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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 18:45:45 UTC

Update Date

2021-09-26 23:14:16 UTC

HMDB ID

HMDB0257722

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

Description

6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid belongs to the class of organic compounds known as flavonoid o-glucuronides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid. Based on a literature review very few articles have been published on 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). (2s,3s,4s,5r)-6-[4-(5,7-dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 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

  Mrv1652308201922482D          

 32 35  0  0  0  0            999 V2000
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
  8  1  2  0  0  0  0
  8  2  1  0  0  0  0
  9  5  2  0  0  0  0
  9  6  1  0  0  0  0
 10  3  2  0  0  0  0
 10  4  1  0  0  0  0
 11  5  1  0  0  0  0
 12  7  1  0  0  0  0
 13  7  1  0  0  0  0
 13  8  1  0  0  0  0
 14  6  2  0  0  0  0
 15 11  2  0  0  0  0
 15 12  1  0  0  0  0
 15 14  1  0  0  0  0
 17 16  1  0  0  0  0
 18 16  1  0  0  0  0
 19 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 18  1  0  0  0  0
 22  9  1  0  0  0  0
 23 11  1  0  0  0  0
 24 12  2  0  0  0  0
 25 16  1  0  0  0  0
 26 17  1  0  0  0  0
 27 18  1  0  0  0  0
 28 20  2  0  0  0  0
 29 20  1  0  0  0  0
 30 10  1  0  0  0  0
 30 21  1  0  0  0  0
 31 13  1  0  0  0  0
 31 14  1  0  0  0  0
 32 19  1  0  0  0  0
 32 21  1  0  0  0  0
M  END

HMDB0257722
     RDKit          3D
(2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,...
 52 55  0  0  0  0  0  0  0  0999 V2000
    6.2442    2.0749   -0.9391 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3387    1.3744   -0.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071    1.6462   -0.7619 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2176    0.3804   -1.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7436    0.4830   -1.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9310   -0.6066   -1.1544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570   -0.4928   -0.9911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0673    0.7129   -0.7584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4181    0.9099   -0.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3957   -0.0942   -0.6251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2645    0.2424   -1.6288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5275   -0.1870   -1.4540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6192   -1.6462   -1.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5879   -2.3337   -1.6391 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8065   -2.3448   -1.2436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2319    0.4925   -0.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3947   -0.2035   -0.0154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3083    0.6033    0.8892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9304    1.9165    1.1291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0732   -0.2298    0.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1176    0.1114    1.6803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2146    1.8363   -0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1276    1.7034   -0.8537 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6697   -0.7223   -0.5346 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7470   -0.8311    0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0052   -1.9443    1.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1171   -1.9912    1.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3442   -3.1229    2.6534 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0086   -0.9460    1.9497 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7728    0.1973    1.1669 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6473    1.2467    1.2232 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6479    0.2208    0.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4316    1.8944    0.2086 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7850    2.4763   -1.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4682    0.2624   -2.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3603   -1.5761   -1.3348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0404   -1.3984   -1.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8852   -1.0699   -0.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0959    0.1296   -2.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8407   -2.9736   -0.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5059    1.5064   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0347   -0.0864   -0.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8588    0.2457    1.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2703    2.5580    0.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3008   -1.2977    0.8804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0555    1.0778    1.8079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6559    2.8092   -0.5099 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8138    2.5725   -0.8073 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3175   -2.7633    1.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8743   -3.9110    2.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8637   -1.0004    2.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5743    2.0885    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 12 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  8 22  1  0
 22 23  2  0
  4 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 32  2  1  0
 23  5  1  0
 32 25  1  0
 20 10  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  6 36  1  0
  7 37  1  0
 10 38  1  0
 12 39  1  0
 15 40  1  0
 16 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 26 49  1  0
 28 50  1  0
 29 51  1  0
 31 52  1  0
M  END

  Mrv1652308201922482D          

 32 35  0  0  0  0            999 V2000
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
  8  1  2  0  0  0  0
  8  2  1  0  0  0  0
  9  5  2  0  0  0  0
  9  6  1  0  0  0  0
 10  3  2  0  0  0  0
 10  4  1  0  0  0  0
 11  5  1  0  0  0  0
 12  7  1  0  0  0  0
 13  7  1  0  0  0  0
 13  8  1  0  0  0  0
 14  6  2  0  0  0  0
 15 11  2  0  0  0  0
 15 12  1  0  0  0  0
 15 14  1  0  0  0  0
 17 16  1  0  0  0  0
 18 16  1  0  0  0  0
 19 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 18  1  0  0  0  0
 22  9  1  0  0  0  0
 23 11  1  0  0  0  0
 24 12  2  0  0  0  0
 25 16  1  0  0  0  0
 26 17  1  0  0  0  0
 27 18  1  0  0  0  0
 28 20  2  0  0  0  0
 29 20  1  0  0  0  0
 30 10  1  0  0  0  0
 30 21  1  0  0  0  0
 31 13  1  0  0  0  0
 31 14  1  0  0  0  0
 32 19  1  0  0  0  0
 32 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0257722

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1C(O)C(OC2=CC=C(C=C2)C2CC(=O)C3=C(O)C=C(O)C=C3O2)OC(C1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O11/c22-9-5-11(23)15-12(24)7-13(31-14(15)6-9)8-1-3-10(4-2-8)30-21-18(27)16(25)17(26)19(32-21)20(28)29/h1-6,13,16-19,21-23,25-27H,7H2,(H,28,29)

> <INCHI_KEY>
DFIUUCDSSKATFP-UHFFFAOYSA-N

> <FORMULA>
C21H20O11

> <MOLECULAR_WEIGHT>
448.38

> <EXACT_MASS>
448.100561464

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
42.98748309580358

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
0.73

> <JCHEM_LOGP>
0.8873144950000008

> <ALOGPS_LOGS>
-2.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.8668018832790745

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.21362575295671

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6868267613771284

> <JCHEM_POLAR_SURFACE_AREA>
183.20999999999998

> <JCHEM_REFRACTIVITY>
103.30159999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.48e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[4-(5,7-dihydroxy-4-oxo-2,3-dihydro-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0257722
     RDKit          3D
(2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,...
 52 55  0  0  0  0  0  0  0  0999 V2000
    6.2442    2.0749   -0.9391 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3387    1.3744   -0.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071    1.6462   -0.7619 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2176    0.3804   -1.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7436    0.4830   -1.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9310   -0.6066   -1.1544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570   -0.4928   -0.9911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0673    0.7129   -0.7584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4181    0.9099   -0.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3957   -0.0942   -0.6251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2645    0.2424   -1.6288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5275   -0.1870   -1.4540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6192   -1.6462   -1.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5879   -2.3337   -1.6391 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8065   -2.3448   -1.2436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2319    0.4925   -0.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3947   -0.2035   -0.0154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3083    0.6033    0.8892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9304    1.9165    1.1291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0732   -0.2298    0.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1176    0.1114    1.6803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2146    1.8363   -0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1276    1.7034   -0.8537 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6697   -0.7223   -0.5346 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7470   -0.8311    0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0052   -1.9443    1.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1171   -1.9912    1.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3442   -3.1229    2.6534 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0086   -0.9460    1.9497 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7728    0.1973    1.1669 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6473    1.2467    1.2232 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6479    0.2208    0.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4316    1.8944    0.2086 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7850    2.4763   -1.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4682    0.2624   -2.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3603   -1.5761   -1.3348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0404   -1.3984   -1.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8852   -1.0699   -0.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0959    0.1296   -2.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8407   -2.9736   -0.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5059    1.5064   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0347   -0.0864   -0.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8588    0.2457    1.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2703    2.5580    0.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3008   -1.2977    0.8804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0555    1.0778    1.8079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6559    2.8092   -0.5099 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8138    2.5725   -0.8073 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3175   -2.7633    1.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8743   -3.9110    2.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8637   -1.0004    2.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5743    2.0885    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 12 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  8 22  1  0
 22 23  2  0
  4 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 32  2  1  0
 23  5  1  0
 32 25  1  0
 20 10  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  6 36  1  0
  7 37  1  0
 10 38  1  0
 12 39  1  0
 15 40  1  0
 16 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 26 49  1  0
 28 50  1  0
 29 51  1  0
 31 52  1  0
M  END

HEADER    PROTEIN                                 20-AUG-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-AUG-19         0                                  
HETATM    1  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.338  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.338  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.004  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.004   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      16.004   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.671  -2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      18.672  -3.080   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      18.672   0.000   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      16.004  -4.620   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      14.671   2.310   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      17.338   2.310   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      14.671  -0.770   0.000  0.00  0.00           O+0
CONECT    1    3    8                                                       
CONECT    2    4    8                                                       
CONECT    3    1   10                                                       
CONECT    4    2   10                                                       
CONECT    5    9   11                                                       
CONECT    6    9   14                                                       
CONECT    7   12   13                                                       
CONECT    8    1    2   13                                                  
CONECT    9    5    6   22                                                  
CONECT   10    3    4   30                                                  
CONECT   11    5   15   23                                                  
CONECT   12    7   15   24                                                  
CONECT   13    7    8   31                                                  
CONECT   14    6   15   31                                                  
CONECT   15   11   12   14                                                  
CONECT   16   17   18   25                                                  
CONECT   17   16   19   26                                                  
CONECT   18   16   21   27                                                  
CONECT   19   17   20   32                                                  
CONECT   20   19   28   29                                                  
CONECT   21   18   30   32                                                  
CONECT   22    9                                                            
CONECT   23   11                                                            
CONECT   24   12                                                            
CONECT   25   16                                                            
CONECT   26   17                                                            
CONECT   27   18                                                            
CONECT   28   20                                                            
CONECT   29   20                                                            
CONECT   30   10   21                                                       
CONECT   31   13   14                                                       
CONECT   32   19   21                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

COMPND    HMDB0257722
HETATM    1  O1  UNL     1       6.244   2.075  -0.939  1.00  0.00           O  
HETATM    2  C1  UNL     1       5.339   1.374  -0.487  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.907   1.646  -0.762  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.218   0.380  -1.263  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.744   0.483  -1.089  1.00  0.00           C  
HETATM    6  C5  UNL     1       0.931  -0.607  -1.154  1.00  0.00           C  
HETATM    7  C6  UNL     1      -0.457  -0.493  -0.991  1.00  0.00           C  
HETATM    8  C7  UNL     1      -1.067   0.713  -0.758  1.00  0.00           C  
HETATM    9  O2  UNL     1      -2.418   0.910  -0.588  1.00  0.00           O  
HETATM   10  C8  UNL     1      -3.396  -0.094  -0.625  1.00  0.00           C  
HETATM   11  O3  UNL     1      -4.264   0.242  -1.629  1.00  0.00           O  
HETATM   12  C9  UNL     1      -5.527  -0.187  -1.454  1.00  0.00           C  
HETATM   13  C10 UNL     1      -5.619  -1.646  -1.450  1.00  0.00           C  
HETATM   14  O4  UNL     1      -4.588  -2.334  -1.639  1.00  0.00           O  
HETATM   15  O5  UNL     1      -6.807  -2.345  -1.244  1.00  0.00           O  
HETATM   16  C11 UNL     1      -6.232   0.493  -0.298  1.00  0.00           C  
HETATM   17  O6  UNL     1      -7.395  -0.204  -0.015  1.00  0.00           O  
HETATM   18  C12 UNL     1      -5.308   0.603   0.889  1.00  0.00           C  
HETATM   19  O7  UNL     1      -4.930   1.916   1.129  1.00  0.00           O  
HETATM   20  C13 UNL     1      -4.073  -0.230   0.693  1.00  0.00           C  
HETATM   21  O8  UNL     1      -3.118   0.111   1.680  1.00  0.00           O  
HETATM   22  C14 UNL     1      -0.215   1.836  -0.693  1.00  0.00           C  
HETATM   23  C15 UNL     1       1.128   1.703  -0.854  1.00  0.00           C  
HETATM   24  O9  UNL     1       3.670  -0.722  -0.535  1.00  0.00           O  
HETATM   25  C16 UNL     1       4.747  -0.831   0.288  1.00  0.00           C  
HETATM   26  C17 UNL     1       5.005  -1.944   1.071  1.00  0.00           C  
HETATM   27  C18 UNL     1       6.117  -1.991   1.883  1.00  0.00           C  
HETATM   28  O10 UNL     1       6.344  -3.123   2.653  1.00  0.00           O  
HETATM   29  C19 UNL     1       7.009  -0.946   1.950  1.00  0.00           C  
HETATM   30  C20 UNL     1       6.773   0.197   1.167  1.00  0.00           C  
HETATM   31  O11 UNL     1       7.647   1.247   1.223  1.00  0.00           O  
HETATM   32  C21 UNL     1       5.648   0.221   0.358  1.00  0.00           C  
HETATM   33  H1  UNL     1       3.432   1.894   0.209  1.00  0.00           H  
HETATM   34  H2  UNL     1       3.785   2.476  -1.484  1.00  0.00           H  
HETATM   35  H3  UNL     1       3.468   0.262  -2.358  1.00  0.00           H  
HETATM   36  H4  UNL     1       1.360  -1.576  -1.335  1.00  0.00           H  
HETATM   37  H5  UNL     1      -1.040  -1.398  -1.055  1.00  0.00           H  
HETATM   38  H6  UNL     1      -2.885  -1.070  -0.817  1.00  0.00           H  
HETATM   39  H7  UNL     1      -6.096   0.130  -2.405  1.00  0.00           H  
HETATM   40  H8  UNL     1      -6.841  -2.974  -0.443  1.00  0.00           H  
HETATM   41  H9  UNL     1      -6.506   1.506  -0.627  1.00  0.00           H  
HETATM   42  H10 UNL     1      -8.035  -0.086  -0.745  1.00  0.00           H  
HETATM   43  H11 UNL     1      -5.859   0.246   1.776  1.00  0.00           H  
HETATM   44  H12 UNL     1      -5.270   2.558   0.474  1.00  0.00           H  
HETATM   45  H13 UNL     1      -4.301  -1.298   0.880  1.00  0.00           H  
HETATM   46  H14 UNL     1      -3.055   1.078   1.808  1.00  0.00           H  
HETATM   47  H15 UNL     1      -0.656   2.809  -0.510  1.00  0.00           H  
HETATM   48  H16 UNL     1       1.814   2.573  -0.807  1.00  0.00           H  
HETATM   49  H17 UNL     1       4.318  -2.763   1.027  1.00  0.00           H  
HETATM   50  H18 UNL     1       6.874  -3.911   2.342  1.00  0.00           H  
HETATM   51  H19 UNL     1       7.864  -1.000   2.584  1.00  0.00           H  
HETATM   52  H20 UNL     1       7.574   2.089   0.742  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   32
CONECT    3    4   33   34
CONECT    4    5   24   35
CONECT    5    6    6   23
CONECT    6    7   36
CONECT    7    8    8   37
CONECT    8    9   22
CONECT    9   10
CONECT   10   11   20   38
CONECT   11   12
CONECT   12   13   16   39
CONECT   13   14   14   15
CONECT   15   40
CONECT   16   17   18   41
CONECT   17   42
CONECT   18   19   20   43
CONECT   19   44
CONECT   20   21   45
CONECT   21   46
CONECT   22   23   23   47
CONECT   23   48
CONECT   24   25
CONECT   25   26   26   32
CONECT   26   27   49
CONECT   27   28   29   29
CONECT   28   50
CONECT   29   30   51
CONECT   30   31   32   32
CONECT   31   52
END

HMDB0257722
     RDKit          3D
(2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,...
 52 55  0  0  0  0  0  0  0  0999 V2000
    6.2442    2.0749   -0.9391 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3387    1.3744   -0.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071    1.6462   -0.7619 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2176    0.3804   -1.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7436    0.4830   -1.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9310   -0.6066   -1.1544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570   -0.4928   -0.9911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0673    0.7129   -0.7584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4181    0.9099   -0.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3957   -0.0942   -0.6251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2645    0.2424   -1.6288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5275   -0.1870   -1.4540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6192   -1.6462   -1.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5879   -2.3337   -1.6391 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8065   -2.3448   -1.2436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2319    0.4925   -0.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3947   -0.2035   -0.0154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3083    0.6033    0.8892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9304    1.9165    1.1291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0732   -0.2298    0.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1176    0.1114    1.6803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2146    1.8363   -0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1276    1.7034   -0.8537 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6697   -0.7223   -0.5346 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7470   -0.8311    0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0052   -1.9443    1.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1171   -1.9912    1.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3442   -3.1229    2.6534 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0086   -0.9460    1.9497 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7728    0.1973    1.1669 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6473    1.2467    1.2232 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6479    0.2208    0.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4316    1.8944    0.2086 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7850    2.4763   -1.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4682    0.2624   -2.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3603   -1.5761   -1.3348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0404   -1.3984   -1.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8852   -1.0699   -0.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0959    0.1296   -2.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8407   -2.9736   -0.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5059    1.5064   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0347   -0.0864   -0.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8588    0.2457    1.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2703    2.5580    0.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3008   -1.2977    0.8804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0555    1.0778    1.8079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6559    2.8092   -0.5099 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8138    2.5725   -0.8073 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3175   -2.7633    1.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8743   -3.9110    2.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8637   -1.0004    2.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5743    2.0885    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 12 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  8 22  1  0
 22 23  2  0
  4 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 32  2  1  0
 23  5  1  0
 32 25  1  0
 20 10  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  6 36  1  0
  7 37  1  0
 10 38  1  0
 12 39  1  0
 15 40  1  0
 16 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 26 49  1  0
 28 50  1  0
 29 51  1  0
 31 52  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
6-[4-(5,7-Dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₂₁H₂₀O₁₁

Average Molecular Weight

448.38

Monoisotopic Molecular Weight

448.100561464

IUPAC Name

6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-[4-(5,7-dihydroxy-4-oxo-2,3-dihydro-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC1C(O)C(OC2=CC=C(C=C2)C2CC(=O)C3=C(O)C=C(O)C=C3O2)OC(C1O)C(O)=O

InChI Identifier

InChI=1S/C21H20O11/c22-9-5-11(23)15-12(24)7-13(31-14(15)6-9)8-1-3-10(4-2-8)30-21-18(27)16(25)17(26)19(32-21)20(28)29/h1-6,13,16-19,21-23,25-27H,7H2,(H,28,29)

InChI Key

DFIUUCDSSKATFP-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid o-glucuronides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid O-glucuronides

Alternative Parents

Substituents

Flavonoid-4p-o-glucuronide
Hydroxyflavonoid
Flavanone
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavan
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Phenolic glycoside
O-glucuronide
1-o-glucuronide
Glucuronic acid or derivatives
Hexose monosaccharide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Chromone
1-benzopyran
Chromane
Benzopyran
Phenoxy compound
Aryl ketone
Aryl alkyl ketone
Phenol ether
Beta-hydroxy acid
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Pyran
Monosaccharide
Benzenoid
Hydroxy acid
Monocyclic benzene moiety
Fatty acyl
Oxane
Vinylogous acid
Secondary alcohol
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Polyol
Organoheterocyclic compound
Oxacycle
Acetal
Ether
Carbonyl group
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aldehyde
Alcohol
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0128083)

Plant

Plant (HMDB: HMDB0128083)

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	0.73	ALOGPS
logP	0.89	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	3.21	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	183.21 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	103.3 m³·mol⁻¹	ChemAxon
Polarizability	42.99 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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+H]+	201.662	30932474
DeepCCS	[M-H]-	199.266	30932474
DeepCCS	[M-2H]-	232.279	30932474
DeepCCS	[M+Na]+	207.68	30932474
AllCCS	[M+H]+	203.1	32859911
AllCCS	[M+H-H2O]+	200.8	32859911
AllCCS	[M+NH4]+	205.2	32859911
AllCCS	[M+Na]+	205.9	32859911
AllCCS	[M-H]-	199.2	32859911
AllCCS	[M+Na-2H]-	199.6	32859911
AllCCS	[M+HCOO]-	200.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	OC1C(O)C(OC2=CC=C(C=C2)C2CC(=O)C3=C(O)C=C(O)C=C3O2)OC(C1O)C(O)=O	5154.7	Standard polar	33892256
(2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	OC1C(O)C(OC2=CC=C(C=C2)C2CC(=O)C3=C(O)C=C(O)C=C3O2)OC(C1O)C(O)=O	4018.9	Standard non polar	33892256
(2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	OC1C(O)C(OC2=CC=C(C=C2)C2CC(=O)C3=C(O)C=C(O)C=C3O2)OC(C1O)C(O)=O	4304.7	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 - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (3 TMS) - 70eV, Positive	splash10-0udj-3352349000-dfa8cb9042cf75b627b5	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a59-9125200000-ef7d29c3cf1ee25dcbed	2017-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-[4-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-11-05	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 - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 10V, Positive-QTOF	splash10-00ea-0290700000-5f5ea6b829455c17d870	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 20V, Positive-QTOF	splash10-05fr-0490000000-4c70573c04a73fd85083	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 40V, Positive-QTOF	splash10-0kmi-1930000000-008fa0b3097795aaf03a	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 10V, Negative-QTOF	splash10-0fdk-1251900000-16bbf6f0839e8d3fc4c8	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 20V, Negative-QTOF	splash10-00di-2391200000-e011276b61a2b2625c86	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 40V, Negative-QTOF	splash10-00di-5590000000-4a1cbbb1494a41016d74	2017-06-28	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 10V, Negative-QTOF	splash10-0002-0000900000-e34b057bc120eef7d6a0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 20V, Negative-QTOF	splash10-0f6t-0900800000-69dacded01f8f8671ced	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 40V, Negative-QTOF	splash10-0002-0591000000-018e08e837bbf313d155	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 10V, Positive-QTOF	splash10-0002-0000900000-6cdaf2bc31caca882f1d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 20V, Positive-QTOF	splash10-0f6t-0900400000-d3bfd499635b3b0942a0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 40V, Positive-QTOF	splash10-0udi-0920000000-2a0db174772f7a158364	2021-09-22	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

FDB086939

KNApSAcK ID

Not Available

Chemspider ID

26458107

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53394091

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 (2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid (HMDB0257722)

MOL for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for HMDB0257722 ((2S,3S,4S,5R)-6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra