.882  1.00  0.00           H  
HETATM   50  H18 UNL     1       5.613  -0.170   0.927  1.00  0.00           H  
HETATM   51  H19 UNL     1       8.187  -0.119  -2.136  1.00  0.00           H  
HETATM   52  H20 UNL     1       6.775  -1.907  -2.038  1.00  0.00           H  
HETATM   53  H21 UNL     1       7.340  -1.949  -0.363  1.00  0.00           H  
HETATM   54  H22 UNL     1       5.296  -2.576   0.125  1.00  0.00           H  
HETATM   55  H23 UNL     1       5.265  -0.233  -2.624  1.00  0.00           H  
HETATM   56  H24 UNL     1       5.490   2.491  -2.242  1.00  0.00           H  
HETATM   57  H25 UNL     1       2.947   1.005   1.199  1.00  0.00           H  
HETATM   58  H26 UNL     1       1.465   0.762   2.880  1.00  0.00           H  
HETATM   59  H27 UNL     1       2.487  -1.261   0.674  1.00  0.00           H  
HETATM   60  H28 UNL     1       1.050  -2.031   2.241  1.00  0.00           H  
HETATM   61  H29 UNL     1       0.677  -1.134  -0.913  1.00  0.00           H  
HETATM   62  H30 UNL     1      -0.561  -2.625  -0.013  1.00  0.00           H  
HETATM   63  H31 UNL     1      -3.745   2.921  -0.138  1.00  0.00           H  
HETATM   64  H32 UNL     1      -2.297   2.141   0.701  1.00  0.00           H  
HETATM   65  H33 UNL     1      -2.503   2.138  -1.131  1.00  0.00           H  
HETATM   66  H34 UNL     1      -4.609   1.338  -1.988  1.00  0.00           H  
HETATM   67  H35 UNL     1      -4.905  -0.368  -1.585  1.00  0.00           H  
HETATM   68  H36 UNL     1      -3.283   0.142  -2.075  1.00  0.00           H  
CONECT    1    2    2   33   34
CONECT    2    3   35
CONECT    3    4    5   32
CONECT    4   36   37   38
CONECT    5    6   39   40
CONECT    6    7   41   42
CONECT    7    8   29   43
CONECT    8    9
CONECT    9   10   27   44
CONECT   10   11
CONECT   11   12   23   45
CONECT   12   13   46   47
CONECT   13   14
CONECT   14   15   21   48
CONECT   15   16
CONECT   16   17   49   50
CONECT   17   18   19   21
CONECT   18   51
CONECT   19   20   52   53
CONECT   20   54
CONECT   21   22   55
CONECT   22   56
CONECT   23   24   25   57
CONECT   24   58
CONECT   25   26   27   59
CONECT   26   60
CONECT   27   28   61
CONECT   28   62
CONECT   29   30   31   32
CONECT   30   63   64   65
CONECT   31   66   67   68
END

HMDB0031367
     RDKit          3D
Linalool oxide D 3-[apiosyl-(1->6)-glucoside]
 68 70  0  0  0  0  0  0  0  0999 V2000
   -7.1886    1.1243   -0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7906   -0.0688    0.3330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4879   -0.2350    1.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9067   -0.1372    2.5640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8830   -1.5485    0.7965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4769   -1.5772    0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7484   -0.2643    0.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6619   -0.1659   -0.3866 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4902    0.2392    0.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0475    1.2878   -0.4545 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4088    1.5361   -0.1966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2082    1.4905   -1.4552 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127    1.6939   -1.4774 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4587    0.9215   -0.9423 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2789    1.6033    0.0016 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1843    0.5586    0.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6147    0.0016   -1.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8920    0.4327   -1.3680 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5445   -1.5090   -1.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3119   -2.0105   -0.6624 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5747    0.5645   -1.9509 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0185    1.7149   -2.5462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8967    0.8307    1.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2716    1.4274    2.1580 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6348   -0.6474    1.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3526   -1.0756    2.3174 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4476   -0.9473    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2013   -2.0729    0.6991 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7571    0.7730   -0.1007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9997    2.0899   -0.1410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1975    0.4507   -1.4888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7397    0.8699    0.8283 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1155    1.2327   -0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5861    2.0084    0.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3771   -0.9437    0.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6631    0.6701    2.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9966    0.2240    3.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2460   -1.1111    2.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5006   -2.0667    0.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0371   -2.2147    1.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9254   -2.3555    0.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3716   -1.9279   -0.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5817   -0.0140    1.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6324    0.4220    1.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3970    2.6461    0.0911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419    2.3273   -2.1030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8688    0.5808   -2.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1591   -0.0123   -0.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0455    0.9342    0.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6132   -0.1703    0.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1872   -0.1189   -2.1357 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7748   -1.9070   -2.0377 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3403   -1.9490   -0.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2957   -2.5757    0.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2654   -0.2334   -2.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4905    2.4911   -2.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9471    1.0051    1.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4655    0.7621    2.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -1.2606    0.6736 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0497   -2.0309    2.2407 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6766   -1.1341   -0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5609   -2.6255   -0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7447    2.9211   -0.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2965    2.1415    0.7015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5026    2.1378   -1.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6088    1.3383   -1.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9053   -0.3683   -1.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2827    0.1416   -2.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  3  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  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 17 21  1  0
 21 22  1  0
 11 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
  7 29  1  0
 29 30  1  0
 29 31  1  0
 29 32  1  0
 32  3  1  0
 27  9  1  0
 21 14  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  4 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  9 44  1  0
 11 45  1  0
 12 46  1  0
 12 47  1  0
 14 48  1  0
 16 49  1  0
 16 50  1  0
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 21 55  1  0
 22 56  1  0
 23 57  1  0
 24 58  1  0
 25 59  1  0
 26 60  1  0
 27 61  1  0
 28 62  1  0
 30 63  1  0
 30 64  1  0
 30 65  1  0
 31 66  1  0
 31 67  1  0
 31 68  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₃₆O₁₁

Average Molecular Weight

464.5039

Monoisotopic Molecular Weight

464.225761994

IUPAC Name

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(6-ethenyl-2,2,6-trimethyloxan-3-yl)oxy]oxane-3,4,5-triol

Traditional Name

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[(6-ethenyl-2,2,6-trimethyloxan-3-yl)oxy]oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC1(C)OC(C)(CCC1OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O)C=C

InChI Identifier

InChI=1S/C21H36O11/c1-5-20(4)7-6-12(19(2,3)32-20)31-17-15(25)14(24)13(23)11(30-17)8-28-18-16(26)21(27,9-22)10-29-18/h5,11-18,22-27H,1,6-10H2,2-4H3

InChI Key

AINNVCLTLJOODL-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Disaccharide
O-glycosyl compound
Oxane
Tertiary alcohol
Tetrahydrofuran
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Acetal
Primary alcohol
Hydrocarbon derivative
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0031367)
Cytoplasm (HMDB: HMDB0031367)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0031367)

Source

Endogenous

Endogenous (HMDB: HMDB0031367)

Plant

Plant (HMDB: HMDB0031367)

Exogenous

Food

Food (HMDB: HMDB0031367)

Tea

Exogenous (HMDB: HMDB0031367)

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	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	11.3 g/L	ALOGPS
logP	-0.5	ALOGPS
logP	-1.4	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	11.7	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	167.53 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	108.13 m³·mol⁻¹	ChemAxon
Polarizability	47.29 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	203.474	31661259
DarkChem	[M-H]-	196.497	31661259
DeepCCS	[M+H]+	205.592	30932474
DeepCCS	[M-H]-	203.234	30932474
DeepCCS	[M-2H]-	237.417	30932474
DeepCCS	[M+Na]+	213.211	30932474
AllCCS	[M+H]+	210.3	32859911
AllCCS	[M+H-H2O]+	208.4	32859911
AllCCS	[M+NH4]+	212.1	32859911
AllCCS	[M+Na]+	212.6	32859911
AllCCS	[M-H]-	206.5	32859911
AllCCS	[M+Na-2H]-	207.9	32859911
AllCCS	[M+HCOO]-	209.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Linalool oxide D 3-[apiosyl-(1->6)-glucoside]	CC1(C)OC(C)(CCC1OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O)C=C	2821.8	Standard polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside]	CC1(C)OC(C)(CCC1OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O)C=C	3045.5	Standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside]	CC1(C)OC(C)(CCC1OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O)C=C	3444.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O)C(O)C(O)C2O)C(C)(C)O1	3360.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TMS,isomer #2	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O)C(O)C(O)C2O)C(C)(C)O1	3332.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TMS,isomer #3	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C)C(O)C(O)C2O)C(C)(C)O1	3373.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TMS,isomer #4	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O[Si](C)(C)C)C(O)C2O)C(C)(C)O1	3329.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TMS,isomer #5	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3293.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TMS,isomer #6	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3305.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O)C(O)C(O)C2O)C(C)(C)O1	3263.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #10	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(C)(C)O1	3278.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #11	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3240.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #12	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3255.1	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #13	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3225.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #14	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3227.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #15	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3224.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #2	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O)C(C)(C)O1	3295.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #3	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O)C(C)(C)O1	3281.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #4	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3253.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #5	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3257.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #6	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O)C(C)(C)O1	3260.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #7	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O)C(C)(C)O1	3233.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #8	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3192.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TMS,isomer #9	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3209.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O)C(C)(C)O1	3181.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #10	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3140.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #11	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(C)(C)O1	3128.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #12	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3075.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #13	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3107.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #14	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3079.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #15	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3101.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #16	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3083.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #17	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3112.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #18	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3129.1	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #19	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3111.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #2	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O)C(C)(C)O1	3165.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #20	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3154.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #3	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3117.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #4	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3140.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #5	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(C)(C)O1	3195.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #6	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3142.1	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #7	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3166.0	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #8	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3148.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TMS,isomer #9	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3154.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(C)(C)O1	3088.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #10	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3064.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #11	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C)(C)O1	2994.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #12	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3007.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #13	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	2995.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #14	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3013.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #15	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3027.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #2	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3035.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #3	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3060.0	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #4	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3041.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #5	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3050.9	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #6	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3036.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #7	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C)(C)O1	3059.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #8	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C)(C)O1	3067.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],4TMS,isomer #9	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	3055.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],5TMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(C)(C)O1	2996.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],5TMS,isomer #2	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(C)(C)O1	2996.1	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],5TMS,isomer #3	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	2984.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],5TMS,isomer #4	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	2977.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],5TMS,isomer #5	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	2988.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],5TMS,isomer #6	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	2938.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],6TMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C)(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(C)(C)O1	2964.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TBDMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O)C(C)(C)O1	3588.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TBDMS,isomer #2	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O)C(C)(C)O1	3544.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TBDMS,isomer #3	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(C)(C)O1	3583.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TBDMS,isomer #4	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(C)(C)O1	3554.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TBDMS,isomer #5	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3517.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],1TBDMS,isomer #6	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3534.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O)C(C)(C)O1	3688.0	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #10	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(C)(C)O1	3689.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #11	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3651.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #12	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3663.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #13	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3649.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #14	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3644.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #15	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3644.1	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #2	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(C)(C)O1	3735.1	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #3	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(C)(C)O1	3713.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #4	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3683.6	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #5	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3688.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #6	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(C)(C)O1	3669.0	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #7	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(C)(C)O1	3656.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #8	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3622.0	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],2TBDMS,isomer #9	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3629.1	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #1	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(C)(C)O1	3806.5	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #10	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3799.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #11	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(C)(C)O1	3769.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #12	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3750.1	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #13	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3744.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #14	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3756.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #15	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3763.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #16	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO[Si](C)(C)C(C)(C)C)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3755.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #17	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[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)C2O)C(C)(C)O1	3771.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #18	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3771.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #19	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3766.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #2	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(C)(C)O1	3788.8	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #20	C=CC1(C)CCC(OC2OC(COC3OCC(O)(CO)C3O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3773.7	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #3	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3774.4	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #4	C=CC1(C)CCC(OC2OC(COC3OCC(CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)C3O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3763.9	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #5	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(C)(C)O1	3828.3	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #6	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3815.2	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #7	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3805.9	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #8	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(C)(C)O1	3802.9	Semi standard non polar	33892256
Linalool oxide D 3-[apiosyl-(1->6)-glucoside],3TBDMS,isomer #9	C=CC1(C)CCC(OC2OC(COC3OCC(CO)(O[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(C)(C)O1	3802.3	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 - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] GC-MS (Non-derivatized) - 70eV, Positive	splash10-000t-3132900000-aadee65ee712eae1489c	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] GC-MS (3 TMS) - 70eV, Positive	splash10-014i-2410129000-37490488c13cc6377cbb	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-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 - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 10V, Positive-QTOF	splash10-00xr-1902500000-9af825d4179ff5c0f694	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 20V, Positive-QTOF	splash10-00di-5901000000-a3cbdba90724db426537	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 40V, Positive-QTOF	splash10-00di-6900000000-447a02b370161381f99b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 10V, Negative-QTOF	splash10-02u1-0832900000-4512cde0753f7c91b759	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 20V, Negative-QTOF	splash10-014i-1910100000-fcf684cfc4f5bfa11e52	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 40V, Negative-QTOF	splash10-00lr-9600000000-3be49817795dae240f2e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 10V, Negative-QTOF	splash10-03di-0001900000-d7db073baa65d8892f35	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 20V, Negative-QTOF	splash10-08n9-7509200000-14c12f3585a5d5340728	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 40V, Negative-QTOF	splash10-0ldl-6900000000-913727a468c7649bdf4b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 10V, Positive-QTOF	splash10-015a-1903800000-59e918016bd350a1c8e7	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 20V, Positive-QTOF	splash10-0f8a-8902200000-673458aeae89976ea4e3	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Linalool oxide D 3-[apiosyl-(1->6)-glucoside] 40V, Positive-QTOF	splash10-0002-4910000000-fe3a490219b5a646671f	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

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

FDB003434

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

131751158

PDB ID

Not Available

ChEBI ID

167984

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for Linalool oxide D 3-[apiosyl-(1->6)-glucoside] (HMDB0031367)

MOL for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

3D MOL for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

3D SDF for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

3D-SDF for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

PDB for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

3D PDB for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

SMILES for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

INCHI for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

Structure for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

3D Structure for HMDB0031367 (Linalool oxide D 3-[apiosyl-(1->6)-glucoside])

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra