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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 03:17:01 UTC

Update Date

2022-03-07 02:57:05 UTC

HMDB ID

HMDB0041590

Secondary Accession Numbers

HMDB41590

Metabolite Identification

Common Name

Lutein 5,6-epoxide

Description

Lutein; 5,6-Epoxide is found in common grape. Paprika oleoresin (also known as paprika extract) is an oil soluble extract from the fruits of Capsicum Annum Linn or Capsicum Frutescens(Indian red chillies), and is primarily used as a colouring and/or flavouring in food products. It is composed of capsaicin, the main flavouring compound giving pungency in higher concentrations, and capsanthin and capsorubin, the main colouring compounds (among other carotenoids).

Structure

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

lutein 5,6-epoxide
  Mrv1572001071617052D          
  Marvin  03020616482D          
 43 45  0  0  0  0            999 V2000
   -6.7893   -0.2309    0.0000 C   0  0  2  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
   -5.3603   -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
   -1.0735   -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
   -0.3591    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  1  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
   -6.0748   -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  1  0  0  0  0  0  0  0  0  0
    8.9291    1.4191    0.0000 O   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
   -6.7893   -1.0559    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0748   -0.6434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1 42  1  0  0  0  0
  1 33  1  0  0  0  0
  1  2  1  1  0  0  0
 42  3  1  0  0  0  0
 33  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  1  0  0  0
 26 31  1  0  0  0  0
 26 36  1  0  0  0  0
 31 27  2  0  0  0  0
 36 28  1  0  0  0  0
 27 38  1  0  0  0  0
  4 40  1  0  0  0  0
 28 38  1  0  0  0  0
 42 29  1  1  0  0  0
 31 30  1  0  0  0  0
 33 32  1  0  0  0  0
 33 34  1  0  0  0  0
 36 35  1  0  0  0  0
 36 37  1  0  0  0  0
 38 39  1  6  0  0  0
 40 41  1  1  0  0  0
 42 43  1  0  0  0  0
  1 43  1  0  0  0  0
M  END

HMDB0041590
     RDKit          3D
Lutein 5,6-epoxide
 99101  0  0  0  0  0  0  0  0999 V2000
    9.6818    0.1161   -4.0197 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3958   -0.0492   -2.7353 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5126    0.9966   -1.9271 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2490    0.7674   -0.6361 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5621    1.9511    0.0143 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5370    0.0512   -0.9848 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2331   -1.3086   -1.5787 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3381   -2.3495   -0.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3801   -1.6260   -2.5525 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9588   -1.3611   -2.3660 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8889   -2.1344   -1.6725 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6777   -1.6743   -1.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7037   -2.5432   -0.7299 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0650   -3.8979   -0.3152 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5254   -2.0288   -0.5549 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4040   -2.6662    0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2463   -2.0101    0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0753   -2.5867    0.7372 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -3.8550    1.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9797   -1.8456    0.6585 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6625   -2.1745    1.1515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2961   -1.2663    0.9370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6540   -1.4565    1.3437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5544   -0.4877    1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9670    0.7284    0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9263   -0.5776    1.2701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7790    0.3859    0.9650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2100    0.2813    1.1479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9736    1.3285    0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2570    2.4685    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4430    1.3330    0.9001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1690    2.3440    0.4782 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6320    2.4054    0.6262 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.0840    3.7256    0.1774 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5483    2.5053   -0.3795 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.1808    2.2339   -1.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0115    2.3304   -0.0837 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4253    2.8554    1.2499 C   0  0  1  0  0  0  0  0  0  0  0  0
  -14.4882    2.0727    1.7325 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3472    2.8993    2.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1633    2.0015    1.9829 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1774    2.1101    3.0938 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6535    0.5704    1.9289 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7946   -0.5330   -4.0965 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3507    1.1763   -4.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3477   -0.1264   -4.8835 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1302    1.9708   -2.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6184    0.1538    0.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
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   11.1308   -1.9269   -3.3378 H   0  0  0  0  0  0  0  0  0  0  0  0
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    9.1141   -3.9664    0.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9337   -4.5917   -1.2081 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3316   -0.9805   -0.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5333   -3.6542    0.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  2  0
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 42 94  1  0
 42 95  1  0
 42 96  1  0
 43 97  1  0
 43 98  1  0
 43 99  1  0
M  END

lutein 5,6-epoxide
  Mrv1572001071617052D          
  Marvin  03020616482D          
 43 45  0  0  0  0            999 V2000
   -6.7893   -0.2309    0.0000 C   0  0  2  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
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    1.7844   -1.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6422   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.5001    1.4191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0748   -1.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0876   -0.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.9291    1.4191    0.0000 O   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
   -6.7893   -1.0559    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0748   -0.6434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1 33  1  0  0  0  0
  1  2  1  1  0  0  0
 42  3  1  0  0  0  0
 33  4  1  0  0  0  0
  2  5  2  0  0  0  0
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  1 43  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0041590

> <DATABASE_NAME>
hmdb

> <SMILES>
C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=C[C@H](O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C40H56O3/c1-29(17-13-19-31(3)21-22-36-33(5)25-34(41)26-37(36,6)7)15-11-12-16-30(2)18-14-20-32(4)23-24-40-38(8,9)27-35(42)28-39(40,10)43-40/h11-25,34-36,41-42H,26-28H2,1-10H3/b12-11+,17-13+,18-14+,22-21+,24-23+,29-15+,30-16+,31-19+,32-20+/t34-,35-,36-,39+,40-/m0/s1

> <INCHI_KEY>
DYUUPIKEWLHQGQ-FJOIUHRLSA-N

> <FORMULA>
C40H56O3

> <MOLECULAR_WEIGHT>
584.885

> <EXACT_MASS>
584.422945663

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
73.60307485636955

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3S,6S)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol

> <ALOGPS_LOGP>
8.39

> <JCHEM_LOGP>
8.003617862999999

> <ALOGPS_LOGS>
-5.85

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.21727233987641

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.139684034106125

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3910077414822246

> <JCHEM_POLAR_SURFACE_AREA>
52.989999999999995

> <JCHEM_REFRACTIVITY>
193.75150000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.24e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
lutein 5,6-epoxide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0041590
     RDKit          3D
Lutein 5,6-epoxide
 99101  0  0  0  0  0  0  0  0999 V2000
    9.6818    0.1161   -4.0197 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3958   -0.0492   -2.7353 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5126    0.9966   -1.9271 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2490    0.7674   -0.6361 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5621    1.9511    0.0143 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5370    0.0512   -0.9848 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2331   -1.3086   -1.5787 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3381   -2.3495   -0.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3801   -1.6260   -2.5525 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9588   -1.3611   -2.3660 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8889   -2.1344   -1.6725 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6777   -1.6743   -1.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7037   -2.5432   -0.7299 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0650   -3.8979   -0.3152 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5254   -2.0288   -0.5549 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0753   -2.5867    0.7372 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -3.8550    1.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2961   -1.2663    0.9370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6540   -1.4565    1.3437 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9670    0.7284    0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9263   -0.5776    1.2701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7790    0.3859    0.9650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2100    0.2813    1.1479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9736    1.3285    0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.4430    1.3330    0.9001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1690    2.3440    0.4782 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6320    2.4054    0.6262 C   0  0  1  0  0  0  0  0  0  0  0  0
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  -11.5483    2.5053   -0.3795 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.1808    2.2339   -1.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0115    2.3304   -0.0837 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4253    2.8554    1.2499 C   0  0  1  0  0  0  0  0  0  0  0  0
  -14.4882    2.0727    1.7325 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3472    2.8993    2.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1633    2.0015    1.9829 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1774    2.1101    3.0938 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6535    0.5704    1.9289 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7946   -0.5330   -4.0965 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3507    1.1763   -4.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3477   -0.1264   -4.8835 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1302    1.9708   -2.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6184    0.1538    0.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9497    2.6488   -0.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0043    0.6394   -1.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.1928   -0.0470   -0.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.8591   -3.2517   -0.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3850   -2.6182   -0.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9855   -1.9068    0.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3109   -1.4072   -1.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
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   13.2661   -1.0083   -3.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1308   -1.9269   -3.3378 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0755   -3.1639   -1.3652 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3981   -0.6950   -1.7047 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4425   -4.3530    0.4695 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1141   -3.9664    0.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9337   -4.5917   -1.2081 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3316   -0.9805   -0.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5333   -3.6542    0.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2331   -1.0097   -0.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1738   -4.7650    0.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9438   -3.9371    2.1220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0996   -0.8681    0.1542 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4450   -3.0960    1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0135   -0.3423    0.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9928   -2.3364    1.8215 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -15.3680    2.5139    1.5878 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.4884    0.0577    2.9245 H   0  0  0  0  0  0  0  0  0  0  0  0
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 10  2  1  0
 35 33  1  0
 41 33  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  3 47  1  0
  4 48  1  1
  5 49  1  0
  6 50  1  0
  6 51  1  0
  8 52  1  0
  8 53  1  0
  8 54  1  0
  9 55  1  0
  9 56  1  0
  9 57  1  0
 10 58  1  6
 11 59  1  0
 12 60  1  0
 14 61  1  0
 14 62  1  0
 14 63  1  0
 15 64  1  0
 16 65  1  0
 17 66  1  0
 19 67  1  0
 19 68  1  0
 19 69  1  0
 20 70  1  0
 21 71  1  0
 22 72  1  0
 23 73  1  0
 25 74  1  0
 25 75  1  0
 25 76  1  0
 26 77  1  0
 27 78  1  0
 28 79  1  0
 30 80  1  0
 30 81  1  0
 30 82  1  0
 31 83  1  0
 32 84  1  0
 36 85  1  0
 36 86  1  0
 36 87  1  0
 37 88  1  0
 37 89  1  0
 38 90  1  6
 39 91  1  0
 40 92  1  0
 40 93  1  0
 42 94  1  0
 42 95  1  0
 42 96  1  0
 43 97  1  0
 43 98  1  0
 43 99  1  0
M  END

HEADER    PROTEIN                                 07-JAN-16   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: lutein 5,6-epoxide                                
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-JAN-16         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     -11.340  -2.741   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.333   2.649   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.667   1.879   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -14.777   1.673   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -14.007   0.339   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -13.237   1.673   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      13.230  -1.765   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      14.000  -0.431   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.770  -1.765   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      15.334   1.879   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      16.668   2.649   0.000  0.00  0.00           O+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
HETATM   42  C   UNK     0     -12.673  -1.971   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0     -11.340  -1.201   0.000  0.00  0.00           O+0
CONECT    1   42   33    2   43                                             
CONECT    2    1    5                                                       
CONECT    3   42   40                                                       
CONECT    4   33   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   31   36                                                  
CONECT   27   31   38                                                       
CONECT   28   36   38                                                       
CONECT   29   42                                                            
CONECT   30   31                                                            
CONECT   31   26   27   30                                                  
CONECT   32   33                                                            
CONECT   33    1    4   32   34                                             
CONECT   34   33                                                            
CONECT   35   36                                                            
CONECT   36   26   28   35   37                                             
CONECT   37   36                                                            
CONECT   38   27   28   39                                                  
CONECT   39   38                                                            
CONECT   40    3    4   41                                                  
CONECT   41   40                                                            
CONECT   42    1    3   29   43                                             
CONECT   43   42    1                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

COMPND    HMDB0041590
HETATM    1  C1  UNL     1       9.682   0.116  -4.020  1.00  0.00           C  
HETATM    2  C2  UNL     1      10.396  -0.049  -2.735  1.00  0.00           C  
HETATM    3  C3  UNL     1      10.513   0.997  -1.927  1.00  0.00           C  
HETATM    4  C4  UNL     1      11.249   0.767  -0.636  1.00  0.00           C  
HETATM    5  O1  UNL     1      11.562   1.951   0.014  1.00  0.00           O  
HETATM    6  C5  UNL     1      12.537   0.051  -0.985  1.00  0.00           C  
HETATM    7  C6  UNL     1      12.233  -1.309  -1.579  1.00  0.00           C  
HETATM    8  C7  UNL     1      12.338  -2.350  -0.488  1.00  0.00           C  
HETATM    9  C8  UNL     1      13.380  -1.626  -2.553  1.00  0.00           C  
HETATM   10  C9  UNL     1      10.959  -1.361  -2.366  1.00  0.00           C  
HETATM   11  C10 UNL     1       9.889  -2.134  -1.673  1.00  0.00           C  
HETATM   12  C11 UNL     1       8.678  -1.674  -1.423  1.00  0.00           C  
HETATM   13  C12 UNL     1       7.704  -2.543  -0.730  1.00  0.00           C  
HETATM   14  C13 UNL     1       8.065  -3.898  -0.315  1.00  0.00           C  
HETATM   15  C14 UNL     1       6.525  -2.029  -0.555  1.00  0.00           C  
HETATM   16  C15 UNL     1       5.404  -2.666   0.083  1.00  0.00           C  
HETATM   17  C16 UNL     1       4.246  -2.010   0.130  1.00  0.00           C  
HETATM   18  C17 UNL     1       3.075  -2.587   0.737  1.00  0.00           C  
HETATM   19  C18 UNL     1       3.057  -3.855   1.427  1.00  0.00           C  
HETATM   20  C19 UNL     1       1.980  -1.846   0.659  1.00  0.00           C  
HETATM   21  C20 UNL     1       0.662  -2.175   1.151  1.00  0.00           C  
HETATM   22  C21 UNL     1      -0.296  -1.266   0.937  1.00  0.00           C  
HETATM   23  C22 UNL     1      -1.654  -1.457   1.344  1.00  0.00           C  
HETATM   24  C23 UNL     1      -2.554  -0.488   1.101  1.00  0.00           C  
HETATM   25  C24 UNL     1      -1.967   0.728   0.423  1.00  0.00           C  
HETATM   26  C25 UNL     1      -3.926  -0.578   1.270  1.00  0.00           C  
HETATM   27  C26 UNL     1      -4.779   0.386   0.965  1.00  0.00           C  
HETATM   28  C27 UNL     1      -6.210   0.281   1.148  1.00  0.00           C  
HETATM   29  C28 UNL     1      -6.974   1.329   0.729  1.00  0.00           C  
HETATM   30  C29 UNL     1      -6.257   2.468   0.117  1.00  0.00           C  
HETATM   31  C30 UNL     1      -8.443   1.333   0.900  1.00  0.00           C  
HETATM   32  C31 UNL     1      -9.169   2.344   0.478  1.00  0.00           C  
HETATM   33  C32 UNL     1     -10.632   2.405   0.626  1.00  0.00           C  
HETATM   34  O2  UNL     1     -11.084   3.726   0.177  1.00  0.00           O  
HETATM   35  C33 UNL     1     -11.548   2.505  -0.379  1.00  0.00           C  
HETATM   36  C34 UNL     1     -11.181   2.234  -1.834  1.00  0.00           C  
HETATM   37  C35 UNL     1     -13.012   2.330  -0.084  1.00  0.00           C  
HETATM   38  C36 UNL     1     -13.425   2.855   1.250  1.00  0.00           C  
HETATM   39  O3  UNL     1     -14.488   2.073   1.732  1.00  0.00           O  
HETATM   40  C37 UNL     1     -12.347   2.899   2.292  1.00  0.00           C  
HETATM   41  C38 UNL     1     -11.163   2.002   1.983  1.00  0.00           C  
HETATM   42  C39 UNL     1     -10.177   2.110   3.094  1.00  0.00           C  
HETATM   43  C40 UNL     1     -11.654   0.570   1.929  1.00  0.00           C  
HETATM   44  H1  UNL     1       8.795  -0.533  -4.097  1.00  0.00           H  
HETATM   45  H2  UNL     1       9.351   1.176  -4.153  1.00  0.00           H  
HETATM   46  H3  UNL     1      10.348  -0.126  -4.883  1.00  0.00           H  
HETATM   47  H4  UNL     1      10.130   1.971  -2.113  1.00  0.00           H  
HETATM   48  H5  UNL     1      10.618   0.154   0.022  1.00  0.00           H  
HETATM   49  H6  UNL     1      10.950   2.649  -0.346  1.00  0.00           H  
HETATM   50  H7  UNL     1      13.004   0.639  -1.823  1.00  0.00           H  
HETATM   51  H8  UNL     1      13.193  -0.047  -0.144  1.00  0.00           H  
HETATM   52  H9  UNL     1      12.859  -3.252  -0.841  1.00  0.00           H  
HETATM   53  H10 UNL     1      11.385  -2.618  -0.030  1.00  0.00           H  
HETATM   54  H11 UNL     1      12.985  -1.907   0.332  1.00  0.00           H  
HETATM   55  H12 UNL     1      14.311  -1.407  -1.955  1.00  0.00           H  
HETATM   56  H13 UNL     1      13.360  -2.707  -2.731  1.00  0.00           H  
HETATM   57  H14 UNL     1      13.266  -1.008  -3.441  1.00  0.00           H  
HETATM   58  H15 UNL     1      11.131  -1.927  -3.338  1.00  0.00           H  
HETATM   59  H16 UNL     1      10.076  -3.164  -1.365  1.00  0.00           H  
HETATM   60  H17 UNL     1       8.398  -0.695  -1.705  1.00  0.00           H  
HETATM   61  H18 UNL     1       7.442  -4.353   0.470  1.00  0.00           H  
HETATM   62  H19 UNL     1       9.114  -3.966   0.073  1.00  0.00           H  
HETATM   63  H20 UNL     1       7.934  -4.592  -1.208  1.00  0.00           H  
HETATM   64  H21 UNL     1       6.332  -0.981  -0.922  1.00  0.00           H  
HETATM   65  H22 UNL     1       5.533  -3.654   0.515  1.00  0.00           H  
HETATM   66  H23 UNL     1       4.233  -1.010  -0.314  1.00  0.00           H  
HETATM   67  H24 UNL     1       3.174  -4.765   0.771  1.00  0.00           H  
HETATM   68  H25 UNL     1       2.187  -3.986   2.117  1.00  0.00           H  
HETATM   69  H26 UNL     1       3.944  -3.937   2.122  1.00  0.00           H  
HETATM   70  H27 UNL     1       2.100  -0.868   0.154  1.00  0.00           H  
HETATM   71  H28 UNL     1       0.445  -3.096   1.664  1.00  0.00           H  
HETATM   72  H29 UNL     1       0.013  -0.342   0.402  1.00  0.00           H  
HETATM   73  H30 UNL     1      -1.993  -2.336   1.821  1.00  0.00           H  
HETATM   74  H31 UNL     1      -1.557   0.393  -0.560  1.00  0.00           H  
HETATM   75  H32 UNL     1      -2.708   1.503   0.350  1.00  0.00           H  
HETATM   76  H33 UNL     1      -1.145   1.138   1.075  1.00  0.00           H  
HETATM   77  H34 UNL     1      -4.394  -1.481   1.706  1.00  0.00           H  
HETATM   78  H35 UNL     1      -4.392   1.309   0.581  1.00  0.00           H  
HETATM   79  H36 UNL     1      -6.721  -0.556   1.594  1.00  0.00           H  
HETATM   80  H37 UNL     1      -6.886   3.227  -0.373  1.00  0.00           H  
HETATM   81  H38 UNL     1      -5.600   2.089  -0.738  1.00  0.00           H  
HETATM   82  H39 UNL     1      -5.599   2.997   0.834  1.00  0.00           H  
HETATM   83  H40 UNL     1      -8.870   0.472   1.380  1.00  0.00           H  
HETATM   84  H41 UNL     1      -8.664   3.178  -0.024  1.00  0.00           H  
HETATM   85  H42 UNL     1     -10.171   2.647  -2.043  1.00  0.00           H  
HETATM   86  H43 UNL     1     -11.247   1.136  -2.037  1.00  0.00           H  
HETATM   87  H44 UNL     1     -11.881   2.714  -2.550  1.00  0.00           H  
HETATM   88  H45 UNL     1     -13.527   3.018  -0.843  1.00  0.00           H  
HETATM   89  H46 UNL     1     -13.420   1.331  -0.330  1.00  0.00           H  
HETATM   90  H47 UNL     1     -13.852   3.897   1.168  1.00  0.00           H  
HETATM   91  H48 UNL     1     -15.368   2.514   1.588  1.00  0.00           H  
HETATM   92  H49 UNL     1     -11.902   3.939   2.333  1.00  0.00           H  
HETATM   93  H50 UNL     1     -12.693   2.669   3.318  1.00  0.00           H  
HETATM   94  H51 UNL     1     -10.572   2.775   3.891  1.00  0.00           H  
HETATM   95  H52 UNL     1      -9.222   2.562   2.763  1.00  0.00           H  
HETATM   96  H53 UNL     1     -10.030   1.129   3.591  1.00  0.00           H  
HETATM   97  H54 UNL     1     -12.767   0.518   1.752  1.00  0.00           H  
HETATM   98  H55 UNL     1     -11.133  -0.047   1.180  1.00  0.00           H  
HETATM   99  H56 UNL     1     -11.488   0.058   2.925  1.00  0.00           H  
CONECT    1    2   44   45   46
CONECT    2    3    3   10
CONECT    3    4   47
CONECT    4    5    6   48
CONECT    5   49
CONECT    6    7   50   51
CONECT    7    8    9   10
CONECT    8   52   53   54
CONECT    9   55   56   57
CONECT   10   11   58
CONECT   11   12   12   59
CONECT   12   13   60
CONECT   13   14   15   15
CONECT   14   61   62   63
CONECT   15   16   64
CONECT   16   17   17   65
CONECT   17   18   66
CONECT   18   19   20   20
CONECT   19   67   68   69
CONECT   20   21   70
CONECT   21   22   22   71
CONECT   22   23   72
CONECT   23   24   24   73
CONECT   24   25   26
CONECT   25   74   75   76
CONECT   26   27   27   77
CONECT   27   28   78
CONECT   28   29   29   79
CONECT   29   30   31
CONECT   30   80   81   82
CONECT   31   32   32   83
CONECT   32   33   84
CONECT   33   34   35   41
CONECT   34   35
CONECT   35   36   37
CONECT   36   85   86   87
CONECT   37   38   88   89
CONECT   38   39   40   90
CONECT   39   91
CONECT   40   41   92   93
CONECT   41   42   43
CONECT   42   94   95   96
CONECT   43   97   98   99
END

HMDB0041590
     RDKit          3D
Lutein 5,6-epoxide
 99101  0  0  0  0  0  0  0  0999 V2000
    9.6818    0.1161   -4.0197 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3958   -0.0492   -2.7353 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5126    0.9966   -1.9271 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2490    0.7674   -0.6361 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5621    1.9511    0.0143 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5370    0.0512   -0.9848 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2331   -1.3086   -1.5787 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3381   -2.3495   -0.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3801   -1.6260   -2.5525 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9588   -1.3611   -2.3660 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8889   -2.1344   -1.6725 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6777   -1.6743   -1.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7037   -2.5432   -0.7299 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0650   -3.8979   -0.3152 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5254   -2.0288   -0.5549 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4040   -2.6662    0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2463   -2.0101    0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0753   -2.5867    0.7372 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -3.8550    1.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9797   -1.8456    0.6585 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6625   -2.1745    1.1515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2961   -1.2663    0.9370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6540   -1.4565    1.3437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5544   -0.4877    1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9670    0.7284    0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9263   -0.5776    1.2701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7790    0.3859    0.9650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2100    0.2813    1.1479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9736    1.3285    0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2570    2.4685    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4430    1.3330    0.9001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1690    2.3440    0.4782 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6320    2.4054    0.6262 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.0840    3.7256    0.1774 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5483    2.5053   -0.3795 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.1808    2.2339   -1.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0115    2.3304   -0.0837 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4253    2.8554    1.2499 C   0  0  1  0  0  0  0  0  0  0  0  0
  -14.4882    2.0727    1.7325 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3472    2.8993    2.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1633    2.0015    1.9829 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1774    2.1101    3.0938 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6535    0.5704    1.9289 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7946   -0.5330   -4.0965 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3507    1.1763   -4.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3477   -0.1264   -4.8835 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1302    1.9708   -2.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6184    0.1538    0.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9497    2.6488   -0.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0043    0.6394   -1.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.1928   -0.0470   -0.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.8591   -3.2517   -0.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3850   -2.6182   -0.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9855   -1.9068    0.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3109   -1.4072   -1.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3599   -2.7071   -2.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.2661   -1.0083   -3.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1308   -1.9269   -3.3378 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0755   -3.1639   -1.3652 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3981   -0.6950   -1.7047 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4425   -4.3530    0.4695 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1141   -3.9664    0.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9337   -4.5917   -1.2081 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3316   -0.9805   -0.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5333   -3.6542    0.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2331   -1.0097   -0.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1738   -4.7650    0.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1867   -3.9860    2.1167 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9438   -3.9371    2.1220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0996   -0.8681    0.1542 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4450   -3.0960    1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0135   -0.3423    0.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9928   -2.3364    1.8215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5568    0.3929   -0.5601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7079    1.5033    0.3500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1454    1.1378    1.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3939   -1.4812    1.7063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3915    1.3091    0.5811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7214   -0.5561    1.5936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8864    3.2270   -0.3734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5998    2.0889   -0.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5994    2.9966    0.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8699    0.4722    1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6640    3.1780   -0.0245 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1706    2.6469   -2.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2474    1.1356   -2.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8811    2.7138   -2.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.5268    3.0183   -0.8435 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4201    1.3314   -0.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8518    3.8966    1.1685 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.3680    2.5139    1.5878 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9024    3.9389    2.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6932    2.6692    3.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5718    2.7748    3.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2224    2.5621    2.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0295    1.1286    3.5912 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7672    0.5182    1.7517 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1332   -0.0469    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4884    0.0577    2.9245 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
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M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Taraxanthin	HMDB

Chemical Formula

C₄₀H₅₆O₃

Average Molecular Weight

584.885

Monoisotopic Molecular Weight

584.422945663

IUPAC Name

(1R,3S,6S)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol

Traditional Name

lutein 5,6-epoxide

CAS Registry Number

28368-08-3

SMILES

C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=C[C@H](O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C

InChI Identifier

InChI=1S/C40H56O3/c1-29(17-13-19-31(3)21-22-36-33(5)25-34(41)26-37(36,6)7)15-11-12-16-30(2)18-14-20-32(4)23-24-40-38(8,9)27-35(42)28-39(40,10)43-40/h11-25,34-36,41-42H,26-28H2,1-10H3/b12-11+,17-13+,18-14+,22-21+,24-23+,29-15+,30-16+,31-19+,32-20+/t34-,35-,36-,39+,40-/m0/s1

InChI Key

DYUUPIKEWLHQGQ-FJOIUHRLSA-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
Oxepane
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

epoxycarotenol (CHEBI:27448 )
C40 isoprenoids (tetraterpenes) (C08602 )
Carotenoids (C08602 )
C40 isoprenoids (tetraterpenes) (LMPR01070275 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0041590)

Source

Endogenous

Endogenous (HMDB: HMDB0041590)

Plant

Plant (HMDB: HMDB0041590)
Poaceae (HMDB: HMDB0041590)

Animal

Animal (HMDB: HMDB0041590)

Exogenous

Food

Food (HMDB: HMDB0041590)

Herb and spice

Herb

Dandelion (FooDB: FOOD00181)

Oilseed crop

Sunflower (FooDB: FOOD00086)

Fruit

Berry

Grape (FooDB: FOOD00369)
Common grape (FooDB: FOOD00204)

Cereal and cereal product

Cereal

Rice (FooDB: FOOD00125)

Vegetable

Leaf vegetable

Swamp cabbage (FooDB: FOOD00091)

Fruit vegetable

Garden tomato (var.) (FooDB: FOOD00173)

Exogenous (HMDB: HMDB0041590)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0041590)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0041590)

Lipid metabolism pathway (HMDB: HMDB0041590)

Cellular process

Cell signaling (HMDB: HMDB0041590)

Biochemical process

Lipid transport (HMDB: HMDB0041590)

Role

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00082 g/L	ALOGPS
logP	8.39	ALOGPS
logP	8	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	15.14	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	52.99 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	193.75 m³·mol⁻¹	ChemAxon
Polarizability	73.6 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
DeepCCS	[M-2H]-	279.856	30932474
DeepCCS	[M+Na]+	253.9	30932474
AllCCS	[M+H]+	263.7	32859911
AllCCS	[M+H-H2O]+	262.0	32859911
AllCCS	[M+NH4]+	265.2	32859911
AllCCS	[M+Na]+	265.6	32859911
AllCCS	[M-H]-	234.9	32859911
AllCCS	[M+Na-2H]-	238.9	32859911
AllCCS	[M+HCOO]-	243.6	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022.	5.27 minutes	32390414
Predicted by Siyang on May 30, 2022	29.8842 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.06 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	5078.3 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	554.1 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	304.6 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	273.1 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	207.4 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	1477.2 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	808.2 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	119.8 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	2671.8 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	956.9 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1748.7 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	1156.8 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	627.1 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	221.5 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	641.5 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	11.1 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Lutein 5,6-epoxide	C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=C[C@H](O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C	6195.7	Standard polar	33892256
Lutein 5,6-epoxide	C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=C[C@H](O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C	4706.2	Standard non polar	33892256
Lutein 5,6-epoxide	C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=C[C@H](O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C	4538.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Lutein 5,6-epoxide,1TMS,isomer #1	CC1=C[C@H](O[Si](C)(C)C)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/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C	4701.2	Semi standard non polar	33892256
Lutein 5,6-epoxide,1TMS,isomer #2	CC1=C[C@H](O)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/[C@@]12O[C@]1(C)C[C@@H](O[Si](C)(C)C)CC2(C)C	4706.0	Semi standard non polar	33892256
Lutein 5,6-epoxide,2TMS,isomer #1	CC1=C[C@H](O[Si](C)(C)C)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/[C@@]12O[C@]1(C)C[C@@H](O[Si](C)(C)C)CC2(C)C	4660.4	Semi standard non polar	33892256
Lutein 5,6-epoxide,1TBDMS,isomer #1	CC1=C[C@H](O[Si](C)(C)C(C)(C)C)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/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C	4921.2	Semi standard non polar	33892256
Lutein 5,6-epoxide,1TBDMS,isomer #2	CC1=C[C@H](O)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/[C@@]12O[C@]1(C)C[C@@H](O[Si](C)(C)C(C)(C)C)CC2(C)C	4926.5	Semi standard non polar	33892256
Lutein 5,6-epoxide,2TBDMS,isomer #1	CC1=C[C@H](O[Si](C)(C)C(C)(C)C)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/[C@@]12O[C@]1(C)C[C@@H](O[Si](C)(C)C(C)(C)C)CC2(C)C	5133.3	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 - Lutein 5,6-epoxide GC-MS (Non-derivatized) - 70eV, Positive	splash10-014i-1000190000-67bb327ab40dd0772065	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Lutein 5,6-epoxide GC-MS (1 TMS) - 70eV, Positive	splash10-000f-9000037000-76289228353979af6a71	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Lutein 5,6-epoxide GC-MS ("Lutein 5,6-epoxide,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Lutein 5,6-epoxide GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Lutein 5,6-epoxide GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Lutein 5,6-epoxide GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Lutein 5,6-epoxide GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Lutein 5,6-epoxide GC-MS (TBDMS_2_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 - Lutein 5,6-epoxide 10V, Positive-QTOF	splash10-014i-0111290000-a7ef643a5a14b81ae242	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 20V, Positive-QTOF	splash10-0292-0796850000-0e749a06fe1d820fe331	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 40V, Positive-QTOF	splash10-03dr-1595110000-8c068fd3666f50103d72	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 10V, Negative-QTOF	splash10-001i-0000090000-fad0bb0baa27e2b42f29	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 20V, Negative-QTOF	splash10-00lr-0100090000-0c4177f6b15091bb72a7	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 40V, Negative-QTOF	splash10-00lj-3600690000-0da3146882ca62b2bdda	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 10V, Positive-QTOF	splash10-014i-0021390000-f89590e2794256d8f6be	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 20V, Positive-QTOF	splash10-066s-0144970000-c02a23d9a5a0b202a058	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 40V, Positive-QTOF	splash10-014i-1269610000-a37db61ec2674b1827cb	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 10V, Negative-QTOF	splash10-001i-0200090000-9e25a89b98ab5c88c472	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 20V, Negative-QTOF	splash10-001i-0403290000-3c235fc40d5c05da811e	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Lutein 5,6-epoxide 40V, Negative-QTOF	splash10-01bc-0619420000-93947538af5fe0d51a11	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Paprika oleoresin

METLIN ID

Not Available

PubChem Compound

5281244

PDB ID

Not Available

ChEBI ID

27448

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for Lutein 5,6-epoxide (HMDB0041590)

MOL for HMDB0041590 (Lutein 5,6-epoxide)

3D MOL for HMDB0041590 (Lutein 5,6-epoxide)

3D SDF for HMDB0041590 (Lutein 5,6-epoxide)

3D-SDF for HMDB0041590 (Lutein 5,6-epoxide)

PDB for HMDB0041590 (Lutein 5,6-epoxide)

3D PDB for HMDB0041590 (Lutein 5,6-epoxide)

SMILES for HMDB0041590 (Lutein 5,6-epoxide)

INCHI for HMDB0041590 (Lutein 5,6-epoxide)

Structure for HMDB0041590 (Lutein 5,6-epoxide)

3D Structure for HMDB0041590 (Lutein 5,6-epoxide)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra