NP-MRD: Showing NP-Card for 3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one (NP0290930)

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Record Information

Version

1.0

Created at

2022-09-09 21:50:06 UTC

Updated at

2022-09-09 21:50:06 UTC

NP-MRD ID

NP0290930

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one

Description

3-{4-[(3-{[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. 3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one is found in Glycyrrhiza aspera. 3-{4-[(3-{[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241506362D          

 50 54  0  0  0  0            999 V2000
    8.0194  -11.9945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5345  -11.3271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8701  -10.5734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3851   -9.9060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7207   -9.1523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2358   -8.4848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5713   -7.7312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0864   -7.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4220   -6.3101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2425   -6.2238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5780   -5.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3985   -5.3839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0931   -4.8027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2726   -4.8889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7877   -4.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9672   -4.3077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4823   -3.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8178   -2.8866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -2.2192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5124   -2.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1769   -3.0591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3564   -3.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0208   -3.8990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0510   -2.5641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2070   -1.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7221   -1.0568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7982    0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.8767   -8.3124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0261   -9.7335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8466   -9.6472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6905  -10.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1755  -11.1546    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
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 11  1  4  0  0  0
 13 14  2  0  0  0  0
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 18 19  1  0  0  0  0
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 22 23  1  0  0  0  0
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 25 27  1  0  0  0  0
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 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
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 36 37  1  0  0  0  0
 34 38  1  0  0  0  0
 31 38  1  0  0  0  0
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 18 40  1  0  0  0  0
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 15 41  1  0  0  0  0
 10 42  1  0  0  0  0
 42 43  1  0  0  0  0
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  7 44  1  0  0  0  0
  5 45  1  0  0  0  0
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 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
  3 49  1  0  0  0  0
 49 50  1  0  0  0  0
M  END

     RDKit          3D

 90 94  0  0  0  0  0  0  0  0999 V2000
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    2.8134    0.4299    0.5610 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.1960   -1.4747   -1.8087 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.7866   -0.8025   -2.8728 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2943   -0.5439   -1.0637 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9957    0.5628   -0.6175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3804    1.7627   -0.9460 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8799    2.3734    0.2352 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9859    2.9610    0.8298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9986    3.2560   -0.2293 C   0  0  2  0  0  0  0  0  0  0  0  0
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   10.8833    0.4955    1.5746 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.9417   -0.2054    2.3862 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8993    0.6828    2.8779 O   0  0  0  0  0  0  0  0  0  0  0  0
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   11.4402    0.7936   -0.8834 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.7062    0.3341   -1.2953 O   0  0  0  0  0  0  0  0  0  0  0  0
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 16 61  1  0
 17 62  1  6
 18 63  1  0
 19 64  1  6
 21 65  1  6
 23 66  1  0
 23 67  1  0
 25 68  1  0
 26 69  1  0
 26 70  1  0
 27 71  1  0
 28 72  1  6
 29 73  1  0
 30 74  1  0
 31 75  1  0
 50 90  1  0
 48 89  1  0
 46 87  1  1
 47 88  1  0
 44 85  1  6
 45 86  1  0
 42 83  1  1
 43 84  1  0
M  END


  Mrv1533004241506362D          

 50 54  0  0  0  0            999 V2000
    8.0194  -11.9945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5345  -11.3271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8701  -10.5734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3851   -9.9060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7207   -9.1523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2358   -8.4848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5713   -7.7312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0864   -7.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4220   -6.3101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2425   -6.2238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5780   -5.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3985   -5.3839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0931   -4.8027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2726   -4.8889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7877   -4.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9672   -4.3077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4823   -3.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8178   -2.8866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -2.2192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5124   -2.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1769   -3.0591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3564   -3.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0208   -3.8990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2004   -3.9852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8715   -2.4779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0510   -2.5641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2070   -1.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7221   -1.0568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0275   -1.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3631   -0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781   -0.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0531   -0.2169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982    0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9136    1.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0177    1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7627    2.4504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331    0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9177    0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6383   -2.8004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1232   -3.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7274   -6.8913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5479   -6.8050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3918   -7.6449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5412   -9.0660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8767   -8.3124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0261   -9.7335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8466   -9.6472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6905  -10.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1755  -11.1546    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
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 11  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 34 38  1  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 18 40  1  0  0  0  0
 40 41  2  0  0  0  0
 15 41  1  0  0  0  0
 10 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
  7 44  1  0  0  0  0
  5 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
  3 49  1  0  0  0  0
 49 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0290930

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC1OC(OC2=CC=C(C(=O)C=CC3=CC=C(OC4OC(CO)C(O)C(O)C4OC4OCC(O)(CO)C4O)C=C3)C(O)=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H40O18/c33-10-20-22(38)24(40)26(42)29(48-20)47-16-6-7-17(19(37)9-16)18(36)8-3-14-1-4-15(5-2-14)46-30-27(25(41)23(39)21(11-34)49-30)50-31-28(43)32(44,12-35)13-45-31/h1-9,20-31,33-35,37-44H,10-13H2

> <INCHI_KEY>
FYJCXNYYSACEJK-UHFFFAOYSA-N

> <FORMULA>
C32H40O18

> <MOLECULAR_WEIGHT>
712.654

> <EXACT_MASS>
712.221464448

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
70.86623542258317

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one

> <ALOGPS_LOGP>
-0.76

> <JCHEM_LOGP>
-2.1830059026666664

> <ALOGPS_LOGS>
-2.64

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.662156951205805

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.052588580167467

> <JCHEM_PKA_STRONGEST_BASIC>
-3.648395345694367

> <JCHEM_POLAR_SURFACE_AREA>
294.97999999999996

> <JCHEM_REFRACTIVITY>
163.77870000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.65e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  O   UNK     0      14.970 -22.390   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      14.064 -21.144   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.691 -19.737   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      13.786 -18.491   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      14.412 -17.084   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      13.507 -15.838   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      14.133 -14.432   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.228 -13.186   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.854 -11.779   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.386 -11.618   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.012 -10.211   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      17.544 -10.050   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      15.107  -8.965   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.576  -9.126   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.670  -7.880   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.139  -8.041   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.234  -6.795   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.860  -5.388   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.955  -4.142   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.423  -4.303   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.797  -5.710   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.265  -5.871   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.639  -7.278   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.107  -7.439   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.360  -4.625   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.829  -4.786   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.986  -3.219   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.081  -1.973   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.518  -3.058   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.144  -1.651   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.239  -0.405   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.699  -0.405   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.223   1.060   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.469   1.965   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.439   3.109   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       7.500   3.109   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       7.024   4.574   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       7.715   1.060   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.180   1.536   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      12.392  -5.227   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      13.297  -6.473   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      16.291 -12.864   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      17.823 -12.703   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      15.665 -14.271   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      15.944 -16.923   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      16.570 -15.516   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      16.849 -18.169   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      18.380 -18.008   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      16.222 -19.576   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      17.128 -20.822   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   49                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   45                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   44                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   42                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   41                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   40                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   20   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   38                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36   38                                             
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36                                                            
CONECT   38   34   31   39                                                  
CONECT   39   38                                                            
CONECT   40   18   41                                                       
CONECT   41   40   15                                                       
CONECT   42   10   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42    7                                                       
CONECT   45    5   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47    3   50                                                  
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  108    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₀O₁₈

Average Mass

712.6540 Da

Monoisotopic Mass

712.22146 Da

IUPAC Name

3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one

Traditional Name

3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one

CAS Registry Number

Not Available

SMILES

OCC1OC(OC2=CC=C(C(=O)C=CC3=CC=C(OC4OC(CO)C(O)C(O)C4OC4OCC(O)(CO)C4O)C=C3)C(O)=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C32H40O18/c33-10-20-22(38)24(40)26(42)29(48-20)47-16-6-7-17(19(37)9-16)18(36)8-3-14-1-4-15(5-2-14)46-30-27(25(41)23(39)21(11-34)49-30)50-31-28(43)32(44,12-35)13-45-31/h1-9,20-31,33-35,37-44H,10-13H2

InChI Key

FYJCXNYYSACEJK-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Glycyrrhiza aspera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid O-glycosides

Alternative Parents

Substituents

Flavonoid o-glycoside
2'-hydroxychalcone
Linear 1,3-diarylpropanoid
Cinnamylphenol
Fatty acyl glycoside of mono- or disaccharide
Fatty acyl glycoside
Phenolic glycoside
Cinnamic acid or derivatives
Alkyl glycoside
Disaccharide
O-glycosyl compound
Glycosyl compound
Aryl ketone
Benzoyl
Styrene
Phenoxy compound
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
1-hydroxy-4-unsubstituted benzenoid
Oxane
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Acryloyl-group
Enone
Vinylogous acid
Alpha,beta-unsaturated ketone
Tertiary alcohol
Oxolane
Secondary alcohol
Ketone
Acetal
Organoheterocyclic compound
Oxacycle
Polyol
Organic oxygen compound
Aldehyde
Alcohol
Hydrocarbon derivative
Organic oxide
Primary alcohol
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	-0.76	ALOGPS
logP	-2.2	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	7.05	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	294.98 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	163.78 m³·mol⁻¹	ChemAxon
Polarizability	70.87 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one (NP0290930)

MOL for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

3D MOL for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

3D SDF for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

3D-SDF for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

PDB for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

3D PDB for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

SMILES for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

INCHI for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

Structure for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)

3D Structure for NP0290930 (3-{4-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy]phenyl}-1-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-en-1-one)