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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2017-09-08 16:53:07 UTC

Update Date

2022-03-07 03:18:07 UTC

HMDB ID

HMDB0112261

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2',3'-Anhydrolutein

Description

2',3'-Anhydrolutein is a carotenoid found in human serum and breast milk (PMID: 9164160 ). Carotenoids are isoprenoid molecules that are widespread in nature and are typically seen as pigments in fruits, flowers, birds and crustacea. Animals are unable to synthesise carotenoids de novo, and rely upon the diet as a source of these compounds. Over recent years there has been considerable interest in dietary carotenoids with respect to their potential in alleviating age-related diseases in humans. This attention has been mirrored by significant advances in cloning most of the carotenoid genes and in the genetic manipulation of crop plants with the intention of increasing levels in the diet. Studies have shown an inverse relationship between the consumption of certain fruits and vegetables and the risk of epithelial cancer. Since carotenoids are among the micronutrients found in cancer preventive foods, detailed qualitative and quantitative determination of these compounds, particularly in fruits and vegetables and in human plasma, have recently become increasingly important. (PMID: 1416048 , 15003396 )

Structure

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

                        
  Mrv1652311101723282D          

 41 42  0  0  0  0            999 V2000
   -6.7893   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0748    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5038   -1.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2182   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3602   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6459    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9314   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6459    1.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2169    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5025   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7880    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0734   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7880    1.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3590    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3554   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0699    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4988    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844   -1.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2133   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9278    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6422   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3567    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6422   -1.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0712   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7857    0.1816    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5001    1.4191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2146    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7893   -1.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0748   -1.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0712    1.4191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7857    1.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9163    0.8961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5038    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0913    0.8961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0876   -0.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5001   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9126   -0.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2146    1.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2182   -1.0559    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.9327   -1.4684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1 29  2  0  0  0  0
  1 34  1  0  0  0  0
  1  2  1  0  0  0  0
 29  3  1  0  0  0  0
 34  4  1  0  0  0  0
  2  5  2  0  0  0  0
  3 40  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 23 25  2  0  0  0  0
 26 25  1  6  0  0  0
 26 32  1  0  0  0  0
 26 37  1  0  0  0  0
 32 27  2  0  0  0  0
 37 28  1  0  0  0  0
  4 40  1  0  0  0  0
 28 39  2  0  0  0  0
 29 30  1  0  0  0  0
 32 31  1  0  0  0  0
 34 33  1  0  0  0  0
 34 35  1  0  0  0  0
 37 36  1  0  0  0  0
 37 38  1  0  0  0  0
 40 41  1  1  0  0  0
 27 39  1  0  0  0  0
M  END

HMDB0112261
     RDKit          3D
2',3'-Anhydrolutein
 95 96  0  0  0  0  0  0  0  0999 V2000
   11.4038    1.9004    0.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0712    0.5488    0.1957 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3561    0.4839    0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0709   -0.7890    0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3118   -1.8521   -0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8462   -1.9167   -0.0747 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3934   -3.1739    0.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4889   -2.2137   -1.5486 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2123   -0.6794    0.3769 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.8633   -0.4055    0.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6738   -0.2057    0.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3243    0.1239   -0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5758    0.9061    1.0252 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5199   -0.2136   -1.0643 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1216    0.1174   -1.0637 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2758    0.0606   -2.0621 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8724    0.4068   -1.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4334    0.3624   -0.3051 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4220    1.3540   -3.0213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6433    1.4893   -2.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.8415    0.8250   -0.3190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1028    1.2856   -0.2168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4412    2.4118   -1.1025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0629    0.5198    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2818    0.8757    0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0903   -0.0761    1.6822 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.6893    1.7676    1.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2398   -0.3825    2.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5870   -1.6570    3.3968 C   0  0  1  0  0  0  0  0  0  0  0  0
  -12.6078   -2.4921    3.8801 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9295   -2.3001    2.2382 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.3907   -2.0417    0.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1022    2.6876   -0.0973 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0749    1.7927    0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0271   -0.7327   -1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7249    0.4689   -0.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6440   -0.2170   -3.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7273    1.2350    0.2531 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0455   -0.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0769   -0.4844    0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2492    0.6249   -3.7003 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3543    0.8062   -1.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -12.5898   -3.3474    3.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.1873   -1.0860    3.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7096   -2.3833    2.1692 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.0883   -2.8824    0.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5536   -1.2127   -0.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
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  6  8  1  0
  6  9  1  0
  9 10  1  0
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 21 22  1  0
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 31 32  1  0
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  9  2  1  0
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 40 92  1  0
 41 93  1  0
 41 94  1  0
 41 95  1  0
M  END

                        
  Mrv1652311101723282D          

 41 42  0  0  0  0            999 V2000
   -6.7893   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0748    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5038   -1.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2182   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3602   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6459    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9314   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6459    1.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2169    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5025   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7880    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0734   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7880    1.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3590    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3554   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0699    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4988    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844   -1.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2133   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9278    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6422   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3567    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6422   -1.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0712   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7857    0.1816    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5001    1.4191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2146    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7893   -1.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0748   -1.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0712    1.4191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7857    1.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9163    0.8961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5038    0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0913    0.8961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0876   -0.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5001   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9126   -0.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2146    1.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2182   -1.0559    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.9327   -1.4684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1 29  2  0  0  0  0
  1 34  1  0  0  0  0
  1  2  1  0  0  0  0
 29  3  1  0  0  0  0
 34  4  1  0  0  0  0
  2  5  2  0  0  0  0
  3 40  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 23 25  2  0  0  0  0
 26 25  1  6  0  0  0
 26 32  1  0  0  0  0
 26 37  1  0  0  0  0
 32 27  2  0  0  0  0
 37 28  1  0  0  0  0
  4 40  1  0  0  0  0
 28 39  2  0  0  0  0
 29 30  1  0  0  0  0
 32 31  1  0  0  0  0
 34 33  1  0  0  0  0
 34 35  1  0  0  0  0
 37 36  1  0  0  0  0
 37 38  1  0  0  0  0
 40 41  1  1  0  0  0
 27 39  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0112261

> <DATABASE_NAME>
hmdb

> <SMILES>
C\C(\C=C\C=C(/C)\C=C\[C@@H]1C(C)=CC=CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C[C@@H](O)CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C40H54O/c1-30(18-13-20-32(3)23-25-37-34(5)22-15-27-39(37,7)8)16-11-12-17-31(2)19-14-21-33(4)24-26-38-35(6)28-36(41)29-40(38,9)10/h11-27,36-37,41H,28-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20+,33-21+/t36-,37-/m1/s1

> <INCHI_KEY>
HBHHQQIZEXNSHZ-AJGOZXJMSA-N

> <FORMULA>
C40H54O

> <MOLECULAR_WEIGHT>
550.871

> <EXACT_MASS>
550.417466359

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
71.84532652444159

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohexa-2,4-dien-1-yl]octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-3-en-1-ol

> <ALOGPS_LOGP>
8.96

> <JCHEM_LOGP>
9.419098740999999

> <ALOGPS_LOGS>
-5.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.907213404525137

> <JCHEM_PKA_STRONGEST_BASIC>
-1.089784856860705

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
194.66450000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.88e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohexa-2,4-dien-1-yl]octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-3-en-1-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0112261
     RDKit          3D
2',3'-Anhydrolutein
 95 96  0  0  0  0  0  0  0  0999 V2000
   11.4038    1.9004    0.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0712    0.5488    0.1957 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3561    0.4839    0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0709   -0.7890    0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3118   -1.8521   -0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8462   -1.9167   -0.0747 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3934   -3.1739    0.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4889   -2.2137   -1.5486 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2123   -0.6794    0.3769 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.8633   -0.4055    0.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6738   -0.2057    0.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3243    0.1239   -0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5758    0.9061    1.0252 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5199   -0.2136   -1.0643 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1216    0.1174   -1.0637 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2758    0.0606   -2.0621 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8724    0.4068   -1.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4334    0.3624   -0.3051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9515    0.6481   -2.6510 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5779    0.9415   -2.3018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4220    1.3540   -3.0213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6433    1.4893   -2.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8782    1.9756   -2.6675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8649    2.4972   -4.0748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8637    1.6019   -1.8964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8375    1.2332   -1.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8415    0.8250   -0.3190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1028    1.2856   -0.2168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4412    2.4118   -1.1025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0629    0.5198    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2818    0.8757    0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0903   -0.0761    1.6822 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2874    0.3752    2.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6893    1.7676    1.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2398   -0.3825    2.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5870   -1.6570    3.3968 C   0  0  1  0  0  0  0  0  0  0  0  0
  -12.6078   -2.4921    3.8801 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9295   -2.3001    2.2382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6920   -1.5033    1.8240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5705   -1.8612    2.6959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3907   -2.0417    0.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1022    2.6876   -0.0973 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1245    2.1185    1.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5574    1.8720   -0.4190 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.9324    1.4297    0.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.1441   -0.8076    0.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.8750   -2.8036   -0.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0744   -3.9834   -0.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5873   -2.9423    1.3800 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2644   -3.5465    1.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6232   -2.8703   -1.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4046   -1.2512   -2.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3423   -2.8092   -1.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3354   -0.8076    1.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7478   -1.2132   -0.9264 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8209    0.7044    1.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9195    0.3102    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0749    1.7927    0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3071    1.4302    1.7139 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0271   -0.7327   -1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7249    0.4689   -0.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6440   -0.2170   -3.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7273    1.2350    0.2531 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0455   -0.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0769   -0.4844    0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2492    0.6249   -3.7003 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3543    0.8062   -1.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2225    1.5499   -4.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7085    1.1559   -1.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6291    3.2712   -4.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0509    1.7111   -4.8117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8810    2.9893   -4.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8345    2.4650   -2.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8704    0.4306   -0.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6939   -0.0196    0.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6851    2.1544   -2.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3538    2.8922   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6547    3.2206   -1.0513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7387   -0.4293    1.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6601    1.8096    0.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6961    1.9712    2.0483 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6594    1.8761    0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9416    2.5149    2.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1751   -0.6037    2.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5088    0.1982    3.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8918   -1.4411    4.2268 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5898   -3.3474    3.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6310   -2.3817    1.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5733   -3.3245    2.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1873   -1.0860    3.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7096   -2.3833    2.1692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9239   -2.7062    3.3829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3776   -2.4513    0.3995 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0883   -2.8824    0.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5536   -1.2127   -0.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 39 40  1  0
 39 41  1  0
  9  2  1  0
 39 32  1  0
  1 42  1  0
  1 43  1  0
  1 44  1  0
  3 45  1  0
  4 46  1  0
  5 47  1  0
  7 48  1  0
  7 49  1  0
  7 50  1  0
  8 51  1  0
  8 52  1  0
  8 53  1  0
  9 54  1  1
 10 55  1  0
 11 56  1  0
 13 57  1  0
 13 58  1  0
 13 59  1  0
 14 60  1  0
 15 61  1  0
 16 62  1  0
 18 63  1  0
 18 64  1  0
 18 65  1  0
 19 66  1  0
 20 67  1  0
 21 68  1  0
 22 69  1  0
 24 70  1  0
 24 71  1  0
 24 72  1  0
 25 73  1  0
 26 74  1  0
 27 75  1  0
 29 76  1  0
 29 77  1  0
 29 78  1  0
 30 79  1  0
 31 80  1  0
 34 81  1  0
 34 82  1  0
 34 83  1  0
 35 84  1  0
 35 85  1  0
 36 86  1  1
 37 87  1  0
 38 88  1  0
 38 89  1  0
 40 90  1  0
 40 91  1  0
 40 92  1  0
 41 93  1  0
 41 94  1  0
 41 95  1  0
M  END

HEADER    PROTEIN                                 10-NOV-17   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-NOV-17         0                                  
HETATM    1  C   UNK     0     -12.673  -0.431   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -11.340   0.339   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -14.007  -2.741   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -15.341  -0.431   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.006  -0.431   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.672   0.339   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.339  -0.431   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.672   1.879   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.005   0.339   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.671  -0.431   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.338   0.339   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.004  -0.431   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.338   1.879   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.670   0.339   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.663  -0.431   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.997   0.339   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.331  -0.431   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.664   0.339   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.331  -1.971   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.998  -0.431   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.332   0.339   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.665  -0.431   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.999   0.339   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.665  -1.971   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.333  -0.431   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.667   0.339   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.000   2.649   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      15.334   0.339   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -12.673  -1.971   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -11.340  -2.741   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.333   2.649   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.667   1.879   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -14.777   1.673   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -14.007   0.339   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -13.237   1.673   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.230  -1.765   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.000  -0.431   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      14.770  -1.765   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      15.334   1.879   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -15.341  -1.971   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0     -16.674  -2.741   0.000  0.00  0.00           O+0
CONECT    1   29   34    2                                                  
CONECT    2    1    5                                                       
CONECT    3   29   40                                                       
CONECT    4   34   40                                                       
CONECT    5    2    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6    9                                                       
CONECT    8    6                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11   14                                                       
CONECT   13   11                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17   20                                                       
CONECT   19   17                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22   25                                                       
CONECT   24   22                                                            
CONECT   25   23   26                                                       
CONECT   26   25   32   37                                                  
CONECT   27   32   39                                                       
CONECT   28   37   39                                                       
CONECT   29    1    3   30                                                  
CONECT   30   29                                                            
CONECT   31   32                                                            
CONECT   32   26   27   31                                                  
CONECT   33   34                                                            
CONECT   34    1    4   33   35                                             
CONECT   35   34                                                            
CONECT   36   37                                                            
CONECT   37   26   28   36   38                                             
CONECT   38   37                                                            
CONECT   39   28   27                                                       
CONECT   40    3    4   41                                                  
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

COMPND    HMDB0112261
HETATM    1  C1  UNL     1      11.404   1.900   0.289  1.00  0.00           C  
HETATM    2  C2  UNL     1      12.071   0.549   0.196  1.00  0.00           C  
HETATM    3  C3  UNL     1      13.356   0.484   0.161  1.00  0.00           C  
HETATM    4  C4  UNL     1      14.071  -0.789   0.047  1.00  0.00           C  
HETATM    5  C5  UNL     1      13.312  -1.852  -0.047  1.00  0.00           C  
HETATM    6  C6  UNL     1      11.846  -1.917  -0.075  1.00  0.00           C  
HETATM    7  C7  UNL     1      11.393  -3.174   0.677  1.00  0.00           C  
HETATM    8  C8  UNL     1      11.489  -2.214  -1.549  1.00  0.00           C  
HETATM    9  C9  UNL     1      11.212  -0.679   0.377  1.00  0.00           C  
HETATM   10  C10 UNL     1       9.863  -0.405   0.235  1.00  0.00           C  
HETATM   11  C11 UNL     1       8.674  -0.206   0.061  1.00  0.00           C  
HETATM   12  C12 UNL     1       7.324   0.124  -0.015  1.00  0.00           C  
HETATM   13  C13 UNL     1       6.576   0.906   1.025  1.00  0.00           C  
HETATM   14  C14 UNL     1       6.520  -0.214  -1.064  1.00  0.00           C  
HETATM   15  C15 UNL     1       5.122   0.117  -1.064  1.00  0.00           C  
HETATM   16  C16 UNL     1       4.276   0.061  -2.062  1.00  0.00           C  
HETATM   17  C17 UNL     1       2.872   0.407  -1.751  1.00  0.00           C  
HETATM   18  C18 UNL     1       2.433   0.362  -0.305  1.00  0.00           C  
HETATM   19  C19 UNL     1       1.952   0.648  -2.651  1.00  0.00           C  
HETATM   20  C20 UNL     1       0.578   0.941  -2.302  1.00  0.00           C  
HETATM   21  C21 UNL     1      -0.422   1.354  -3.021  1.00  0.00           C  
HETATM   22  C22 UNL     1      -1.643   1.489  -2.322  1.00  0.00           C  
HETATM   23  C23 UNL     1      -2.878   1.976  -2.668  1.00  0.00           C  
HETATM   24  C24 UNL     1      -2.865   2.497  -4.075  1.00  0.00           C  
HETATM   25  C25 UNL     1      -3.864   1.602  -1.896  1.00  0.00           C  
HETATM   26  C26 UNL     1      -4.837   1.233  -1.135  1.00  0.00           C  
HETATM   27  C27 UNL     1      -5.841   0.825  -0.319  1.00  0.00           C  
HETATM   28  C28 UNL     1      -7.103   1.286  -0.217  1.00  0.00           C  
HETATM   29  C29 UNL     1      -7.441   2.412  -1.102  1.00  0.00           C  
HETATM   30  C30 UNL     1      -8.063   0.520   0.586  1.00  0.00           C  
HETATM   31  C31 UNL     1      -9.282   0.876   0.873  1.00  0.00           C  
HETATM   32  C32 UNL     1     -10.090  -0.076   1.682  1.00  0.00           C  
HETATM   33  C33 UNL     1     -11.287   0.375   2.073  1.00  0.00           C  
HETATM   34  C34 UNL     1     -11.689   1.768   1.664  1.00  0.00           C  
HETATM   35  C35 UNL     1     -12.240  -0.382   2.907  1.00  0.00           C  
HETATM   36  C36 UNL     1     -11.587  -1.657   3.397  1.00  0.00           C  
HETATM   37  O1  UNL     1     -12.608  -2.492   3.880  1.00  0.00           O  
HETATM   38  C37 UNL     1     -10.930  -2.300   2.238  1.00  0.00           C  
HETATM   39  C38 UNL     1      -9.692  -1.503   1.824  1.00  0.00           C  
HETATM   40  C39 UNL     1      -8.570  -1.861   2.696  1.00  0.00           C  
HETATM   41  C40 UNL     1      -9.391  -2.042   0.398  1.00  0.00           C  
HETATM   42  H1  UNL     1      12.102   2.688  -0.097  1.00  0.00           H  
HETATM   43  H2  UNL     1      11.124   2.119   1.314  1.00  0.00           H  
HETATM   44  H3  UNL     1      10.557   1.872  -0.419  1.00  0.00           H  
HETATM   45  H4  UNL     1      13.932   1.430   0.223  1.00  0.00           H  
HETATM   46  H5  UNL     1      15.144  -0.808   0.049  1.00  0.00           H  
HETATM   47  H6  UNL     1      13.875  -2.804  -0.103  1.00  0.00           H  
HETATM   48  H7  UNL     1      11.074  -3.983  -0.010  1.00  0.00           H  
HETATM   49  H8  UNL     1      10.587  -2.942   1.380  1.00  0.00           H  
HETATM   50  H9  UNL     1      12.264  -3.546   1.291  1.00  0.00           H  
HETATM   51  H10 UNL     1      10.623  -2.870  -1.590  1.00  0.00           H  
HETATM   52  H11 UNL     1      11.405  -1.251  -2.080  1.00  0.00           H  
HETATM   53  H12 UNL     1      12.342  -2.809  -1.978  1.00  0.00           H  
HETATM   54  H13 UNL     1      11.335  -0.808   1.585  1.00  0.00           H  
HETATM   55  H14 UNL     1       9.748  -1.213  -0.926  1.00  0.00           H  
HETATM   56  H15 UNL     1       8.821   0.704   1.172  1.00  0.00           H  
HETATM   57  H16 UNL     1       5.919   0.310   1.646  1.00  0.00           H  
HETATM   58  H17 UNL     1       6.075   1.793   0.519  1.00  0.00           H  
HETATM   59  H18 UNL     1       7.307   1.430   1.714  1.00  0.00           H  
HETATM   60  H19 UNL     1       7.027  -0.733  -1.855  1.00  0.00           H  
HETATM   61  H20 UNL     1       4.725   0.469  -0.090  1.00  0.00           H  
HETATM   62  H21 UNL     1       4.644  -0.217  -3.007  1.00  0.00           H  
HETATM   63  H22 UNL     1       2.727   1.235   0.253  1.00  0.00           H  
HETATM   64  H23 UNL     1       1.429  -0.045  -0.155  1.00  0.00           H  
HETATM   65  H24 UNL     1       3.077  -0.484   0.157  1.00  0.00           H  
HETATM   66  H25 UNL     1       2.249   0.625  -3.700  1.00  0.00           H  
HETATM   67  H26 UNL     1       0.354   0.806  -1.206  1.00  0.00           H  
HETATM   68  H27 UNL     1      -0.223   1.550  -4.057  1.00  0.00           H  
HETATM   69  H28 UNL     1      -1.708   1.156  -1.242  1.00  0.00           H  
HETATM   70  H29 UNL     1      -3.629   3.271  -4.149  1.00  0.00           H  
HETATM   71  H30 UNL     1      -3.051   1.711  -4.812  1.00  0.00           H  
HETATM   72  H31 UNL     1      -1.881   2.989  -4.256  1.00  0.00           H  
HETATM   73  H32 UNL     1      -4.834   2.465  -2.452  1.00  0.00           H  
HETATM   74  H33 UNL     1      -3.870   0.431  -0.506  1.00  0.00           H  
HETATM   75  H34 UNL     1      -5.694  -0.020   0.416  1.00  0.00           H  
HETATM   76  H35 UNL     1      -7.685   2.154  -2.137  1.00  0.00           H  
HETATM   77  H36 UNL     1      -8.354   2.892  -0.623  1.00  0.00           H  
HETATM   78  H37 UNL     1      -6.655   3.221  -1.051  1.00  0.00           H  
HETATM   79  H38 UNL     1      -7.739  -0.429   1.002  1.00  0.00           H  
HETATM   80  H39 UNL     1      -9.660   1.810   0.529  1.00  0.00           H  
HETATM   81  H40 UNL     1     -12.696   1.971   2.048  1.00  0.00           H  
HETATM   82  H41 UNL     1     -11.659   1.876   0.560  1.00  0.00           H  
HETATM   83  H42 UNL     1     -10.942   2.515   2.074  1.00  0.00           H  
HETATM   84  H43 UNL     1     -13.175  -0.604   2.335  1.00  0.00           H  
HETATM   85  H44 UNL     1     -12.509   0.198   3.834  1.00  0.00           H  
HETATM   86  H45 UNL     1     -10.892  -1.441   4.227  1.00  0.00           H  
HETATM   87  H46 UNL     1     -12.590  -3.347   3.387  1.00  0.00           H  
HETATM   88  H47 UNL     1     -11.631  -2.382   1.374  1.00  0.00           H  
HETATM   89  H48 UNL     1     -10.573  -3.325   2.527  1.00  0.00           H  
HETATM   90  H49 UNL     1      -8.187  -1.086   3.393  1.00  0.00           H  
HETATM   91  H50 UNL     1      -7.710  -2.383   2.169  1.00  0.00           H  
HETATM   92  H51 UNL     1      -8.924  -2.706   3.383  1.00  0.00           H  
HETATM   93  H52 UNL     1      -8.378  -2.451   0.399  1.00  0.00           H  
HETATM   94  H53 UNL     1     -10.088  -2.882   0.227  1.00  0.00           H  
HETATM   95  H54 UNL     1      -9.554  -1.213  -0.334  1.00  0.00           H  
CONECT    1    2   42   43   44
CONECT    2    3    3    9
CONECT    3    4   45
CONECT    4    5    5   46
CONECT    5    6   47
CONECT    6    7    8    9
CONECT    7   48   49   50
CONECT    8   51   52   53
CONECT    9   10   54
CONECT   10   11   11   55
CONECT   11   12   56
CONECT   12   13   14   14
CONECT   13   57   58   59
CONECT   14   15   60
CONECT   15   16   16   61
CONECT   16   17   62
CONECT   17   18   19   19
CONECT   18   63   64   65
CONECT   19   20   66
CONECT   20   21   21   67
CONECT   21   22   68
CONECT   22   23   23   69
CONECT   23   24   25
CONECT   24   70   71   72
CONECT   25   26   26   73
CONECT   26   27   74
CONECT   27   28   28   75
CONECT   28   29   30
CONECT   29   76   77   78
CONECT   30   31   31   79
CONECT   31   32   80
CONECT   32   33   33   39
CONECT   33   34   35
CONECT   34   81   82   83
CONECT   35   36   84   85
CONECT   36   37   38   86
CONECT   37   87
CONECT   38   39   88   89
CONECT   39   40   41
CONECT   40   90   91   92
CONECT   41   93   94   95
END

HMDB0112261
     RDKit          3D
2',3'-Anhydrolutein
 95 96  0  0  0  0  0  0  0  0999 V2000
   11.4038    1.9004    0.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0712    0.5488    0.1957 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3561    0.4839    0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0709   -0.7890    0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3118   -1.8521   -0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8462   -1.9167   -0.0747 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3934   -3.1739    0.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4889   -2.2137   -1.5486 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2123   -0.6794    0.3769 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.8633   -0.4055    0.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6738   -0.2057    0.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3243    0.1239   -0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5758    0.9061    1.0252 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5199   -0.2136   -1.0643 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1216    0.1174   -1.0637 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2758    0.0606   -2.0621 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8724    0.4068   -1.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4334    0.3624   -0.3051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9515    0.6481   -2.6510 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5779    0.9415   -2.3018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4220    1.3540   -3.0213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6433    1.4893   -2.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8782    1.9756   -2.6675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8649    2.4972   -4.0748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8637    1.6019   -1.8964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8375    1.2332   -1.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8415    0.8250   -0.3190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1028    1.2856   -0.2168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4412    2.4118   -1.1025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0629    0.5198    0.5865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2818    0.8757    0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0903   -0.0761    1.6822 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2874    0.3752    2.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6893    1.7676    1.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2398   -0.3825    2.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5870   -1.6570    3.3968 C   0  0  1  0  0  0  0  0  0  0  0  0
  -12.6078   -2.4921    3.8801 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9295   -2.3001    2.2382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6920   -1.5033    1.8240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5705   -1.8612    2.6959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3907   -2.0417    0.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1022    2.6876   -0.0973 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1245    2.1185    1.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5574    1.8720   -0.4190 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.9324    1.4297    0.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.1441   -0.8076    0.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.8750   -2.8036   -0.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0744   -3.9834   -0.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5873   -2.9423    1.3800 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2644   -3.5465    1.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6232   -2.8703   -1.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4046   -1.2512   -2.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3423   -2.8092   -1.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3354   -0.8076    1.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7478   -1.2132   -0.9264 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8209    0.7044    1.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9195    0.3102    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0749    1.7927    0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3071    1.4302    1.7139 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0271   -0.7327   -1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7249    0.4689   -0.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6440   -0.2170   -3.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7273    1.2350    0.2531 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0455   -0.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0769   -0.4844    0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2492    0.6249   -3.7003 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3543    0.8062   -1.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2225    1.5499   -4.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7085    1.1559   -1.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6291    3.2712   -4.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0509    1.7111   -4.8117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8810    2.9893   -4.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8345    2.4650   -2.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8704    0.4306   -0.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6939   -0.0196    0.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6851    2.1544   -2.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3538    2.8922   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6547    3.2206   -1.0513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7387   -0.4293    1.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6601    1.8096    0.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6961    1.9712    2.0483 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6594    1.8761    0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9416    2.5149    2.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1751   -0.6037    2.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5088    0.1982    3.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8918   -1.4411    4.2268 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5898   -3.3474    3.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6310   -2.3817    1.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5733   -3.3245    2.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1873   -1.0860    3.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7096   -2.3833    2.1692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9239   -2.7062    3.3829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3776   -2.4513    0.3995 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0883   -2.8824    0.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5536   -1.2127   -0.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
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 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  2  0
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 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
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 32 33  2  0
 33 34  1  0
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  9  2  1  0
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  1 42  1  0
  1 43  1  0
  1 44  1  0
  3 45  1  0
  4 46  1  0
  5 47  1  0
  7 48  1  0
  7 49  1  0
  7 50  1  0
  8 51  1  0
  8 52  1  0
  8 53  1  0
  9 54  1  1
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 37 87  1  0
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 40 92  1  0
 41 93  1  0
 41 94  1  0
 41 95  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(3R,6'R)-3-hydroxy-2',3'-didehydro-β,ε-carotene	SMPDB, HMDB
(3R,6'R)-3-hydroxy-2',3'-didehydro-beta,epsilon-carotene	SMPDB, HMDB
2',3'-Anhydrolutein	SMPDB
(3R,6'R)-2',3'-didehydro-β,ε-caroten-3-ol	HMDB
(3R,6'R)-2',3'-didehydro-beta,epsilon-caroten-3-ol	HMDB
2',3'-didehydro-α-caroten-3-ol	HMDB
2',3'-didehydro-alpha-caroten-3-ol	HMDB

Chemical Formula

C₄₀H₅₄O

Average Molecular Weight

550.871

Monoisotopic Molecular Weight

550.417466359

IUPAC Name

(1R)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohexa-2,4-dien-1-yl]octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-3-en-1-ol

Traditional Name

(1R)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohexa-2,4-dien-1-yl]octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-3-en-1-ol

CAS Registry Number

92760-19-5

SMILES

C\C(\C=C\C=C(/C)\C=C\[C@@H]1C(C)=CC=CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C[C@@H](O)CC1(C)C

InChI Identifier

InChI=1S/C40H54O/c1-30(18-13-20-32(3)23-25-37-34(5)22-15-27-39(37,7)8)16-11-12-17-31(2)19-14-21-33(4)24-26-38-35(6)28-36(41)29-40(38,9)10/h11-27,36-37,41H,28-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20+,33-21+/t36-,37-/m1/s1

InChI Key

HBHHQQIZEXNSHZ-AJGOZXJMSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Tetraterpenoids

Direct Parent

Xanthophylls

Alternative Parents

Substituents

Xanthophyll
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Breast Milk (PMID: 9164160)

Non-excretory biofluid

Blood (PMID: 9164160)

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
logP	8.96	ALOGPS
logP	9.42	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	18.91	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	194.66 m³·mol⁻¹	ChemAxon
Polarizability	71.85 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	256.704	30932474
DeepCCS	[M-H]-	254.824	30932474
DeepCCS	[M-2H]-	288.242	30932474
DeepCCS	[M+Na]+	262.405	30932474
AllCCS	[M+H]+	252.5	32859911
AllCCS	[M+H-H2O]+	250.7	32859911
AllCCS	[M+NH4]+	254.2	32859911
AllCCS	[M+Na]+	254.7	32859911
AllCCS	[M-H]-	224.1	32859911
AllCCS	[M+Na-2H]-	226.9	32859911
AllCCS	[M+HCOO]-	230.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2',3'-Anhydrolutein	C\C(\C=C\C=C(/C)\C=C\[C@@H]1C(C)=CC=CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C[C@@H](O)CC1(C)C	5670.8	Standard polar	33892256
2',3'-Anhydrolutein	C\C(\C=C\C=C(/C)\C=C\[C@@H]1C(C)=CC=CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C[C@@H](O)CC1(C)C	4587.9	Standard non polar	33892256
2',3'-Anhydrolutein	C\C(\C=C\C=C(/C)\C=C\[C@@H]1C(C)=CC=CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C[C@@H](O)CC1(C)C	4135.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2',3'-Anhydrolutein,1TMS,isomer #1	CC1=CC=CC(C)(C)[C@@H]1/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)C[C@@H](O[Si](C)(C)C)CC1(C)C	4665.6	Semi standard non polar	33892256
2',3'-Anhydrolutein,1TBDMS,isomer #1	CC1=CC=CC(C)(C)[C@@H]1/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)C[C@@H](O[Si](C)(C)C(C)(C)C)CC1(C)C	4852.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2',3'-Anhydrolutein GC-MS ("2',3'-Anhydrolutein,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2',3'-Anhydrolutein GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2',3'-Anhydrolutein GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-10-15	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 - 2',3'-Anhydrolutein 10V, Positive-QTOF	splash10-0f89-0524190000-1e02685f864d4398d7f4	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 20V, Positive-QTOF	splash10-0002-0849100000-6f9630a2e1b4f4a7d8a2	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 40V, Positive-QTOF	splash10-000b-0559100000-0c9fb166a1407029df16	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 10V, Negative-QTOF	splash10-0002-0000090000-41b1c053e1e4d235aee0	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 20V, Negative-QTOF	splash10-0002-0000090000-4398e765e8ece96df97b	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 40V, Negative-QTOF	splash10-001i-0525190000-be086b830e4986cd5674	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 10V, Positive-QTOF	splash10-0ufu-0456960000-9fe311e67e18bacfd40d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 20V, Positive-QTOF	splash10-059i-0579420000-17a05d03fb902a9282dd	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 40V, Positive-QTOF	splash10-03di-0789100000-c5cb71a2c7841303f1f2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 10V, Negative-QTOF	splash10-0002-0002090000-d245c75cd19588a03e96	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 20V, Negative-QTOF	splash10-0002-0335190000-999fb2b02ad985c493ff	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2',3'-Anhydrolutein 40V, Negative-QTOF	splash10-0532-0739110000-9042f2060acceb7d73fd	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Breast Milk

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Female	Normal	9164160	details
Breast Milk	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Female	Normal	9164160	details

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

Not Available

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

101638875

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Khachik F, Beecher GR, Goli MB, Lusby WR, Smith JC Jr: Separation and identification of carotenoids and their oxidation products in the extracts of human plasma. Anal Chem. 1992 Sep 15;64(18):2111-22. [PubMed:1416048 ]
Fraser PD, Bramley PM: The biosynthesis and nutritional uses of carotenoids. Prog Lipid Res. 2004 May;43(3):228-65. [PubMed:15003396 ]
Khachik F, Spangler CJ, Smith JC Jr, Canfield LM, Steck A, Pfander H: Identification, quantification, and relative concentrations of carotenoids and their metabolites in human milk and serum. Anal Chem. 1997 May 15;69(10):1873-81. [PubMed:9164160 ]
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 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 2',3'-Anhydrolutein (HMDB0112261)

MOL for HMDB0112261 (2',3'-Anhydrolutein)

3D MOL for HMDB0112261 (2',3'-Anhydrolutein)

3D SDF for HMDB0112261 (2',3'-Anhydrolutein)

3D-SDF for HMDB0112261 (2',3'-Anhydrolutein)

PDB for HMDB0112261 (2',3'-Anhydrolutein)

3D PDB for HMDB0112261 (2',3'-Anhydrolutein)

SMILES for HMDB0112261 (2',3'-Anhydrolutein)

INCHI for HMDB0112261 (2',3'-Anhydrolutein)

Structure for HMDB0112261 (2',3'-Anhydrolutein)

3D Structure for HMDB0112261 (2',3'-Anhydrolutein)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra