NP-MRD: Showing NP-Card for 1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone (NP0138140)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-05-31 16:59:56 UTC

Updated at

2022-05-31 16:59:56 UTC

NP-MRD ID

NP0138140

Secondary Accession Numbers

NP0030932

Natural Product Identification

Common Name

1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone

Description

3,4,5,8-Tetrahydroxy-1,2-bis(3-methylbut-2-en-1-yl)-9H-xanthen-9-one belongs to the class of organic compounds known as 8-prenylated xanthones. These are organic compounds containing a C5-isoprenoid group linked to a xanthone moiety at the 8-position. Xanthone is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring that carries a ketone group. Based on a literature review very few articles have been published on 3,4,5,8-tetrahydroxy-1,2-bis(3-methylbut-2-en-1-yl)-9H-xanthen-9-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100093D          

 53 55  0  0  0  0            999 V2000
    5.1795    3.8823   -0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6702    2.4941   -0.7106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7383    1.5377   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    2.2064   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6642    0.8916   -0.8142 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8172    0.4672    0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4388   -0.1608    1.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7959   -0.3452    1.5599 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6982   -0.6360    2.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -1.2565    3.5757 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3174   -0.4868    2.5863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2978   -0.9998    3.7013 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6499   -0.8583    3.8324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2240   -1.3538    5.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4553   -1.9437    5.9707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936   -1.2630    5.2290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4068   -0.6702    4.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8399   -0.1763    3.0901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6987    0.3877    2.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4575   -0.2670    2.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8230    0.2430    1.6512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5534    0.7017    0.7803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3406    0.1599    1.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4015    0.6755    0.4233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2879    1.4340   -0.7085 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7819    0.5233   -1.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5849    0.6231   -3.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1780    1.7179   -3.8257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673   -0.4059   -4.0680 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9331    3.8458    0.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6354    4.3195   -1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    4.5568   -0.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2593    1.9447   -2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3533    0.5569   -1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4715    1.3863   -0.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    3.0101   -0.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3653    0.0803   -1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650    0.9693   -1.7234 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2358    0.3071    0.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973   -1.2589    3.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318   -1.9259    5.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0248   -1.6527    6.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4793   -0.5944    4.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1684    0.6621    1.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3914    2.2020   -1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1157    2.0342   -0.3199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3931   -0.3053   -1.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4508    2.1891   -4.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0644    1.3043   -4.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5103    2.5116   -3.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3700   -0.8876   -4.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8644    0.0678   -4.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7133   -1.1921   -3.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 18  1  0  0  0  0
 18 20  2  0  0  0  0
 21 22  2  0  0  0  0
 23 21  1  0  0  0  0
 18 19  1  0  0  0  0
 11 12  1  0  0  0  0
 14 15  1  0  0  0  0
 12 13  1  0  0  0  0
  9 10  1  0  0  0  0
 20 21  1  0  0  0  0
  7  8  1  0  0  0  0
  6 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 23  1  0  0  0  0
  6  5  1  0  0  0  0
 20 13  1  0  0  0  0
  5  4  1  0  0  0  0
 23 11  2  0  0  0  0
  4  2  2  3  0  0  0
 13 14  2  0  0  0  0
  2  1  1  0  0  0  0
  9  7  2  0  0  0  0
 25 26  1  0  0  0  0
 14 16  1  0  0  0  0
 26 27  2  3  0  0  0
 11  9  1  0  0  0  0
 27 28  1  0  0  0  0
 16 17  2  0  0  0  0
 27 29  1  0  0  0  0
  7  6  1  0  0  0  0
  2  3  1  0  0  0  0
 16 42  1  0  0  0  0
 17 43  1  0  0  0  0
 19 44  1  0  0  0  0
 15 41  1  0  0  0  0
 10 40  1  0  0  0  0
  8 39  1  0  0  0  0
 25 45  1  0  0  0  0
 25 46  1  0  0  0  0
  5 37  1  0  0  0  0
  5 38  1  0  0  0  0
  4 36  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
 26 47  1  0  0  0  0
 28 48  1  0  0  0  0
 28 49  1  0  0  0  0
 28 50  1  0  0  0  0
 29 51  1  0  0  0  0
 29 52  1  0  0  0  0
 29 53  1  0  0  0  0
  3 33  1  0  0  0  0
  3 34  1  0  0  0  0
  3 35  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    5.1795    3.8823   -0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6702    2.4941   -0.7106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7383    1.5377   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    2.2064   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6642    0.8916   -0.8142 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8172    0.4672    0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4388   -0.1608    1.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7959   -0.3452    1.5599 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6982   -0.6360    2.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -1.2565    3.5757 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3174   -0.4868    2.5863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2978   -0.9998    3.7013 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6499   -0.8583    3.8324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2240   -1.3538    5.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4553   -1.9437    5.9707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936   -1.2630    5.2290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4068   -0.6702    4.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8399   -0.1763    3.0901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6987    0.3877    2.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4575   -0.2670    2.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8230    0.2430    1.6512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5534    0.7017    0.7803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3406    0.1599    1.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4015    0.6755    0.4233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2879    1.4340   -0.7085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7819    0.5233   -1.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5849    0.6231   -3.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1780    1.7179   -3.8257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673   -0.4059   -4.0680 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9331    3.8458    0.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6354    4.3195   -1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    4.5568   -0.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2593    1.9447   -2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3533    0.5569   -1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4715    1.3863   -0.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    3.0101   -0.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3653    0.0803   -1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650    0.9693   -1.7234 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2358    0.3071    0.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973   -1.2589    3.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318   -1.9259    5.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0248   -1.6527    6.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4793   -0.5944    4.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1684    0.6621    1.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3914    2.2020   -1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1157    2.0342   -0.3199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3931   -0.3053   -1.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4508    2.1891   -4.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0644    1.3043   -4.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5103    2.5116   -3.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3700   -0.8876   -4.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8644    0.0678   -4.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7133   -1.1921   -3.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 18  1  0
 18 20  2  0
 21 22  2  0
 23 21  1  0
 18 19  1  0
 11 12  1  0
 14 15  1  0
 12 13  1  0
  9 10  1  0
 20 21  1  0
  7  8  1  0
  6 24  2  0
 24 25  1  0
 24 23  1  0
  6  5  1  0
 20 13  1  0
  5  4  1  0
 23 11  2  0
  4  2  2  3
 13 14  2  0
  2  1  1  0
  9  7  2  0
 25 26  1  0
 14 16  1  0
 26 27  2  3
 11  9  1  0
 27 28  1  0
 16 17  2  0
 27 29  1  0
  7  6  1  0
  2  3  1  0
 16 42  1  0
 17 43  1  0
 19 44  1  0
 15 41  1  0
 10 40  1  0
  8 39  1  0
 25 45  1  0
 25 46  1  0
  5 37  1  0
  5 38  1  0
  4 36  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 26 47  1  0
 28 48  1  0
 28 49  1  0
 28 50  1  0
 29 51  1  0
 29 52  1  0
 29 53  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
M  END


  Mrv1652306202100093D          

 53 55  0  0  0  0            999 V2000
    5.1795    3.8823   -0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6702    2.4941   -0.7106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7383    1.5377   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    2.2064   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6642    0.8916   -0.8142 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8172    0.4672    0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4388   -0.1608    1.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7959   -0.3452    1.5599 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6982   -0.6360    2.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -1.2565    3.5757 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3174   -0.4868    2.5863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2978   -0.9998    3.7013 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6499   -0.8583    3.8324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2240   -1.3538    5.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4553   -1.9437    5.9707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936   -1.2630    5.2290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4068   -0.6702    4.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8399   -0.1763    3.0901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6987    0.3877    2.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4575   -0.2670    2.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8230    0.2430    1.6512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5534    0.7017    0.7803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3406    0.1599    1.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4015    0.6755    0.4233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2879    1.4340   -0.7085 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7819    0.5233   -1.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5849    0.6231   -3.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1780    1.7179   -3.8257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673   -0.4059   -4.0680 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9331    3.8458    0.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6354    4.3195   -1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    4.5568   -0.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2593    1.9447   -2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3533    0.5569   -1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4715    1.3863   -0.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    3.0101   -0.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3653    0.0803   -1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650    0.9693   -1.7234 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2358    0.3071    0.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973   -1.2589    3.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318   -1.9259    5.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0248   -1.6527    6.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4793   -0.5944    4.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1684    0.6621    1.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3914    2.2020   -1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1157    2.0342   -0.3199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3931   -0.3053   -1.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4508    2.1891   -4.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0644    1.3043   -4.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5103    2.5116   -3.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3700   -0.8876   -4.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8644    0.0678   -4.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7133   -1.1921   -3.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 18  1  0  0  0  0
 18 20  2  0  0  0  0
 21 22  2  0  0  0  0
 23 21  1  0  0  0  0
 18 19  1  0  0  0  0
 11 12  1  0  0  0  0
 14 15  1  0  0  0  0
 12 13  1  0  0  0  0
  9 10  1  0  0  0  0
 20 21  1  0  0  0  0
  7  8  1  0  0  0  0
  6 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 23  1  0  0  0  0
  6  5  1  0  0  0  0
 20 13  1  0  0  0  0
  5  4  1  0  0  0  0
 23 11  2  0  0  0  0
  4  2  2  3  0  0  0
 13 14  2  0  0  0  0
  2  1  1  0  0  0  0
  9  7  2  0  0  0  0
 25 26  1  0  0  0  0
 14 16  1  0  0  0  0
 26 27  2  3  0  0  0
 11  9  1  0  0  0  0
 27 28  1  0  0  0  0
 16 17  2  0  0  0  0
 27 29  1  0  0  0  0
  7  6  1  0  0  0  0
  2  3  1  0  0  0  0
 16 42  1  0  0  0  0
 17 43  1  0  0  0  0
 19 44  1  0  0  0  0
 15 41  1  0  0  0  0
 10 40  1  0  0  0  0
  8 39  1  0  0  0  0
 25 45  1  0  0  0  0
 25 46  1  0  0  0  0
  5 37  1  0  0  0  0
  5 38  1  0  0  0  0
  4 36  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
 26 47  1  0  0  0  0
 28 48  1  0  0  0  0
 28 49  1  0  0  0  0
 28 50  1  0  0  0  0
 29 51  1  0  0  0  0
 29 52  1  0  0  0  0
 29 53  1  0  0  0  0
  3 33  1  0  0  0  0
  3 34  1  0  0  0  0
  3 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138140

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2OC3=C(C(=O)C2=C(O[H])C([H])=C1[H])C(=C(C(O[H])=C3O[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O6/c1-11(2)5-7-13-14(8-6-12(3)4)19(26)21(28)23-17(13)20(27)18-15(24)9-10-16(25)22(18)29-23/h5-6,9-10,24-26,28H,7-8H2,1-4H3

> <INCHI_KEY>
SHZLJVCQGYKZLS-UHFFFAOYSA-N

> <FORMULA>
C23H24O6

> <MOLECULAR_WEIGHT>
396.439

> <EXACT_MASS>
396.157288493

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
43.20313369786342

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,4,5,8-tetrahydroxy-1,2-bis(3-methylbut-2-en-1-yl)-9H-xanthen-9-one

> <ALOGPS_LOGP>
4.18

> <JCHEM_LOGP>
5.852512932333334

> <ALOGPS_LOGS>
-4.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.344679769889183

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.273625700583685

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8493501886407997

> <JCHEM_POLAR_SURFACE_AREA>
107.22

> <JCHEM_REFRACTIVITY>
113.22549999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.91e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,4,5,8-tetrahydroxy-1,2-bis(3-methylbut-2-en-1-yl)xanthen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    5.1795    3.8823   -0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6702    2.4941   -0.7106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7383    1.5377   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    2.2064   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6642    0.8916   -0.8142 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8172    0.4672    0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4388   -0.1608    1.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7959   -0.3452    1.5599 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6982   -0.6360    2.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -1.2565    3.5757 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3174   -0.4868    2.5863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2978   -0.9998    3.7013 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6499   -0.8583    3.8324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2240   -1.3538    5.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4553   -1.9437    5.9707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936   -1.2630    5.2290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4068   -0.6702    4.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8399   -0.1763    3.0901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6987    0.3877    2.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4575   -0.2670    2.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8230    0.2430    1.6512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5534    0.7017    0.7803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3406    0.1599    1.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4015    0.6755    0.4233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2879    1.4340   -0.7085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7819    0.5233   -1.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5849    0.6231   -3.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1780    1.7179   -3.8257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673   -0.4059   -4.0680 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9331    3.8458    0.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6354    4.3195   -1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    4.5568   -0.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2593    1.9447   -2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3533    0.5569   -1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4715    1.3863   -0.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    3.0101   -0.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3653    0.0803   -1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650    0.9693   -1.7234 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2358    0.3071    0.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973   -1.2589    3.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318   -1.9259    5.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0248   -1.6527    6.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4793   -0.5944    4.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1684    0.6621    1.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3914    2.2020   -1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1157    2.0342   -0.3199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3931   -0.3053   -1.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4508    2.1891   -4.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0644    1.3043   -4.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5103    2.5116   -3.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3700   -0.8876   -4.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8644    0.0678   -4.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7133   -1.1921   -3.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 18  1  0
 18 20  2  0
 21 22  2  0
 23 21  1  0
 18 19  1  0
 11 12  1  0
 14 15  1  0
 12 13  1  0
  9 10  1  0
 20 21  1  0
  7  8  1  0
  6 24  2  0
 24 25  1  0
 24 23  1  0
  6  5  1  0
 20 13  1  0
  5  4  1  0
 23 11  2  0
  4  2  2  3
 13 14  2  0
  2  1  1  0
  9  7  2  0
 25 26  1  0
 14 16  1  0
 26 27  2  3
 11  9  1  0
 27 28  1  0
 16 17  2  0
 27 29  1  0
  7  6  1  0
  2  3  1  0
 16 42  1  0
 17 43  1  0
 19 44  1  0
 15 41  1  0
 10 40  1  0
  8 39  1  0
 25 45  1  0
 25 46  1  0
  5 37  1  0
  5 38  1  0
  4 36  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 26 47  1  0
 28 48  1  0
 28 49  1  0
 28 50  1  0
 29 51  1  0
 29 52  1  0
 29 53  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       5.180   3.882  -0.412  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.670   2.494  -0.711  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.738   1.538  -1.167  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.360   2.206  -0.578  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.664   0.892  -0.814  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.817   0.467   0.376  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.439  -0.161   1.467  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.796  -0.345   1.560  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.698  -0.636   2.544  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.357  -1.256   3.576  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.317  -0.487   2.586  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.298  -1.000   3.701  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.650  -0.858   3.832  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.224  -1.354   5.006  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.455  -1.944   5.971  0.00  0.00           O+0
HETATM   16  C   UNK     0      -3.594  -1.263   5.229  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.407  -0.670   4.264  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.840  -0.176   3.090  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.699   0.388   2.185  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.458  -0.267   2.874  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.823   0.243   1.651  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.553   0.702   0.780  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.341   0.160   1.532  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.402   0.676   0.423  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.288   1.434  -0.709  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.782   0.523  -1.802  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.585   0.623  -3.133  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.178   1.718  -3.826  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.167  -0.406  -4.068  0.00  0.00           C+0
HETATM   30  H   UNK     0       5.933   3.846   0.381  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.635   4.319  -1.307  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.383   4.557  -0.082  0.00  0.00           H+0
HETATM   33  H   UNK     0       6.259   1.945  -2.040  0.00  0.00           H+0
HETATM   34  H   UNK     0       5.353   0.557  -1.452  0.00  0.00           H+0
HETATM   35  H   UNK     0       6.471   1.386  -0.368  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.691   3.010  -0.265  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.365   0.080  -1.036  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.065   0.969  -1.723  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.236   0.307   0.986  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.297  -1.259   3.302  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.532  -1.926   5.652  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.025  -1.653   6.147  0.00  0.00           H+0
HETATM   43  H   UNK     0      -5.479  -0.594   4.423  0.00  0.00           H+0
HETATM   44  H   UNK     0      -4.168   0.662   1.402  0.00  0.00           H+0
HETATM   45  H   UNK     0       0.391   2.202  -1.087  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.116   2.034  -0.320  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.393  -0.305  -1.442  0.00  0.00           H+0
HETATM   48  H   UNK     0      -0.451   2.189  -4.589  0.00  0.00           H+0
HETATM   49  H   UNK     0       1.064   1.304  -4.318  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.510   2.512  -3.154  0.00  0.00           H+0
HETATM   51  H   UNK     0      -0.370  -0.888  -4.644  0.00  0.00           H+0
HETATM   52  H   UNK     0      -1.864   0.068  -4.767  0.00  0.00           H+0
HETATM   53  H   UNK     0      -1.713  -1.192  -3.536  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    4    1    3                                                  
CONECT    3    2   33   34   35                                             
CONECT    4    5    2   36                                                  
CONECT    5    6    4   37   38                                             
CONECT    6   24    5    7                                                  
CONECT    7    8    9    6                                                  
CONECT    8    7   39                                                       
CONECT    9   10    7   11                                                  
CONECT   10    9   40                                                       
CONECT   11   12   23    9                                                  
CONECT   12   11   13                                                       
CONECT   13   12   20   14                                                  
CONECT   14   15   13   16                                                  
CONECT   15   14   41                                                       
CONECT   16   14   17   42                                                  
CONECT   17   18   16   43                                                  
CONECT   18   17   20   19                                                  
CONECT   19   18   44                                                       
CONECT   20   18   21   13                                                  
CONECT   21   22   23   20                                                  
CONECT   22   21                                                            
CONECT   23   21   24   11                                                  
CONECT   24    6   25   23                                                  
CONECT   25   24   26   45   46                                             
CONECT   26   25   27   47                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27   48   49   50                                             
CONECT   29   27   51   52   53                                             
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    3                                                            
CONECT   34    3                                                            
CONECT   35    3                                                            
CONECT   36    4                                                            
CONECT   37    5                                                            
CONECT   38    5                                                            
CONECT   39    8                                                            
CONECT   40   10                                                            
CONECT   41   15                                                            
CONECT   42   16                                                            
CONECT   43   17                                                            
CONECT   44   19                                                            
CONECT   45   25                                                            
CONECT   46   25                                                            
CONECT   47   26                                                            
CONECT   48   28                                                            
CONECT   49   28                                                            
CONECT   50   28                                                            
CONECT   51   29                                                            
CONECT   52   29                                                            
CONECT   53   29                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  110    0
END

RDKit          3D

53 55  0  0  0  0  0  0  0  0999 V2000
    5.1795    3.8823   -0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6702    2.4941   -0.7106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7383    1.5377   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    2.2064   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6642    0.8916   -0.8142 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8172    0.4672    0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4388   -0.1608    1.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7959   -0.3452    1.5599 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6982   -0.6360    2.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -1.2565    3.5757 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3174   -0.4868    2.5863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2978   -0.9998    3.7013 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6499   -0.8583    3.8324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2240   -1.3538    5.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4553   -1.9437    5.9707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936   -1.2630    5.2290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4068   -0.6702    4.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8399   -0.1763    3.0901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6987    0.3877    2.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4575   -0.2670    2.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8230    0.2430    1.6512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5534    0.7017    0.7803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3406    0.1599    1.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4015    0.6755    0.4233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2879    1.4340   -0.7085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7819    0.5233   -1.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5849    0.6231   -3.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1780    1.7179   -3.8257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673   -0.4059   -4.0680 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9331    3.8458    0.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6354    4.3195   -1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    4.5568   -0.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2593    1.9447   -2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3533    0.5569   -1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4715    1.3863   -0.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    3.0101   -0.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3653    0.0803   -1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650    0.9693   -1.7234 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2358    0.3071    0.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2973   -1.2589    3.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318   -1.9259    5.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0248   -1.6527    6.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4793   -0.5944    4.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1684    0.6621    1.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3914    2.2020   -1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1157    2.0342   -0.3199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3931   -0.3053   -1.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4508    2.1891   -4.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0644    1.3043   -4.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5103    2.5116   -3.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3700   -0.8876   -4.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8644    0.0678   -4.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7133   -1.1921   -3.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 18  1  0
 18 20  2  0
 21 22  2  0
 23 21  1  0
 18 19  1  0
 11 12  1  0
 14 15  1  0
 12 13  1  0
  9 10  1  0
 20 21  1  0
  7  8  1  0
  6 24  2  0
 24 25  1  0
 24 23  1  0
  6  5  1  0
 20 13  1  0
  5  4  1  0
 23 11  2  0
  4  2  2  3
 13 14  2  0
  2  1  1  0
  9  7  2  0
 25 26  1  0
 14 16  1  0
 26 27  2  3
 11  9  1  0
 27 28  1  0
 16 17  2  0
 27 29  1  0
  7  6  1  0
  2  3  1  0
 16 42  1  0
 17 43  1  0
 19 44  1  0
 15 41  1  0
 10 40  1  0
  8 39  1  0
 25 45  1  0
 25 46  1  0
  5 37  1  0
  5 38  1  0
  4 36  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 26 47  1  0
 28 48  1  0
 28 49  1  0
 28 50  1  0
 29 51  1  0
 29 52  1  0
 29 53  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₄O₆

Average Mass

396.4390 Da

Monoisotopic Mass

396.15729 Da

IUPAC Name

3,4,5,8-tetrahydroxy-1,2-bis(3-methylbut-2-en-1-yl)-9H-xanthen-9-one

Traditional Name

3,4,5,8-tetrahydroxy-1,2-bis(3-methylbut-2-en-1-yl)xanthen-9-one

CAS Registry Number

776325-66-7

SMILES

[H]OC1=C2OC3=C(C(=O)C2=C(O[H])C([H])=C1[H])C(=C(C(O[H])=C3O[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C23H24O6/c1-11(2)5-7-13-14(8-6-12(3)4)19(26)21(28)23-17(13)20(27)18-15(24)9-10-16(25)22(18)29-23/h5-6,9-10,24-26,28H,7-8H2,1-4H3

InChI Key

SHZLJVCQGYKZLS-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-prenylated xanthones. These are organic compounds containing a C5-isoprenoid group linked to a xanthone moiety at the 8-position. Xanthone is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring that carries a ketone group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

8-prenylated xanthones

Alternative Parents

Substituents

2-prenylated xanthone
8-prenylated xanthone
Chromone
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Polyol
Oxacycle
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.18	ALOGPS
logP	5.85	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	7.27	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	113.23 m³·mol⁻¹	ChemAxon
Polarizability	43.2 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

8267670

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone (NP0138140)

MOL for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

3D MOL for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

3D SDF for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

3D-SDF for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

PDB for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

3D PDB for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

SMILES for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

INCHI for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

Structure for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)

3D Structure for NP0138140 (1,4,5,6-Tetrahydroxy-7,8-diprenylxanthone)