NP-MRD: Showing NP-Card for (2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate (NP0291093)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 22:03:28 UTC

Updated at

2022-09-09 22:03:28 UTC

NP-MRD ID

NP0291093

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

Description

MEGxp0_000989 belongs to the class of organic compounds known as hydroxycinnamic acid glycosides. These are glycosylated hydoxycinnamic acids derivatives. (2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate is found in Brassica napus. Based on a literature review very few articles have been published on MEGxp0_000989.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102200032D          

 53 56  0  0  1  0            999 V2000
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1460   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.8605   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.5749   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.0039   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -5.3625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.5749   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  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  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  1  0  0  0
 13 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 11 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 39 42  2  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 44 47  2  0  0  0  0
 37 47  1  0  0  0  0
  5 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 49 52  2  0  0  0  0
  3 52  1  0  0  0  0
 52 53  1  0  0  0  0
M  END

     RDKit          3D

 95 98  0  0  0  0  0  0  0  0999 V2000
    5.5029    4.5534   -0.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3417    3.6326    0.1889 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9989    2.3136    0.4445 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7946    1.7464    0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4648    0.4186    0.3574 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1624   -0.1421    0.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1184    0.5939   -0.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7900    0.0859   -0.5962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6308   -1.1861   -0.7428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3019    0.8215   -0.7877 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6096    0.5613   -1.1389 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0056    1.2789   -2.1772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9419    2.2415   -2.0691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5785    3.4636   -2.8633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5096    4.1772   -2.5412 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2327    3.7095   -2.5794 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2986    3.7721   -1.3240 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6332    4.9483   -0.7584 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4083    5.2638    0.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1366    6.4882    0.9240 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5359    6.0768   -1.7538 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9740    7.2943   -1.2560 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3325    5.6306   -2.9618 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5502    6.6127   -3.8899 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5337    4.5164   -3.6130 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4316    3.7246   -4.3052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1262    2.6685   -0.6185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9862    3.7305   -0.5521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5135    1.4744    0.1951 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6117    1.8663    1.5615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5377    0.3890    0.0222 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0729   -0.9343    0.0499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8448   -1.8328    1.0736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1304   -1.3881    2.0423 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3516   -3.1926    1.0868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1414   -4.0509    2.0494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6555   -5.4164    2.0369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4080   -6.2707    3.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8188   -7.5780    3.1666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5425   -8.3627    4.2656 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8562   -7.9931    5.4191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5180   -8.1238    2.1082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9558   -9.4462    2.1105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7748   -7.2884    1.0165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4635   -7.8574   -0.0220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8228   -7.2738   -1.2190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3470   -5.9777    1.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4090   -0.3466    0.9989 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6281    0.1788    1.3668 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5844   -0.5766    2.0202 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3032   -1.9156    2.3462 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9373    1.5040    1.0959 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1635    2.0263    1.4640 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4626    4.2492   -0.6033 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4467    5.5190    0.1223 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8882    4.8576   -1.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0557    2.3399   -0.4147 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0197   -1.2272   -0.0514 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2478    1.6888   -0.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5427   -0.5619   -1.5207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9400    1.9049   -2.4355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6339    3.1403   -3.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4861    4.1577   -2.7897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1252    2.6492   -2.9166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6439    4.9507   -0.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3896    5.3503   -0.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4572    4.4309    1.0745 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5936    6.4272    1.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5025    6.1959   -2.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2210    7.9528   -1.2271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3090    5.2480   -2.5888 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6051    7.4874   -3.4700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1682    4.9843   -4.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673    2.9029   -3.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0880    2.9487   -0.2542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6062    4.4790    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5628    1.1341   -0.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3766    2.4874    1.6030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9092    0.4277    0.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9407   -3.4876    0.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5544   -3.7263    2.8900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8455   -5.8341    3.9602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0657   -6.9608    5.7740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7569   -7.9889    5.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9572   -8.7339    6.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4801   -9.8489    1.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7697   -6.1897   -1.1750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0910   -7.6428   -1.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8190   -7.5711   -1.6161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5634   -5.3665    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1633   -1.3994    1.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1841   -2.3285    2.8867 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4045   -1.9090    3.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0525   -2.5224    1.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3736    2.9869    1.2361 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  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 13 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
 33 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  2  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 39 42  2  0
 42 43  1  0
 42 44  1  0
 44 45  1  0
 45 46  1  0
 44 47  2  0
  5 48  2  0
 48 49  1  0
 49 50  1  0
 50 51  1  0
 49 52  2  0
 52 53  1  0
 52  3  1  0
 31 11  1  0
 47 37  1  0
 25 16  1  0
  1 54  1  0
  1 55  1  0
  1 56  1  0
  4 57  1  0
  6 58  1  0
  7 59  1  0
 11 60  1  6
 13 61  1  6
 14 62  1  0
 14 63  1  0
 16 64  1  6
 18 65  1  1
 19 66  1  0
 19 67  1  0
 20 68  1  0
 21 69  1  6
 22 70  1  0
 23 71  1  1
 24 72  1  0
 25 73  1  6
 26 74  1  0
 27 75  1  1
 28 76  1  0
 29 77  1  6
 30 78  1  0
 31 79  1  1
 35 80  1  0
 36 81  1  0
 38 82  1  0
 41 83  1  0
 41 84  1  0
 41 85  1  0
 43 86  1  0
 46 87  1  0
 46 88  1  0
 46 89  1  0
 47 90  1  0
 48 91  1  0
 51 92  1  0
 51 93  1  0
 51 94  1  0
 53 95  1  0
M  END


  Mrv1652309102200032D          

 53 56  0  0  1  0            999 V2000
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1460   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.8605   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.5749   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.0039   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -5.3625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.5749   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  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  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  1  0  0  0
 13 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 11 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 39 42  2  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 44 47  2  0  0  0  0
 37 47  1  0  0  0  0
  5 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 49 52  2  0  0  0  0
  3 52  1  0  0  0  0
 52 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0291093

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)O[C@@H]2O[C@H](CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2OC(=O)\C=C\C2=CC(OC)=C(O)C(OC)=C2)=CC(OC)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C34H42O19/c1-45-17-9-15(10-18(46-2)25(17)38)5-7-23(36)52-32-30(43)28(41)22(14-49-33-31(44)29(42)27(40)21(13-35)50-33)51-34(32)53-24(37)8-6-16-11-19(47-3)26(39)20(12-16)48-4/h5-12,21-22,27-35,38-44H,13-14H2,1-4H3/b7-5+,8-6+/t21-,22-,27-,28-,29+,30+,31-,32-,33-,34+/m1/s1

> <INCHI_KEY>
MBGNTECDWBKCKH-QGDNGYMSSA-N

> <FORMULA>
C34H42O19

> <MOLECULAR_WEIGHT>
754.691

> <EXACT_MASS>
754.232029132

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
75.31480924714273

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-{[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
0.12659086633333325

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.588544662879798

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.987170695214031

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083422322401

> <JCHEM_POLAR_SURFACE_AREA>
279.04999999999995

> <JCHEM_REFRACTIVITY>
177.2867

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-{[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.004  -7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      18.672  -9.240   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      17.338 -11.550   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      20.005 -11.550   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      21.339 -12.320   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      22.673 -11.550   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      22.673 -10.010   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      24.006  -9.240   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      24.006  -7.700   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      25.340  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      25.340  -5.390   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      26.674  -4.620   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      26.674  -7.700   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      28.007  -6.930   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      26.674  -9.240   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      28.007 -10.010   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      25.340 -10.010   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      25.340 -11.550   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      22.673 -14.630   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      20.005 -16.170   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      17.338 -14.630   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      17.338 -16.170   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      18.672 -16.940   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      16.004 -16.940   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      16.004 -18.480   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.670 -19.250   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      14.670 -20.790   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.337 -21.560   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      13.337 -23.100   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      14.670 -23.870   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      12.003 -20.790   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      10.669 -21.560   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      12.003 -19.250   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      10.669 -18.480   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      10.669 -16.940   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      13.337 -18.480   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      10.669  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   52                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   48                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   31                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25                                                            
CONECT   27   13   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   11   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   47                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   42                                                  
CONECT   40   39   41                                                       
CONECT   41   40                                                            
CONECT   42   39   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   47                                                  
CONECT   45   44   46                                                       
CONECT   46   45                                                            
CONECT   47   44   37                                                       
CONECT   48    5   49                                                       
CONECT   49   48   50   52                                                  
CONECT   50   49   51                                                       
CONECT   51   50                                                            
CONECT   52   49    3   53                                                  
CONECT   53   52                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₂O₁₉

Average Mass

754.6910 Da

Monoisotopic Mass

754.23203 Da

IUPAC Name

(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-{[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)O[C@@H]2O[C@H](CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2OC(=O)\C=C\C2=CC(OC)=C(O)C(OC)=C2)=CC(OC)=C1O

InChI Identifier

InChI=1S/C34H42O19/c1-45-17-9-15(10-18(46-2)25(17)38)5-7-23(36)52-32-30(43)28(41)22(14-49-33-31(44)29(42)27(40)21(13-35)50-33)51-34(32)53-24(37)8-6-16-11-19(47-3)26(39)20(12-16)48-4/h5-12,21-22,27-35,38-44H,13-14H2,1-4H3/b7-5+,8-6+/t21-,22-,27-,28-,29+,30+,31-,32-,33-,34+/m1/s1

InChI Key

MBGNTECDWBKCKH-QGDNGYMSSA-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
Brassica napus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxycinnamic acid glycosides. These are glycosylated hydoxycinnamic acids derivatives.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Hydroxycinnamic acid glycosides

Alternative Parents

Substituents

Hydroxycinnamic acid glycoside
O-cinnamoyl glycoside
Cinnamic acid ester
Coumaric acid or derivatives
O-glycosyl compound
Glycosyl compound
Disaccharide
Dimethoxybenzene
Methoxyphenol
M-dimethoxybenzene
Phenol ether
Anisole
Phenoxy compound
Methoxybenzene
Styrene
Fatty acid ester
Phenol
Alkyl aryl ether
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Fatty acyl
Benzenoid
Oxane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Polyol
Organoheterocyclic compound
Ether
Oxacycle
Acetal
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Carbonyl group
Alcohol
Organooxygen compound
Organic oxygen compound
Primary 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	0.13	ChemAxon
pKa (Strongest Acidic)	8.99	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	279.05 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	177.29 m³·mol⁻¹	ChemAxon
Polarizability	75.31 Å³	ChemAxon
Number of Rings	4	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

9403063

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11228013

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate (NP0291093)

MOL for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D MOL for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D SDF for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D-SDF for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

PDB for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D PDB for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

SMILES for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

INCHI for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

Structure for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D Structure for NP0291093 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy}-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)