NP-MRD: Showing NP-Card for (2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate (NP0196549)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 14:39:26 UTC

Updated at

2022-09-04 14:39:27 UTC

NP-MRD ID

NP0196549

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate

Description

Scorodioside belongs to the class of organic compounds known as cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid. (2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate is found in Oreosolen wattii and Scrophularia scorodonia. (2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate was first documented in 2019 (PMID: 30684931). Based on a literature review very few articles have been published on Scorodioside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216392D          

 48 53  0  0  1  0            999 V2000
    5.1057    4.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4237    4.9613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4847    5.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6807    4.6027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6197    3.7800    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3018    3.3158    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0448    3.6744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2408    2.4931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9228    2.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4978    2.1345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8157    2.5987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0727    2.2401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0118    1.4174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6415    0.8845    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1467    0.2322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    0.1208    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3547   -0.7038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0815   -1.0941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5066    0.1818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9107   -0.3888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1070   -1.1901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5111   -1.7608    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7074   -2.5621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1115   -3.1327    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3078   -3.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0999   -4.1647    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6805   -2.9020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2764   -3.4726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8768   -2.1007    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6689   -1.8700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2810   -1.5300    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4772   -0.7287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1186   -0.1581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776    0.6432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182    1.2138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3103    0.9831    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8767    3.4214    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1947    3.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2557    4.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9987    5.0669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5736    5.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8306    4.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1486    5.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5944    4.9196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2764    5.3838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2154    6.2065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4724    6.5651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2096    6.1009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  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
 13 36  1  0  0  0  0
 19 36  1  0  0  0  0
 11 37  1  0  0  0  0
  5 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 43 48  1  0  0  0  0
M  END

     RDKit          3D

 88 93  0  0  0  0  0  0  0  0999 V2000
    1.1640   -4.7256    1.9639 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3430   -3.8636    2.2344 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4745   -4.2606    1.9223 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2199   -2.6336    2.8222 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2444   -1.7354    3.1270 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2561   -1.2966    4.5820 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1876   -0.2427    4.6549 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8994   -0.6880    4.8814 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8110   -1.7257    4.8923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6102    0.4188    4.0929 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6967    0.1312    2.7307 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4711    1.3111    2.0334 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3200    1.2693    1.2953 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5573    1.5039   -0.2075 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8542    2.8798   -0.4884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4447    2.3691   -0.7468 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7770    2.3691   -2.2009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0034    1.9366   -2.5649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4122    2.6280    0.3465 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6142    1.8366    0.5186 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5782    1.9650   -0.4693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2928    0.7723   -0.6028 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3455    0.3344   -1.8952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9717   -0.9305   -1.8772 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8887   -1.4949   -3.2756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5820   -1.6457   -3.6959 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4134   -0.8566   -1.4836 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8660   -2.1427   -1.2351 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6544   -0.0426   -0.2377 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.9578    0.4717   -0.3634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7360    1.1487   -0.2190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7687    1.8420    0.9675 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3359    2.3550    1.7217 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5882    2.3246    2.8774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734    2.3948    2.8395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4948    2.5107    1.6032 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0291   -0.4171    2.3459 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1239   -0.6017    0.9701 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1869   -0.0330    0.2769 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0209    0.6287    0.9433 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3626   -0.1764   -1.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3944    0.3883   -1.7508 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6932    0.3316   -3.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8868   -0.3362   -4.0310 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1744   -0.3875   -5.3810 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2877    0.2337   -5.8992 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1178    0.9142   -5.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8212    0.9591   -3.6961 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3348   -5.7258    2.3994 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0146   -4.7912    0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2526   -4.3269    2.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2582   -2.0677    2.8590 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4384   -2.0941    5.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1926    0.2021    5.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9809   -0.3071    5.9280 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2360   -2.6766    5.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2749   -1.8510    3.9497 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0494   -1.4321    5.6693 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9040   -0.6101    2.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2993    0.3930    1.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0301    0.7307   -0.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5060    3.3768   -2.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0298    1.6630   -2.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9743    1.4287   -3.3977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6926    3.7222    0.2996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4491    0.8036    0.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9234   -0.0256    0.0906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4090   -1.5497   -1.1512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3682   -0.7163   -3.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5074   -2.4168   -3.3677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0611   -2.0065   -2.9542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0162   -0.4616   -2.3256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7158   -2.1824   -0.7345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5510   -0.6880    0.6512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0311    1.1605    0.3593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0873    1.8315   -1.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9277    2.8073    0.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1204    2.2409    3.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7444    2.3655    3.7792 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992    3.4405    1.6245 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8811    0.2246    2.7196 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6656   -0.7311   -1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0907    0.9532   -1.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0108   -0.8381   -3.6843 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5286   -0.9172   -6.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4987    0.1829   -6.9726 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9956    1.4015   -5.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4679    1.4956   -2.9917 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  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  1  0
 16 17  1  6
 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
 11 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  2  0
 39 41  1  0
 41 42  2  0
 42 43  1  0
 43 44  2  0
 44 45  1  0
 45 46  2  0
 46 47  1  0
 47 48  2  0
 37  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
 36 13  1  0
 31 22  1  0
 48 43  1  0
 16 14  1  0
 20 19  1  0
  9 56  1  0
  9 57  1  0
  9 58  1  0
  8 55  1  1
 11 59  1  6
 13 60  1  6
 14 61  1  6
 17 62  1  0
 17 63  1  0
 18 64  1  0
 19 65  1  6
 36 80  1  1
 35 79  1  0
 34 78  1  0
 20 66  1  1
 22 67  1  1
 24 68  1  1
 25 69  1  0
 25 70  1  0
 26 71  1  0
 27 72  1  6
 28 73  1  0
 29 74  1  1
 30 75  1  0
 31 76  1  6
 32 77  1  0
 37 81  1  1
 41 82  1  0
 42 83  1  0
 44 84  1  0
 45 85  1  0
 46 86  1  0
 47 87  1  0
 48 88  1  0
  5 52  1  6
  1 49  1  0
  1 50  1  0
  1 51  1  0
  6 53  1  1
  7 54  1  0
M  END


  Mrv1652309042216392D          

 48 53  0  0  1  0            999 V2000
    5.1057    4.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4237    4.9613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4847    5.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6807    4.6027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6197    3.7800    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3018    3.3158    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0448    3.6744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2408    2.4931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9228    2.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4978    2.1345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8157    2.5987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0727    2.2401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0118    1.4174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6415    0.8845    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1467    0.2322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    0.1208    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3547   -0.7038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0815   -1.0941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5066    0.1818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9107   -0.3888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1070   -1.1901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5111   -1.7608    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7074   -2.5621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1115   -3.1327    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3078   -3.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0999   -4.1647    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6805   -2.9020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2764   -3.4726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8768   -2.1007    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6689   -1.8700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2810   -1.5300    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4772   -0.7287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1186   -0.1581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776    0.6432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182    1.2138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3103    0.9831    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8767    3.4214    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1947    3.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2557    4.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9987    5.0669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5736    5.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8306    4.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1486    5.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5944    4.9196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2764    5.3838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2154    6.2065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4724    6.5651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2096    6.1009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  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
 13 36  1  0  0  0  0
 19 36  1  0  0  0  0
 11 37  1  0  0  0  0
  5 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 43 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196549

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@@H](O[C@@H]2[C@@H]3O[C@]3(CO)[C@@H]3[C@H]2C=CO[C@H]3O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](OC(=O)\C=C\C2=CC=CC=C2)[C@H](OC(C)=O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H40O16/c1-14-21(37)26(43-15(2)35)27(45-19(36)9-8-16-6-4-3-5-7-16)31(42-14)46-25-17-10-11-41-29(20(17)32(13-34)28(25)48-32)47-30-24(40)23(39)22(38)18(12-33)44-30/h3-11,14,17-18,20-31,33-34,37-40H,12-13H2,1-2H3/b9-8+/t14-,17+,18+,20+,21-,22+,23-,24+,25-,26+,27+,28-,29-,30-,31-,32+/m0/s1

> <INCHI_KEY>
IBXDTZNDJHAVNK-DGUYHALFSA-N

> <FORMULA>
C32H40O16

> <MOLECULAR_WEIGHT>
680.656

> <EXACT_MASS>
680.231635208

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
66.3407850127399

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4R,5S,6S)-4-(acetyloxy)-5-hydroxy-2-{[(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_LOGP>
-0.6807131603333345

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.884902073495173

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.15191130407337

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601929344

> <JCHEM_POLAR_SURFACE_AREA>
232.65999999999997

> <JCHEM_REFRACTIVITY>
156.78029999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R,5S,6S)-4-(acetyloxy)-5-hydroxy-2-{[(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       9.531   8.395   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.258   9.261   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.371  10.797   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.871   8.592   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.757   7.056   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.030   6.190   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.417   6.859   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.916   4.654   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.189   3.787   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.529   3.984   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.256   4.851   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.869   4.182   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.755   2.646   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.931   1.651   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.874   0.433   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.348   0.226   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.395  -1.314   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.752  -2.042   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.812   0.339   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.700  -0.726   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.066  -2.222   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.954  -3.287   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.320  -4.783   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.208  -5.848   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.575  -7.343   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.053  -7.774   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.270  -5.417   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -2.383  -6.482   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.637  -3.921   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -3.115  -3.491   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.524  -2.856   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -0.891  -1.360   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       0.221  -0.295   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -0.145   1.201   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.967   2.266   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.446   1.835   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.370   6.387   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       4.097   7.253   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       4.211   8.789   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       5.598   9.458   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.937   9.655   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.551   8.986   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.277   9.853   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -1.110   9.183   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -2.383  10.050   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -2.269  11.585   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -0.882  12.255   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       0.391  11.388   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   37                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   37                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   36                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14   16                                                       
CONECT   16   15   14   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   13   19                                                  
CONECT   37   11    5   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   48                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   43                                                       
MASTER        0    0    0    0    0    0    0    0   48    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₀O₁₆

Average Mass

680.6560 Da

Monoisotopic Mass

680.23164 Da

IUPAC Name

(2S,3R,4R,5S,6S)-4-(acetyloxy)-5-hydroxy-2-{[(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2E)-3-phenylprop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@@H](O[C@@H]2[C@@H]3O[C@]3(CO)[C@@H]3[C@H]2C=CO[C@H]3O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](OC(=O)\C=C\C2=CC=CC=C2)[C@H](OC(C)=O)[C@H]1O

InChI Identifier

InChI=1S/C32H40O16/c1-14-21(37)26(43-15(2)35)27(45-19(36)9-8-16-6-4-3-5-7-16)31(42-14)46-25-17-10-11-41-29(20(17)32(13-34)28(25)48-32)47-30-24(40)23(39)22(38)18(12-33)44-30/h3-11,14,17-18,20-31,33-34,37-40H,12-13H2,1-2H3/b9-8+/t14-,17+,18+,20+,21-,22+,23-,24+,25-,26+,27+,28-,29-,30-,31-,32+/m0/s1

InChI Key

IBXDTZNDJHAVNK-DGUYHALFSA-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
Oreosolen wattii	LOTUS Database	35616633
Scrophularia scorodonia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Cinnamic acid esters

Direct Parent

Cinnamic acid esters

Alternative Parents

Substituents

Cinnamic acid ester
Glycosyl compound
O-glycosyl compound
Styrene
Fatty acid ester
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Fatty acyl
Benzenoid
Monosaccharide
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Secondary alcohol
Acetal
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Organic oxide
Primary alcohol
Organooxygen compound
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	-0.68	ChemAxon
pKa (Strongest Acidic)	12.15	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	232.66 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	156.78 m³·mol⁻¹	ChemAxon
Polarizability	66.34 Å³	ChemAxon
Number of Rings	6	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

C00034220

Chemspider ID

22913319

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23757227

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Luca SV, Czerwinska ME, Miron A, Aprotosoaie AC, Marcourt L, Wolfender JL, Granica S, Skalicka-Wozniak K: High-performance countercurrent chromatographic isolation of acylated iridoid diglycosides from Verbascum ovalifolium Donn ex Sims and evaluation of their inhibitory potential on IL-8 and TNF-alpha production. J Pharm Biomed Anal. 2019 Mar 20;166:295-303. doi: 10.1016/j.jpba.2019.01.031. Epub 2019 Jan 18. [PubMed:30684931 ]
LOTUS database [Link]

Showing NP-Card for (2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate (NP0196549)

MOL for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

3D MOL for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

3D SDF for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

3D-SDF for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

PDB for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

3D PDB for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

SMILES for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

INCHI for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

Structure for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)

3D Structure for NP0196549 ((2s,3r,4r,5s,6s)-4-(acetyloxy)-5-hydroxy-2-{[(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2e)-3-phenylprop-2-enoate)