NP-MRD: Showing NP-Card for 2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol (NP0265214)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 09:07:02 UTC

Updated at

2022-09-08 09:07:02 UTC

NP-MRD ID

NP0265214

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Description

2-[4-({4-[(3,5-Dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-5-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones. 2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol is found in Pyracantha coccinea. 2-[4-({4-[(3,5-Dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-5-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181502062D          

 52 56  0  0  0  0            999 V2000
   -5.6091    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    1.8777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7982   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0531   -2.6919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8781   -2.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3631   -3.3593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1331   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9177   -1.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5308   -2.2043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3593   -3.0113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9724   -3.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8008   -4.3703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0162   -4.6253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7570   -3.3084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3701   -3.8604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1986   -4.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4139   -4.9223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2424   -5.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4578   -5.9843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2863   -6.7912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8555   -6.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6840   -7.0883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6401   -6.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2532   -6.5784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8117   -5.2194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5963   -4.9645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9285   -2.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7131   -2.2465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3262   -2.7985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3154   -1.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235   -0.5973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    1.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0380    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0380   -0.1848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4669   -1.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4669   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1814   -0.5973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4669    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1814    1.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525    1.8777    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  1  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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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
 16 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  0  0  0  0
 19 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  2  0  0  0  0
 14 35  1  0  0  0  0
  5 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  2  0  0  0  0
  3 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 44 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
 42 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END

     RDKit          3D

100104  0  0  0  0  0  0  0  0999 V2000
   -5.0455    0.7459    3.9355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6892    0.8763    2.6934 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9504    0.7655    1.5388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5963    0.5289    1.5758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8343    0.4144    0.4103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3734    0.1504    0.4823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6185    1.4255    0.5634 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7782    2.3631   -0.5900 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3918    3.0584   -0.6980 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3116    2.6156    0.2390 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5792    2.8049   -0.1910 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8953    1.2327    0.6092 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3527    0.2170   -0.3642 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7942   -0.0024   -0.3603 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4122   -0.7994    0.6058 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7617   -1.0279    0.5880 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3380   -1.8241    1.5653 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5352   -2.3924    2.5698 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5674   -0.4645   -0.4077 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9184   -0.7276   -0.3762 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8696    0.0473    0.3538 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3869   -0.6585    1.4129 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3855   -1.5501    1.1303 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9127   -2.9592    0.8475 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0649   -3.0690   -0.2247 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3294   -1.1326    0.0489 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0571   -1.7478   -1.1718 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2827    0.3791   -0.0593 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.2134    0.8105   -0.9821 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8790    0.7256   -0.5183 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.7807    0.3331   -1.8598 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9790    0.3254   -1.3725 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7781    0.8933   -2.3741 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1567    1.7000   -3.3590 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997    0.5391   -1.3273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5058    0.5498   -0.7796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8848    0.7910   -0.8176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5327    0.9227   -2.0333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8294    0.8148   -3.2394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6259    0.9022    0.3329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9877    1.1397    0.2919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9210    0.0387    0.2052 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.6462    0.0894    1.3661 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7594   -0.7094    1.4323 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.4524   -2.1832    1.5280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7537   -2.7056    0.4760 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7506   -0.4130    0.3221 C   0  0  2  0  0  0  0  0  0  0  0  0
  -11.8112   -1.2760    0.3951 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0809   -0.3947   -1.0330 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.0266   -1.6497   -1.6207 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7747    0.3199   -1.0028 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.0480    1.7033   -1.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6892   -0.3175    3.9930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1906    1.4450    3.9439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7630    0.9517    4.7689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0469    0.4193    2.5039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0955   -0.4932   -0.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1833   -0.4262    1.3986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9095    1.9407    1.5187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5922    3.1072   -0.4332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9878    1.7838   -1.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1218    3.2980    1.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1366    3.0393    0.6181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1522    0.9502    1.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0230    0.5668   -1.3834 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8832   -0.7888   -0.1659 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7909   -1.2350    1.3746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1139   -3.0251    3.2698 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7380   -3.0054    2.1095 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0478   -1.5319    3.1006 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2475    0.8704    0.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9895   -1.6437    2.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4571   -3.4334    1.7313 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8529   -3.5471    0.6327 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4740   -3.6035   -0.9447 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3611   -1.4104    0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6818   -1.3459   -1.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4735    0.7863    0.9519 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6282    1.6360   -0.5921 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7827    1.8404   -0.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5835    1.1291   -2.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6151    2.5411   -2.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4026    1.1249   -3.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8869    2.1062   -4.0833 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2356    1.1652   -2.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9666    0.4684   -1.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5306    1.1068   -4.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5621   -0.2510   -3.4761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9009    1.3912   -3.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3492   -0.9143    0.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2952   -0.4551    2.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8352   -2.3458    2.4495 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3920   -2.7585    1.6439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9568   -3.6717    0.4088 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1200    0.6205    0.5075 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0029   -1.5627    1.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7675    0.2221   -1.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1293   -1.5445   -2.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2179    0.0917   -1.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4509    2.1722   -0.4108 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 23 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 19 32  1  0
 32 33  1  0
 33 34  1  0
 32 35  2  0
  5 36  2  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 37 40  2  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 44 47  1  0
 47 48  1  0
 47 49  1  0
 49 50  1  0
 49 51  1  0
 51 52  1  0
 40  3  1  0
 51 42  1  0
 12  7  1  0
 35 14  1  0
 30 21  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
  4 56  1  0
  6 57  1  0
  6 58  1  0
  7 59  1  1
  8 60  1  0
  8 61  1  0
 10 62  1  1
 11 63  1  0
 12 64  1  1
 13 65  1  0
 13 66  1  0
 15 67  1  0
 18 68  1  0
 18 69  1  0
 18 70  1  0
 21 71  1  1
 23 72  1  1
 24 73  1  0
 24 74  1  0
 25 75  1  0
 26 76  1  1
 27 77  1  0
 28 78  1  1
 29 79  1  0
 30 80  1  6
 31 81  1  0
 34 82  1  0
 34 83  1  0
 34 84  1  0
 35 85  1  0
 36 86  1  0
 39 87  1  0
 39 88  1  0
 39 89  1  0
 42 90  1  6
 44 91  1  1
 45 92  1  0
 45 93  1  0
 46 94  1  0
 47 95  1  1
 48 96  1  0
 49 97  1  6
 50 98  1  0
 51 99  1  6
 52100  1  0
M  END


  Mrv1533004181502062D          

 52 56  0  0  0  0            999 V2000
   -5.6091    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    1.8777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7982   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0531   -2.6919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8781   -2.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3631   -3.3593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1331   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9177   -1.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5308   -2.2043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3593   -3.0113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9724   -3.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8008   -4.3703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0162   -4.6253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7570   -3.3084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3701   -3.8604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1986   -4.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4139   -4.9223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2424   -5.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4578   -5.9843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2863   -6.7912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8555   -6.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6840   -7.0883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6401   -6.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2532   -6.5784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8117   -5.2194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5963   -4.9645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9285   -2.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7131   -2.2465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3262   -2.7985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3154   -1.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235   -0.5973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    1.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0380    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0380   -0.1848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4669   -1.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4669   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1814   -0.5973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4669    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1814    1.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525    1.8777    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  1  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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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
 16 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  0  0  0  0
 19 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  2  0  0  0  0
 14 35  1  0  0  0  0
  5 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  2  0  0  0  0
  3 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 44 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
 42 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0265214

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(CC2COC(O)C2CC2=CC(OC)=C(OC3OC(CO)C(O)C(O)C3O)C(OC)=C2)=CC(OC)=C1OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C34H48O18/c1-44-18-7-14(8-19(45-2)30(18)51-33-28(41)26(39)24(37)22(11-35)49-33)5-16-13-48-32(43)17(16)6-15-9-20(46-3)31(21(10-15)47-4)52-34-29(42)27(40)25(38)23(12-36)50-34/h7-10,16-17,22-29,32-43H,5-6,11-13H2,1-4H3

> <INCHI_KEY>
AFVGJDQXVZFGRJ-UHFFFAOYSA-N

> <FORMULA>
C34H48O18

> <MOLECULAR_WEIGHT>
744.74

> <EXACT_MASS>
744.284064706

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
73.49749323943276

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.32

> <JCHEM_LOGP>
-1.8354887376666666

> <ALOGPS_LOGS>
-2.99

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.162643781318762

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.711597681148271

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923662076965

> <JCHEM_POLAR_SURFACE_AREA>
265.13999999999993

> <JCHEM_REFRACTIVITY>
174.07720000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.66e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0     -10.470   4.275   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -9.137   3.505   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -9.137   1.965   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.803   1.195   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.803  -0.345   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.469  -1.115   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.469  -2.655   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.223  -3.560   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -5.699  -5.025   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -7.239  -5.025   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -8.144  -6.271   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -7.715  -3.560   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -9.180  -3.084   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -10.324  -4.115   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.004  -5.621   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -11.148  -6.652   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0     -10.828  -8.158   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -9.364  -8.634   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -12.613  -6.176   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0     -13.757  -7.206   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0     -13.437  -8.712   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0     -11.973  -9.188   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0     -11.653 -10.695   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -10.188 -11.171   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -9.868 -12.677   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0     -12.797 -11.725   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0     -12.477 -13.232   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0     -14.262 -11.249   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0     -15.406 -12.280   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0     -14.582  -9.743   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0     -16.046  -9.267   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0     -12.933  -4.669   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0     -14.398  -4.193   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0     -15.542  -5.224   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -11.789  -3.639   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -9.137  -1.115   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -10.470  -0.345   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -11.804  -1.115   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0     -11.804  -2.655   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -10.470   1.195   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0     -11.804   1.965   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0     -13.138   1.195   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0     -13.138  -0.345   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0     -14.471  -1.115   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -14.471  -2.655   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0     -15.805  -3.425   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0     -15.805  -0.345   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0     -17.139  -1.115   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0     -15.805   1.195   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0     -17.139   1.965   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0     -14.471   1.965   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0     -14.471   3.505   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   40                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   36                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    7   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   35                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   32                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   21   31                                                  
CONECT   31   30                                                            
CONECT   32   19   33   35                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   32   14                                                       
CONECT   36    5   37                                                       
CONECT   37   36   38   40                                                  
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   37    3   41                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43   51                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   47                                                  
CONECT   45   44   46                                                       
CONECT   46   45                                                            
CONECT   47   44   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   42   52                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₈O₁₈

Average Mass

744.7400 Da

Monoisotopic Mass

744.28406 Da

IUPAC Name

2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

COC1=CC(CC2COC(O)C2CC2=CC(OC)=C(OC3OC(CO)C(O)C(O)C3O)C(OC)=C2)=CC(OC)=C1OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C34H48O18/c1-44-18-7-14(8-19(45-2)30(18)51-33-28(41)26(39)24(37)22(11-35)49-33)5-16-13-48-32(43)17(16)6-15-9-20(46-3)31(21(10-15)47-4)52-34-29(42)27(40)25(38)23(12-36)50-34/h7-10,16-17,22-29,32-43H,5-6,11-13H2,1-4H3

InChI Key

AFVGJDQXVZFGRJ-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

Species Name	Source	Reference
Pyracantha coccinea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan glycosides

Sub Class

Not Available

Direct Parent

Lignan glycosides

Alternative Parents

Substituents

Lignan glycoside
Dibenzylbutyrolactol
Furanoid lignan
Tetrahydrofuran lignan
9,9p-epoxylignan
Phenolic glycoside
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
M-dimethoxybenzene
Dimethoxybenzene
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Benzenoid
Oxane
Monocyclic benzene moiety
Monosaccharide
Fatty acyl
Tetrahydrofuran
Secondary alcohol
Hemiacetal
Polyol
Acetal
Organoheterocyclic compound
Ether
Oxacycle
Organooxygen compound
Organic oxygen compound
Primary alcohol
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	-0.32	ALOGPS
logP	-1.8	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	11.71	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	265.14 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	174.08 m³·mol⁻¹	ChemAxon
Polarizability	73.5 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol (NP0265214)

MOL for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0265214 (2-[4-({4-[(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-2-hydroxyoxolan-3-yl}methyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)