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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 03:36:58 UTC

Update Date

2022-03-07 02:57:09 UTC

HMDB ID

HMDB0041697

Secondary Accession Numbers

HMDB41697

Metabolite Identification

Common Name

6'-Hydroxyenterolactone

Description

6'-Hydroxyenterolactone belongs to the class of organic compounds known as dibenzylbutyrolactone lignans. These are lignan compounds containing a 3,4-dibenzyloxolan-2-one moiety. Based on a literature review very few articles have been published on 6'-Hydroxyenterolactone.

Structure

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

HMDB0041697
     RDKit          3D
6'-Hydroxyenterolactone
 41 43  0  0  0  0  0  0  0  0999 V2000
   -0.7152   -3.7955    1.8778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151   -2.9162    1.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1548   -2.9718    0.6680 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2426   -2.0175   -0.3763 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3273   -0.8929    0.0554 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0058    0.0467    1.0270 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2025    0.6906    0.4943 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4457    0.2512    0.8864 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5964    0.8360    0.4012 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8493    0.3755    0.8118 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5514    1.8763   -0.4891 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3138    2.3306   -0.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.7341   -0.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9492    2.2380   -0.8453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7329   -1.6302    0.8274 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9926   -1.9013    0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7077   -0.6884   -0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5512   -0.0795   -1.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2649    1.0818   -1.8869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1380    1.6263   -0.9708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3136    1.0284    0.2563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1901    1.5713    1.1806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5997   -0.1022    0.5178 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8285   -2.4888   -1.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2770   -1.7261   -0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1291   -0.3715   -0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2096    0.7929    1.3175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1984   -0.5397    1.9489 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5271   -0.5842    1.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9158   -0.3848    1.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4602    2.3507   -0.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2949    3.1504   -1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8792    3.0002   -1.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9913   -1.0709    1.7778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6944   -2.5423   -0.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6780   -2.5282    0.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8922   -0.4714   -2.3273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1075    1.5318   -2.8601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6954    2.5241   -1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1487    1.2444    1.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7280   -0.5781    1.4715 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  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  5 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 15  2  1  0
 23 17  1  0
 13  7  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  6
  6 27  1  0
  6 28  1  0
  8 29  1  0
 10 30  1  0
 11 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  1
 16 35  1  0
 16 36  1  0
 18 37  1  0
 19 38  1  0
 20 39  1  0
 22 40  1  0
 23 41  1  0
M  END


  Mrv0541 02271201272D          

 23 25  0  0  0  0            999 V2000
   -0.1499    2.0795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8174    1.5946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5624    0.8099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2626    0.8099    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5175    1.5946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6020    1.8495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0474    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7475    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7240    1.0686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9035    0.9824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5680    0.2287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0529   -0.4387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8734   -0.3525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2089    0.4012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0239    1.0686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5088    0.4012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1732   -0.3525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3528   -0.4387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8678    0.2287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2034    0.9824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6582   -1.0199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3583   -1.0199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4186    1.6498    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
  1  5  1  0  0  0  0
  2  6  2  0  0  0  0
  3  7  1  1  0  0  0
  4  8  1  6  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
  8 11  1  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
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 15 20  2  0  0  0  0
  7 19  1  0  0  0  0
 17 21  1  0  0  0  0
 13 22  1  0  0  0  0
 10 23  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0041697

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1=CC=CC(C[C@@H]2[C@@H](CC3=CC(O)=CC=C3O)COC2=O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H18O5/c19-14-3-1-2-11(6-14)7-16-13(10-23-18(16)22)8-12-9-15(20)4-5-17(12)21/h1-6,9,13,16,19-21H,7-8,10H2/t13-,16+/m0/s1

> <INCHI_KEY>
OUWRXHXCIKQNEC-XJKSGUPXSA-N

> <FORMULA>
C18H18O5

> <MOLECULAR_WEIGHT>
314.3325

> <EXACT_MASS>
314.115423686

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
32.4816430901947

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4R)-4-[(2,5-dihydroxyphenyl)methyl]-3-[(3-hydroxyphenyl)methyl]oxolan-2-one

> <ALOGPS_LOGP>
2.57

> <JCHEM_LOGP>
3.303559720666666

> <ALOGPS_LOGS>
-4.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.809120825103808

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.206622907665636

> <JCHEM_PKA_STRONGEST_BASIC>
-5.8940652287189765

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
84.6889

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.99e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4R)-4-[(2,5-dihydroxyphenyl)methyl]-3-[(3-hydroxyphenyl)methyl]oxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0041697
     RDKit          3D
6'-Hydroxyenterolactone
 41 43  0  0  0  0  0  0  0  0999 V2000
   -0.7152   -3.7955    1.8778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151   -2.9162    1.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1548   -2.9718    0.6680 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2426   -2.0175   -0.3763 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3273   -0.8929    0.0554 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0058    0.0467    1.0270 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2025    0.6906    0.4943 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4457    0.2512    0.8864 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5964    0.8360    0.4012 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8493    0.3755    0.8118 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5514    1.8763   -0.4891 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3138    2.3306   -0.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.7341   -0.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9492    2.2380   -0.8453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7329   -1.6302    0.8274 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9926   -1.9013    0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7077   -0.6884   -0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5512   -0.0795   -1.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2649    1.0818   -1.8869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1380    1.6263   -0.9708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3136    1.0284    0.2563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1901    1.5713    1.1806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5997   -0.1022    0.5178 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8285   -2.4888   -1.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2770   -1.7261   -0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1291   -0.3715   -0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2096    0.7929    1.3175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1984   -0.5397    1.9489 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5271   -0.5842    1.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9158   -0.3848    1.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4602    2.3507   -0.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2949    3.1504   -1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8792    3.0002   -1.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9913   -1.0709    1.7778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6944   -2.5423   -0.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6780   -2.5282    0.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8922   -0.4714   -2.3273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1075    1.5318   -2.8601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6954    2.5241   -1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1487    1.2444    1.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7280   -0.5781    1.4715 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  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  5 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 15  2  1  0
 23 17  1  0
 13  7  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  6
  6 27  1  0
  6 28  1  0
  8 29  1  0
 10 30  1  0
 11 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  1
 16 35  1  0
 16 36  1  0
 18 37  1  0
 19 38  1  0
 20 39  1  0
 22 40  1  0
 23 41  1  0
M  END

HEADER    PROTEIN                                 27-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-FEB-12         0                                  
HETATM    1  O   UNK     0      -0.280   3.882   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.526   2.977   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.050   1.512   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.490   1.512   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.966   2.977   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.990   3.452   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.955   0.266   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.395   0.266   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.085   1.995   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.553   1.834   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.927   0.427   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.832  -0.819   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.364  -0.658   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.990   0.749   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.645   1.995   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.550   0.749   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.923  -0.658   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.392  -0.819   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.487   0.427   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.113   1.834   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -6.829  -1.904   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       6.269  -1.904   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.648   3.080   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    3    6                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    1                                                       
CONECT    6    2                                                            
CONECT    7    3   19                                                       
CONECT    8    4   11                                                       
CONECT    9   10   14                                                       
CONECT   10    9   11   23                                                  
CONECT   11   10   12    8                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13    9                                                       
CONECT   15   16   20                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20    7                                                  
CONECT   20   19   15                                                       
CONECT   21   17                                                            
CONECT   22   13                                                            
CONECT   23   10                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

COMPND    HMDB0041697
HETATM    1  O1  UNL     1      -0.715  -3.796   1.878  1.00  0.00           O  
HETATM    2  C1  UNL     1      -0.115  -2.916   1.189  1.00  0.00           C  
HETATM    3  O2  UNL     1       1.155  -2.972   0.668  1.00  0.00           O  
HETATM    4  C2  UNL     1       1.243  -2.018  -0.376  1.00  0.00           C  
HETATM    5  C3  UNL     1       0.327  -0.893   0.055  1.00  0.00           C  
HETATM    6  C4  UNL     1       1.006   0.047   1.027  1.00  0.00           C  
HETATM    7  C5  UNL     1       2.202   0.691   0.494  1.00  0.00           C  
HETATM    8  C6  UNL     1       3.446   0.251   0.886  1.00  0.00           C  
HETATM    9  C7  UNL     1       4.596   0.836   0.401  1.00  0.00           C  
HETATM   10  O3  UNL     1       5.849   0.375   0.812  1.00  0.00           O  
HETATM   11  C8  UNL     1       4.551   1.876  -0.489  1.00  0.00           C  
HETATM   12  C9  UNL     1       3.314   2.331  -0.894  1.00  0.00           C  
HETATM   13  C10 UNL     1       2.156   1.734  -0.399  1.00  0.00           C  
HETATM   14  O4  UNL     1       0.949   2.238  -0.845  1.00  0.00           O  
HETATM   15  C11 UNL     1      -0.733  -1.630   0.827  1.00  0.00           C  
HETATM   16  C12 UNL     1      -1.993  -1.901   0.047  1.00  0.00           C  
HETATM   17  C13 UNL     1      -2.708  -0.688  -0.373  1.00  0.00           C  
HETATM   18  C14 UNL     1      -2.551  -0.079  -1.580  1.00  0.00           C  
HETATM   19  C15 UNL     1      -3.265   1.082  -1.887  1.00  0.00           C  
HETATM   20  C16 UNL     1      -4.138   1.626  -0.971  1.00  0.00           C  
HETATM   21  C17 UNL     1      -4.314   1.028   0.256  1.00  0.00           C  
HETATM   22  O5  UNL     1      -5.190   1.571   1.181  1.00  0.00           O  
HETATM   23  C18 UNL     1      -3.600  -0.102   0.518  1.00  0.00           C  
HETATM   24  H1  UNL     1       0.829  -2.489  -1.291  1.00  0.00           H  
HETATM   25  H2  UNL     1       2.277  -1.726  -0.527  1.00  0.00           H  
HETATM   26  H3  UNL     1      -0.129  -0.372  -0.792  1.00  0.00           H  
HETATM   27  H4  UNL     1       0.210   0.793   1.317  1.00  0.00           H  
HETATM   28  H5  UNL     1       1.198  -0.540   1.949  1.00  0.00           H  
HETATM   29  H6  UNL     1       3.527  -0.584   1.600  1.00  0.00           H  
HETATM   30  H7  UNL     1       5.916  -0.385   1.463  1.00  0.00           H  
HETATM   31  H8  UNL     1       5.460   2.351  -0.884  1.00  0.00           H  
HETATM   32  H9  UNL     1       3.295   3.150  -1.596  1.00  0.00           H  
HETATM   33  H10 UNL     1       0.879   3.000  -1.499  1.00  0.00           H  
HETATM   34  H11 UNL     1      -0.991  -1.071   1.778  1.00  0.00           H  
HETATM   35  H12 UNL     1      -1.694  -2.542  -0.821  1.00  0.00           H  
HETATM   36  H13 UNL     1      -2.678  -2.528   0.649  1.00  0.00           H  
HETATM   37  H14 UNL     1      -1.892  -0.471  -2.327  1.00  0.00           H  
HETATM   38  H15 UNL     1      -3.108   1.532  -2.860  1.00  0.00           H  
HETATM   39  H16 UNL     1      -4.695   2.524  -1.197  1.00  0.00           H  
HETATM   40  H17 UNL     1      -6.149   1.244   1.140  1.00  0.00           H  
HETATM   41  H18 UNL     1      -3.728  -0.578   1.471  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   15
CONECT    3    4
CONECT    4    5   24   25
CONECT    5    6   15   26
CONECT    6    7   27   28
CONECT    7    8    8   13
CONECT    8    9   29
CONECT    9   10   11   11
CONECT   10   30
CONECT   11   12   31
CONECT   12   13   13   32
CONECT   13   14
CONECT   14   33
CONECT   15   16   34
CONECT   16   17   35   36
CONECT   17   18   18   23
CONECT   18   19   37
CONECT   19   20   20   38
CONECT   20   21   39
CONECT   21   22   23   23
CONECT   22   40
CONECT   23   41
END

HMDB0041697
     RDKit          3D
6'-Hydroxyenterolactone
 41 43  0  0  0  0  0  0  0  0999 V2000
   -0.7152   -3.7955    1.8778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151   -2.9162    1.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1548   -2.9718    0.6680 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2426   -2.0175   -0.3763 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3273   -0.8929    0.0554 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0058    0.0467    1.0270 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2025    0.6906    0.4943 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4457    0.2512    0.8864 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5964    0.8360    0.4012 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8493    0.3755    0.8118 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5514    1.8763   -0.4891 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3138    2.3306   -0.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.7341   -0.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9492    2.2380   -0.8453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7329   -1.6302    0.8274 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9926   -1.9013    0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7077   -0.6884   -0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5512   -0.0795   -1.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2649    1.0818   -1.8869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1380    1.6263   -0.9708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3136    1.0284    0.2563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1901    1.5713    1.1806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5997   -0.1022    0.5178 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8285   -2.4888   -1.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2770   -1.7261   -0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1291   -0.3715   -0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2096    0.7929    1.3175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1984   -0.5397    1.9489 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5271   -0.5842    1.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9158   -0.3848    1.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4602    2.3507   -0.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2949    3.1504   -1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8792    3.0002   -1.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9913   -1.0709    1.7778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6944   -2.5423   -0.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6780   -2.5282    0.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8922   -0.4714   -2.3273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1075    1.5318   -2.8601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6954    2.5241   -1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1487    1.2444    1.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7280   -0.5781    1.4715 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  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  5 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 15  2  1  0
 23 17  1  0
 13  7  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  6
  6 27  1  0
  6 28  1  0
  8 29  1  0
 10 30  1  0
 11 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  1
 16 35  1  0
 16 36  1  0
 18 37  1  0
 19 38  1  0
 20 39  1  0
 22 40  1  0
 23 41  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₈H₁₈O₅

Average Molecular Weight

314.3325

Monoisotopic Molecular Weight

314.115423686

IUPAC Name

(3R,4R)-4-[(2,5-dihydroxyphenyl)methyl]-3-[(3-hydroxyphenyl)methyl]oxolan-2-one

Traditional Name

(3R,4R)-4-[(2,5-dihydroxyphenyl)methyl]-3-[(3-hydroxyphenyl)methyl]oxolan-2-one

CAS Registry Number

Not Available

SMILES

OC1=CC=CC(C[C@@H]2[C@@H](CC3=CC(O)=CC=C3O)COC2=O)=C1

InChI Identifier

InChI=1S/C18H18O5/c19-14-3-1-2-11(6-14)7-16-13(10-23-18(16)22)8-12-9-15(20)4-5-17(12)21/h1-6,9,13,16,19-21H,7-8,10H2/t13-,16+/m0/s1

InChI Key

OUWRXHXCIKQNEC-XJKSGUPXSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzylbutyrolactone lignans. These are lignan compounds containing a 3,4-dibenzyloxolan-2-one moiety.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Furanoid lignans

Sub Class

Tetrahydrofuran lignans

Direct Parent

Dibenzylbutyrolactone lignans

Alternative Parents

Substituents

Dibenzylbutyrolactone
Lignan lactone
Hydroquinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Gamma butyrolactone
Benzenoid
Tetrahydrofuran
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0041697)

Cellular substructure

Membrane (HMDB: HMDB0041697)

Source

Exogenous

Food

Food (HMDB: HMDB0041697)

Not Available

Nutrient (HMDB: HMDB0041697)

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	0.03 g/L	ALOGPS
logP	2.57	ALOGPS
logP	3.3	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	9.21	ChemAxon
pKa (Strongest Basic)	-5.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	84.69 m³·mol⁻¹	ChemAxon
Polarizability	32.48 Å³	ChemAxon
Number of Rings	3	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
DarkChem	[M+H]+	174.468	31661259
DarkChem	[M-H]-	172.306	31661259
DeepCCS	[M+H]+	187.558	30932474
DeepCCS	[M-H]-	185.2	30932474
DeepCCS	[M-2H]-	218.641	30932474
DeepCCS	[M+Na]+	193.869	30932474
AllCCS	[M+H]+	175.1	32859911
AllCCS	[M+H-H2O]+	171.6	32859911
AllCCS	[M+NH4]+	178.4	32859911
AllCCS	[M+Na]+	179.3	32859911
AllCCS	[M-H]-	177.1	32859911
AllCCS	[M+Na-2H]-	176.7	32859911
AllCCS	[M+HCOO]-	176.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6'-Hydroxyenterolactone	OC1=CC=CC(C[C@@H]2[C@@H](CC3=CC(O)=CC=C3O)COC2=O)=C1	4714.6	Standard polar	33892256
6'-Hydroxyenterolactone	OC1=CC=CC(C[C@@H]2[C@@H](CC3=CC(O)=CC=C3O)COC2=O)=C1	3182.4	Standard non polar	33892256
6'-Hydroxyenterolactone	OC1=CC=CC(C[C@@H]2[C@@H](CC3=CC(O)=CC=C3O)COC2=O)=C1	3287.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6'-Hydroxyenterolactone,1TMS,isomer #1	C[Si](C)(C)OC1=CC=CC(C[C@H]2C(=O)OC[C@@H]2CC2=CC(O)=CC=C2O)=C1	3000.2	Semi standard non polar	33892256
6'-Hydroxyenterolactone,1TMS,isomer #2	C[Si](C)(C)OC1=CC=C(O)C(C[C@H]2COC(=O)[C@@H]2CC2=CC=CC(O)=C2)=C1	2998.7	Semi standard non polar	33892256
6'-Hydroxyenterolactone,1TMS,isomer #3	C[Si](C)(C)OC1=CC=C(O)C=C1C[C@H]1COC(=O)[C@@H]1CC1=CC=CC(O)=C1	2990.0	Semi standard non polar	33892256
6'-Hydroxyenterolactone,2TMS,isomer #1	C[Si](C)(C)OC1=CC=CC(C[C@H]2C(=O)OC[C@@H]2CC2=CC(O[Si](C)(C)C)=CC=C2O)=C1	3012.0	Semi standard non polar	33892256
6'-Hydroxyenterolactone,2TMS,isomer #2	C[Si](C)(C)OC1=CC=CC(C[C@H]2C(=O)OC[C@@H]2CC2=CC(O)=CC=C2O[Si](C)(C)C)=C1	2979.3	Semi standard non polar	33892256
6'-Hydroxyenterolactone,2TMS,isomer #3	C[Si](C)(C)OC1=CC=C(O[Si](C)(C)C)C(C[C@H]2COC(=O)[C@@H]2CC2=CC=CC(O)=C2)=C1	2960.7	Semi standard non polar	33892256
6'-Hydroxyenterolactone,3TMS,isomer #1	C[Si](C)(C)OC1=CC=CC(C[C@H]2C(=O)OC[C@@H]2CC2=CC(O[Si](C)(C)C)=CC=C2O[Si](C)(C)C)=C1	3042.0	Semi standard non polar	33892256
6'-Hydroxyenterolactone,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=CC(C[C@H]2C(=O)OC[C@@H]2CC2=CC(O)=CC=C2O)=C1	3282.9	Semi standard non polar	33892256
6'-Hydroxyenterolactone,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(O)C(C[C@H]2COC(=O)[C@@H]2CC2=CC=CC(O)=C2)=C1	3277.0	Semi standard non polar	33892256
6'-Hydroxyenterolactone,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC=C(O)C=C1C[C@H]1COC(=O)[C@@H]1CC1=CC=CC(O)=C1	3280.1	Semi standard non polar	33892256
6'-Hydroxyenterolactone,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=CC(C[C@H]2C(=O)OC[C@@H]2CC2=CC(O[Si](C)(C)C(C)(C)C)=CC=C2O)=C1	3495.1	Semi standard non polar	33892256
6'-Hydroxyenterolactone,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=CC(C[C@H]2C(=O)OC[C@@H]2CC2=CC(O)=CC=C2O[Si](C)(C)C(C)(C)C)=C1	3494.1	Semi standard non polar	33892256
6'-Hydroxyenterolactone,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC=C(O[Si](C)(C)C(C)(C)C)C(C[C@H]2COC(=O)[C@@H]2CC2=CC=CC(O)=C2)=C1	3461.7	Semi standard non polar	33892256
6'-Hydroxyenterolactone,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=CC(C[C@H]2C(=O)OC[C@@H]2CC2=CC(O[Si](C)(C)C(C)(C)C)=CC=C2O[Si](C)(C)C(C)(C)C)=C1	3765.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 6'-Hydroxyenterolactone GC-MS (Non-derivatized) - 70eV, Positive	splash10-00di-1910000000-6748c1a0586cc4726fe3	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6'-Hydroxyenterolactone GC-MS (3 TMS) - 70eV, Positive	splash10-00xr-2440940000-84671d54153bf880bccb	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6'-Hydroxyenterolactone GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 10V, Positive-QTOF	splash10-014i-0489000000-41431926a2776672cd9a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 20V, Positive-QTOF	splash10-0aos-0981000000-4fb11df61f9f3b0b65f4	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 40V, Positive-QTOF	splash10-0aov-4910000000-6ab53020317e2f08b614	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 10V, Negative-QTOF	splash10-03di-0019000000-7277f2c4cbe9d5e99359	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 20V, Negative-QTOF	splash10-07vi-0394000000-2c4f08091c4746019e20	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 40V, Negative-QTOF	splash10-05mk-0930000000-c2d6f724dea89de1821a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 10V, Negative-QTOF	splash10-03di-0009000000-17c33a15798bfddeb855	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 20V, Negative-QTOF	splash10-03di-0967000000-182eb81b7f3f2be006b2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 40V, Negative-QTOF	splash10-0006-9450000000-13eac8f05741bd79ad1f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 10V, Positive-QTOF	splash10-066r-0369000000-9a3f354a4726527690dc	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 20V, Positive-QTOF	splash10-0a4i-6920000000-aac48cdb5f328090f045	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6'-Hydroxyenterolactone 40V, Positive-QTOF	splash10-0a4i-5930000000-737d19551554f67ec02c	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

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

FDB029862

KNApSAcK ID

Not Available

Chemspider ID

30777600

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131753184

PDB ID

Not Available

ChEBI ID

175038

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

Neveu V, Perez-Jimenez J, Vos F, Crespy V, du Chaffaut L, Mennen L, Knox C, Eisner R, Cruz J, Wishart D, Scalbert A: Phenol-Explorer: an online comprehensive database on polyphenol contents in foods. Database (Oxford). 2010;2010:bap024. doi: 10.1093/database/bap024. Epub 2010 Jan 8. [PubMed:20428313 ]

Showing metabocard for 6'-Hydroxyenterolactone (HMDB0041697)

MOL for HMDB0041697 (6'-Hydroxyenterolactone)

3D MOL for HMDB0041697 (6'-Hydroxyenterolactone)

3D SDF for HMDB0041697 (6'-Hydroxyenterolactone)

3D-SDF for HMDB0041697 (6'-Hydroxyenterolactone)

PDB for HMDB0041697 (6'-Hydroxyenterolactone)

3D PDB for HMDB0041697 (6'-Hydroxyenterolactone)

SMILES for HMDB0041697 (6'-Hydroxyenterolactone)

INCHI for HMDB0041697 (6'-Hydroxyenterolactone)

Structure for HMDB0041697 (6'-Hydroxyenterolactone)

3D Structure for HMDB0041697 (6'-Hydroxyenterolactone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra