NP-MRD: Showing NP-Card for Exiguaflavanone H (NP0055836)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 01:46:17 UTC

Updated at

2022-04-28 01:46:17 UTC

NP-MRD ID

NP0055836

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Exiguaflavanone H

Description

(2S)-5-hydroxy-8,8-dimethyl-10-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-2-(2,4,6-trihydroxyphenyl)-2H,3H,4H,8H-pyrano[3,2-g]chromen-4-one belongs to the class of organic compounds known as 8-prenylated flavanones. These are flavanones that features a C5-isoprenoid substituent at the 8-position. Exiguaflavanone H is found in Sophora exigua. Based on a literature review very few articles have been published on (2S)-5-hydroxy-8,8-dimethyl-10-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-2-(2,4,6-trihydroxyphenyl)-2H,3H,4H,8H-pyrano[3,2-g]chromen-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282203462D          

 37 40  0  0  1  0            999 V2000
    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 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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   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 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
   -0.4372   -0.6996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8245   -0.0288    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  1  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
   -1.4289   -1.6500    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
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  1  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    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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    0.0000    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   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  1 10  1  0  0  0  0
  8 11  1  0  0  0  0
  8 12  1  0  0  0  0
  5 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  3 26  1  0  0  0  0
 26 27  2  0  0  0  0
 24 28  1  1  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 31 35  1  0  0  0  0
 29 36  1  0  0  0  0
  2 37  1  0  0  0  0
M  END

     RDKit          3D

 71 74  0  0  0  0  0  0  0  0999 V2000
    1.9050   -0.2677   -2.4788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0833   -0.2014   -1.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2889    0.5185   -0.6848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1303   -0.8563   -0.2657 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8899   -1.9697    0.4624 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8415   -1.4906    1.4654 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1232   -1.8308    1.5093 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6860   -2.7493    0.5129 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0405   -1.2979    2.5666 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3386   -0.0404    0.6941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4562    1.0310    0.0993 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0204    2.2984   -0.1080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7502    3.2686   -0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0435    2.9131   -1.1238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7752    3.8811   -1.7221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5173    1.6403   -0.9128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7622    0.6697   -0.3069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2175   -0.6179   -0.0835 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6268   -0.8524   -0.2038 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9514   -2.2684   -0.0187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7237   -2.8505    1.2113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1947   -2.1068    2.2846 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9876   -4.1739    1.4863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5072   -4.9356    0.4587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7994   -6.2732    0.6559 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7417   -4.3785   -0.7731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4685   -3.0558   -1.0183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7306   -2.5751   -2.2792 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0943   -0.2350   -1.4756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8735    1.2516   -1.3185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7513    2.0909   -1.5104 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2797    4.6334   -0.8641 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8957    4.9917   -0.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7707    4.0183    0.2661 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1063    4.0782   -0.4858 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0067    4.4521    1.7203 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2854    2.7205    0.2624 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5826    0.2007   -3.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0602   -0.8025   -2.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2755    0.8403    0.3540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2077   -0.1318   -0.8097 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4548    1.4110   -1.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3812   -1.4382   -0.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4603   -2.5130   -0.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2007   -2.7060    0.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4770   -0.8036    2.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5966   -2.4297   -0.5265 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1318   -3.7358    0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7525   -3.0012    0.7180 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0027   -1.0104    2.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2189   -2.0399    3.3729 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5698   -0.4001    3.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0067    0.3864    1.4999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3288   -0.7560    1.2418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6610    3.8714   -2.0833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0787   -0.2602    0.6415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9777   -1.1145    2.1382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8019   -4.6113    2.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6338   -6.7146    1.5663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1460   -4.9999   -1.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1043   -3.1246   -3.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1752   -0.4215   -1.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4412   -0.5467   -2.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9094    5.3906   -1.3617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2316    6.0429   -0.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8813    3.4779    0.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4875    5.1190   -0.5318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9423    3.7531   -1.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9744    4.0487    2.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    5.5475    1.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1421    4.0420    2.2861 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  9  1  0
  7  6  2  3
  6  5  1  0
  5  4  1  0
  4 10  1  0
 10 11  1  0
 11 12  2  0
 12 37  1  0
 37 34  1  0
 34 35  1  6
 34 36  1  0
 34 33  1  0
 33 32  2  0
 32 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 29  1  0
 29 30  1  0
 30 31  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
 17 11  1  0
 27 20  1  0
 13 12  1  0
 30 16  1  0
  8 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
  9 51  1  0
  9 52  1  0
  6 46  1  0
  5 44  1  0
  5 45  1  0
  4 43  1  6
 10 53  1  0
 10 54  1  0
 35 66  1  0
 35 67  1  0
 35 68  1  0
 36 69  1  0
 36 70  1  0
 36 71  1  0
 33 65  1  0
 32 64  1  0
 15 55  1  0
 19 56  1  1
 29 62  1  0
 29 63  1  0
 22 57  1  0
 23 58  1  0
 25 59  1  0
 26 60  1  0
 28 61  1  0
  3 40  1  0
  3 41  1  0
  3 42  1  0
  1 38  1  0
  1 39  1  0
M  END


  Mrv1652304282203462D          

 37 40  0  0  1  0            999 V2000
    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 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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   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 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
   -0.4372   -0.6996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8245   -0.0288    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  1  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
   -1.4289   -1.6500    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
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  1  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    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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    0.0000    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   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  1 10  1  0  0  0  0
  8 11  1  0  0  0  0
  8 12  1  0  0  0  0
  5 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  3 26  1  0  0  0  0
 26 27  2  0  0  0  0
 24 28  1  1  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 31 35  1  0  0  0  0
 29 36  1  0  0  0  0
  2 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0055836

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC[C@@H](CC1=C2OC(C)(C)C=CC2=C(O)C2=C1O[C@@H](CC2=O)C1=C(O)C=C(O)C=C1O)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C30H34O7/c1-15(2)7-8-17(16(3)4)11-20-28-19(9-10-30(5,6)37-28)27(35)26-23(34)14-24(36-29(20)26)25-21(32)12-18(31)13-22(25)33/h7,9-10,12-13,17,24,31-33,35H,3,8,11,14H2,1-2,4-6H3/t17-,24-/m0/s1

> <INCHI_KEY>
SFDUGGMUNSJGJB-XDHUDOTRSA-N

> <FORMULA>
C30H34O7

> <MOLECULAR_WEIGHT>
506.595

> <EXACT_MASS>
506.230453435

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
53.85066409947456

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5S)-9-hydroxy-13,13-dimethyl-2-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-5-(2,4,6-trihydroxyphenyl)-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1,3(8),9,11-tetraen-7-one

> <ALOGPS_LOGP>
4.90

> <JCHEM_LOGP>
6.720831506666666

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.177134677474145

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.577460304604456

> <JCHEM_PKA_STRONGEST_BASIC>
-4.638723379076953

> <JCHEM_POLAR_SURFACE_AREA>
116.45000000000002

> <JCHEM_REFRACTIVITY>
144.58460000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.10e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5S)-9-hydroxy-13,13-dimethyl-2-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-5-(2,4,6-trihydroxyphenyl)-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1,3(8),9,11-tetraen-7-one

> <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       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.816  -1.306   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.539  -0.054   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
CONECT    1    2    6   10                                                  
CONECT    2    1    3   37                                                  
CONECT    3    2    4   26                                                  
CONECT    4    3    5   23                                                  
CONECT    5    4    6   13                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11   12                                             
CONECT    9    8   10                                                       
CONECT   10    9    1                                                       
CONECT   11    8                                                            
CONECT   12    8                                                            
CONECT   13    5   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   14   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23    4   24                                                       
CONECT   24   23   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25    3   27                                                  
CONECT   27   26                                                            
CONECT   28   24   29   33                                                  
CONECT   29   28   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   35                                                  
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33                                                            
CONECT   35   31                                                            
CONECT   36   29                                                            
CONECT   37    2                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₄O₇

Average Mass

506.5950 Da

Monoisotopic Mass

506.23045 Da

IUPAC Name

(5S)-9-hydroxy-13,13-dimethyl-2-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-5-(2,4,6-trihydroxyphenyl)-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1,3(8),9,11-tetraen-7-one

Traditional Name

(5S)-9-hydroxy-13,13-dimethyl-2-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-5-(2,4,6-trihydroxyphenyl)-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1,3(8),9,11-tetraen-7-one

CAS Registry Number

Not Available

SMILES

CC(C)=CC[C@@H](CC1=C2OC(C)(C)C=CC2=C(O)C2=C1O[C@@H](CC2=O)C1=C(O)C=C(O)C=C1O)C(C)=C

InChI Identifier

InChI=1S/C30H34O7/c1-15(2)7-8-17(16(3)4)11-20-28-19(9-10-30(5,6)37-28)27(35)26-23(34)14-24(36-29(20)26)25-21(32)12-18(31)13-22(25)33/h7,9-10,12-13,17,24,31-33,35H,3,8,11,14H2,1-2,4-6H3/t17-,24-/m0/s1

InChI Key

SFDUGGMUNSJGJB-XDHUDOTRSA-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
Sophora exigua	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-prenylated flavanones. These are flavanones that features a C5-isoprenoid substituent at the 8-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

8-prenylated flavanones

Alternative Parents

Substituents

8-prenylated flavanone
Pyranoflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Flavanone
Hydroxyflavonoid
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Aromatic monoterpenoid
Chromane
Benzopyran
Monoterpenoid
1-benzopyran
Benzenetriol
Phloroglucinol derivative
Aryl ketone
Aryl alkyl ketone
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Ketone
Polyol
Organoheterocyclic compound
Ether
Oxacycle
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
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	4.9	ALOGPS
logP	6.72	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.58	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	144.58 m³·mol⁻¹	ChemAxon
Polarizability	53.85 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

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

163006484

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Exiguaflavanone H (NP0055836)

MOL for NP0055836 (Exiguaflavanone H)

3D MOL for NP0055836 (Exiguaflavanone H)

3D SDF for NP0055836 (Exiguaflavanone H)

3D-SDF for NP0055836 (Exiguaflavanone H)

PDB for NP0055836 (Exiguaflavanone H)

3D PDB for NP0055836 (Exiguaflavanone H)

SMILES for NP0055836 (Exiguaflavanone H)

INCHI for NP0055836 (Exiguaflavanone H)

Structure for NP0055836 (Exiguaflavanone H)

3D Structure for NP0055836 (Exiguaflavanone H)