NP-MRD: Showing NP-Card for Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside (NP0054596)

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Record Information

Version

2.0

Created at

2022-04-28 00:54:02 UTC

Updated at

2022-04-28 00:54:02 UTC

NP-MRD ID

NP0054596

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside

Description

7-Hydroxy-5-(beta-D-glucopyranosyloxy)-2-(4-hydroxy-3-methoxyphenyl)-3-[6-O-[(E)-3-[3-(beta-D-glucopyranosyloxy)-4-hydroxyphenyl]propenoyl]-beta-D-glucopyranosyloxy]-1-benzopyrylium belongs to the class of organic compounds known as flavonoid 3-o-p-coumaroyl glycosides. These are flavonoid 3-O-glycosides where the carbohydrate moiety is esterified with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring. Thus, 7-hydroxy-5-(beta-D-glucopyranosyloxy)-2-(4-hydroxy-3-methoxyphenyl)-3-[6-O-[(e)-3-[3-(beta-D-glucopyranosyloxy)-4-hydroxyphenyl]propenoyl]-beta-D-glucopyranosyloxy]-1-benzopyrylium is considered to be a flavonoid. Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside is found in Arabidopsis thaliana and Ipomoea nil . Based on a literature review very few articles have been published on 7-Hydroxy-5-(beta-D-glucopyranosyloxy)-2-(4-hydroxy-3-methoxyphenyl)-3-[6-O-[(E)-3-[3-(beta-D-glucopyranosyloxy)-4-hydroxyphenyl]propenoyl]-beta-D-glucopyranosyloxy]-1-benzopyrylium.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282202542D          

 67 73  0  0  1  0            999 V2000
   -0.7145   -0.4125    0.0000 C   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 C   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
    1.4289   -0.0000    0.0000 O   0  3  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
    2.8579   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  2  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   -4.1250    0.0000 C   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
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7171   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   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
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    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
  5  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
  4 10  1  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 16 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 28 30  1  0  0  0  0
 31 30  1  6  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
 35 36  1  0  0  0  0
 31 36  1  0  0  0  0
 35 37  1  6  0  0  0
 37 38  1  0  0  0  0
 34 39  1  1  0  0  0
 33 40  1  6  0  0  0
 32 41  1  1  0  0  0
 27 42  1  0  0  0  0
 15 43  1  1  0  0  0
 14 44  1  6  0  0  0
 13 45  1  1  0  0  0
  8 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 46 51  1  0  0  0  0
 50 52  1  0  0  0  0
 52 53  1  0  0  0  0
 49 54  1  0  0  0  0
  3 55  1  0  0  0  0
 56 55  1  1  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
 60 61  1  0  0  0  0
 56 61  1  0  0  0  0
 60 62  1  1  0  0  0
 62 63  1  0  0  0  0
 59 64  1  6  0  0  0
 58 65  1  1  0  0  0
 57 66  1  6  0  0  0
  1 67  1  0  0  0  0
M  CHG  1   7   1
M  END

     RDKit          3D

116122  0  0  0  0  0  0  0  0999 V2000
   -6.7949    0.2011    8.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4362   -1.1664    8.1872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0092   -1.6319    6.9504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9228   -0.8461    5.8380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5006   -1.2755    4.5820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4837   -0.2915    3.5089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9544    0.9092    3.7283 O   0  0  0  0  0  3  0  0  0  0  0  0
   -5.9763    1.8473    2.8203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4962    3.1024    3.1639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5218    4.0981    2.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0580    5.3190    2.6569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0656    3.9174    0.9529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5334    2.6754    0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1090    2.5052   -0.6715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6832    2.0146   -1.7601 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.8548    1.3768   -3.8387 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2059    0.5966   -3.9119 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7534   -0.6706   -3.6012 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.3924    2.0852   -5.3828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1704    2.7255   -3.0552 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3524    3.4001   -2.8460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5153    1.6804    1.5430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9972    0.4274    1.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9871   -0.5408    2.2297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4820   -1.7494    2.0015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5387   -2.2140    1.1327 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0375   -1.1625    0.3027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7600   -1.6171   -0.0508 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8459   -0.4778   -0.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4992   -0.7973   -0.5276 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3968    0.2813   -0.5288 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2641   -1.1423   -1.1801 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6809   -1.2935   -1.4829 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0435   -2.5467   -1.9779 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3667   -2.7768   -2.2540 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3465   -1.8163   -2.0592 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6884   -2.1154   -2.3617 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.8418    0.4111   -1.3417 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1843    0.5808   -1.4944 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.8094    0.7309   -0.2077 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1758    0.5476   -0.4861 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.9381    0.2615    0.7698 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8451    1.2993    1.7030 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.7392    1.7953   -1.1347 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0067    1.4800   -1.6113 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8828    2.2818   -2.2655 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.9542    3.6958   -2.2467 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.8598    1.8429   -3.4412 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6069   -0.3260   -1.2777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8382   -2.6535   -1.1128 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.1151   -3.4622   -1.0100 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9298   -3.2283   -2.1219 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2173    0.2056    5.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8550    3.2239    4.1678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0938    6.0692    1.9908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0967    4.7041    0.2362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0580    0.9323   -1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7685   -0.0073   -2.5103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0302    2.3698   -4.2815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9436    1.4007   -3.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7739    0.4292   -4.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7330   -0.6720   -3.6134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2625    1.1165   -3.8629 H   0  0  0  0  0  0  0  0  0  0  0  0
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 63113  1  0
M  CHG  1   7   1
M  END


  Mrv1652304282202542D          

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M  CHG  1   7   1
M  END
> <DATABASE_ID>
NP0054596

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC=C1O)C1=[O+]C2=CC(O)=CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2C=C1O[C@@H]1O[C@H](COC(=O)\C=C\C2=CC=C(O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C43H48O24/c1-59-24-9-17(4-6-20(24)47)40-26(12-19-22(61-40)10-18(46)11-23(19)62-41-37(56)34(53)31(50)27(13-44)65-41)64-43-39(58)36(55)33(52)29(67-43)15-60-30(49)7-3-16-2-5-21(48)25(8-16)63-42-38(57)35(54)32(51)28(14-45)66-42/h2-12,27-29,31-39,41-45,50-58H,13-15H2,1H3,(H2-,46,47,48,49)/p+1/t27-,28-,29-,31-,32-,33-,34+,35+,36+,37-,38-,39-,41-,42-,43-/m1/s1

> <INCHI_KEY>
MRYLLGRTCPVXBO-CKUBBGCWSA-O

> <FORMULA>
C43H49O24

> <MOLECULAR_WEIGHT>
949.84

> <EXACT_MASS>
949.260828878

> <JCHEM_ACCEPTOR_COUNT>
23

> <JCHEM_ATOM_COUNT>
116

> <JCHEM_AVERAGE_POLARIZABILITY>
91.12925733072868

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
14

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2E)-3-(4-hydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoyl]oxy}methyl)oxan-2-yl]oxy}-1lambda4-chromen-1-ylium

> <ALOGPS_LOGP>
1.00

> <JCHEM_LOGP>
-1.7786000000000046

> <ALOGPS_LOGS>
-3.39

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.37860555096424

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.661111240919055

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6789477956099885

> <JCHEM_POLAR_SURFACE_AREA>
387.2700000000001

> <JCHEM_REFRACTIVITY>
228.55810000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.01e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2E)-3-(4-hydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoyl]oxy}methyl)oxan-2-yl]oxy}-1lambda4-chromen-1-ylium

> <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      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+1
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.670  -2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.004  -3.080   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      17.338  -5.390   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      21.339  -3.080   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      20.005  -2.310   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      18.672  -3.080   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      20.005  -0.770   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      21.339   0.000   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      22.673  -2.310   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      22.673  -5.390   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      20.005  -6.930   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      17.338  -2.310   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   63  O   UNK     0      -6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0      -5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   65  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   66  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   67  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
CONECT    1    2    6   67                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   55                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   46                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    4                                                       
CONECT   11    9   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14   45                                                  
CONECT   14   13   15   44                                                  
CONECT   15   14   16   43                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   12                                                       
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   42                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28   24                                                       
CONECT   30   28   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33   41                                                  
CONECT   33   32   34   40                                                  
CONECT   34   33   35   39                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35   31                                                       
CONECT   37   35   38                                                       
CONECT   38   37                                                            
CONECT   39   34                                                            
CONECT   40   33                                                            
CONECT   41   32                                                            
CONECT   42   27                                                            
CONECT   43   15                                                            
CONECT   44   14                                                            
CONECT   45   13                                                            
CONECT   46    8   47   51                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50   54                                                  
CONECT   50   49   51   52                                                  
CONECT   51   50   46                                                       
CONECT   52   50   53                                                       
CONECT   53   52                                                            
CONECT   54   49                                                            
CONECT   55    3   56                                                       
CONECT   56   55   57   61                                                  
CONECT   57   56   58   66                                                  
CONECT   58   57   59   65                                                  
CONECT   59   58   60   64                                                  
CONECT   60   59   61   62                                                  
CONECT   61   60   56                                                       
CONECT   62   60   63                                                       
CONECT   63   62                                                            
CONECT   64   59                                                            
CONECT   65   58                                                            
CONECT   66   57                                                            
CONECT   67    1                                                            
MASTER        0    0    0    0    0    0    0    0   67    0  146    0
END

View in JSmol

Synonyms

Value	Source
7-Hydroxy-5-(b-D-glucopyranosyloxy)-2-(4-hydroxy-3-methoxyphenyl)-3-[6-O-[(e)-3-[3-(b-D-glucopyranosyloxy)-4-hydroxyphenyl]propenoyl]-b-D-glucopyranosyloxy]-1-benzopyrylium	Generator
7-Hydroxy-5-(β-D-glucopyranosyloxy)-2-(4-hydroxy-3-methoxyphenyl)-3-[6-O-[(e)-3-[3-(β-D-glucopyranosyloxy)-4-hydroxyphenyl]propenoyl]-β-D-glucopyranosyloxy]-1-benzopyrylium	Generator

Chemical Formula

C₄₃H₄₉O₂₄

Average Mass

949.8400 Da

Monoisotopic Mass

949.26083 Da

IUPAC Name

7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2E)-3-(4-hydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoyl]oxy}methyl)oxan-2-yl]oxy}-1lambda4-chromen-1-ylium

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC=C1O)C1=[O+]C2=CC(O)=CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2C=C1O[C@@H]1O[C@H](COC(=O)\C=C\C2=CC=C(O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C43H48O24/c1-59-24-9-17(4-6-20(24)47)40-26(12-19-22(61-40)10-18(46)11-23(19)62-41-37(56)34(53)31(50)27(13-44)65-41)64-43-39(58)36(55)33(52)29(67-43)15-60-30(49)7-3-16-2-5-21(48)25(8-16)63-42-38(57)35(54)32(51)28(14-45)66-42/h2-12,27-29,31-39,41-45,50-58H,13-15H2,1H3,(H2-,46,47,48,49)/p+1/t27-,28-,29-,31-,32-,33-,34+,35+,36+,37-,38-,39-,41-,42-,43-/m1/s1

InChI Key

MRYLLGRTCPVXBO-CKUBBGCWSA-O

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
Arabidopsis thaliana	Plant	KNApSAcK
Ipomoea nil	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid 3-o-p-coumaroyl glycosides. These are flavonoid 3-O-glycosides where the carbohydrate moiety is esterified with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid 3-O-p-coumaroyl glycosides

Alternative Parents

Substituents

Flavonoid 3-o-6-p-coumaroyl-glycoside
Anthocyanidin-3-o-glycoside
Anthocyanidin-5-o-glycoside
Anthocyanin
Flavonoid-3-o-glycoside
3p-methoxyflavonoid-skeleton
4'-hydroxyflavonoid
7-hydroxyflavonoid
Hydroxyflavonoid
Anthocyanidin
Phenolic glycoside
Cinnamic acid or derivatives
Cinnamic acid ester
Hydroxycinnamic acid or derivatives
Coumaric acid or derivatives
O-glycosyl compound
Glycosyl compound
Benzopyran
Methoxyphenol
1-benzopyran
Methoxybenzene
Styrene
Phenol ether
Phenoxy compound
Anisole
Alkyl aryl ether
Phenol
Fatty acid ester
1-hydroxy-2-unsubstituted benzenoid
Fatty acyl
Oxane
Monocyclic benzene moiety
Benzenoid
Monosaccharide
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Heteroaromatic compound
Carboxylic acid ester
Secondary alcohol
Acetal
Polyol
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Primary alcohol
Alcohol
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organic cation
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	ALOGPS
logP	-1.8	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	6.66	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	23	ChemAxon
Hydrogen Donor Count	14	ChemAxon
Polar Surface Area	387.27 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	228.56 m³·mol⁻¹	ChemAxon
Polarizability	91.13 Å³	ChemAxon
Number of Rings	7	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

101695775

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside (NP0054596)

MOL for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

3D MOL for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

3D SDF for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

3D-SDF for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

PDB for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

3D PDB for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

SMILES for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

INCHI for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

Structure for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)

3D Structure for NP0054596 (Peonidin 3-[6-(3-glucosylcaffeyl)glucoside]-5-glucoside)