NP-MRD: Showing NP-Card for xanthohumol B (NP0027944)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2021-06-19 19:57:44 UTC

Updated at

2021-06-29 23:54:24 UTC

NP-MRD ID

NP0027944

Secondary Accession Numbers

None

Natural Product Identification

Common Name

xanthohumol B

Provided By

JEOL Database JEOL Logo

Description

xanthohumol B is found in Humulus lupulus. It was first documented in 2005 (Zhao, F., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192121573D          

 49 51  0  0  0  0            999 V2000
    1.8126    1.6175   -0.7630 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6398    0.8907   -0.4130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.1724    0.7539 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7970   -0.0035    1.5410 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7402   -0.7074    2.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5308   -1.2127    3.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6134   -1.0560    2.4291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7856   -1.5776    2.9243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5595   -0.3982    1.1825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8156   -0.3199    0.3897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8876   -0.2301    0.9882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7519   -0.4706   -1.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8549   -0.2718   -1.8254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8942   -0.4112   -3.2868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0505   -0.9309   -3.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1402   -1.0579   -5.2752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0730   -0.6520   -6.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1160   -0.7563   -7.4265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9251   -0.1191   -5.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8371    0.0068   -4.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4574   -1.9301    4.5457 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7249   -1.7151    5.3710 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6344   -0.4453    6.0382 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9898   -1.7830    4.4868 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2154   -3.1835    3.8919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2328   -1.4054    5.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9304   -0.8175    3.4150 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6398    0.9382   -0.9922 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    2.3303    0.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913    2.1890   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7626    0.3931    1.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5338   -1.1864    2.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8096   -0.7660   -1.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7964   -0.0082   -1.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8906   -1.2496   -3.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0437   -1.4704   -5.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9728   -1.1365   -7.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1029    0.2042   -6.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9398    0.4464   -3.6791 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3191   -2.9997    4.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4081   -1.5684    5.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7703   -2.4689    6.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6728    0.2417    5.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258   -3.2015    3.2812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3120   -3.9389    4.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4022   -3.4866    3.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1389   -1.4635    4.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3591   -2.0660    6.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779   -0.3704    5.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  2  0  0  0  0
 12 13  2  0  0  0  0
 16 17  1  0  0  0  0
  9  3  2  0  0  0  0
 17 19  2  0  0  0  0
 10 11  2  0  0  0  0
 19 20  1  0  0  0  0
 20 14  2  0  0  0  0
  3  4  1  0  0  0  0
 17 18  1  0  0  0  0
 13 14  1  0  0  0  0
  5  4  2  0  0  0  0
  6  5  1  0  0  0  0
  7  8  1  0  0  0  0
  9 10  1  0  0  0  0
  3  2  1  0  0  0  0
  7  9  1  0  0  0  0
  2  1  1  0  0  0  0
  6 21  1  0  0  0  0
  5 27  1  0  0  0  0
 27 24  1  0  0  0  0
 24 22  1  0  0  0  0
 22 21  1  0  0  0  0
 10 12  1  0  0  0  0
 22 23  1  0  0  0  0
 14 15  1  0  0  0  0
 24 25  1  0  0  0  0
  6  7  2  0  0  0  0
 24 26  1  0  0  0  0
 12 33  1  0  0  0  0
 13 34  1  0  0  0  0
  8 32  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
 15 35  1  0  0  0  0
 16 36  1  0  0  0  0
 19 38  1  0  0  0  0
 20 39  1  0  0  0  0
 18 37  1  0  0  0  0
  4 31  1  0  0  0  0
 22 42  1  0  0  0  0
 21 40  1  0  0  0  0
 21 41  1  0  0  0  0
 23 43  1  0  0  0  0
 25 44  1  0  0  0  0
 25 45  1  0  0  0  0
 25 46  1  0  0  0  0
 26 47  1  0  0  0  0
 26 48  1  0  0  0  0
 26 49  1  0  0  0  0
M  END

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    1.8126    1.6175   -0.7630 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6398    0.8907   -0.4130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.1724    0.7539 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7970   -0.0035    1.5410 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7402   -0.7074    2.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5308   -1.2127    3.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6134   -1.0560    2.4291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7856   -1.5776    2.9243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5595   -0.3982    1.1825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8156   -0.3199    0.3897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8876   -0.2301    0.9882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7519   -0.4706   -1.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8549   -0.2718   -1.8254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8942   -0.4112   -3.2868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0505   -0.9309   -3.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1402   -1.0579   -5.2752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0730   -0.6520   -6.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1160   -0.7563   -7.4265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9251   -0.1191   -5.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8371    0.0068   -4.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4574   -1.9301    4.5457 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7249   -1.7151    5.3710 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6344   -0.4453    6.0382 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9898   -1.7830    4.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2154   -3.1835    3.8919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2328   -1.4054    5.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9304   -0.8175    3.4150 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6398    0.9382   -0.9922 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    2.3303    0.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913    2.1890   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7626    0.3931    1.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5338   -1.1864    2.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8096   -0.7660   -1.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7964   -0.0082   -1.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8906   -1.2496   -3.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0437   -1.4704   -5.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9728   -1.1365   -7.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1029    0.2042   -6.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9398    0.4464   -3.6791 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3191   -2.9997    4.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4081   -1.5684    5.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7703   -2.4689    6.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6728    0.2417    5.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258   -3.2015    3.2812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3120   -3.9389    4.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4022   -3.4866    3.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1389   -1.4635    4.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3591   -2.0660    6.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779   -0.3704    5.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  2  0
 12 13  2  0
 16 17  1  0
  9  3  2  0
 17 19  2  0
 10 11  2  0
 19 20  1  0
 20 14  2  0
  3  4  1  0
 17 18  1  0
 13 14  1  0
  5  4  2  0
  6  5  1  0
  7  8  1  0
  9 10  1  0
  3  2  1  0
  7  9  1  0
  2  1  1  0
  6 21  1  0
  5 27  1  0
 27 24  1  0
 24 22  1  0
 22 21  1  0
 10 12  1  0
 22 23  1  0
 14 15  1  0
 24 25  1  0
  6  7  2  0
 24 26  1  0
 12 33  1  0
 13 34  1  0
  8 32  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 15 35  1  0
 16 36  1  0
 19 38  1  0
 20 39  1  0
 18 37  1  0
  4 31  1  0
 22 42  1  0
 21 40  1  0
 21 41  1  0
 23 43  1  0
 25 44  1  0
 25 45  1  0
 25 46  1  0
 26 47  1  0
 26 48  1  0
 26 49  1  0
M  END


  Mrv1652306192121573D          

 49 51  0  0  0  0            999 V2000
    1.8126    1.6175   -0.7630 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6398    0.8907   -0.4130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.1724    0.7539 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7970   -0.0035    1.5410 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7402   -0.7074    2.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5308   -1.2127    3.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6134   -1.0560    2.4291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7856   -1.5776    2.9243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5595   -0.3982    1.1825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8156   -0.3199    0.3897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8876   -0.2301    0.9882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7519   -0.4706   -1.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8549   -0.2718   -1.8254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8942   -0.4112   -3.2868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0505   -0.9309   -3.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1402   -1.0579   -5.2752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0730   -0.6520   -6.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1160   -0.7563   -7.4265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9251   -0.1191   -5.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8371    0.0068   -4.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4574   -1.9301    4.5457 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7249   -1.7151    5.3710 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6344   -0.4453    6.0382 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9898   -1.7830    4.4868 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2154   -3.1835    3.8919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2328   -1.4054    5.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9304   -0.8175    3.4150 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6398    0.9382   -0.9922 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    2.3303    0.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913    2.1890   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7626    0.3931    1.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5338   -1.1864    2.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8096   -0.7660   -1.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7964   -0.0082   -1.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8906   -1.2496   -3.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0437   -1.4704   -5.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9728   -1.1365   -7.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1029    0.2042   -6.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9398    0.4464   -3.6791 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3191   -2.9997    4.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4081   -1.5684    5.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7703   -2.4689    6.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6728    0.2417    5.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258   -3.2015    3.2812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3120   -3.9389    4.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4022   -3.4866    3.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1389   -1.4635    4.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3591   -2.0660    6.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779   -0.3704    5.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  2  0  0  0  0
 12 13  2  0  0  0  0
 16 17  1  0  0  0  0
  9  3  2  0  0  0  0
 17 19  2  0  0  0  0
 10 11  2  0  0  0  0
 19 20  1  0  0  0  0
 20 14  2  0  0  0  0
  3  4  1  0  0  0  0
 17 18  1  0  0  0  0
 13 14  1  0  0  0  0
  5  4  2  0  0  0  0
  6  5  1  0  0  0  0
  7  8  1  0  0  0  0
  9 10  1  0  0  0  0
  3  2  1  0  0  0  0
  7  9  1  0  0  0  0
  2  1  1  0  0  0  0
  6 21  1  0  0  0  0
  5 27  1  0  0  0  0
 27 24  1  0  0  0  0
 24 22  1  0  0  0  0
 22 21  1  0  0  0  0
 10 12  1  0  0  0  0
 22 23  1  0  0  0  0
 14 15  1  0  0  0  0
 24 25  1  0  0  0  0
  6  7  2  0  0  0  0
 24 26  1  0  0  0  0
 12 33  1  0  0  0  0
 13 34  1  0  0  0  0
  8 32  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
 15 35  1  0  0  0  0
 16 36  1  0  0  0  0
 19 38  1  0  0  0  0
 20 39  1  0  0  0  0
 18 37  1  0  0  0  0
  4 31  1  0  0  0  0
 22 42  1  0  0  0  0
 21 40  1  0  0  0  0
 21 41  1  0  0  0  0
 23 43  1  0  0  0  0
 25 44  1  0  0  0  0
 25 45  1  0  0  0  0
 25 46  1  0  0  0  0
 26 47  1  0  0  0  0
 26 48  1  0  0  0  0
 26 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0027944

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(\C([H])=C(/[H])C(=O)C2=C(OC([H])([H])[H])C([H])=C3OC(C([H])([H])[H])(C([H])([H])[H])[C@@]([H])(O[H])C([H])([H])C3=C2O[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O6/c1-21(2)18(24)10-14-16(27-21)11-17(26-3)19(20(14)25)15(23)9-6-12-4-7-13(22)8-5-12/h4-9,11,18,22,24-25H,10H2,1-3H3/b9-6+/t18-/m0/s1

> <INCHI_KEY>
GUQGMEWOCKDLDE-YOCVDRLZSA-N

> <FORMULA>
C21H22O6

> <MOLECULAR_WEIGHT>
370.401

> <EXACT_MASS>
370.141638428

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
39.93734156137141

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-1-[(3S)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one

> <ALOGPS_LOGP>
3.21

> <JCHEM_LOGP>
3.7245573916666666

> <ALOGPS_LOGS>
-4.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.043975345178815

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.341817914200762

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3326512486799613

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
102.0943

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.32e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-1-[(3S)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    1.8126    1.6175   -0.7630 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6398    0.8907   -0.4130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.1724    0.7539 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7970   -0.0035    1.5410 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7402   -0.7074    2.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5308   -1.2127    3.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6134   -1.0560    2.4291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7856   -1.5776    2.9243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5595   -0.3982    1.1825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8156   -0.3199    0.3897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8876   -0.2301    0.9882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7519   -0.4706   -1.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8549   -0.2718   -1.8254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8942   -0.4112   -3.2868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0505   -0.9309   -3.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1402   -1.0579   -5.2752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0730   -0.6520   -6.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1160   -0.7563   -7.4265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9251   -0.1191   -5.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8371    0.0068   -4.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4574   -1.9301    4.5457 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7249   -1.7151    5.3710 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6344   -0.4453    6.0382 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9898   -1.7830    4.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2154   -3.1835    3.8919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2328   -1.4054    5.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9304   -0.8175    3.4150 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6398    0.9382   -0.9922 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    2.3303    0.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913    2.1890   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7626    0.3931    1.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5338   -1.1864    2.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8096   -0.7660   -1.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7964   -0.0082   -1.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8906   -1.2496   -3.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0437   -1.4704   -5.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9728   -1.1365   -7.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1029    0.2042   -6.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9398    0.4464   -3.6791 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3191   -2.9997    4.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4081   -1.5684    5.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7703   -2.4689    6.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6728    0.2417    5.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258   -3.2015    3.2812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3120   -3.9389    4.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4022   -3.4866    3.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1389   -1.4635    4.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3591   -2.0660    6.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779   -0.3704    5.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  2  0
 12 13  2  0
 16 17  1  0
  9  3  2  0
 17 19  2  0
 10 11  2  0
 19 20  1  0
 20 14  2  0
  3  4  1  0
 17 18  1  0
 13 14  1  0
  5  4  2  0
  6  5  1  0
  7  8  1  0
  9 10  1  0
  3  2  1  0
  7  9  1  0
  2  1  1  0
  6 21  1  0
  5 27  1  0
 27 24  1  0
 24 22  1  0
 22 21  1  0
 10 12  1  0
 22 23  1  0
 14 15  1  0
 24 25  1  0
  6  7  2  0
 24 26  1  0
 12 33  1  0
 13 34  1  0
  8 32  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 15 35  1  0
 16 36  1  0
 19 38  1  0
 20 39  1  0
 18 37  1  0
  4 31  1  0
 22 42  1  0
 21 40  1  0
 21 41  1  0
 23 43  1  0
 25 44  1  0
 25 45  1  0
 25 46  1  0
 26 47  1  0
 26 48  1  0
 26 49  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       1.813   1.617  -0.763  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.640   0.891  -0.413  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.653   0.172   0.754  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.797  -0.004   1.541  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.740  -0.707   2.748  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.531  -1.213   3.223  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.613  -1.056   2.429  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.786  -1.578   2.924  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.560  -0.398   1.183  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.816  -0.320   0.390  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.888  -0.230   0.988  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.752  -0.471  -1.088  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.855  -0.272  -1.825  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.894  -0.411  -3.287  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.051  -0.931  -3.886  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.140  -1.058  -5.275  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.073  -0.652  -6.068  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.116  -0.756  -7.426  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.925  -0.119  -5.496  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.837   0.007  -4.107  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.457  -1.930   4.546  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.725  -1.715   5.371  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.634  -0.445   6.038  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.990  -1.783   4.487  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.215  -3.184   3.892  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.233  -1.405   5.310  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.930  -0.818   3.415  0.00  0.00           O+0
HETATM   28  H   UNK     0       2.640   0.938  -0.992  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.087   2.330   0.021  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.591   2.189  -1.670  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.763   0.393   1.242  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.534  -1.186   2.418  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.810  -0.766  -1.532  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.796  -0.008  -1.346  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.891  -1.250  -3.272  0.00  0.00           H+0
HETATM   36  H   UNK     0      -5.044  -1.470  -5.713  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.973  -1.137  -7.681  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.103   0.204  -6.128  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.940   0.446  -3.679  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.319  -3.000   4.348  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.408  -1.568   5.114  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.770  -2.469   6.165  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.673   0.242   5.347  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.126  -3.201   3.281  0.00  0.00           H+0
HETATM   45  H   UNK     0       3.312  -3.939   4.679  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.402  -3.487   3.225  0.00  0.00           H+0
HETATM   47  H   UNK     0       5.139  -1.464   4.695  0.00  0.00           H+0
HETATM   48  H   UNK     0       4.359  -2.066   6.174  0.00  0.00           H+0
HETATM   49  H   UNK     0       4.178  -0.370   5.665  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    3    1                                                       
CONECT    3    9    4    2                                                  
CONECT    4    3    5   31                                                  
CONECT    5    4    6   27                                                  
CONECT    6    5   21    7                                                  
CONECT    7    8    9    6                                                  
CONECT    8    7   32                                                       
CONECT    9    3   10    7                                                  
CONECT   10   11    9   12                                                  
CONECT   11   10                                                            
CONECT   12   13   10   33                                                  
CONECT   13   12   14   34                                                  
CONECT   14   20   13   15                                                  
CONECT   15   16   14   35                                                  
CONECT   16   15   17   36                                                  
CONECT   17   16   19   18                                                  
CONECT   18   17   37                                                       
CONECT   19   17   20   38                                                  
CONECT   20   19   14   39                                                  
CONECT   21    6   22   40   41                                             
CONECT   22   24   21   23   42                                             
CONECT   23   22   43                                                       
CONECT   24   27   22   25   26                                             
CONECT   25   24   44   45   46                                             
CONECT   26   24   47   48   49                                             
CONECT   27    5   24                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    4                                                            
CONECT   32    8                                                            
CONECT   33   12                                                            
CONECT   34   13                                                            
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   18                                                            
CONECT   38   19                                                            
CONECT   39   20                                                            
CONECT   40   21                                                            
CONECT   41   21                                                            
CONECT   42   22                                                            
CONECT   43   23                                                            
CONECT   44   25                                                            
CONECT   45   25                                                            
CONECT   46   25                                                            
CONECT   47   26                                                            
CONECT   48   26                                                            
CONECT   49   26                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  102    0
END

RDKit          3D

49 51  0  0  0  0  0  0  0  0999 V2000
    1.8126    1.6175   -0.7630 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6398    0.8907   -0.4130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    0.1724    0.7539 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7970   -0.0035    1.5410 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7402   -0.7074    2.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5308   -1.2127    3.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6134   -1.0560    2.4291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7856   -1.5776    2.9243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5595   -0.3982    1.1825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8156   -0.3199    0.3897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8876   -0.2301    0.9882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7519   -0.4706   -1.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8549   -0.2718   -1.8254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8942   -0.4112   -3.2868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0505   -0.9309   -3.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1402   -1.0579   -5.2752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0730   -0.6520   -6.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1160   -0.7563   -7.4265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9251   -0.1191   -5.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8371    0.0068   -4.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4574   -1.9301    4.5457 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7249   -1.7151    5.3710 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6344   -0.4453    6.0382 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9898   -1.7830    4.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2154   -3.1835    3.8919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2328   -1.4054    5.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9304   -0.8175    3.4150 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6398    0.9382   -0.9922 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0875    2.3303    0.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913    2.1890   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7626    0.3931    1.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5338   -1.1864    2.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8096   -0.7660   -1.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7964   -0.0082   -1.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8906   -1.2496   -3.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0437   -1.4704   -5.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9728   -1.1365   -7.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1029    0.2042   -6.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9398    0.4464   -3.6791 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3191   -2.9997    4.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4081   -1.5684    5.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7703   -2.4689    6.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6728    0.2417    5.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258   -3.2015    3.2812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3120   -3.9389    4.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4022   -3.4866    3.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1389   -1.4635    4.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3591   -2.0660    6.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779   -0.3704    5.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  2  0
 12 13  2  0
 16 17  1  0
  9  3  2  0
 17 19  2  0
 10 11  2  0
 19 20  1  0
 20 14  2  0
  3  4  1  0
 17 18  1  0
 13 14  1  0
  5  4  2  0
  6  5  1  0
  7  8  1  0
  9 10  1  0
  3  2  1  0
  7  9  1  0
  2  1  1  0
  6 21  1  0
  5 27  1  0
 27 24  1  0
 24 22  1  0
 22 21  1  0
 10 12  1  0
 22 23  1  0
 14 15  1  0
 24 25  1  0
  6  7  2  0
 24 26  1  0
 12 33  1  0
 13 34  1  0
  8 32  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 15 35  1  0
 16 36  1  0
 19 38  1  0
 20 39  1  0
 18 37  1  0
  4 31  1  0
 22 42  1  0
 21 40  1  0
 21 41  1  0
 23 43  1  0
 25 44  1  0
 25 45  1  0
 25 46  1  0
 26 47  1  0
 26 48  1  0
 26 49  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₂O₆

Average Mass

370.4010 Da

Monoisotopic Mass

370.14164 Da

IUPAC Name

(2E)-1-[(3S)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one

Traditional Name

(2E)-1-[(3S)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(\C([H])=C(/[H])C(=O)C2=C(OC([H])([H])[H])C([H])=C3OC(C([H])([H])[H])(C([H])([H])[H])[C@@]([H])(O[H])C([H])([H])C3=C2O[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C21H22O6/c1-21(2)18(24)10-14-16(27-21)11-17(26-3)19(20(14)25)15(23)9-6-12-4-7-13(22)8-5-12/h4-9,11,18,22,24-25H,10H2,1-3H3/b9-6+/t18-/m0/s1

InChI Key

GUQGMEWOCKDLDE-YOCVDRLZSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, 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

Species Name	Source	Reference
Humulus lupulus	JEOL database	Zhao, F., et al, J. Nat. Prod. 68, 43 (2005)

Chemical Taxonomy

Classification

Not classified

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	3.21	ALOGPS
logP	3.72	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	7.34	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	102.09 m³·mol⁻¹	ChemAxon
Polarizability	39.94 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Zhao, F., et al. (2005). Zhao, F., et al, J. Nat. Prod. 68, 43 (2005). J. Nat. Prod..

Showing NP-Card for xanthohumol B (NP0027944)

MOL for NP0027944 (xanthohumol B)

3D MOL for NP0027944 (xanthohumol B)

3D SDF for NP0027944 (xanthohumol B)

3D-SDF for NP0027944 (xanthohumol B)

PDB for NP0027944 (xanthohumol B)

3D PDB for NP0027944 (xanthohumol B)

SMILES for NP0027944 (xanthohumol B)

INCHI for NP0027944 (xanthohumol B)

Structure for NP0027944 (xanthohumol B)

3D Structure for NP0027944 (xanthohumol B)