NP-MRD: Showing NP-Card for (2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate (NP0215222)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 14:45:50 UTC

Updated at

2022-09-05 14:45:50 UTC

NP-MRD ID

NP0215222

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate

Description

Isomacrophylloside belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. (2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate is found in Gentiana tibetica. Based on a literature review very few articles have been published on Isomacrophylloside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052216452D          

 62 67  0  0  1  0            999 V2000
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 25  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 26 35  1  0  0  0  0
 35 36  1  1  0  0  0
 14 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 37 42  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  6  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  2  0  0  0  0
 46 52  1  0  0  0  0
 52 53  1  0  0  0  0
  4 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 56 57  1  0  0  0  0
 57 58  2  0  0  0  0
 57 59  1  0  0  0  0
 59 60  1  0  0  0  0
 60 61  1  0  0  0  0
 62 61  1  1  0  0  0
 56 62  1  0  0  0  0
  3 62  1  0  0  0  0
M  END

     RDKit          3D

106111  0  0  0  0  0  0  0  0999 V2000
   -2.6437   -3.1932   -2.0482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6780   -2.6627   -1.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8690   -2.7385    0.0644 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9079   -1.3071    0.5386 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6247   -0.8217    0.5877 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3815    0.2340   -0.2915 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5545   -0.2343   -1.2558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2863    0.2124   -1.3692 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7029   -0.8335   -1.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3165   -1.2969   -3.1035 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0563   -2.2834   -3.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6783   -2.8004   -5.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0768   -2.7091   -3.1579 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2539    0.8934   -0.0936 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5266    1.4407   -0.4424 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7213    1.0048    0.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6612    0.0845    0.9203 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9197    1.6875   -0.3711 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7940    2.7718   -1.2540 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8881    3.4810   -1.6815 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1443    3.1437   -1.2495 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3063    2.0705   -0.3699 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5972    1.8027    0.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1737    1.3555    0.0505 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4151    0.2905    0.9148 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5553   -1.0360    0.4755 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7509   -1.9589    1.1334 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3944   -2.9246    1.8398 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4906   -3.5615    2.9029 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2445   -4.5483    3.5845 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6651   -2.4913    2.5168 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1709   -3.6510    3.1557 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6595   -2.0263    1.4878 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5274   -1.0924    1.9943 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9464   -1.5588    0.2725 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8234   -2.7176   -0.5647 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6966    1.9980    0.1743 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2884    2.9041    1.1715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0022    4.2316    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4184    5.0990    2.0569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1170    4.6166   -0.2599 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0926    1.5126    0.3760 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9309    2.5781   -0.1197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7108    3.3036    0.7992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6295    2.9729    1.9832 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5625    4.3937    0.3142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5716    4.6843   -1.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3555    5.6986   -1.5058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1477    6.4483   -0.6360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1453    6.1716    0.6993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9397    6.9290    1.5440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3331    5.1220    1.1688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4049    4.9265    2.5225 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6268   -1.1294    1.7411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9199   -1.6390    1.7679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1437   -2.7913    1.1333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4701   -3.4010    1.0914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4686   -2.7704    1.5429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5661   -4.6731    0.5442 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6617   -5.1196   -0.4682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7169   -4.0022   -0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0751   -3.5232    0.4212 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5681   -3.1017   -3.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8737   -3.7166   -1.4857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4325   -2.1453   -2.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9783   -3.2834    0.4485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4577   -0.7212   -0.2475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3965    0.3816   -0.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2979    1.0009   -2.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8355   -1.6526   -1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6954   -0.3183   -1.8994 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5203   -3.9048   -4.9799 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4221   -2.6035   -5.8927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3053   -2.3711   -5.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3023    0.1040    0.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8137    3.0329   -1.5874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8161    4.3155   -2.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0000    3.6922   -1.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8180    1.1181    0.7022 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1358   -1.0057   -0.5936 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6570   -3.7650    1.1646 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1880   -2.7615    3.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6185   -4.0110    2.3893 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3575   -5.3103    2.9890 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4803   -1.7573    3.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9886   -3.9830    2.7260 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2889   -2.9186    1.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4746   -1.3835    2.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5316   -0.8651   -0.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2665   -2.3956   -1.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7100    2.6143   -0.7852 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4620    5.4444    1.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2347    6.0110    2.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2837    4.5948    3.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2386    1.4642    1.4922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9500    4.0860   -1.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3643    5.9313   -2.5778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7518    7.2385   -1.0365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9346    6.7162    2.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9416    4.2721    3.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7512   -1.1658    2.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1862   -5.4767   -1.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0079   -5.9475   -0.0914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9009   -4.4118   -1.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2185   -3.1841   -1.4004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8116   -4.4241    1.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 13  2  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4 54  1  0
 54 55  1  0
 55 56  2  0
 56 62  1  0
 62 61  1  0
 61 60  1  0
 60 59  1  0
 59 57  1  0
 57 58  2  0
 62  3  1  0
  3  2  1  0
  2  1  2  3
  6 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  2  0
 44 46  1  0
 46 47  2  0
 47 48  1  0
 48 49  2  0
 49 50  1  0
 50 51  1  0
 50 52  2  0
 52 53  1  0
 42 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 39 41  2  0
 37 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 28 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 14  8  1  0
 24 18  1  0
 35 26  1  0
  3  4  1  0
 52 46  1  0
 57 56  1  0
 12 72  1  0
 12 73  1  0
 12 74  1  0
  9 70  1  0
  9 71  1  0
  8 69  1  6
  6 68  1  6
  4 67  1  6
 55101  1  0
 62106  1  1
 61104  1  0
 61105  1  0
 60102  1  0
 60103  1  0
  3 66  1  1
  2 65  1  0
  1 63  1  0
  1 64  1  0
 42 95  1  1
 47 96  1  0
 48 97  1  0
 49 98  1  0
 51 99  1  0
 53100  1  0
 37 91  1  6
 40 92  1  0
 40 93  1  0
 40 94  1  0
 14 75  1  1
 19 76  1  0
 20 77  1  0
 21 78  1  0
 23 79  1  0
 26 80  1  6
 28 81  1  6
 29 82  1  0
 29 83  1  0
 30 84  1  0
 31 85  1  1
 32 86  1  0
 33 87  1  6
 34 88  1  0
 35 89  1  6
 36 90  1  0
M  END


  Mrv1652309052216452D          

 62 67  0  0  1  0            999 V2000
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 25  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 26 35  1  0  0  0  0
 35 36  1  1  0  0  0
 14 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 37 42  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  6  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  2  0  0  0  0
 46 52  1  0  0  0  0
 52 53  1  0  0  0  0
  4 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 56 57  1  0  0  0  0
 57 58  2  0  0  0  0
 57 59  1  0  0  0  0
 59 60  1  0  0  0  0
 60 61  1  0  0  0  0
 62 61  1  1  0  0  0
 56 62  1  0  0  0  0
  3 62  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0215222

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@H]1O[C@@H](O[C@@H]2OC=C3[C@@H](CCOC3=O)[C@H]2C=C)[C@H](OC(=O)C2=CC=CC(O)=C2O)[C@@H](OC(C)=O)[C@@H]1OC(=O)C1=CC=CC(O)=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H44O22/c1-4-18-19-11-12-53-35(50)22(19)14-55-38(18)62-40-34(60-36(51)20-7-5-9-23(44)27(20)46)33(56-17(3)43)32(26(58-40)15-54-16(2)42)59-37(52)21-8-6-10-24(45)31(21)61-39-30(49)29(48)28(47)25(13-41)57-39/h4-10,14,18-19,25-26,28-30,32-34,38-41,44-49H,1,11-13,15H2,2-3H3/t18-,19+,25-,26-,28-,29+,30-,32-,33+,34-,38+,39+,40+/m1/s1

> <INCHI_KEY>
PCQHAARAQYTSDQ-FCUWADEDSA-N

> <FORMULA>
C40H44O22

> <MOLECULAR_WEIGHT>
876.77

> <EXACT_MASS>
876.232423057

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
106

> <JCHEM_AVERAGE_POLARIZABILITY>
82.02259086833867

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5R,6S)-6-{[(3S,4R,4aS)-4-ethenyl-8-oxo-3H,4H,4aH,5H,6H,8H-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate

> <JCHEM_LOGP>
1.9113264076666678

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.740915879367762

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.090889467688582

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923575028783

> <JCHEM_POLAR_SURFACE_AREA>
319.26

> <JCHEM_REFRACTIVITY>
199.46300000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5R,6S)-6-{[(3S,4R,4aS)-4-ethenyl-8-oxo-3H,4H,4aH,5H,6H-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -5.335   0.000   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.336   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -9.336   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -8.002   6.160   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.335   4.620   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -6.668   6.930   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -8.002   9.240   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -8.002  10.780   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -5.335   9.240   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -5.335  10.780   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -4.001   8.470   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -2.667   9.240   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -2.667   6.160   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   62                                                  
CONECT    4    3    5   54                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   42                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    8   15   37                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   18   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   35                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   26   36                                                  
CONECT   36   35                                                            
CONECT   37   14   38   42                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   37    6   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   52                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50   46   53                                                  
CONECT   53   52                                                            
CONECT   54    4   55                                                       
CONECT   55   54   56                                                       
CONECT   56   55   57   62                                                  
CONECT   57   56   58   59                                                  
CONECT   58   57                                                            
CONECT   59   57   60                                                       
CONECT   60   59   61                                                       
CONECT   61   60   62                                                       
CONECT   62   61   56    3                                                  
MASTER        0    0    0    0    0    0    0    0   62    0  134    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₄₄O₂₂

Average Mass

876.7700 Da

Monoisotopic Mass

876.23242 Da

IUPAC Name

(2R,3R,4S,5R,6S)-6-{[(3S,4R,4aS)-4-ethenyl-8-oxo-3H,4H,4aH,5H,6H,8H-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate

Traditional Name

(2R,3R,4S,5R,6S)-6-{[(3S,4R,4aS)-4-ethenyl-8-oxo-3H,4H,4aH,5H,6H-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@H]1O[C@@H](O[C@@H]2OC=C3[C@@H](CCOC3=O)[C@H]2C=C)[C@H](OC(=O)C2=CC=CC(O)=C2O)[C@@H](OC(C)=O)[C@@H]1OC(=O)C1=CC=CC(O)=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C40H44O22/c1-4-18-19-11-12-53-35(50)22(19)14-55-38(18)62-40-34(60-36(51)20-7-5-9-23(44)27(20)46)33(56-17(3)43)32(26(58-40)15-54-16(2)42)59-37(52)21-8-6-10-24(45)31(21)61-39-30(49)29(48)28(47)25(13-41)57-39/h4-10,14,18-19,25-26,28-30,32-34,38-41,44-49H,1,11-13,15H2,2-3H3/t18-,19+,25-,26-,28-,29+,30-,32-,33+,34-,38+,39+,40+/m1/s1

InChI Key

PCQHAARAQYTSDQ-FCUWADEDSA-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
Gentiana tibetica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Phenolic glycoside
M-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Glycosyl compound
O-glycosyl compound
Benzoate ester
Salicylic acid or derivatives
Benzoic acid or derivatives
Phenoxy compound
Benzoyl
Catechol
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Delta valerolactone
Delta_valerolactone
Phenol
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Vinylogous acid
Lactone
Secondary alcohol
Carboxylic acid ester
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Primary alcohol
Carbonyl group
Organic oxygen compound
Alcohol
Organic oxide
Hydrocarbon derivative
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	1.91	ChemAxon
pKa (Strongest Acidic)	9.09	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	319.26 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	199.46 m³·mol⁻¹	ChemAxon
Polarizability	82.02 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

Not Available

Chemspider ID

58116517

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102316723

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,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate (NP0215222)

MOL for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

3D MOL for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

3D SDF for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

3D-SDF for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

PDB for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

3D PDB for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

SMILES for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

INCHI for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

Structure for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)

3D Structure for NP0215222 ((2r,3r,4s,5r,6s)-6-{[(3s,4r,4as)-4-ethenyl-8-oxo-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-3-yl]oxy}-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,3-dihydroxybenzoyloxy)oxan-3-yl 3-hydroxy-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate)