NP-MRD: Showing NP-Card for (2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid (NP0205321)

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Record Information

Version

2.0

Created at

2022-09-05 01:12:20 UTC

Updated at

2022-09-05 01:12:20 UTC

NP-MRD ID

NP0205321

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid

Description

(Z)-3-[4-[(6-O-Galloyl-beta-D-glucopyranosyl)oxy]phenyl]propenoic acid belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Based on a literature review very few articles have been published on (Z)-3-[4-[(6-O-Galloyl-beta-D-glucopyranosyl)oxy]phenyl]propenoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052203122D          

 34 36  0  0  1  0            999 V2000
   -7.1447   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -0.4125    0.0000 C   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
   -5.7158   -0.0000    0.0000 C   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
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   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   -2.8875    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  2  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   -5.3625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.8592   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    0.0000 C   0  0  1  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
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 18 26  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 11 31  1  0  0  0  0
 31 32  1  1  0  0  0
  9 33  1  0  0  0  0
 33 34  2  0  0  0  0
  6 34  1  0  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
    8.7683    3.3025   -1.6962 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8895    2.5430   -1.1317 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6072    2.9209   -1.4097 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4210    1.4813   -0.3459 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7676    0.5600    0.2669 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3496    0.3774    0.2810 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7443   -0.1034    1.4682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4222   -0.4059    1.5199 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5758   -0.2623    0.4064 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3339   -0.5684    0.5376 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0879   -0.8684    0.6446 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3013   -0.1676    1.5800 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0055   -0.1845    1.0880 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9169    0.7238    1.8421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2080    0.6598    1.3061 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5404    1.0110    0.0380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6516    1.4335   -0.7437 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9309    0.9165   -0.4748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2303    1.2825   -1.7660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5081    1.2125   -2.2877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8174    1.5803   -3.5903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5208    0.7594   -1.4859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8270    0.6769   -1.9854 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2594    0.3826   -0.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3037   -0.0761    0.6170 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9585    0.4629    0.3200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6065   -1.5676    1.1102 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6532   -1.5930    0.1901 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6604   -2.6599    0.7947 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9415   -3.7289    1.6790 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7818   -2.3418    0.9286 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4839   -3.0769   -0.0300 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1479    0.2031   -0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4886    0.4988   -0.7827 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3221    3.0502   -2.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5480    1.4766   -0.2713 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3614   -0.1716    0.8454 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4271   -0.2033    2.3132 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0221   -0.7693    2.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5439   -0.6959   -0.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9420    0.1442    0.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0146    0.3615    2.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5937    1.7867    1.8227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4367    1.6413   -2.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0581    1.9199   -4.1908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0236    0.9488   -2.9295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1702   -0.3602    1.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7551    0.1689    1.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0779   -1.6889    2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2422   -1.4721   -0.7096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8728   -3.0923   -0.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3286   -4.4655    1.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1057   -2.5535    1.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1129   -2.5215   -0.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5370    0.3386   -1.6740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9047    0.7731   -1.7556 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  2  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
  6 34  1  0
 34 33  2  0
 11 31  1  0
 31 32  1  0
 31 29  1  0
 29 30  1  0
 29 27  1  0
 26 18  1  0
 33  9  1  0
 28 50  1  0
 27 49  1  1
 13 41  1  6
 14 42  1  0
 14 43  1  0
 19 44  1  0
 21 45  1  0
 23 46  1  0
 25 47  1  0
 26 48  1  0
 11 40  1  6
  8 39  1  0
  7 38  1  0
  5 37  1  0
  4 36  1  0
  3 35  1  0
 34 56  1  0
 33 55  1  0
 31 53  1  1
 32 54  1  0
 29 51  1  6
 30 52  1  0
M  END


  Mrv1652309052203122D          

 34 36  0  0  1  0            999 V2000
   -7.1447   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -0.4125    0.0000 C   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
   -5.7158   -0.0000    0.0000 C   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
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   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   -2.8875    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  2  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   -5.3625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.8592   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    0.0000 C   0  0  1  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
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 18 26  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 11 31  1  0  0  0  0
 31 32  1  1  0  0  0
  9 33  1  0  0  0  0
 33 34  2  0  0  0  0
  6 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0205321

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1[C@@H](COC(=O)C2=CC(O)=C(O)C(O)=C2)O[C@@H](OC2=CC=C(\C=C/C(O)=O)C=C2)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H22O12/c23-13-7-11(8-14(24)17(13)27)21(31)32-9-15-18(28)19(29)20(30)22(34-15)33-12-4-1-10(2-5-12)3-6-16(25)26/h1-8,15,18-20,22-24,27-30H,9H2,(H,25,26)/b6-3-/t15-,18-,19+,20-,22-/m1/s1

> <INCHI_KEY>
UQIFTTHBJDWQSZ-ADUYLMGXSA-N

> <FORMULA>
C22H22O12

> <MOLECULAR_WEIGHT>
478.406

> <EXACT_MASS>
478.111126148

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
44.8206385929806

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z)-3-(4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid

> <JCHEM_LOGP>
1.1490567286666664

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.107871347991635

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.22339146346935

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6491104813346213

> <JCHEM_POLAR_SURFACE_AREA>
203.43999999999997

> <JCHEM_REFRACTIVITY>
112.94990000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-3-(4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  O   UNK     0     -13.337  -0.000   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0     -12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0     -12.003  -2.310   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0     -10.669  -0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0     -10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0     -10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0     -12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0     -13.337 -12.320   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0     -13.337 -13.860   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0     -14.670 -14.630   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0     -12.003 -14.630   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -10.669 -13.860   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -8.002 -13.860   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -9.336 -16.170   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -8.002 -16.940   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0     -10.669 -16.940   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0     -10.669 -18.480   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0     -12.003 -16.170   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -14.670 -10.010   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0     -14.670  -6.930   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0     -12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0     -12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   34                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   33                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   31                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   18                                                       
CONECT   27   13   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   11   32                                                  
CONECT   32   31                                                            
CONECT   33    9   34                                                       
CONECT   34   33    6                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

View in JSmol

Synonyms

Value	Source
(Z)-3-[4-[(6-O-Galloyl-b-D-glucopyranosyl)oxy]phenyl]propenoate	Generator
(Z)-3-[4-[(6-O-Galloyl-b-D-glucopyranosyl)oxy]phenyl]propenoic acid	Generator
(Z)-3-[4-[(6-O-Galloyl-beta-D-glucopyranosyl)oxy]phenyl]propenoate	Generator
(Z)-3-[4-[(6-O-Galloyl-β-D-glucopyranosyl)oxy]phenyl]propenoate	Generator
(Z)-3-[4-[(6-O-Galloyl-β-D-glucopyranosyl)oxy]phenyl]propenoic acid	Generator

Chemical Formula

C₂₂H₂₂O₁₂

Average Mass

478.4060 Da

Monoisotopic Mass

478.11113 Da

IUPAC Name

(2Z)-3-(4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid

Traditional Name

(2Z)-3-(4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

O[C@@H]1[C@@H](COC(=O)C2=CC(O)=C(O)C(O)=C2)O[C@@H](OC2=CC=C(\C=C/C(O)=O)C=C2)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C22H22O12/c23-13-7-11(8-14(24)17(13)27)21(31)32-9-15-18(28)19(29)20(30)22(34-15)33-12-4-1-10(2-5-12)3-6-16(25)26/h1-8,15,18-20,22-24,27-30H,9H2,(H,25,26)/b6-3-/t15-,18-,19+,20-,22-/m1/s1

InChI Key

UQIFTTHBJDWQSZ-ADUYLMGXSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Galloyl ester
Cinnamic acid
Cinnamic acid or derivatives
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
O-glycosyl compound
P-hydroxybenzoic acid ester
Benzoate ester
Benzoic acid or derivatives
Benzenetriol
Pyrogallol derivative
Phenoxy compound
Phenol ether
Benzoyl
Styrene
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Monocyclic benzene moiety
Oxane
Monosaccharide
Dicarboxylic acid or derivatives
Benzenoid
Carboxylic acid ester
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Carboxylic acid
Organic oxide
Carbonyl group
Hydrocarbon derivative
Alcohol
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	1.15	ChemAxon
pKa (Strongest Acidic)	3.22	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	203.44 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	112.95 m³·mol⁻¹	ChemAxon
Polarizability	44.82 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

102023506

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid (NP0205321)

MOL for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

3D MOL for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

3D SDF for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

3D-SDF for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

PDB for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

3D PDB for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

SMILES for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

INCHI for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

Structure for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)

3D Structure for NP0205321 ((2z)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl]oxy}phenyl)prop-2-enoic acid)