NP-MRD: Showing NP-Card for (3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate (NP0325774)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 06:47:03 UTC

Updated at

2022-09-12 06:47:04 UTC

NP-MRD ID

NP0325774

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122208472D          

 59 64  0  0  1  0            999 V2000
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -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
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   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
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    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
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  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
    0.0000   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -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
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    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
    4.2868   -4.1250    0.0000 C   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
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 O   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
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  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
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  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
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  6 17  2  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 39 37  1  4  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 43 46  2  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 48 51  2  0  0  0  0
 41 51  1  0  0  0  0
 35 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
 19 54  1  0  0  0  0
 54 55  1  0  0  0  0
  5 56  2  0  0  0  0
 56 57  1  0  0  0  0
 57 58  2  0  0  0  0
  3 58  1  0  0  0  0
 58 59  1  0  0  0  0
M  END

     RDKit          3D

101106  0  0  0  0  0  0  0  0999 V2000
    1.1579    3.4164    3.7827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1901    3.6205    4.1033 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0662    4.0783    3.0636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322    4.2783    1.8099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3317    4.7148    0.7988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9032    4.8539   -0.5650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6105    5.7160   -1.3066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3670    5.9531   -2.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1452    6.8613   -3.2869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8317    7.0615   -4.6110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6005    7.9600   -5.3540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8219    6.4318   -5.2294 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027    5.5065   -4.5705 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9364    4.9175   -5.1404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2834    5.2828   -3.2456 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4465    4.3867   -2.4640 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1636    4.1525   -1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8666    3.2577   -0.3648 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8479    2.4314   -1.0150 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0516    1.5816   -1.7710 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9048    0.2614   -1.3089 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9329   -0.5999   -1.9281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8355   -1.9341   -1.5616 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8086   -2.6518   -2.2699 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1879   -3.3178   -3.3679 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3062   -3.6533   -4.1844 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8212   -3.7121   -5.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8095   -4.6709   -5.6748 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8254   -4.9679   -3.6230 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1839   -5.0753   -3.8443 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5649   -4.9783   -2.1154 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2595   -5.4049   -1.9151 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7014   -3.5519   -1.5647 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5783   -3.5327   -0.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8885    0.3415    0.1548 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3181   -0.7457    0.8102 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5320   -0.5515    1.8812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7241    0.6796    2.1986 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2257   -1.5604    2.6838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9390   -1.1287    3.7064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6823   -2.0749    4.5754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -1.6023    5.8004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9237   -2.4929    6.5795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3989   -2.1229    7.7542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8526   -1.7537    8.8878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1946   -3.7748    6.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9522   -4.6741    6.8404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7246   -4.2483    4.8466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0380   -5.4777    4.4680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7501   -6.2012    3.3087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9862   -3.3335    4.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3706    0.5253    0.5492 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4217    0.5579    1.9247 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7870    1.8512   -0.0487 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1871    2.7685    0.9376 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6750    4.9382    1.1091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2036    4.7365    2.3621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3361    4.2815    3.3836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9080    4.0884    4.6653 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2689    2.7659    2.8783 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6701    2.8888    4.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258    4.4306    3.5757 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4977    4.1108    1.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9541    7.3639   -2.8059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4339    7.5748   -5.8325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5909    6.6019   -6.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2360    3.8847   -2.9892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3665    3.0829   -1.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0857   -0.0434   -1.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9767   -0.2318   -1.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7440   -0.5477   -3.0648 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4442   -1.8639   -2.8213 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0680   -2.8467   -4.0415 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5929   -4.0010   -6.3474 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3856   -2.7122   -5.8569 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9091   -4.2496   -5.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2338   -5.7676   -4.0883 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4024   -6.0483   -3.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2514   -5.6419   -1.6258 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7597   -5.5493   -2.7810 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7798   -3.2201   -1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4987   -3.5586    0.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4190    1.3087    0.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1676   -2.5918    2.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0301   -0.1023    3.9815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9468   -0.6316    6.1688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1638   -1.8798    9.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8293   -2.2533    9.2435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1339   -0.6536    8.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2920   -4.3405    7.7392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8922   -5.5884    2.3800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5610   -6.9873    3.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7935   -6.7274    3.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6108   -3.6516    3.1715 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9258   -0.3356    0.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3729    0.6326    2.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7518    1.6470   -0.6171 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8274    3.6620    0.7686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3368    5.2956    0.3327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2200    4.8982    2.6352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9181    4.1968    4.7641 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 56  2  0
 56 57  1  0
 57 58  2  0
 58 59  1  0
  5  6  1  0
  6 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 21 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  2  0
 37 39  1  0
 39 40  2  0
 40 41  1  0
 41 42  2  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 43 46  2  0
 46 47  1  0
 46 48  1  0
 48 49  1  0
 49 50  1  0
 48 51  2  0
 35 52  1  0
 52 53  1  0
 52 54  1  0
 54 55  1  0
 17 16  1  0
 16 15  2  0
 15 13  1  0
 13 14  2  0
 13 12  1  0
 12 10  2  0
 10 11  1  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
 58  3  1  0
  7  6  1  0
 54 19  1  0
  8 15  1  0
 33 24  1  0
 51 41  1  0
  1 60  1  0
  1 61  1  0
  1 62  1  0
  4 63  1  0
 56 99  1  0
 57100  1  0
 59101  1  0
 19 68  1  6
 21 69  1  6
 22 70  1  0
 22 71  1  0
 24 72  1  6
 26 73  1  6
 27 74  1  0
 27 75  1  0
 28 76  1  0
 29 77  1  6
 30 78  1  0
 31 79  1  1
 32 80  1  0
 33 81  1  1
 34 82  1  0
 35 83  1  6
 39 84  1  0
 40 85  1  0
 42 86  1  0
 45 87  1  0
 45 88  1  0
 45 89  1  0
 47 90  1  0
 50 91  1  0
 50 92  1  0
 50 93  1  0
 51 94  1  0
 52 95  1  6
 53 96  1  0
 54 97  1  6
 55 98  1  0
 16 67  1  0
 12 66  1  0
 11 65  1  0
  9 64  1  0
M  END


  Mrv1652309122208472D          

 59 64  0  0  1  0            999 V2000
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -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
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   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
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    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
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  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
    0.0000   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -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
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    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
    4.2868   -4.1250    0.0000 C   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
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 O   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
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  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
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  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
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  6 17  2  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 39 37  1  4  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 43 46  2  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 48 51  2  0  0  0  0
 41 51  1  0  0  0  0
 35 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
 19 54  1  0  0  0  0
 54 55  1  0  0  0  0
  5 56  2  0  0  0  0
 56 57  1  0  0  0  0
 57 58  2  0  0  0  0
  3 58  1  0  0  0  0
 58 59  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325774

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC=C1O)C1=C(O[C@@H]2OC(CO[C@@H]3OC(CO)[C@@H](O)C(O)C3O)[C@@H](OC(=O)C=CC3=CC(OC)=C(O)C(OC)=C3)C(O)C2O)C=C2C(=O)C=C(O)C=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C39H42O20/c1-51-23-10-17(5-6-20(23)42)36-26(13-19-21(43)11-18(41)12-22(19)55-36)56-39-35(50)33(48)37(28(58-39)15-54-38-34(49)32(47)31(46)27(14-40)57-38)59-29(44)7-4-16-8-24(52-2)30(45)25(9-16)53-3/h4-13,27-28,31-35,37-42,45-50H,14-15H2,1-3H3/t27?,28?,31-,32?,33?,34?,35?,37-,38-,39-/m1/s1

> <INCHI_KEY>
KXMBVCSQAMEENC-GPVCNSJHSA-N

> <FORMULA>
C39H42O20

> <MOLECULAR_WEIGHT>
830.745

> <EXACT_MASS>
830.226943752

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
81.25464371333308

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,6S)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxo-5H-chromen-3-yl]oxy}-2-({[(2R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
-0.49411465933333515

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.894128499054622

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.543258562736921

> <JCHEM_PKA_STRONGEST_BASIC>
2.545121789628125

> <JCHEM_POLAR_SURFACE_AREA>
299.28

> <JCHEM_REFRACTIVITY>
202.7271

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6S)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       6.668 -11.550   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       0.000  -9.240   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       5.335 -16.940   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       5.335 -18.480   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       2.667 -18.480   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       0.000 -16.940   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   58                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   56                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    8   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16    6   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   54                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   35                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   24   34                                                  
CONECT   34   33                                                            
CONECT   35   21   36   52                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   51                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   46                                                  
CONECT   44   43   45                                                       
CONECT   45   44                                                            
CONECT   46   43   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49   51                                                  
CONECT   49   48   50                                                       
CONECT   50   49                                                            
CONECT   51   48   41                                                       
CONECT   52   35   53   54                                                  
CONECT   53   52                                                            
CONECT   54   52   19   55                                                  
CONECT   55   54                                                            
CONECT   56    5   57                                                       
CONECT   57   56   58                                                       
CONECT   58   57    3   59                                                  
CONECT   59   58                                                            
MASTER        0    0    0    0    0    0    0    0   59    0  128    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₄₂O₂₀

Average Mass

830.7450 Da

Monoisotopic Mass

830.22694 Da

IUPAC Name

(3S,6S)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxo-5H-chromen-3-yl]oxy}-2-({[(2R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

Traditional Name

(3S,6S)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC=C1O)C1=C(O[C@@H]2OC(CO[C@@H]3OC(CO)[C@@H](O)C(O)C3O)[C@@H](OC(=O)C=CC3=CC(OC)=C(O)C(OC)=C3)C(O)C2O)C=C2C(=O)C=C(O)C=C2O1

InChI Identifier

InChI=1S/C39H42O20/c1-51-23-10-17(5-6-20(23)42)36-26(13-19-21(43)11-18(41)12-22(19)55-36)56-39-35(50)33(48)37(28(58-39)15-54-38-34(49)32(47)31(46)27(14-40)57-38)59-29(44)7-4-16-8-24(52-2)30(45)25(9-16)53-3/h4-13,27-28,31-35,37-42,45-50H,14-15H2,1-3H3/t27?,28?,31-,32?,33?,34?,35?,37-,38-,39-/m1/s1

InChI Key

KXMBVCSQAMEENC-GPVCNSJHSA-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
Dioscorea alata	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	-0.49	ChemAxon
pKa (Strongest Acidic)	7.54	ChemAxon
pKa (Strongest Basic)	2.55	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	299.28 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	202.73 m³·mol⁻¹	ChemAxon
Polarizability	81.25 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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate (NP0325774)

MOL for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D MOL for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D SDF for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D-SDF for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

PDB for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D PDB for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

SMILES for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

INCHI for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

Structure for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)

3D Structure for NP0325774 ((3s,6s)-4,5-dihydroxy-6-{[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-oxochromen-3-yl]oxy}-2-({[(2r,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-3-yl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate)