NP-MRD: Showing NP-Card for (2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0228847)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 08:39:56 UTC

Updated at

2022-09-06 08:39:56 UTC

NP-MRD ID

NP0228847

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Description

Unduloside belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton. Based on a literature review very few articles have been published on Unduloside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062210392D          

 47 51  0  0  1  0            999 V2000
   -1.4087    4.6671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6636    3.8824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1116    3.2693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3665    2.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8145    1.8716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0694    1.0870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5174    0.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7723   -0.3107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5793   -0.4822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203   -0.9238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752   -1.7084    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    0.7541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358    1.3672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    2.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.6021    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0668    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    2.1896    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4957    2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4957    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371   -2.6646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3441   -2.8361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822   -1.8800    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8342   -1.2669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0075    2.0431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2474    2.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3046    3.4409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0497    4.2255    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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 16  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 22 21  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 24 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
 22 31  1  0  0  0  0
 31 32  1  1  0  0  0
 20 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 36 35  1  1  0  0  0
 14 36  1  0  0  0  0
 19 36  1  0  0  0  0
 12 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 11 42  1  0  0  0  0
 42 43  1  1  0  0  0
  5 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
  3 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END

     RDKit          3D

 87 91  0  0  0  0  0  0  0  0999 V2000
    7.9512    0.8397   -3.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0529    1.9776   -2.2566 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3708    2.2788   -1.1118 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4310    1.4230   -0.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7331    1.7187    0.5918 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7642    0.7674    1.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0385    0.9319    2.1928 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0878   -0.0977    2.6241 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4107    0.0857    3.6594 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9061   -1.2788    1.9256 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9988   -2.2649    2.3323 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9856   -2.4585    1.2218 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0946   -1.6338    1.4048 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2213   -0.7064    0.3725 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2735    0.6762    0.8369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4467    1.2374    0.5760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8099    2.6375    0.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9162    2.6958    1.7796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3508    0.2463   -0.0828 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0996    0.8622   -1.2094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4836    0.7693   -1.0630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1400    1.9476   -0.8856 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8294    2.1065    0.2877 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8444    1.1993    0.4145 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4255    0.1464    1.4205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1762    0.7796    2.6477 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2799    0.5217   -0.8483 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.6379    0.1825   -0.6940 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1939    1.4019   -2.0640 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.0494    0.5660   -3.1662 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0382    2.3485   -2.0330 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5632    3.6204   -1.6987 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6846    0.5393   -2.5102 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7826   -0.4406   -2.7761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1975   -1.1331   -1.8541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4904   -0.8824   -0.4248 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6365   -3.7987    1.0719 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6878   -4.5619    0.5907 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6747   -4.4643   -0.9209 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0273   -4.0856    1.0981 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9035   -5.1627    1.1342 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8035   -3.5584    2.5120 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9856   -3.2869    3.1591 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0106    2.9084    1.1894 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9539    3.7844    0.6567 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6434    3.4826   -0.4959 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5829    4.3601   -1.0206 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8733    0.2206   -2.8544 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0761    0.2007   -2.8532 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0096    1.1594   -4.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2100    0.4767   -1.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6071   -0.1729    0.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1526    1.8326    2.7600 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4451   -2.0176    3.2521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4937   -2.1769    0.2733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6175   -0.9001   -0.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5417    1.2234    1.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9775    3.1206    1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0042    3.2031    0.0231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8050    2.1430    2.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0855   -0.1369    0.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9183    1.9810   -1.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3498    2.7640   -0.8792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7231    1.7289    0.8773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1679   -0.6687    1.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4553   -0.2876    1.0950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8163    0.4164    3.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7307   -0.4338   -0.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1762    0.9217   -0.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1592    1.9614   -2.2445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8862    0.0806   -3.3830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5382    2.3538   -2.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5231    4.2497   -2.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5174   -0.6803   -3.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4794   -1.9140   -2.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9868   -1.8391   -0.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5951   -5.6322    0.8413 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3673   -5.1984   -1.3827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0465   -3.4637   -1.2099 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6434   -4.5718   -1.3268 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4268   -3.2325    0.5162 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9787   -5.6029    0.2521 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1782   -4.3194    3.0198 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7210   -3.4918    2.5163 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4756    3.1658    2.1019 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1321    4.7235    1.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0977    4.1569   -1.8610 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  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 36  1  0
 36 35  1  0
 35 34  2  0
 34 33  1  0
 33 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 12 37  1  0
 37 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
  5 44  2  0
 44 45  1  0
 45 46  2  0
 46 47  1  0
 46  3  1  0
 42 11  1  0
 36 14  1  0
 31 22  1  0
 20 19  1  0
  1 48  1  0
  1 49  1  0
  1 50  1  0
  4 51  1  0
  6 52  1  0
  7 53  1  0
 11 54  1  1
 12 55  1  6
 14 56  1  6
 15 57  1  0
 17 58  1  0
 17 59  1  0
 18 60  1  0
 19 61  1  1
 36 76  1  1
 35 75  1  0
 34 74  1  0
 20 62  1  1
 22 63  1  1
 24 64  1  1
 25 65  1  0
 25 66  1  0
 26 67  1  0
 27 68  1  6
 28 69  1  0
 29 70  1  6
 30 71  1  0
 31 72  1  6
 32 73  1  0
 38 77  1  6
 39 78  1  0
 39 79  1  0
 39 80  1  0
 40 81  1  6
 41 82  1  0
 42 83  1  1
 43 84  1  0
 44 85  1  0
 45 86  1  0
 47 87  1  0
M  END


  Mrv1652309062210392D          

 47 51  0  0  1  0            999 V2000
   -1.4087    4.6671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6636    3.8824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1116    3.2693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3665    2.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8145    1.8716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0694    1.0870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5174    0.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7723   -0.3107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5793   -0.4822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203   -0.9238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752   -1.7084    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    0.7541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358    1.3672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    2.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.6021    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0668    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    2.1896    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4957    2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4957    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371   -2.6646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3441   -2.8361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822   -1.8800    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8342   -1.2669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0075    2.0431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2474    2.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3046    3.4409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0497    4.2255    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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 16  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 22 21  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 24 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
 22 31  1  0  0  0  0
 31 32  1  1  0  0  0
 20 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 36 35  1  1  0  0  0
 14 36  1  0  0  0  0
 19 36  1  0  0  0  0
 12 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 11 42  1  0  0  0  0
 42 43  1  1  0  0  0
  5 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
  3 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0228847

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)O[C@H]2[C@H](O[C@@H]3C=C(CO)[C@@H]4[C@H]3C=CO[C@H]4O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[C@@H](C)[C@H](O)[C@H]2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C31H40O16/c1-13-23(36)26(39)28(46-21(35)6-4-14-3-5-17(34)19(9-14)41-2)31(43-13)44-18-10-15(11-32)22-16(18)7-8-42-29(22)47-30-27(40)25(38)24(37)20(12-33)45-30/h3-10,13,16,18,20,22-34,36-40H,11-12H2,1-2H3/b6-4+/t13-,16-,18+,20+,22+,23-,24+,25-,26+,27+,28+,29-,30-,31-/m0/s1

> <INCHI_KEY>
JKLCTVDYVIZSMA-CXLKIWCRSA-N

> <FORMULA>
C31H40O16

> <MOLECULAR_WEIGHT>
668.645

> <EXACT_MASS>
668.231635208

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
67.00408901526733

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4R,5R,6S)-2-{[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,7aH-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
-1.3331414506666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.09659480704479

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.8651474374298

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7415130639193954

> <JCHEM_POLAR_SURFACE_AREA>
243.51999999999995

> <JCHEM_REFRACTIVITY>
158.05820000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4R,5R,6S)-2-{[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,7aH-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.629   8.712   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.105   7.247   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.075   6.103   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.551   4.638   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.520   3.494   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.996   2.029   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.966   0.885   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.442  -0.580   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.948  -0.900   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -0.411  -1.724   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.887  -3.189   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.650  -4.013   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.650   1.408   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.680   2.552   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.924   1.777   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.258   2.547   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.258   4.087   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.591   4.857   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.591   6.397   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.925   7.167   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.925   4.087   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.259   4.857   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.925   2.547   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.259   1.777   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.591   1.777   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.591   0.237   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       6.258  -0.533   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.333  -5.798   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.839  -6.118   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -2.315  -7.583   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.869  -4.974   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -4.376  -5.294   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -2.393  -3.509   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -3.424  -2.365   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -0.014   3.814   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       0.462   5.278   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -0.569   6.423   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -0.093   7.888   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   46                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   44                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   42                                                  
CONECT   12   11   13   37                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   36                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   36                                                  
CONECT   20   19   21   33                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   31                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   22   32                                                  
CONECT   32   31                                                            
CONECT   33   20   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   14   19                                                  
CONECT   37   12   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   11   43                                                  
CONECT   43   42                                                            
CONECT   44    5   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45    3   47                                                  
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₀O₁₆

Average Mass

668.6450 Da

Monoisotopic Mass

668.23164 Da

IUPAC Name

(2R,3R,4R,5R,6S)-2-{[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,7aH-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)O[C@H]2[C@H](O[C@@H]3C=C(CO)[C@@H]4[C@H]3C=CO[C@H]4O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[C@@H](C)[C@H](O)[C@H]2O)=CC=C1O

InChI Identifier

InChI=1S/C31H40O16/c1-13-23(36)26(39)28(46-21(35)6-4-14-3-5-17(34)19(9-14)41-2)31(43-13)44-18-10-15(11-32)22-16(18)7-8-42-29(22)47-30-27(40)25(38)24(37)20(12-33)45-30/h3-10,13,16,18,20,22-34,36-40H,11-12H2,1-2H3/b6-4+/t13-,16-,18+,20+,22+,23-,24+,25-,26+,27+,28+,29-,30-,31-/m0/s1

InChI Key

JKLCTVDYVIZSMA-CXLKIWCRSA-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 iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Iridoid O-glycosides

Alternative Parents

Substituents

Iridoid o-glycoside
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Glycosyl compound
Iridoid-skeleton
O-glycosyl compound
Methoxyphenol
Monoterpenoid
Bicyclic monoterpenoid
Aromatic monoterpenoid
Phenoxy compound
Methoxybenzene
Anisole
Styrene
Phenol ether
Fatty acid ester
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Fatty acyl
Monosaccharide
Oxane
Benzenoid
Monocyclic benzene moiety
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Acetal
Organooxygen compound
Carbonyl group
Organic oxide
Alcohol
Organic oxygen compound
Primary alcohol
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-1.3	ChemAxon
pKa (Strongest Acidic)	9.87	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	243.52 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	158.06 m³·mol⁻¹	ChemAxon
Polarizability	67 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

101713480

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0228847)

MOL for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D MOL for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D SDF for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D-SDF for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

PDB for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D PDB for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

SMILES for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

INCHI for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

Structure for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D Structure for NP0228847 ((2r,3r,4r,5r,6s)-2-{[(1s,4ar,5s,7as)-7-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,7ah-cyclopenta[c]pyran-5-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)