NP-MRD: Showing NP-Card for Sterenin H (NP0013061)

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Record Information

Version

1.0

Created at

2021-01-05 22:32:43 UTC

Updated at

2021-07-15 17:13:28 UTC

NP-MRD ID

NP0013061

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Sterenin H

Provided By

NPAtlas

Description

Sterenin H is found in Stereum hirsutum. It was first documented in 2014 (PMID: 25029175). Based on a literature review very few articles have been published on Sterenin H.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119323D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306242119323D          

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    5.8891   -1.9437    1.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6483   -3.2768   -0.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9724   -1.8167   -2.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7994   -0.8580   -3.2543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0982   -1.2419    2.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9060   -1.8875    0.7111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6384   -0.9254    1.8052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1440   -3.8290    0.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3274   -2.3528    1.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2408   -2.1547   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5055   -3.6443    0.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5860   -3.4615   -1.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0774   -4.6456    0.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3788    1.1416    0.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  3  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 22 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28  4  1  0  0  0  0
 20 13  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
  3 33  1  0  0  0  0
  3 34  1  0  0  0  0
  6 35  1  0  0  0  0
  6 36  1  0  0  0  0
  7 37  1  0  0  0  0
  8 38  1  0  0  0  0
 15 39  1  0  0  0  0
 15 40  1  0  0  0  0
 15 41  1  0  0  0  0
 16 42  1  0  0  0  0
 18 43  1  0  0  0  0
 19 44  1  0  0  0  0
 21 45  1  0  0  0  0
 23 46  1  0  0  0  0
 23 47  1  0  0  0  0
 24 48  1  0  0  0  0
 26 49  1  0  0  0  0
 26 50  1  0  0  0  0
 26 51  1  0  0  0  0
 27 52  1  0  0  0  0
 27 53  1  0  0  0  0
 27 54  1  0  0  0  0
 29 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0013061

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(=C(C(=O)OC2=C([H])C(=C(C(O[H])=C2C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])OC([H])([H])[H])C([H])([H])O[H])C(O[H])=C1[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O7/c1-12(2)5-6-16-19(8-14(10-23)17(11-28-4)21(16)26)29-22(27)20-13(3)7-15(24)9-18(20)25/h5,7-9,23-26H,6,10-11H2,1-4H3

> <INCHI_KEY>
QBAPFNYOABZILN-UHFFFAOYSA-N

> <FORMULA>
C22H26O7

> <MOLECULAR_WEIGHT>
402.443

> <EXACT_MASS>
402.167853177

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
43.08720807808868

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-hydroxy-5-(hydroxymethyl)-4-(methoxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoate

> <ALOGPS_LOGP>
2.82

> <JCHEM_LOGP>
4.724400621333333

> <ALOGPS_LOGS>
-4.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.795133533466199

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.107227126609668

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9275815210766476

> <JCHEM_POLAR_SURFACE_AREA>
116.45

> <JCHEM_REFRACTIVITY>
111.47059999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.11e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-5-(hydroxymethyl)-4-(methoxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
   -2.4665    4.2483    1.2129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8247    4.3417   -0.0906 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0876    3.0962   -0.7167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9935    2.1585   -0.3601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7468    2.4950   -0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4532    3.7931   -1.5678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2084    3.5428   -2.9300 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2469    1.6384   -0.5416 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508    0.4588    0.2651 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2296   -0.2489    0.4980 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1247   -0.5366   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6454   -0.2014   -1.6861 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4477   -1.1162   -0.4756 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0436   -1.3344    0.7358 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3922   -1.0965    2.0376 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4006   -1.7423    0.7577 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1097   -1.9187   -0.3980 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4686   -2.3135   -0.4027 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4794   -1.6980   -1.5994 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1494   -1.2920   -1.6495 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6692   -1.0981   -2.9418 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1905    0.1688    0.7331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4894   -1.1464    1.3836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8928   -1.5467    1.2612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3464   -2.5525    0.6293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8299   -2.7840    0.6171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5594   -3.5852   -0.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2420    1.0565    0.4148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4787    0.7369    0.8908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2220    3.8147    1.8704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4406    3.7414    1.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2222    5.2868    1.5794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0286    2.7614   -0.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2501    3.1399   -1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7290    3.9308   -1.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8110    4.7249   -1.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0652    3.0658   -3.2515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2780    1.8589   -0.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2338   -1.0342    2.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0141   -0.0610    2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7304   -1.8561    2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8891   -1.9437    1.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6483   -3.2768   -0.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9724   -1.8167   -2.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7994   -0.8580   -3.2543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0982   -1.2419    2.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9060   -1.8875    0.7111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6384   -0.9254    1.8052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1440   -3.8290    0.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3274   -2.3528    1.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2408   -2.1547   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5055   -3.6443    0.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5860   -3.4615   -1.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0774   -4.6456    0.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3788    1.1416    0.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
  9 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  3
 25 26  1  0
 25 27  1  0
 22 28  2  0
 28 29  1  0
 28  4  1  0
 20 13  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
 15 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 18 43  1  0
 19 44  1  0
 21 45  1  0
 23 46  1  0
 23 47  1  0
 24 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
 27 52  1  0
 27 53  1  0
 27 54  1  0
 29 55  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.466   4.248   1.213  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.825   4.342  -0.091  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.088   3.096  -0.717  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.994   2.159  -0.360  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.747   2.495  -0.867  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.453   3.793  -1.568  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.208   3.543  -2.930  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.247   1.638  -0.542  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.051   0.459   0.265  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.230  -0.249   0.498  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.125  -0.537  -0.573  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.645  -0.201  -1.686  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.448  -1.116  -0.476  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.044  -1.334   0.736  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.392  -1.097   2.038  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.401  -1.742   0.758  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.110  -1.919  -0.398  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.469  -2.313  -0.403  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.479  -1.698  -1.599  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.149  -1.292  -1.650  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.669  -1.098  -2.942  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.190   0.169   0.733  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.489  -1.146   1.384  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.893  -1.547   1.261  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.346  -2.553   0.629  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.830  -2.784   0.617  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.559  -3.585  -0.041  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.242   1.056   0.415  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.479   0.737   0.891  0.00  0.00           O+0
HETATM   30  H   UNK     0      -3.222   3.815   1.870  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.441   3.741   1.321  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.222   5.287   1.579  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.029   2.761  -0.168  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.250   3.140  -1.745  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.729   3.931  -1.252  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.811   4.725  -1.243  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.065   3.066  -3.252  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.278   1.859  -0.885  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.234  -1.034   2.794  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.014  -0.061   2.134  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.730  -1.856   2.430  0.00  0.00           H+0
HETATM   42  H   UNK     0       5.889  -1.944   1.691  0.00  0.00           H+0
HETATM   43  H   UNK     0       7.648  -3.277  -0.423  0.00  0.00           H+0
HETATM   44  H   UNK     0       5.972  -1.817  -2.542  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.799  -0.858  -3.254  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.098  -1.242   2.368  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.906  -1.888   0.711  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.638  -0.925   1.805  0.00  0.00           H+0
HETATM   49  H   UNK     0      -5.144  -3.829   0.523  0.00  0.00           H+0
HETATM   50  H   UNK     0      -5.327  -2.353   1.555  0.00  0.00           H+0
HETATM   51  H   UNK     0      -5.241  -2.155  -0.233  0.00  0.00           H+0
HETATM   52  H   UNK     0      -1.506  -3.644   0.314  0.00  0.00           H+0
HETATM   53  H   UNK     0      -2.586  -3.462  -1.126  0.00  0.00           H+0
HETATM   54  H   UNK     0      -3.077  -4.646   0.187  0.00  0.00           H+0
HETATM   55  H   UNK     0      -4.379   1.142   0.814  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   33   34                                             
CONECT    4    3    5   28                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    7   35   36                                             
CONECT    7    6   37                                                       
CONECT    8    5    9   38                                                  
CONECT    9    8   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   20                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14   39   40   41                                             
CONECT   16   14   17   42                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   43                                                       
CONECT   19   17   20   44                                                  
CONECT   20   19   21   13                                                  
CONECT   21   20   45                                                       
CONECT   22    9   23   28                                                  
CONECT   23   22   24   46   47                                             
CONECT   24   23   25   48                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   49   50   51                                             
CONECT   27   25   52   53   54                                             
CONECT   28   22   29    4                                                  
CONECT   29   28   55                                                       
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    3                                                            
CONECT   34    3                                                            
CONECT   35    6                                                            
CONECT   36    6                                                            
CONECT   37    7                                                            
CONECT   38    8                                                            
CONECT   39   15                                                            
CONECT   40   15                                                            
CONECT   41   15                                                            
CONECT   42   16                                                            
CONECT   43   18                                                            
CONECT   44   19                                                            
CONECT   45   21                                                            
CONECT   46   23                                                            
CONECT   47   23                                                            
CONECT   48   24                                                            
CONECT   49   26                                                            
CONECT   50   26                                                            
CONECT   51   26                                                            
CONECT   52   27                                                            
CONECT   53   27                                                            
CONECT   54   27                                                            
CONECT   55   29                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  112    0
END

RDKit          3D

55 56  0  0  0  0  0  0  0  0999 V2000
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   -2.5594   -3.5852   -0.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4406    3.7414    1.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2222    5.2868    1.5794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0286    2.7614   -0.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2501    3.1399   -1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7290    3.9308   -1.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8110    4.7249   -1.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0652    3.0658   -3.2515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2780    1.8589   -0.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2338   -1.0342    2.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0141   -0.0610    2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7304   -1.8561    2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8891   -1.9437    1.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6483   -3.2768   -0.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9724   -1.8167   -2.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7994   -0.8580   -3.2543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0982   -1.2419    2.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9060   -1.8875    0.7111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6384   -0.9254    1.8052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1440   -3.8290    0.5234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3274   -2.3528    1.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2408   -2.1547   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5055   -3.6443    0.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5860   -3.4615   -1.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0774   -4.6456    0.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3788    1.1416    0.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  2  0
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 13 14  2  0
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  9 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  3
 25 26  1  0
 25 27  1  0
 22 28  2  0
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 28  4  1  0
 20 13  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
 15 39  1  0
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 18 43  1  0
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 21 45  1  0
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 27 52  1  0
 27 53  1  0
 27 54  1  0
 29 55  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-Hydroxy-5-(hydroxymethyl)-4-(methoxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoic acid	Generator

Chemical Formula

C₂₂H₂₆O₇

Average Mass

402.4430 Da

Monoisotopic Mass

402.16785 Da

IUPAC Name

3-hydroxy-5-(hydroxymethyl)-4-(methoxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoate

Traditional Name

3-hydroxy-5-(hydroxymethyl)-4-(methoxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoate

CAS Registry Number

Not Available

SMILES

COCC1=C(O)C(CC=C(C)C)=C(OC(=O)C2=C(O)C=C(O)C=C2C)C=C1CO

InChI Identifier

InChI=1S/C22H26O7/c1-12(2)5-6-16-19(8-14(10-23)17(11-28-4)21(16)26)29-22(27)20-13(3)7-15(24)9-18(20)25/h5,7-9,23-26H,6,10-11H2,1-4H3

InChI Key

QBAPFNYOABZILN-UHFFFAOYSA-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
Stereum hirsutum	NPAtlas	25029175

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	2.82	ALOGPS
logP	4.72	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	8.11	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	111.47 m³·mol⁻¹	ChemAxon
Polarizability	43.09 Å³	ChemAxon
Number of Rings	2	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

NPAtlas ID

NPA009861

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435353

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

77461066

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wang BT, Qi QY, Ma K, Pei YF, Han JJ, Xu W, Li EW, Liu HW: Depside alpha-glucosidase inhibitors from a culture of the mushroom Stereum hirsutum. Planta Med. 2014 Jul;80(11):918-24. doi: 10.1055/s-0034-1382828. Epub 2014 Jul 16. [PubMed:25029175 ]

Showing NP-Card for Sterenin H (NP0013061)

MOL for NP0013061 (Sterenin H)

3D MOL for NP0013061 (Sterenin H)

3D SDF for NP0013061 (Sterenin H)

3D-SDF for NP0013061 (Sterenin H)

PDB for NP0013061 (Sterenin H)

3D PDB for NP0013061 (Sterenin H)

SMILES for NP0013061 (Sterenin H)

INCHI for NP0013061 (Sterenin H)

Structure for NP0013061 (Sterenin H)

3D Structure for NP0013061 (Sterenin H)