NP-MRD: Showing NP-Card for (2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate (NP0220994)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 22:27:15 UTC

Updated at

2022-09-05 22:27:15 UTC

NP-MRD ID

NP0220994

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate

Description

4',5,7-Trihydroxy-3-[6-O-[3-O-(2-O,3-O,4-O-triacetyl-alpha-L-rhamnopyranosyl)-2-O,4-O-diacetyl-alpha-L-rhamnopyranosyl]-beta-D-glucopyranosyloxy]flavone belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. (2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate is found in Camellia reticulata and Camellia semiserrata. Based on a literature review very few articles have been published on 4',5,7-Trihydroxy-3-[6-O-[3-O-(2-O,3-O,4-O-triacetyl-alpha-L-rhamnopyranosyl)-2-O,4-O-diacetyl-alpha-L-rhamnopyranosyl]-beta-D-glucopyranosyloxy]flavone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062200272D          

 67 72  0  0  1  0            999 V2000
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -8.6625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  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  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
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  1  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
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  1  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
    0.0000   -2.4750    0.0000 C   0  0  1  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  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 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
   -0.7145    1.2375    0.0000 C   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
    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
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  2  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
   -0.7145   -3.7125    0.0000 C   0  0  1  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
    0.0000   -4.1250    0.0000 C   0  0  2  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
    2.1434   -6.1875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 O   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
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  2  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
    2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 29 35  1  0  0  0  0
 28 36  1  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
 39 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
 37 44  1  0  0  0  0
 44 45  1  0  0  0  0
 27 45  1  0  0  0  0
 45 46  2  0  0  0  0
 25 47  1  0  0  0  0
 47 48  1  1  0  0  0
 47 49  1  0  0  0  0
 49 50  1  6  0  0  0
 49 51  1  0  0  0  0
 23 51  1  0  0  0  0
 51 52  1  1  0  0  0
 20 53  1  0  0  0  0
 11 53  1  0  0  0  0
 53 54  1  1  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  2  0  0  0  0
  9 58  1  0  0  0  0
 58 59  1  1  0  0  0
 59 60  1  0  0  0  0
 60 61  1  0  0  0  0
 60 62  2  0  0  0  0
 58 63  1  0  0  0  0
  5 63  1  0  0  0  0
 63 64  1  1  0  0  0
 64 65  1  0  0  0  0
 65 66  1  0  0  0  0
 65 67  2  0  0  0  0
M  END

     RDKit          3D

117122  0  0  0  0  0  0  0  0999 V2000
    9.0033    1.7349   -5.5547 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2768    2.0657   -4.3137 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6839    3.0536   -3.5746 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1662    1.4335   -3.8076 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4917    1.7583   -2.6323 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0456    2.0457   -2.9419 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8585    3.5459   -2.8089 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1865    1.4161   -2.1119 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4070    1.2809   -0.8065 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5428    0.3429   -0.1979 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9254    0.8531    0.9459 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1014   -0.0836    2.1134 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9465    0.6782    3.3199 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9600    0.6630    4.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7519    1.4849    5.5144 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9721   -0.0084    4.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0044   -1.1322    2.1151 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5183   -2.4223    2.6732 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6054   -1.3766    0.7755 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8227   -0.3078    0.3539 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4513   -0.3781    0.9364 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5005   -0.3516    0.0526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7575   -0.5869    0.9782 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8635   -0.5506    0.2725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9643   -1.2422    0.6021 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7057   -1.6561   -0.5431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0055   -2.0870   -0.5516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0979   -1.2777   -0.5493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0550    0.1714   -0.5599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9548    0.8849   -0.9399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9482    2.2672   -0.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0889    2.9380   -0.4732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0864    4.3257   -0.4390 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2004    2.2512   -0.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1820    0.8878   -0.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3218   -1.8416   -0.5444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5107   -3.1242   -0.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8089   -3.6683   -0.5527 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0568   -5.0061   -0.5724 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2632   -5.6456   -0.5643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9102   -5.8317   -0.5886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6555   -5.3387   -0.5811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5109   -6.1534   -0.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4386   -3.9731   -0.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1585   -3.4680   -0.5588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2050   -4.2864   -0.5733 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6953   -2.3510    1.5959 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5930   -1.7242    2.8787 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3140   -2.9379    1.3498 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1882   -3.1080   -0.0084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3704   -1.8036    1.7680 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4287   -1.6115    3.1366 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4628    1.0289    0.6765 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2179    1.9444   -0.3839 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4540    3.0840   -0.2196 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2039    4.0470   -1.3379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0469    3.3200    0.9014 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8232    0.9320   -0.4572 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4234    2.1697   -0.0254 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0300    2.3253    1.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6224    3.6700    1.5451 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0942    1.4181    2.0217 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5939    0.5557   -1.6961 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9314    0.3995   -1.3069 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7500   -0.6792   -1.5195 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1674   -0.7064   -1.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3312   -1.6796   -2.1336 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8379    2.4559   -6.3874 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8603    0.6816   -5.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1056    1.8316   -5.3204 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9792    2.6117   -2.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8123    1.7829   -3.9953 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2864    3.9953   -3.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3717    3.8167   -1.8278 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8394    4.0838   -2.7783 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1572    2.2500   -0.2612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3802    1.8655    1.1826 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1039   -0.5695    2.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4019    1.1777    6.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0873    2.5186    5.2105 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6968    1.4963    5.8342 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1448   -0.8007    2.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1542   -3.3081    2.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0722   -2.5896    3.7014 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5946   -2.4689    2.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7025   -0.3341   -0.7291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4546   -1.1577   -0.6698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6239    0.6014   -0.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6620    0.3036    1.6751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7082   -0.5500    1.1580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0858    0.3959   -1.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0953    2.8597   -1.1949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7765    4.7959    0.4281 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1284    2.7313    0.2585 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0602    0.3332    0.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6178   -2.9672   -0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7902   -5.6649   -1.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0376   -6.9089   -0.6068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7129   -7.1531   -0.6174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4302   -3.1450    1.6202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6076   -0.7418    2.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2086   -3.8338    1.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2886   -3.3335   -0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3350   -2.1732    1.5448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5138   -1.4020    3.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9487    1.4721    1.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2785    4.9504   -0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3268    3.5979   -2.1815 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2278    4.4107   -1.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9172    0.1669    0.3381 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0820    4.1400    2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6681    4.2644    0.6318 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6652    3.4386    1.8932 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1497   -0.3021   -2.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1151   -1.0794    0.0279 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7291   -1.4167   -1.6608 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6138    0.2931   -1.0292 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 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  2  0
 28 36  1  0
 36 37  1  0
 37 38  2  0
 38 39  1  0
 39 40  1  0
 39 41  2  0
 41 42  1  0
 42 43  1  0
 42 44  2  0
 44 45  1  0
 45 46  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 32 34  1  0
 34 35  2  0
 25 47  1  0
 47 48  1  0
 47 49  1  0
 49 50  1  0
 49 51  1  0
 51 52  1  0
 20 53  1  0
 53 54  1  0
 54 55  1  0
 55 56  1  0
 55 57  2  0
 53 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 63  1  0
 63 64  1  0
 64 65  1  0
 65 66  1  0
 65 67  2  0
 63 58  1  0
 58 59  1  0
 59 60  1  0
 60 61  1  0
 60 62  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 12 17  1  0
 51 23  1  0
 58  9  1  0
 45 27  1  0
 35 29  1  0
 44 37  1  0
 18 83  1  0
 18 84  1  0
 18 85  1  0
 17 82  1  1
 20 86  1  6
 22 87  1  0
 22 88  1  0
 23 89  1  1
 25 90  1  1
 38 96  1  0
 40 97  1  0
 41 98  1  0
 43 99  1  0
 30 91  1  0
 31 92  1  0
 33 93  1  0
 34 94  1  0
 35 95  1  0
 47100  1  1
 48101  1  0
 49102  1  1
 50103  1  0
 51104  1  6
 52105  1  0
 53106  1  1
 56107  1  0
 56108  1  0
 56109  1  0
 11 77  1  1
  9 76  1  1
  6 72  1  6
  7 73  1  0
  7 74  1  0
  7 75  1  0
  5 71  1  1
  1 68  1  0
  1 69  1  0
  1 70  1  0
 63114  1  6
 66115  1  0
 66116  1  0
 66117  1  0
 58110  1  1
 61111  1  0
 61112  1  0
 61113  1  0
 12 78  1  1
 15 79  1  0
 15 80  1  0
 15 81  1  0
M  END


  Mrv1652309062200272D          

 67 72  0  0  1  0            999 V2000
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -8.6625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  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  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
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  1  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
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  1  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
    0.0000   -2.4750    0.0000 C   0  0  1  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  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 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
   -0.7145    1.2375    0.0000 C   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
    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
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  2  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
   -0.7145   -3.7125    0.0000 C   0  0  1  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
    0.0000   -4.1250    0.0000 C   0  0  2  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
    2.1434   -6.1875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 O   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
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  2  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
    2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 29 35  1  0  0  0  0
 28 36  1  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
 39 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
 37 44  1  0  0  0  0
 44 45  1  0  0  0  0
 27 45  1  0  0  0  0
 45 46  2  0  0  0  0
 25 47  1  0  0  0  0
 47 48  1  1  0  0  0
 47 49  1  0  0  0  0
 49 50  1  6  0  0  0
 49 51  1  0  0  0  0
 23 51  1  0  0  0  0
 51 52  1  1  0  0  0
 20 53  1  0  0  0  0
 11 53  1  0  0  0  0
 53 54  1  1  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  2  0  0  0  0
  9 58  1  0  0  0  0
 58 59  1  1  0  0  0
 59 60  1  0  0  0  0
 60 61  1  0  0  0  0
 60 62  2  0  0  0  0
 58 63  1  0  0  0  0
  5 63  1  0  0  0  0
 63 64  1  1  0  0  0
 64 65  1  0  0  0  0
 65 66  1  0  0  0  0
 65 67  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0220994

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=C(OC4=CC(O)=CC(O)=C4C3=O)C3=CC=C(O)C=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](OC(C)=O)[C@H](O[C@@H]2O[C@@H](C)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]2OC(C)=O)[C@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C43H50O24/c1-15-34(60-18(4)45)38(67-43-40(63-21(7)48)37(61-19(5)46)33(16(2)58-43)59-17(3)44)39(62-20(6)47)42(57-15)56-14-27-29(52)31(54)32(55)41(65-27)66-36-30(53)28-25(51)12-24(50)13-26(28)64-35(36)22-8-10-23(49)11-9-22/h8-13,15-16,27,29,31-34,37-43,49-52,54-55H,14H2,1-7H3/t15-,16-,27+,29+,31-,32+,33-,34-,37+,38+,39+,40+,41-,42+,43-/m0/s1

> <INCHI_KEY>
BDSBDFMORMRKJV-CRUVEKOYSA-N

> <FORMULA>
C43H50O24

> <MOLECULAR_WEIGHT>
950.849

> <EXACT_MASS>
950.26920249

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
117

> <JCHEM_AVERAGE_POLARIZABILITY>
91.1087130030017

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4R,5S,6S)-4,5-bis(acetyloxy)-2-{[(2R,3R,4R,5S,6S)-3,5-bis(acetyloxy)-2-{[(2R,3S,4S,5R,6S)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate

> <JCHEM_LOGP>
0.9165057193333331

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.869704432198856

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.372348425375802

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6486860463826885

> <JCHEM_POLAR_SURFACE_AREA>
334.55999999999995

> <JCHEM_REFRACTIVITY>
214.79130000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R,5S,6S)-4,5-bis(acetyloxy)-2-{[(2R,3R,4R,5S,6S)-3,5-bis(acetyloxy)-2-{[(2R,3S,4S,5R,6S)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      12.003 -14.630   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.003 -16.170   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      13.337 -16.940   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      10.669 -16.940   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.336 -16.170   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.002 -13.860   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.335 -13.860   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.002 -12.320   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       0.000  -9.240   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0       2.667 -12.320   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       4.001 -14.630   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0       6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0       5.335 -16.940   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0       5.335 -18.480   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0       4.001 -19.250   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0       6.668 -19.250   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0       8.002 -16.940   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0       8.002 -18.480   0.000  0.00  0.00           O+0
HETATM   65  C   UNK     0       9.336 -19.250   0.000  0.00  0.00           C+0
HETATM   66  C   UNK     0      10.669 -18.480   0.000  0.00  0.00           C+0
HETATM   67  O   UNK     0       9.336 -20.790   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   63                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   58                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   53                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   53                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   51                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   47                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   45                                                  
CONECT   28   27   29   36                                                  
CONECT   29   28   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   29                                                       
CONECT   36   28   37                                                       
CONECT   37   36   38   44                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   37   45                                                  
CONECT   45   44   27   46                                                  
CONECT   46   45                                                            
CONECT   47   25   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   23   52                                                  
CONECT   52   51                                                            
CONECT   53   20   11   54                                                  
CONECT   54   53   55                                                       
CONECT   55   54   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55                                                            
CONECT   58    9   59   63                                                  
CONECT   59   58   60                                                       
CONECT   60   59   61   62                                                  
CONECT   61   60                                                            
CONECT   62   60                                                            
CONECT   63   58    5   64                                                  
CONECT   64   63   65                                                       
CONECT   65   64   66   67                                                  
CONECT   66   65                                                            
CONECT   67   65                                                            
MASTER        0    0    0    0    0    0    0    0   67    0  144    0
END

View in JSmol

Synonyms

Value	Source
4',5,7-Trihydroxy-3-[6-O-[3-O-(2-O,3-O,4-O-triacetyl-a-L-rhamnopyranosyl)-2-O,4-O-diacetyl-a-L-rhamnopyranosyl]-b-D-glucopyranosyloxy]flavone	Generator
4',5,7-Trihydroxy-3-[6-O-[3-O-(2-O,3-O,4-O-triacetyl-α-L-rhamnopyranosyl)-2-O,4-O-diacetyl-α-L-rhamnopyranosyl]-β-D-glucopyranosyloxy]flavone	Generator

Chemical Formula

C₄₃H₅₀O₂₄

Average Mass

950.8490 Da

Monoisotopic Mass

950.26920 Da

IUPAC Name

(2S,3R,4R,5S,6S)-4,5-bis(acetyloxy)-2-{[(2R,3R,4R,5S,6S)-3,5-bis(acetyloxy)-2-{[(2R,3S,4S,5R,6S)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate

Traditional Name

(2S,3R,4R,5S,6S)-4,5-bis(acetyloxy)-2-{[(2R,3R,4R,5S,6S)-3,5-bis(acetyloxy)-2-{[(2R,3S,4S,5R,6S)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=C(OC4=CC(O)=CC(O)=C4C3=O)C3=CC=C(O)C=C3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](OC(C)=O)[C@H](O[C@@H]2O[C@@H](C)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]2OC(C)=O)[C@H]1OC(C)=O

InChI Identifier

InChI=1S/C43H50O24/c1-15-34(60-18(4)45)38(67-43-40(63-21(7)48)37(61-19(5)46)33(16(2)58-43)59-17(3)44)39(62-20(6)47)42(57-15)56-14-27-29(52)31(54)32(55)41(65-27)66-36-30(53)28-25(51)12-24(50)13-26(28)64-35(36)22-8-10-23(49)11-9-22/h8-13,15-16,27,29,31-34,37-43,49-52,54-55H,14H2,1-7H3/t15-,16-,27+,29+,31-,32+,33-,34-,37+,38+,39+,40+,41-,42+,43-/m0/s1

InChI Key

BDSBDFMORMRKJV-CRUVEKOYSA-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
Camellia reticulata	LOTUS Database	35616633
Camellia semiserrata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-3-O-glycosides

Alternative Parents

Substituents

Oligosaccharide
Flavonoid-3-o-glycoside
4'-hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Hydroxyflavonoid
Flavone
Pentacarboxylic acid or derivatives
O-glycosyl compound
Chromone
Glycosyl compound
1-benzopyran
Benzopyran
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Monocyclic benzene moiety
Benzenoid
Pyran
Oxane
Vinylogous acid
Heteroaromatic compound
Secondary alcohol
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Acetal
Polyol
Organic oxide
Carbonyl group
Organic oxygen compound
Alcohol
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	0.92	ChemAxon
pKa (Strongest Acidic)	6.37	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	334.56 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	214.79 m³·mol⁻¹	ChemAxon
Polarizability	91.11 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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102476664

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,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate (NP0220994)

MOL for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

3D MOL for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

3D SDF for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

3D-SDF for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

PDB for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

3D PDB for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

SMILES for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

INCHI for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

Structure for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)

3D Structure for NP0220994 ((2s,3r,4r,5s,6s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4r,5s,6s)-3,5-bis(acetyloxy)-2-{[(2r,3s,4s,5r,6s)-6-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxan-4-yl]oxy}-6-methyloxan-3-yl acetate)