NP-MRD: Showing NP-Card for Haploside C (NP0053989)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 00:29:06 UTC

Updated at

2022-04-28 00:29:06 UTC

NP-MRD ID

NP0053989

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Haploside C

Description

[(2S,3S,4S,5S,6S)-6-{[3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-4-oxo-4H-chromen-7-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetate belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Haploside C is found in Haplophyllum acutifolium and Haplophyllum perforatum. Based on a literature review very few articles have been published on [(2S,3S,4S,5S,6S)-6-{[3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-4-oxo-4H-chromen-7-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282202292D          

 49 53  0  0  1  0            999 V2000
   -0.7145   -0.4125    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 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
    0.7145   -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
    0.0000    0.8250    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
    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
    2.1434   -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
    2.8579   -1.6500    0.0000 O   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 C   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
    4.2868   -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
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   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  1  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  1  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
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    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
   -4.2868   -1.6500    0.0000 O   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
   -2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 O   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
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 23  1  0  0  0  0
  3 24  1  0  0  0  0
  1 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  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 26 31  1  0  0  0  0
 30 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 29 37  1  1  0  0  0
 28 38  1  6  0  0  0
 27 39  1  6  0  0  0
 40 39  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  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
 40 45  1  0  0  0  0
 44 46  1  6  0  0  0
 43 47  1  6  0  0  0
 42 48  1  6  0  0  0
 41 49  1  1  0  0  0
M  END

     RDKit          3D

 85 89  0  0  0  0  0  0  0  0999 V2000
    9.9718    0.1174   -1.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5401    1.4216   -0.8601 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2172    1.6282   -0.5091 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3320    0.5335   -0.4805 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0256    0.6676   -0.1428 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0223   -0.3796    0.0080 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7368   -0.0091   -0.1536 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7303   -0.8252   -0.0517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4182   -0.3826   -0.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3035    0.9912   -0.5197 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1927    1.9379    0.5324 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3266   -1.2015   -0.1397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9099   -0.6132   -0.3499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1581   -1.1927   -0.3096 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7478   -1.4711   -1.5285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9773   -2.0529   -1.4679 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8127   -3.5245   -1.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0494   -4.1826   -2.1519 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7775   -5.5298   -2.0638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9816   -6.2603   -3.0847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2269   -6.1643   -1.0694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9707   -1.4725   -0.5251 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1436   -2.2112   -0.5478 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3392   -1.4524    0.8499 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2432   -0.8477    1.7088 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1184   -0.5051    0.6381 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6988    0.5845   -0.0095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7230    1.7502    0.6928 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0233    2.1562    1.0394 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8730    3.2101    1.9396 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1886    3.6481    2.5323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2373    4.4119    1.2795 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9014    4.7504    0.1270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8044    4.0083    0.9083 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1628    5.0046    0.2106 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9949    2.8248   -0.0500 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8263    2.3390   -0.5657 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5184   -2.5239    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7916   -2.9970    0.3330 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0425   -4.3479    0.6305 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8983   -2.1603    0.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1668   -2.6066    0.4146 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3620   -3.8037    0.6756 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2408   -1.6897    0.2977 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4560   -2.2248    0.5101 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6282    1.9857    0.1720 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4828    3.0542    0.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8065    2.9010   -0.1971 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6877    3.9719   -0.2286 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4183   -0.3039   -2.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0524    0.0992   -1.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7427   -0.5397   -0.3122 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7123   -0.4345   -0.7971 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2104    2.9594    0.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2646    1.7684    1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0364    1.8135    1.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0158   -2.2274    0.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4926   -2.0467   -2.4811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7894   -4.0501   -1.1018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3092   -3.7312   -0.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4904   -7.1664   -2.6360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6928   -6.6538   -3.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2504   -5.6188   -3.5963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1906   -0.4060   -0.7815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5567   -2.1105   -1.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0032   -2.4268    1.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0759   -1.3819    1.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7366   -0.3073    1.6304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2197    1.5760    1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1941    2.9013    2.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4331    3.0638    3.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1025    4.6935    2.8303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9904    3.5735    1.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1578    5.2222    2.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6726    4.1347    0.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2743    3.6389    1.7930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8965    5.7723    0.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6757    3.2421   -0.8541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6637    2.7007   -1.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3137   -3.2084    0.2309 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3219   -5.0366    0.7223 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3303   -1.8710    0.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5861    2.1263    0.4480 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1588    4.0709    0.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3555    4.8984    0.0045 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 46  2  0
 46 47  1  0
 47 48  2  0
 48 49  1  0
  5  6  1  0
  6 44  2  0
 44 45  1  0
 44 42  1  0
 42 43  2  0
 42 41  1  0
 41 39  2  0
 39 40  1  0
 39 38  1  0
 38 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 16 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 12  9  1  0
  9 10  1  0
 10 11  1  0
  9  8  2  0
  8  7  1  0
 48  3  1  0
  7  6  1  0
  8 41  1  0
 26 14  1  0
 36 28  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
  4 53  1  0
 46 83  1  0
 47 84  1  0
 49 85  1  0
 45 82  1  0
 40 81  1  0
 38 80  1  0
 14 57  1  1
 16 58  1  6
 17 59  1  0
 17 60  1  0
 20 61  1  0
 20 62  1  0
 20 63  1  0
 22 64  1  6
 23 65  1  0
 24 66  1  1
 25 67  1  0
 26 68  1  1
 28 69  1  1
 30 70  1  1
 31 71  1  0
 31 72  1  0
 31 73  1  0
 32 74  1  1
 33 75  1  0
 34 76  1  1
 35 77  1  0
 36 78  1  6
 37 79  1  0
 11 54  1  0
 11 55  1  0
 11 56  1  0
M  END


  Mrv1652304282202292D          

 49 53  0  0  1  0            999 V2000
   -0.7145   -0.4125    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 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
    0.7145   -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
    0.0000    0.8250    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
    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
    2.1434   -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
    2.8579   -1.6500    0.0000 O   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 C   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
    4.2868   -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
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   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  1  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  1  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
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    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
   -4.2868   -1.6500    0.0000 O   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
   -2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 O   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
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 23  1  0  0  0  0
  3 24  1  0  0  0  0
  1 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  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 26 31  1  0  0  0  0
 30 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 29 37  1  1  0  0  0
 28 38  1  6  0  0  0
 27 39  1  6  0  0  0
 40 39  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  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
 40 45  1  0  0  0  0
 44 46  1  6  0  0  0
 43 47  1  6  0  0  0
 42 48  1  6  0  0  0
 41 49  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0053989

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC=C1O)C1=C(O)C(=O)C2=C(O)C=C(O[C@@H]3O[C@@H](COC(C)=O)[C@@H](O)[C@H](O)[C@@H]3O[C@@H]3O[C@H](C)[C@H](O)[C@H](O)[C@H]3O)C(OC)=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C31H36O18/c1-10-19(35)22(38)25(41)30(45-10)49-29-23(39)20(36)17(9-44-11(2)32)47-31(29)46-16-8-14(34)18-21(37)24(40)26(48-28(18)27(16)43-4)12-5-6-13(33)15(7-12)42-3/h5-8,10,17,19-20,22-23,25,29-31,33-36,38-41H,9H2,1-4H3/t10-,17+,19+,20-,22+,23+,25-,29+,30+,31-/m1/s1

> <INCHI_KEY>
JGGRFKDDIGORCC-GWMNVLECSA-N

> <FORMULA>
C31H36O18

> <MOLECULAR_WEIGHT>
696.611

> <EXACT_MASS>
696.190164319

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
66.56635649134925

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2S,3S,4S,5S,6S)-6-{[3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-4-oxo-4H-chromen-7-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetate

> <ALOGPS_LOGP>
0.64

> <JCHEM_LOGP>
-0.4063461076666665

> <ALOGPS_LOGS>
-2.64

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.767230681400239

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.557080257508948

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6121826294490695

> <JCHEM_POLAR_SURFACE_AREA>
269.81999999999994

> <JCHEM_REFRACTIVITY>
159.9732

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.61e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2S,3S,4S,5S,6S)-6-{[3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-4-oxochromen-7-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -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  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -3.080   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  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -8.002   0.000   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -5.335   1.540   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -9.336   3.850   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -9.336   2.310   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -8.002   1.540   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0     -10.669   1.540   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0     -10.669   4.620   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      -8.002   6.160   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      -5.335   4.620   0.000  0.00  0.00           O+0
CONECT    1    2    6   25                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    5   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11    4   13                                                  
CONECT   13   12                                                            
CONECT   14   11                                                            
CONECT   15   10   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19   15                                                       
CONECT   21   19   22                                                       
CONECT   22   21                                                            
CONECT   23   18                                                            
CONECT   24    3                                                            
CONECT   25    1   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28   39                                                  
CONECT   28   27   29   38                                                  
CONECT   29   28   30   37                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30   26                                                       
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   29                                                            
CONECT   38   28                                                            
CONECT   39   27   40                                                       
CONECT   40   39   41   45                                                  
CONECT   41   40   42   49                                                  
CONECT   42   41   43   48                                                  
CONECT   43   42   44   47                                                  
CONECT   44   43   45   46                                                  
CONECT   45   44   40                                                       
CONECT   46   44                                                            
CONECT   47   43                                                            
CONECT   48   42                                                            
CONECT   49   41                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Value	Source
[(2S,3S,4S,5S,6S)-6-{[3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-4-oxo-4H-chromen-7-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetic acid	Generator

Chemical Formula

C₃₁H₃₆O₁₈

Average Mass

696.6110 Da

Monoisotopic Mass

696.19016 Da

IUPAC Name

Traditional Name

[(2S,3S,4S,5S,6S)-6-{[3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-4-oxochromen-7-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC=C1O)C1=C(O)C(=O)C2=C(O)C=C(O[C@@H]3O[C@@H](COC(C)=O)[C@@H](O)[C@H](O)[C@@H]3O[C@@H]3O[C@H](C)[C@H](O)[C@H](O)[C@H]3O)C(OC)=C2O1

InChI Identifier

InChI=1S/C31H36O18/c1-10-19(35)22(38)25(41)30(45-10)49-29-23(39)20(36)17(9-44-11(2)32)47-31(29)46-16-8-14(34)18-21(37)24(40)26(48-28(18)27(16)43-4)12-5-6-13(33)15(7-12)42-3/h5-8,10,17,19-20,22-23,25,29-31,33-36,38-41H,9H2,1-4H3/t10-,17+,19+,20-,22+,23+,25-,29+,30+,31-/m1/s1

InChI Key

JGGRFKDDIGORCC-GWMNVLECSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Haplophyllum acutifolium	LOTUS Database	35616633
Haplophyllum perforatum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

Flavonoid-7-o-glycoside
3-hydroxyflavone
8-methoxyflavonoid-skeleton
3p-methoxyflavonoid-skeleton
Hydroxyflavonoid
Flavone
5-hydroxyflavonoid
4'-hydroxyflavonoid
3-hydroxyflavonoid
Phenolic glycoside
O-glycosyl compound
Glycosyl compound
Disaccharide
Chromone
1-benzopyran
Methoxyphenol
Benzopyran
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Alkyl aryl ether
Benzenoid
Pyran
Oxane
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	0.64	ALOGPS
logP	-0.41	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	7.56	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	269.82 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	159.97 m³·mol⁻¹	ChemAxon
Polarizability	66.57 Å³	ChemAxon
Number of Rings	5	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

162961595

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Haploside C (NP0053989)

MOL for NP0053989 (Haploside C)

3D MOL for NP0053989 (Haploside C)

3D SDF for NP0053989 (Haploside C)

3D-SDF for NP0053989 (Haploside C)

PDB for NP0053989 (Haploside C)

3D PDB for NP0053989 (Haploside C)

SMILES for NP0053989 (Haploside C)

INCHI for NP0053989 (Haploside C)

Structure for NP0053989 (Haploside C)

3D Structure for NP0053989 (Haploside C)