NP-MRD: Showing NP-Card for 6-Hydroxyluteolin 7-(6''-malonylglucoside) (NP0052706)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-27 23:39:56 UTC

Updated at

2022-04-27 23:39:56 UTC

NP-MRD ID

NP0052706

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-Hydroxyluteolin 7-(6''-malonylglucoside)

Description

6-Hydroxyluteolin 7-(6''-malonylglucoside) 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. Thus, 6-hydroxyluteolin 7-(6''-malonylglucoside) is considered to be a flavonoid. 6-Hydroxyluteolin 7-(6''-malonylglucoside) is found in Bryum capillare. Based on a literature review very few articles have been published on 6-hydroxyluteolin 7-(6''-malonylglucoside).

Structure

MOL 3D MOL SDF PDB SMILES InChI

  Mrv1652304282201392D          

 39 42  0  0  1  0            999 V2000
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    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
   -3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    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   -0.8250    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
   -2.8579   -0.8250    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
   -5.0013   -0.4125    0.0000 C   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
   -6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    0.4125    0.0000 C   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
   -5.0013    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  1  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   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  2  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  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    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
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 O   0  0  0  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
   -2.8579   -5.7750    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
  5  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
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 16 18  1  0  0  0  0
 15 19  1  0  0  0  0
  3 20  1  0  0  0  0
  2 21  1  0  0  0  0
  1 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  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 28  1  0  0  0  0
 27 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 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
 26 37  1  1  0  0  0
 25 38  1  6  0  0  0
 24 39  1  1  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
    5.7058   -4.7621    2.4305 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5022   -4.0448    3.4486 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1331   -4.3655    4.6383 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6073   -2.8619    3.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0413   -2.6833    2.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3812   -3.4918    1.1679 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1630   -1.6693    1.7427 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6349   -1.5015    0.4527 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6522   -1.2328   -0.6151 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1262   -1.0708   -1.8621 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4820    0.1503   -2.0989 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2666    0.2617   -1.5051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0042    0.4860   -1.9086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0249    0.5276   -0.9277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3384    0.7454   -1.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2597    0.7749   -0.2534 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5318    0.9802   -0.4801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4703    0.9936    0.6589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8083    1.1929    0.4743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6539    1.2029    1.5521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1654    1.0128    2.8276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9946    1.0174    3.9377 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8206    0.8094    3.0443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3394    0.6181    4.3433 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9782    0.8011    1.9537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9193    1.1731   -1.7817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0090    1.1550   -2.8347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3483    1.3288   -4.0197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6868    0.9342   -2.5271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7119    0.9017   -3.5314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1157    1.0967   -4.8275 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3691    0.6767   -3.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5675    0.6501   -4.2225 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4264    1.3108   -1.7554 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5305    1.2046   -2.6103 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9206    1.2421   -0.3473 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9324    1.4863    0.5916 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5666   -0.1111   -0.1679 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8009   -0.1618   -0.8023 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1536   -4.3143    4.6749 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2219   -1.9963    3.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8136   -3.0460    4.1834 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0412   -2.4108    0.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9237   -0.6267    0.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3189   -2.1300   -0.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4056    0.2054   -3.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287    0.3763    0.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2280    1.3430   -0.4890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7200    1.3622    1.3956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9955    1.1593    3.8723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9974    0.6320    5.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9216    0.6460    2.0766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9536    1.3450   -2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508    1.1018   -5.6363 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3348    0.7837   -5.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615    2.2414   -1.8981 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6684    0.2499   -2.8899 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7034    2.0192   -0.2299 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4637    2.3123    0.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7481   -0.2439    0.9201 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5466   -0.3358   -0.1869 H   0  0  0  0  0  0  0  0  0  0  0  0
 37 36  1  0
 36 38  1  0
 38 39  1  0
 38  9  1  0
  9  8  1  0
  8  7  1  0
  7  5  1  0
  5  6  2  0
  5  4  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 32  2  0
 32 33  1  0
 32 30  1  0
 30 31  1  0
 30 29  2  0
 29 27  1  0
 27 28  2  0
 27 26  1  0
 26 17  2  0
 17 16  1  0
 16 15  1  0
 15 14  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 11 34  1  0
 34 35  1  0
 34 36  1  0
 14 13  1  0
 25 18  1  0
 15 29  1  0
 37 59  1  0
 36 58  1  6
 38 60  1  1
 39 61  1  0
  9 45  1  6
  8 43  1  0
  8 44  1  0
  4 41  1  0
  4 42  1  0
  3 40  1  0
 11 46  1  6
 33 55  1  0
 31 54  1  0
 26 53  1  0
 14 47  1  0
 19 48  1  0
 20 49  1  0
 22 50  1  0
 24 51  1  0
 25 52  1  0
 34 56  1  1
 35 57  1  0
M  END

  Mrv1652304282201392D          

 39 42  0  0  1  0            999 V2000
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    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
   -3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    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   -0.8250    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
   -2.8579   -0.8250    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
   -5.0013   -0.4125    0.0000 C   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
   -6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    0.4125    0.0000 C   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
   -5.0013    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  1  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   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  2  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  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    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
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 O   0  0  0  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
   -2.8579   -5.7750    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
  5  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
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 16 18  1  0  0  0  0
 15 19  1  0  0  0  0
  3 20  1  0  0  0  0
  2 21  1  0  0  0  0
  1 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  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 28  1  0  0  0  0
 27 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 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
 26 37  1  1  0  0  0
 25 38  1  6  0  0  0
 24 39  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0052706

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@H]1[C@H](O)[C@@H](COC(=O)CC(O)=O)O[C@@H](OC2=C(O)C(O)=C3C(=O)C=C(OC3=C2)C2=CC=C(O)C(O)=C2)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H22O15/c25-9-2-1-8(3-10(9)26)12-4-11(27)18-13(37-12)5-14(19(31)21(18)33)38-24-23(35)22(34)20(32)15(39-24)7-36-17(30)6-16(28)29/h1-5,15,20,22-26,31-35H,6-7H2,(H,28,29)/t15-,20-,22+,23-,24-/m1/s1

> <INCHI_KEY>
GCZGYYNUSHMJGX-ZRKQWZGSSA-N

> <FORMULA>
C24H22O15

> <MOLECULAR_WEIGHT>
550.425

> <EXACT_MASS>
550.095870008

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
51.31523883739773

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-{[(2R,3S,4S,5R,6S)-6-{[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxo-4H-chromen-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3-oxopropanoic acid

> <ALOGPS_LOGP>
1.25

> <JCHEM_LOGP>
0.16484425333333397

> <ALOGPS_LOGS>
-2.71

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.514951475597055

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.346879694533757

> <JCHEM_PKA_STRONGEST_BASIC>
-3.649103045691378

> <JCHEM_POLAR_SURFACE_AREA>
249.96999999999997

> <JCHEM_REFRACTIVITY>
124.51569999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.07e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{[(2R,3S,4S,5R,6S)-6-{[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3-oxopropanoic acid

> <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      -5.335  -6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.668  -3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -8.002  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -10.669  -1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -12.003   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.669   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -9.336   0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0     -10.669   3.080   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0     -13.337   1.540   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -2.667  -6.160   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.334  -8.470   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.667  -6.160   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       6.668  -8.470   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       0.000 -10.780   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -2.667 -12.320   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -5.335 -10.780   0.000  0.00  0.00           O+0
CONECT    1    2    6   22                                                  
CONECT    2    1    3   21                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   12                                                       
CONECT   18   16                                                            
CONECT   19   15                                                            
CONECT   20    3                                                            
CONECT   21    2                                                            
CONECT   22    1   23                                                       
CONECT   23   22   24   28                                                  
CONECT   24   23   25   39                                                  
CONECT   25   24   26   38                                                  
CONECT   26   25   27   37                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27   23                                                       
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   26                                                            
CONECT   38   25                                                            
CONECT   39   24                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₂O₁₅

Average Mass

550.4250 Da

Monoisotopic Mass

550.09587 Da

IUPAC Name

3-{[(2R,3S,4S,5R,6S)-6-{[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxo-4H-chromen-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3-oxopropanoic acid

Traditional Name

3-{[(2R,3S,4S,5R,6S)-6-{[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3-oxopropanoic acid

CAS Registry Number

Not Available

SMILES

O[C@H]1[C@H](O)[C@@H](COC(=O)CC(O)=O)O[C@@H](OC2=C(O)C(O)=C3C(=O)C=C(OC3=C2)C2=CC=C(O)C(O)=C2)[C@@H]1O

InChI Identifier

InChI=1S/C24H22O15/c25-9-2-1-8(3-10(9)26)12-4-11(27)18-13(37-12)5-14(19(31)21(18)33)38-24-23(35)22(34)20(32)15(39-24)7-36-17(30)6-16(28)29/h1-5,15,20,22-26,31-35H,6-7H2,(H,28,29)/t15-,20-,22+,23-,24-/m1/s1

InChI Key

GCZGYYNUSHMJGX-ZRKQWZGSSA-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
Bryum capillare	-	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
Hydroxyflavonoid
Flavone
6-hydroxyflavonoid
5-hydroxyflavonoid
4'-hydroxyflavonoid
3'-hydroxyflavonoid
Phenolic glycoside
O-glycosyl compound
Glycosyl compound
Chromone
1-benzopyran
Benzopyran
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Benzenoid
1,3-dicarbonyl compound
Pyran
Oxane
Monosaccharide
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid
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	1.25	ALOGPS
logP	0.16	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	3.35	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	249.97 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	124.52 m³·mol⁻¹	ChemAxon
Polarizability	51.32 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00004395

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

163104088

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 6-Hydroxyluteolin 7-(6''-malonylglucoside) (NP0052706)

MOL for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

3D MOL for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

3D SDF for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

3D-SDF for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

PDB for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

3D PDB for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

SMILES for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

INCHI for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

Structure for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))

3D Structure for NP0052706 (6-Hydroxyluteolin 7-(6''-malonylglucoside))