NP-MRD: Showing NP-Card for 4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid (NP0060057)

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Record Information

Version

2.0

Created at

2022-04-28 05:10:37 UTC

Updated at

2022-04-28 05:10:37 UTC

NP-MRD ID

NP0060057

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid

Description

Isoetin 4'-glucuronide 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. Thus, isoetin 4'-glucuronide is considered to be a flavonoid. 4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid is found in Adonis aleppica. Based on a literature review very few articles have been published on Isoetin 4'-glucuronide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282207102D          

 34 37  0  0  1  0            999 V2000
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 O   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
   -5.7158    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -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
    2.1434   -0.4125    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
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 13 15  1  1  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 12 18  1  6  0  0  0
 11 19  1  1  0  0  0
 10 20  1  6  0  0  0
  3 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 22 28  2  0  0  0  0
 25 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 24 32  2  0  0  0  0
 31 33  1  0  0  0  0
 29 34  1  0  0  0  0
M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    6.5164   -1.9039    1.1842 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4639   -1.5731    0.5995 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2769   -2.1514    0.9836 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5057   -0.5859   -0.4757 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3154   -0.2519   -1.0508 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4273    0.4687   -0.2483 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5059   -0.3731    0.2573 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1428   -0.4392    0.2342 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5217   -1.5129    0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8461   -1.6404    0.9230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3864   -2.7424    1.6173 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6670   -0.7387    0.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1096   -0.8045    0.2665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8257   -1.7759    0.8665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2225   -1.7659    0.7922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8928   -2.6822    1.3584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8254   -0.7549    0.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2040   -0.7228    0.0145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9259   -1.7418    0.6453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8163    0.2810   -0.6711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0321    1.2453   -1.2632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7162    2.2552   -1.9562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6635    1.2207   -1.1807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0420    0.1971   -0.4817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7594    0.1335   -0.3780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0653    0.3258   -0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3030    0.4552   -0.3915 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8757    1.5493   -1.0791 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2602    1.1847    0.8406 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5161    2.2539    1.3378 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4427    1.7777    0.1041 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0296    2.8263    0.7853 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3890    0.6201   -0.1310 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3363    0.8881   -1.0848 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9905   -3.0891    0.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0992   -1.0909   -1.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0294    1.3439   -0.8398 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1611   -2.2361    1.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7766   -3.3832    2.0661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4017   -2.6065    1.4297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9224   -1.7497    0.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9003    0.2773   -0.7213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1554    2.9727   -2.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0658    1.9862   -1.6519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6470    1.0897   -0.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3073    2.2212   -1.5461 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5529    0.4895    1.6319 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0762    3.0474    1.5332 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0903    2.0940   -0.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6552    3.6680    0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8443    0.3915    0.8709 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2346    1.0528   -0.6558 H   0  0  0  0  0  0  0  0  0  0  0  0
 32 31  1  0
 31 29  1  0
 29 30  1  0
 29  6  1  0
  6  7  1  0
  7  8  1  0
  8 27  2  0
 27 28  1  0
 27 26  1  0
 26 12  2  0
 12 10  1  0
 10 11  1  0
 10  9  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
  6  5  1  0
  5  4  1  0
  4 33  1  0
 33 34  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
 33 31  1  0
  9  8  1  0
 25 13  1  0
 24 17  1  0
 32 50  1  0
 31 49  1  6
 29 47  1  1
 30 48  1  0
  6 37  1  6
 28 46  1  0
 26 45  1  0
 11 39  1  0
  9 38  1  0
 14 40  1  0
 19 41  1  0
 20 42  1  0
 22 43  1  0
 23 44  1  0
  4 36  1  6
 33 51  1  1
 34 52  1  0
  3 35  1  0
M  END


  Mrv1652304282207102D          

 34 37  0  0  1  0            999 V2000
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 O   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
   -5.7158    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -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
    2.1434   -0.4125    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
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 13 15  1  1  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 12 18  1  6  0  0  0
 11 19  1  1  0  0  0
 10 20  1  6  0  0  0
  3 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 22 28  2  0  0  0  0
 25 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 24 32  2  0  0  0  0
 31 33  1  0  0  0  0
 29 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0060057

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1[C@@H](O)[C@H](OC2=C(O)C=C(C(O)=C2)C2=CC(=O)C3=C(O)C=C(O)C=C3O2)O[C@@H]([C@H]1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H18O13/c22-6-1-10(25)15-11(26)5-12(32-14(15)2-6)7-3-9(24)13(4-8(7)23)33-21-18(29)16(27)17(28)19(34-21)20(30)31/h1-5,16-19,21-25,27-29H,(H,30,31)/t16-,17-,18+,19-,21+/m0/s1

> <INCHI_KEY>
RWFFSMNHMCPJTQ-ZFORQUDYSA-N

> <FORMULA>
C21H18O13

> <MOLECULAR_WEIGHT>
478.362

> <EXACT_MASS>
478.07474064

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
44.10368775507772

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-2,5-dihydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
1.31

> <JCHEM_LOGP>
0.15176493499999974

> <ALOGPS_LOGS>
-2.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.5732281928951055

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8310830459062992

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7319986700221444

> <JCHEM_POLAR_SURFACE_AREA>
223.66999999999996

> <JCHEM_REFRACTIVITY>
108.88749999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.69e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)-2,5-dihydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -6.668  -2.310   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0     -10.669   0.000   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -8.002   0.000   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0     -12.003  -2.310   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0     -12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   22                                                  
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11   20                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    9                                                       
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   12                                                            
CONECT   19   11                                                            
CONECT   20   10                                                            
CONECT   21    3                                                            
CONECT   22    2   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   32                                                  
CONECT   25   24   26   29                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   22                                                       
CONECT   29   25   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31   24                                                       
CONECT   33   31                                                            
CONECT   34   29                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₈O₁₃

Average Mass

478.3620 Da

Monoisotopic Mass

478.07474 Da

IUPAC Name

(2S,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-2,5-dihydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

(2S,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)-2,5-dihydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

O[C@@H]1[C@@H](O)[C@H](OC2=C(O)C=C(C(O)=C2)C2=CC(=O)C3=C(O)C=C(O)C=C3O2)O[C@@H]([C@H]1O)C(O)=O

InChI Identifier

InChI=1S/C21H18O13/c22-6-1-10(25)15-11(26)5-12(32-14(15)2-6)7-3-9(24)13(4-8(7)23)33-21-18(29)16(27)17(28)19(34-21)20(30)31/h1-5,16-19,21-25,27-29H,(H,30,31)/t16-,17-,18+,19-,21+/m0/s1

InChI Key

RWFFSMNHMCPJTQ-ZFORQUDYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Adonis aleppica	Plant	KNApSAcK

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
3'-hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavone
Phenolic glycoside
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Alkyl glycoside
Hexose monosaccharide
O-glycosyl compound
Glycosyl compound
Chromone
Benzopyran
1-benzopyran
Phenol ether
Hydroquinone
Phenoxy compound
Beta-hydroxy acid
Phenol
1-hydroxy-2-unsubstituted benzenoid
Pyranone
1-hydroxy-4-unsubstituted benzenoid
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Pyran
Oxane
Monosaccharide
Hydroxy acid
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Monocarboxylic acid or derivatives
Polyol
Acetal
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Organoheterocyclic compound
Organic oxygen compound
Organooxygen compound
Organic oxide
Carbonyl group
Alcohol
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	1.31	ALOGPS
logP	0.15	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	2.83	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	223.67 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	108.89 m³·mol⁻¹	ChemAxon
Polarizability	44.1 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00013711

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

101921624

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid (NP0060057)

MOL for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

3D MOL for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

3D SDF for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

3D-SDF for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

PDB for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

3D PDB for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

SMILES for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

INCHI for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

Structure for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)

3D Structure for NP0060057 (4-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2,5-dihydroxyphenyl beta-D-glucopyranosiduronic acid)