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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 22:15:20 UTC

Update Date

2021-09-26 22:53:27 UTC

HMDB ID

HMDB0245156

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2-Hydroxyestradiol 17-sulfate

Description

2-Hydroxyestradiol 17-sulfate belongs to the class of organic compounds known as sulfated steroids. These are sterol lipids containing a sulfate group attached to the steroid skeleton. Based on a literature review a small amount of articles have been published on 2-Hydroxyestradiol 17-sulfate. This compound has been identified in human blood as reported by (PMID: 31557052 ). 2-hydroxyestradiol 17-sulfate is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 2-Hydroxyestradiol 17-sulfate is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

  Mrv1652309112100152D          

 25 28  0  0  0  0            999 V2000
    4.3228    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939    1.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1111    1.5050    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.9284    1.3922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2240    2.3223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9983    0.6878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492    1.6739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.1221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
 12 15  1  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
  5 23  1  0  0  0  0
 18 23  1  0  0  0  0
 21 24  1  0  0  0  0
 20 25  1  0  0  0  0
M  END

HMDB0245156
     RDKit          3D
2-Hydroxyestradiol 17-sulfate
 49 52  0  0  0  0  0  0  0  0999 V2000
   -1.6350   -1.5436   -1.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7053   -0.2673   -0.6388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0946    0.9099   -1.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3812    0.9539   -1.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120   -0.1555   -0.4467 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4237    0.2303   -0.0482 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    1.1871   -0.7092 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3969    1.5103   -0.3103 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0615    2.5065   -1.0285 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0174    0.8874    0.7506 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3038    1.1779    1.1862 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2610   -0.0875    1.3908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9785   -0.4348    1.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2817   -1.5062    1.7992 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8468   -1.7016    1.4004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3008   -0.4203    0.8715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1630   -0.3277    0.7813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9637   -1.4600    1.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3601   -1.1063    0.7971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1715   -0.0472   -0.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0040   -0.2264   -1.3565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9190    1.1380   -1.6874 S   0  0  0  0  0  6  0  0  0  0  0  0
   -4.0830    2.2695   -2.1905 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9108    0.7645   -2.7557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7334    1.6846   -0.3191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4199   -1.2998   -2.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9133   -2.2810   -1.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6224   -2.0923   -1.4312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4642    0.9610   -2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5001    1.8271   -0.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7987    0.9244   -2.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7471    1.9329   -0.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1588   -1.0725   -1.0502 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6233    1.6770   -1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9857    2.7713   -0.7781 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8511    1.8758    0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7582   -0.5844    2.2383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2752   -1.1444    2.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8683   -2.4541    1.8046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2439   -2.1457    2.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8537   -2.4801    0.5884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6626    0.3917    1.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5530    0.6038    1.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6629   -2.4389    0.8709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9740   -1.5191    2.4106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8797   -1.9989    0.4006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9678   -0.7061    1.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2980    0.9736    0.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2040    2.3432    0.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  2  0
 22 25  1  0
 17  2  1  0
 20  2  1  0
 16  5  1  0
 13  6  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  7 34  1  0
  9 35  1  0
 11 36  1  0
 12 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  0
 25 49  1  0
M  END

  Mrv1652309112100152D          

 25 28  0  0  0  0            999 V2000
    4.3228    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939    1.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1111    1.5050    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.9284    1.3922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2240    2.3223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9983    0.6878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492    1.6739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.1221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
 12 15  1  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
  5 23  1  0  0  0  0
 18 23  1  0  0  0  0
 21 24  1  0  0  0  0
 20 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0245156

> <DATABASE_NAME>
hmdb

> <SMILES>
CC12CCC3C(CCC4=CC(O)=C(O)C=C34)C1CCC2OS(O)(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H24O6S/c1-18-7-6-11-12(14(18)4-5-17(18)24-25(21,22)23)3-2-10-8-15(19)16(20)9-13(10)11/h8-9,11-12,14,17,19-20H,2-7H2,1H3,(H,21,22,23)

> <INCHI_KEY>
LKEXGMTXKRKYSA-UHFFFAOYSA-N

> <FORMULA>
C18H24O6S

> <MOLECULAR_WEIGHT>
368.44

> <EXACT_MASS>
368.129359667

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
38.857287730252956

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{4,5-dihydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2,4,6-trien-14-yl}oxidanesulfonic acid

> <ALOGPS_LOGP>
0.43

> <JCHEM_LOGP>
3.496921774666667

> <ALOGPS_LOGS>
-3.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.67035955738885

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.4409711144298205

> <JCHEM_PKA_STRONGEST_BASIC>
-6.2531169711728625

> <JCHEM_POLAR_SURFACE_AREA>
104.06000000000002

> <JCHEM_REFRACTIVITY>
91.8774

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{4,5-dihydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2,4,6-trien-14-yl}oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0245156
     RDKit          3D
2-Hydroxyestradiol 17-sulfate
 49 52  0  0  0  0  0  0  0  0999 V2000
   -1.6350   -1.5436   -1.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7053   -0.2673   -0.6388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0946    0.9099   -1.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3812    0.9539   -1.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120   -0.1555   -0.4467 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4237    0.2303   -0.0482 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    1.1871   -0.7092 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3969    1.5103   -0.3103 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0615    2.5065   -1.0285 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0174    0.8874    0.7506 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3038    1.1779    1.1862 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2610   -0.0875    1.3908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9785   -0.4348    1.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2817   -1.5062    1.7992 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8468   -1.7016    1.4004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3008   -0.4203    0.8715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1630   -0.3277    0.7813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9637   -1.4600    1.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3601   -1.1063    0.7971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1715   -0.0472   -0.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0040   -0.2264   -1.3565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9190    1.1380   -1.6874 S   0  0  0  0  0  6  0  0  0  0  0  0
   -4.0830    2.2695   -2.1905 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9108    0.7645   -2.7557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7334    1.6846   -0.3191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4199   -1.2998   -2.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9133   -2.2810   -1.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6224   -2.0923   -1.4312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4642    0.9610   -2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5001    1.8271   -0.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7987    0.9244   -2.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7471    1.9329   -0.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1588   -1.0725   -1.0502 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6233    1.6770   -1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9857    2.7713   -0.7781 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8511    1.8758    0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7582   -0.5844    2.2383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2752   -1.1444    2.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8683   -2.4541    1.8046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2439   -2.1457    2.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8537   -2.4801    0.5884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6626    0.3917    1.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5530    0.6038    1.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6629   -2.4389    0.8709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9740   -1.5191    2.4106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8797   -1.9989    0.4006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9678   -0.7061    1.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2980    0.9736    0.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2040    2.3432    0.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  2  0
 22 25  1  0
 17  2  1  0
 20  2  1  0
 16  5  1  0
 13  6  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  7 34  1  0
  9 35  1  0
 11 36  1  0
 12 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  0
 25 49  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       8.069   3.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.366   1.312   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.358   0.135   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.874   0.406   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.365   0.325   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.937   1.804   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.882   3.020   0.000  0.00  0.00           O+0
HETATM   12  S   UNK     0      11.407   2.809   0.000  0.00  0.00           S+0
HETATM   13  O   UNK     0      12.933   2.599   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      11.618   4.335   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      11.197   1.284   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.182   0.499   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.850   1.041   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.652   3.125   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -1.698   0.228   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7   10                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7   16                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    2   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12                                                            
CONECT   16    6   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22    5   18                                                  
CONECT   24   21                                                            
CONECT   25   20                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

COMPND    HMDB0245156
HETATM    1  C1  UNL     1      -1.635  -1.544  -1.377  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.705  -0.267  -0.639  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.095   0.910  -1.314  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.381   0.954  -1.228  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.012  -0.155  -0.447  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.424   0.230  -0.048  1.00  0.00           C  
HETATM    7  C7  UNL     1       3.111   1.187  -0.709  1.00  0.00           C  
HETATM    8  C8  UNL     1       4.397   1.510  -0.310  1.00  0.00           C  
HETATM    9  O1  UNL     1       5.061   2.506  -1.029  1.00  0.00           O  
HETATM   10  C9  UNL     1       5.017   0.887   0.751  1.00  0.00           C  
HETATM   11  O2  UNL     1       6.304   1.178   1.186  1.00  0.00           O  
HETATM   12  C10 UNL     1       4.261  -0.088   1.391  1.00  0.00           C  
HETATM   13  C11 UNL     1       2.978  -0.435   1.021  1.00  0.00           C  
HETATM   14  C12 UNL     1       2.282  -1.506   1.799  1.00  0.00           C  
HETATM   15  C13 UNL     1       0.847  -1.702   1.400  1.00  0.00           C  
HETATM   16  C14 UNL     1       0.301  -0.420   0.871  1.00  0.00           C  
HETATM   17  C15 UNL     1      -1.163  -0.328   0.781  1.00  0.00           C  
HETATM   18  C16 UNL     1      -1.964  -1.460   1.303  1.00  0.00           C  
HETATM   19  C17 UNL     1      -3.360  -1.106   0.797  1.00  0.00           C  
HETATM   20  C18 UNL     1      -3.172  -0.047  -0.270  1.00  0.00           C  
HETATM   21  O3  UNL     1      -4.004  -0.226  -1.356  1.00  0.00           O  
HETATM   22  S1  UNL     1      -4.919   1.138  -1.687  1.00  0.00           S  
HETATM   23  O4  UNL     1      -4.083   2.269  -2.191  1.00  0.00           O  
HETATM   24  O5  UNL     1      -5.911   0.764  -2.756  1.00  0.00           O  
HETATM   25  O6  UNL     1      -5.733   1.685  -0.319  1.00  0.00           O  
HETATM   26  H1  UNL     1      -1.420  -1.300  -2.460  1.00  0.00           H  
HETATM   27  H2  UNL     1      -0.913  -2.281  -1.019  1.00  0.00           H  
HETATM   28  H3  UNL     1      -2.622  -2.092  -1.431  1.00  0.00           H  
HETATM   29  H4  UNL     1      -1.464   0.961  -2.381  1.00  0.00           H  
HETATM   30  H5  UNL     1      -1.500   1.827  -0.837  1.00  0.00           H  
HETATM   31  H6  UNL     1       0.799   0.924  -2.257  1.00  0.00           H  
HETATM   32  H7  UNL     1       0.747   1.933  -0.799  1.00  0.00           H  
HETATM   33  H8  UNL     1       1.159  -1.072  -1.050  1.00  0.00           H  
HETATM   34  H9  UNL     1       2.623   1.677  -1.544  1.00  0.00           H  
HETATM   35  H10 UNL     1       5.986   2.771  -0.778  1.00  0.00           H  
HETATM   36  H11 UNL     1       6.851   1.876   0.731  1.00  0.00           H  
HETATM   37  H12 UNL     1       4.758  -0.584   2.238  1.00  0.00           H  
HETATM   38  H13 UNL     1       2.275  -1.144   2.868  1.00  0.00           H  
HETATM   39  H14 UNL     1       2.868  -2.454   1.805  1.00  0.00           H  
HETATM   40  H15 UNL     1       0.244  -2.146   2.216  1.00  0.00           H  
HETATM   41  H16 UNL     1       0.854  -2.480   0.588  1.00  0.00           H  
HETATM   42  H17 UNL     1       0.663   0.392   1.567  1.00  0.00           H  
HETATM   43  H18 UNL     1      -1.553   0.604   1.278  1.00  0.00           H  
HETATM   44  H19 UNL     1      -1.663  -2.439   0.871  1.00  0.00           H  
HETATM   45  H20 UNL     1      -1.974  -1.519   2.411  1.00  0.00           H  
HETATM   46  H21 UNL     1      -3.880  -1.999   0.401  1.00  0.00           H  
HETATM   47  H22 UNL     1      -3.968  -0.706   1.631  1.00  0.00           H  
HETATM   48  H23 UNL     1      -3.298   0.974   0.144  1.00  0.00           H  
HETATM   49  H24 UNL     1      -5.204   2.343   0.186  1.00  0.00           H  
CONECT    1    2   26   27   28
CONECT    2    3   17   20
CONECT    3    4   29   30
CONECT    4    5   31   32
CONECT    5    6   16   33
CONECT    6    7    7   13
CONECT    7    8   34
CONECT    8    9   10   10
CONECT    9   35
CONECT   10   11   12
CONECT   11   36
CONECT   12   13   13   37
CONECT   13   14
CONECT   14   15   38   39
CONECT   15   16   40   41
CONECT   16   17   42
CONECT   17   18   43
CONECT   18   19   44   45
CONECT   19   20   46   47
CONECT   20   21   48
CONECT   21   22
CONECT   22   23   23   24   24
CONECT   22   25
CONECT   25   49
END

HMDB0245156
     RDKit          3D
2-Hydroxyestradiol 17-sulfate
 49 52  0  0  0  0  0  0  0  0999 V2000
   -1.6350   -1.5436   -1.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7053   -0.2673   -0.6388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0946    0.9099   -1.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3812    0.9539   -1.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120   -0.1555   -0.4467 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4237    0.2303   -0.0482 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    1.1871   -0.7092 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3969    1.5103   -0.3103 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0615    2.5065   -1.0285 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0174    0.8874    0.7506 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3038    1.1779    1.1862 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2610   -0.0875    1.3908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9785   -0.4348    1.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2817   -1.5062    1.7992 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8468   -1.7016    1.4004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3008   -0.4203    0.8715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1630   -0.3277    0.7813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9637   -1.4600    1.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3601   -1.1063    0.7971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1715   -0.0472   -0.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0040   -0.2264   -1.3565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9190    1.1380   -1.6874 S   0  0  0  0  0  6  0  0  0  0  0  0
   -4.0830    2.2695   -2.1905 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9108    0.7645   -2.7557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7334    1.6846   -0.3191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4199   -1.2998   -2.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9133   -2.2810   -1.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6224   -2.0923   -1.4312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4642    0.9610   -2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5001    1.8271   -0.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7987    0.9244   -2.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7471    1.9329   -0.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1588   -1.0725   -1.0502 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6233    1.6770   -1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9857    2.7713   -0.7781 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8511    1.8758    0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7582   -0.5844    2.2383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2752   -1.1444    2.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8683   -2.4541    1.8046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2439   -2.1457    2.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8537   -2.4801    0.5884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6626    0.3917    1.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5530    0.6038    1.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6629   -2.4389    0.8709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9740   -1.5191    2.4106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8797   -1.9989    0.4006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9678   -0.7061    1.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2980    0.9736    0.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2040    2.3432    0.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  2  0
 22 25  1  0
 17  2  1  0
 20  2  1  0
 16  5  1  0
 13  6  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  7 34  1  0
  9 35  1  0
 11 36  1  0
 12 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  0
 25 49  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-Hydroxyestradiol 17-sulfuric acid	Generator
2-Hydroxyestradiol 17-sulphate	Generator
2-Hydroxyestradiol 17-sulphuric acid	Generator

Chemical Formula

C₁₈H₂₄O₆S

Average Molecular Weight

368.44

Monoisotopic Molecular Weight

368.129359667

IUPAC Name

{4,5-dihydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2,4,6-trien-14-yl}oxidanesulfonic acid

Traditional Name

{4,5-dihydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2,4,6-trien-14-yl}oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

CC12CCC3C(CCC4=CC(O)=C(O)C=C34)C1CCC2OS(O)(=O)=O

InChI Identifier

InChI=1S/C18H24O6S/c1-18-7-6-11-12(14(18)4-5-17(18)24-25(21,22)23)3-2-10-8-15(19)16(20)9-13(10)11/h8-9,11-12,14,17,19-20H,2-7H2,1H3,(H,21,22,23)

InChI Key

LKEXGMTXKRKYSA-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sulfated steroids. These are sterol lipids containing a sulfate group attached to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Sulfated steroids

Direct Parent

Sulfated steroids

Alternative Parents

Substituents

Sulfated steroid skeleton
Estrogen-skeleton
3-hydroxysteroid
Estrane-skeleton
2-hydroxysteroid
Hydroxysteroid
Phenanthrene
Tetralin
Phenol
1-hydroxy-2-unsubstituted benzenoid
Alkyl sulfate
Sulfate-ester
Sulfuric acid monoester
Sulfuric acid ester
Benzenoid
Organic sulfuric acid or derivatives
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

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	0.43	ALOGPS
logP	3.5	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	-1.4	ChemAxon
pKa (Strongest Basic)	-6.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	91.88 m³·mol⁻¹	ChemAxon
Polarizability	38.86 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	219.109	30932474
DeepCCS	[M+Na]+	194.675	30932474
AllCCS	[M+H]+	185.8	32859911
AllCCS	[M+H-H2O]+	183.3	32859911
AllCCS	[M+NH4]+	188.2	32859911
AllCCS	[M+Na]+	188.8	32859911
AllCCS	[M-H]-	181.8	32859911
AllCCS	[M+Na-2H]-	181.8	32859911
AllCCS	[M+HCOO]-	181.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-Hydroxyestradiol 17-sulfate	CC12CCC3C(CCC4=CC(O)=C(O)C=C34)C1CCC2OS(O)(=O)=O	4764.0	Standard polar	33892256
2-Hydroxyestradiol 17-sulfate	CC12CCC3C(CCC4=CC(O)=C(O)C=C34)C1CCC2OS(O)(=O)=O	2651.0	Standard non polar	33892256
2-Hydroxyestradiol 17-sulfate	CC12CCC3C(CCC4=CC(O)=C(O)C=C34)C1CCC2OS(O)(=O)=O	3390.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-Hydroxyestradiol 17-sulfate,3TMS,isomer #1	CC12CCC3C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4CCC3C1CCC2OS(=O)(=O)O[Si](C)(C)C	3349.0	Semi standard non polar	33892256
2-Hydroxyestradiol 17-sulfate,3TMS,isomer #1	CC12CCC3C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4CCC3C1CCC2OS(=O)(=O)O[Si](C)(C)C	3505.6	Standard non polar	33892256
2-Hydroxyestradiol 17-sulfate,3TMS,isomer #1	CC12CCC3C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4CCC3C1CCC2OS(=O)(=O)O[Si](C)(C)C	3794.0	Standard polar	33892256
2-Hydroxyestradiol 17-sulfate,3TBDMS,isomer #1	CC12CCC3C4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4CCC3C1CCC2OS(=O)(=O)O[Si](C)(C)C(C)(C)C	3980.0	Semi standard non polar	33892256
2-Hydroxyestradiol 17-sulfate,3TBDMS,isomer #1	CC12CCC3C4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4CCC3C1CCC2OS(=O)(=O)O[Si](C)(C)C(C)(C)C	4373.4	Standard non polar	33892256
2-Hydroxyestradiol 17-sulfate,3TBDMS,isomer #1	CC12CCC3C4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4CCC3C1CCC2OS(=O)(=O)O[Si](C)(C)C(C)(C)C	3991.0	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (Non-derivatized) - 70eV, Positive	splash10-004r-0985000000-878ca3dd417b4a5280c9	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxyestradiol 17-sulfate GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-03	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-Hydroxyestradiol 17-sulfate 10V, Positive-QTOF	splash10-014i-0019000000-738dd232721517c0e4f2	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxyestradiol 17-sulfate 20V, Positive-QTOF	splash10-00di-0390000000-15f943db1c4ca4ca50b4	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxyestradiol 17-sulfate 40V, Positive-QTOF	splash10-07e3-0950000000-7a0d1b2a9e7bf6ba38e2	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxyestradiol 17-sulfate 10V, Negative-QTOF	splash10-014i-0009000000-75e71d515551aa019f78	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxyestradiol 17-sulfate 20V, Negative-QTOF	splash10-014i-1009000000-346c01b67c570001dbd9	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxyestradiol 17-sulfate 40V, Negative-QTOF	splash10-052b-9028000000-3e7249dede82ab813f94	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

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	Not Specified	Not Specified	Normal	31557052	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

78169433

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 2-Hydroxyestradiol 17-sulfate (HMDB0245156)

MOL for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

3D MOL for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

3D SDF for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

3D-SDF for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

PDB for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

3D PDB for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

SMILES for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

INCHI for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

Structure for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

3D Structure for HMDB0245156 (2-Hydroxyestradiol 17-sulfate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra