NP-MRD: Showing NP-Card for 3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid (NP0247930)

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Record Information

Version

2.0

Created at

2022-09-07 09:57:34 UTC

Updated at

2022-09-07 09:57:34 UTC

NP-MRD ID

NP0247930

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid

Description

3-Methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. 3-Methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251511562D          

 58 62  0  0  0  0            999 V2000
   -8.5737   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -0.4125    0.0000 O   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
   -7.1447   -1.6500    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
   -7.8592   -2.8875    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
   -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  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
   -9.2881   -1.2375    0.0000 O   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
   -5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    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
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   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
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    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
    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 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
    1.4289    0.8250    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 O   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
    0.7145    2.0625    0.0000 C   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
    1.4289    2.4750    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 O   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
   -2.1434   -1.2375    0.0000 O   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 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 O   0  0  0  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
   -6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 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
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 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
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 36 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 39 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 34 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 32 51  1  0  0  0  0
 51 52  1  0  0  0  0
 18 53  1  0  0  0  0
 53 54  1  0  0  0  0
 53 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  1  0  0  0  0
 16 57  1  0  0  0  0
 57 58  1  0  0  0  0
M  END

     RDKit          3D

100104  0  0  0  0  0  0  0  0999 V2000
    0.1244    2.8883    3.7389 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7545    2.0782    2.7939 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1281    1.4418    1.7526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2112    1.5939    1.6029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8720    0.9729    0.5743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3350    1.1551    0.4289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9537    0.5777   -0.4970 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9720    1.9503    1.3082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3182    2.2587    1.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1586    1.0644    1.6704 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0954    0.0854    0.7345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1697   -0.7921    0.6934 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.2162   -0.3379   -0.1028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8261   -0.9415   -1.1670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4168   -2.1887   -1.5773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0220   -2.8161   -2.6527 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0477   -2.1986   -3.3316 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7101   -2.8294   -4.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3427   -3.9732   -4.8534 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7394   -2.2134   -5.1593 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4426   -0.9530   -2.9071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8726   -0.3018   -1.8530 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2484    0.9539   -1.4007 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2831    1.6628   -2.0266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7375   -0.9990    2.0952 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.8115   -1.8797    2.0444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2671    0.3293    2.6300 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.9330    0.3930    3.9765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6161    1.4806    1.8884 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5524    2.6142    2.7267 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1457    0.1826   -0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2341    0.0459   -0.1329 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9069    0.6613    0.8905 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2276    0.5708    1.1165 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2383   -0.1068    0.4156 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1240    0.8367   -0.0140 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4370    0.5423   -0.1480 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8221   -0.1262   -1.4554 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1894   -0.3742   -1.4560 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2072    0.5440   -1.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9297    1.7605   -1.3146 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5849    0.0841   -1.3911 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9308   -1.2359   -1.4663 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2344   -1.6810   -1.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5250   -3.0329   -1.5447 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5013   -4.0067   -1.6271 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2415   -0.7414   -1.3868 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5800   -1.0789   -1.3796 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9199    0.6176   -1.3087 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9338    1.5505   -1.2293 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6354    2.9238   -1.1504 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6046    1.0350   -1.3103 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0525   -0.1025    1.0515 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0764   -0.9771    0.6157 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0866   -0.8056    1.9524 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7202    0.0361    3.0053 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8309   -1.2291    1.2236 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1347   -2.3532    0.4640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4971    2.2681    4.4197 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9187    3.3565    4.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4547    3.6571    3.2007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    2.2092    2.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5336    3.0558    2.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6621    2.7194    0.4045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7989    0.6467    2.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7590   -1.7725    0.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6189   -2.7631   -1.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7148   -3.8033   -2.9937 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6187   -1.2332   -5.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2588   -0.4716   -3.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1861    2.7304   -1.7491 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1605    1.5489   -3.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2866    1.3345   -1.6898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9441   -1.3600    2.7751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5665   -2.7679    1.7014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3637    0.3445    2.4945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6501    0.0526    4.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0680    1.7278    0.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2647    3.2552    2.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6797   -0.2977   -1.1158 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7429   -0.5755   -0.8466 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7273   -0.6038   -0.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9567    1.5640   -0.2195 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5832    0.6185   -2.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3003   -1.0741   -1.6398 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1025   -1.9455   -1.5284 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0680   -4.0339   -2.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6682   -3.8108   -0.9214 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9760   -4.9860   -1.4374 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.2846   -0.3636   -1.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9155    3.1674   -0.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1369    3.3053   -2.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5468    3.5334   -1.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3193    2.0877   -1.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6072    0.6327    1.7089 H   0  0  0  0  0  0  0  0  0  0  0  0
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 20 69  1  0
M  END


  Mrv1533004251511562D          

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 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
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 40 41  2  0  0  0  0
 36 41  1  0  0  0  0
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 39 44  1  0  0  0  0
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 44 46  1  0  0  0  0
 34 47  1  0  0  0  0
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 55 57  1  0  0  0  0
 16 57  1  0  0  0  0
 57 58  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0247930

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC=C1OC1OC(COC(=O)C2=CC=C(OC3OC(COC(=O)C4=CC(OC)=C(O)C(OC)=C4)C(O)C(O)C3O)C(OC)=C2)C(O)C(O)C1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C37H42O21/c1-49-20-9-15(33(45)46)5-7-18(20)55-36-31(43)29(41)27(39)24(57-36)13-53-34(47)16-6-8-19(21(10-16)50-2)56-37-32(44)30(42)28(40)25(58-37)14-54-35(48)17-11-22(51-3)26(38)23(12-17)52-4/h5-12,24-25,27-32,36-44H,13-14H2,1-4H3,(H,45,46)

> <INCHI_KEY>
MINRACKXAPJYCO-UHFFFAOYSA-N

> <FORMULA>
C37H42O21

> <MOLECULAR_WEIGHT>
822.722

> <EXACT_MASS>
822.221858372

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
78.96065775518743

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid

> <ALOGPS_LOGP>
1.14

> <JCHEM_LOGP>
0.5439112069999988

> <ALOGPS_LOGS>
-3.45

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.434939260251156

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.097337122538397

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6491105015658105

> <JCHEM_POLAR_SURFACE_AREA>
305.34999999999997

> <JCHEM_REFRACTIVITY>
189.04250000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.89e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0     -16.004  -0.000   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -14.670  -0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0     -14.670  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -13.337  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -13.337  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -14.670  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -16.004  -4.620   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0     -17.338  -5.390   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0     -18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -16.004  -3.080   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0     -17.338  -2.310   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0     -12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0     -10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0     -12.003  -6.930   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0     -10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -8.002 -12.320   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -5.335 -13.860   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0     -10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0     -10.669 -13.860   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0     -12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0     -13.337 -12.320   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0     -12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0     -13.337  -9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7    3   11                                                  
CONECT   11   10                                                            
CONECT   12    5   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   57                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   53                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   20   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   23   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   51                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   47                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   36   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   39   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   34   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   32   52                                                  
CONECT   52   51                                                            
CONECT   53   18   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   16   58                                                  
CONECT   58   57                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  124    0
END

View in JSmol

Synonyms

Value	Source
3-Methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoate	Generator

Chemical Formula

C₃₇H₄₂O₂₁

Average Mass

822.7220 Da

Monoisotopic Mass

822.22186 Da

IUPAC Name

3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid

Traditional Name

3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC=C1OC1OC(COC(=O)C2=CC=C(OC3OC(COC(=O)C4=CC(OC)=C(O)C(OC)=C4)C(O)C(O)C3O)C(OC)=C2)C(O)C(O)C1O)C(O)=O

InChI Identifier

InChI=1S/C37H42O21/c1-49-20-9-15(33(45)46)5-7-18(20)55-36-31(43)29(41)27(39)24(57-36)13-53-34(47)16-6-8-19(21(10-16)50-2)56-37-32(44)30(42)28(40)25(58-37)14-54-35(48)17-11-22(51-3)26(38)23(12-17)52-4/h5-12,24-25,27-32,36-44H,13-14H2,1-4H3,(H,45,46)

InChI Key

MINRACKXAPJYCO-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Phenolic glycoside
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
Glycosyl compound
M-methoxybenzoic acid or derivatives
O-glycosyl compound
Methoxyphenol
M-dimethoxybenzene
Dimethoxybenzene
Benzoate ester
Benzoic acid or derivatives
Benzoic acid
Tricarboxylic acid or derivatives
Phenoxy compound
Phenol ether
Benzoyl
Methoxybenzene
Anisole
Phenol
Sugar acid
Alkyl aryl ether
Oxane
Monosaccharide
Monocyclic benzene moiety
Benzenoid
Secondary alcohol
Carboxylic acid ester
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Ether
Carboxylic acid
Organic oxygen compound
Organic oxide
Organooxygen compound
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	1.14	ALOGPS
logP	0.54	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	4.1	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	305.35 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	189.04 m³·mol⁻¹	ChemAxon
Polarizability	78.96 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

74342566

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid (NP0247930)

MOL for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

3D MOL for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

3D SDF for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

3D-SDF for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

PDB for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

3D PDB for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

SMILES for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

INCHI for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

Structure for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)

3D Structure for NP0247930 (3-methoxy-4-[(3,4,5-trihydroxy-6-{[3-methoxy-4-({3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyloxy)methyl]oxan-2-yl}oxy)benzoyloxy]methyl}oxan-2-yl)oxy]benzoic acid)