NP-MRD: Showing NP-Card for 6-O-Galloylsucrose (NP0086324)

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Record Information

Version

2.0

Created at

2022-04-29 06:38:21 UTC

Updated at

2022-04-29 06:38:21 UTC

NP-MRD ID

NP0086324

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-O-Galloylsucrose

Description

2-O-(6-O-Galloyl-alpha-D-glucopyranosyl)-beta-D-fructofuranose belongs to the class of organic compounds known as galloyl esters. These are organic compounds that contain an ester derivative of 3,4,5-trihydroxybenzoic acid. 6-O-Galloylsucrose is found in Rheum spp. Based on a literature review very few articles have been published on 2-O-(6-O-Galloyl-alpha-D-glucopyranosyl)-beta-D-fructofuranose.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292208382D          

 34 36  0  0  1  0            999 V2000
   -0.0759    7.9497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4762    7.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2831    7.5081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5381    8.2927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8352    6.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6421    7.0665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5802    6.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7732    5.9389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    5.1542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2887    4.9827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5436    4.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3506    4.0266    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6055    3.2419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4125    3.0704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6674    2.2858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1154    1.6727    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4480    1.1878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5634    2.2858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7564    2.1143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7828    1.1878    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5675    1.4427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5279    0.4032    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0128   -0.2643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7029    0.4032    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2180   -0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5535   -1.0180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9645    3.6835    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7715    3.5120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7096    4.4681    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2616    5.0812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9026    4.6397    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6477    5.4243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0703    4.5411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2212    6.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 16 18  1  1  0  0  0
 18 19  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  6  0  0  0
  9 33  2  0  0  0  0
  8 34  2  0  0  0  0
  2 34  1  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
    4.1581   -1.6268   -2.1661 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1499   -0.9241   -1.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9521   -0.6313   -0.4925 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7486   -1.1357   -1.0405 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5471   -0.7146   -0.2175 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5648   -1.2413   -0.8128 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7522   -1.0267   -0.1303 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1622    0.2753   -0.1105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3817    0.5068   -0.7317 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3272    0.2168   -2.2150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3312    0.9873   -2.8350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6732    1.8842   -0.6311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9978    2.0207   -0.9713 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6240    3.2242   -0.2523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5337    3.0481    1.1482 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7195    0.7705   -0.5580 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3383    0.1241   -1.6111 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5594   -0.1011   -0.0590 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5011    0.0849    1.2944 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6089   -1.6437    1.2409 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6690   -0.7167    2.2647 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2596   -2.3563    1.3857 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0671   -3.2788    0.3807 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7902   -1.2611    1.1898 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4922   -0.2299    2.0957 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4144   -0.4080   -0.5686 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6139   -0.6864   -1.1792 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7766   -0.1930   -0.6400 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9712   -0.4866   -1.2724 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7449    0.5691    0.4949 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9614    1.0377    0.9886 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5462    0.8459    1.1031 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5399    1.6137    2.2420 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3884    0.3608    0.5751 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5884   -0.7418   -2.0682 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7539   -2.2477   -1.1031 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5521    0.3972   -0.1827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5277   -1.6282   -0.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0766   -0.8378   -2.4507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2970    0.4134   -2.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7707    1.8041   -3.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1759    2.1731   -2.0449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1697    4.1648   -0.5727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7106    3.2794   -0.4642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6192    3.1555    1.4718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4514    0.9183    0.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6477    0.7209   -2.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7750   -1.1410   -0.3667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9535   -0.6013    1.8342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3735   -2.4221    1.4458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8426    0.1968    1.9920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2131   -2.7967    2.3801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9025   -3.6392    0.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7990   -1.6510    1.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2768   -0.1368    2.7030 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6440   -1.2926   -2.0827 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0213   -1.0408   -2.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9859    1.5988    1.8163 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7109    1.8607    2.7450 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4502    0.5858    1.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12  9  1  0
  9 10  1  0
 10 11  1  0
  9  8  1  1
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 28 30  2  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  2  0
  5 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  1  0
 22 20  1  0
 20 21  1  0
  9 18  1  0
 18 19  1  0
 18 16  1  0
 16 17  1  0
 16 13  1  0
 20  7  1  0
 34 26  1  0
 15 45  1  0
 14 43  1  0
 14 44  1  0
 13 42  1  6
 10 39  1  0
 10 40  1  0
 11 41  1  0
  7 38  1  6
  5 37  1  1
  4 35  1  0
  4 36  1  0
 27 56  1  0
 29 57  1  0
 31 58  1  0
 33 59  1  0
 34 60  1  0
 24 54  1  6
 25 55  1  0
 22 52  1  1
 23 53  1  0
 20 50  1  1
 21 51  1  0
 18 48  1  1
 19 49  1  0
 16 46  1  1
 17 47  1  0
M  END


  Mrv1652304292208382D          

 34 36  0  0  1  0            999 V2000
   -0.0759    7.9497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4762    7.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2831    7.5081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5381    8.2927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8352    6.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6421    7.0665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5802    6.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7732    5.9389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    5.1542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2887    4.9827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5436    4.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3506    4.0266    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6055    3.2419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4125    3.0704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6674    2.2858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1154    1.6727    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4480    1.1878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7564    2.1143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7828    1.1878    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5675    1.4427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5279    0.4032    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0128   -0.2643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7029    0.4032    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2180   -0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5535   -1.0180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9645    3.6835    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7715    3.5120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7096    4.4681    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2616    5.0812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9026    4.6397    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6477    5.4243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0703    4.5411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2212    6.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
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 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 16 18  1  1  0  0  0
 18 19  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  6  0  0  0
  9 33  2  0  0  0  0
  8 34  2  0  0  0  0
  2 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086324

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](COC(=O)C3=CC(O)=C(O)C(O)=C3)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O15/c20-3-9-13(26)16(29)19(5-21,33-9)34-18-15(28)14(27)12(25)10(32-18)4-31-17(30)6-1-7(22)11(24)8(23)2-6/h1-2,9-10,12-16,18,20-29H,3-5H2/t9-,10-,12-,13-,14+,15-,16+,18-,19+/m1/s1

> <INCHI_KEY>
SNSUBUCSOCHKOG-RDWBPHHJSA-N

> <FORMULA>
C19H26O15

> <MOLECULAR_WEIGHT>
494.402

> <EXACT_MASS>
494.127170137

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
45.537039216705864

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3S,4S,5R,6R)-6-{[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

> <ALOGPS_LOGP>
-1.55

> <JCHEM_LOGP>
-2.9442310800000002

> <ALOGPS_LOGS>
-1.18

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.181569412316472

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.10782248377458

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6490951360291204

> <JCHEM_POLAR_SURFACE_AREA>
256.28999999999996

> <JCHEM_REFRACTIVITY>
104.53880000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.26e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4S,5R,6R)-6-{[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0      -0.142  14.839   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       0.889  13.695   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.395  14.015   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.871  15.480   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.426  12.871   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.932  13.191   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.950  11.406   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.443  11.086   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.968   9.621   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.539   9.301   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.015   7.836   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.521   7.516   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.997   6.052   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -4.503   5.731   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.979   4.267   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -3.949   3.122   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.703   2.217   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.918   4.267   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.412   3.947   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -5.195   2.217   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -6.659   2.693   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.719   0.753   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.624  -0.493   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -3.179   0.753   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.274  -0.493   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.900  -1.900   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.534   6.876   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -7.040   6.556   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -5.058   8.341   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -6.088   9.485   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -3.552   8.661   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -3.076  10.125   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       1.998   8.477   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       0.413  12.230   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   34                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   34                                                  
CONECT    9    8   10   33                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   31                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18   20                                             
CONECT   17   16   24                                                       
CONECT   18   16   19                                                       
CONECT   19   18                                                            
CONECT   20   16   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   17   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   14   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   12   32                                                  
CONECT   32   31                                                            
CONECT   33    9                                                            
CONECT   34    8    2                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

View in JSmol

Synonyms

Value	Source
2-O-(6-O-Galloyl-a-D-glucopyranosyl)-b-D-fructofuranose	Generator
2-O-(6-O-Galloyl-α-D-glucopyranosyl)-β-D-fructofuranose	Generator

Chemical Formula

C₁₉H₂₆O₁₅

Average Mass

494.4020 Da

Monoisotopic Mass

494.12717 Da

IUPAC Name

[(2R,3S,4S,5R,6R)-6-{[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

Traditional Name

[(2R,3S,4S,5R,6R)-6-{[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](COC(=O)C3=CC(O)=C(O)C(O)=C3)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C19H26O15/c20-3-9-13(26)16(29)19(5-21,33-9)34-18-15(28)14(27)12(25)10(32-18)4-31-17(30)6-1-7(22)11(24)8(23)2-6/h1-2,9-10,12-16,18,20-29H,3-5H2/t9-,10-,12-,13-,14+,15-,16+,18-,19+/m1/s1

InChI Key

SNSUBUCSOCHKOG-RDWBPHHJSA-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
Rheum spp.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as galloyl esters. These are organic compounds that contain an ester derivative of 3,4,5-trihydroxybenzoic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Galloyl esters

Alternative Parents

Substituents

Galloyl ester
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
O-glycosyl compound
Glycosyl compound
Disaccharide
C-glycosyl compound
Benzoate ester
Benzenetriol
Pyrogallol derivative
Benzoyl
Ketal
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Oxane
Tetrahydrofuran
Secondary alcohol
Carboxylic acid ester
Acetal
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Alcohol
Organic oxygen compound
Primary alcohol
Organic oxide
Hydrocarbon derivative
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	-1.6	ALOGPS
logP	-2.9	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	8.11	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	256.29 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	104.54 m³·mol⁻¹	ChemAxon
Polarizability	45.54 Å³	ChemAxon
Number of Rings	3	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

C00056525

Chemspider ID

103881733

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14055558

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 6-O-Galloylsucrose (NP0086324)

MOL for NP0086324 (6-O-Galloylsucrose)

3D MOL for NP0086324 (6-O-Galloylsucrose)

3D SDF for NP0086324 (6-O-Galloylsucrose)

3D-SDF for NP0086324 (6-O-Galloylsucrose)

PDB for NP0086324 (6-O-Galloylsucrose)

3D PDB for NP0086324 (6-O-Galloylsucrose)

SMILES for NP0086324 (6-O-Galloylsucrose)

INCHI for NP0086324 (6-O-Galloylsucrose)

Structure for NP0086324 (6-O-Galloylsucrose)

3D Structure for NP0086324 (6-O-Galloylsucrose)