NP-MRD: Showing NP-Card for Tetrahydrobostrycin (NP0007978)

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Record Information

Version

2.0

Created at

2020-12-09 05:35:31 UTC

Updated at

2021-07-15 16:59:05 UTC

NP-MRD ID

NP0007978

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Tetrahydrobostrycin

Provided By

NPAtlas

Description

Tetrahydrobostrycin belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings. Tetrahydrobostrycin is found in Aspergillus sp. Tetrahydrobostrycin was first documented in 2008 (PMID: 18776653). Based on a literature review very few articles have been published on Tetrahydrobostrycin.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106053D          

 44 46  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306242106053D          

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M  END
> <DATABASE_ID>
NP0007978

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)[C@@]3([H])[C@]([H])(O[H])[C@@]([H])(O[H])[C@](O[H])(C([H])([H])[H])C([H])([H])[C@]3([H])[C@@]([H])(O[H])C2=C(O[H])C(OC([H])([H])[H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H20O8/c1-16(23)4-5-8(14(21)15(16)22)13(20)9-6(17)3-7(24-2)12(19)10(9)11(5)18/h3,5,8,11,14-15,17-19,21-23H,4H2,1-2H3/t5-,8-,11+,14-,15+,16-/m0/s1

> <INCHI_KEY>
BECCUNGYVJUQCO-BJVFMSSPSA-N

> <FORMULA>
C16H20O8

> <MOLECULAR_WEIGHT>
340.328

> <EXACT_MASS>
340.115817604

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
33.59194707457376

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3S,4aS,9aR,10R)-1,2,3,5,8,10-hexahydroxy-6-methoxy-3-methyl-1,2,3,4,4a,9,9a,10-octahydroanthracen-9-one

> <ALOGPS_LOGP>
-0.43

> <JCHEM_LOGP>
-0.8311593883333335

> <ALOGPS_LOGS>
-1.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.405144786750665

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.965008837660836

> <JCHEM_PKA_STRONGEST_BASIC>
-3.250515644233909

> <JCHEM_POLAR_SURFACE_AREA>
147.68

> <JCHEM_REFRACTIVITY>
81.5898

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.30e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3S,4aS,9aR,10R)-1,2,3,5,8,10-hexahydroxy-6-methoxy-3-methyl-1,2,4,4a,9a,10-hexahydroanthracen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
    6.2676    0.6907   -0.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0838    1.1255   -0.7377 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8943    0.4851   -0.3779 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8449   -0.5216    0.5360 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6342   -1.1040    0.8375 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5740   -2.1290    1.7649 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4622   -0.7039    0.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5069    0.3289   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7337    0.9288   -1.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8456    1.9402   -1.9200 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2560    0.8351   -1.3435 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2395    2.2436   -1.4056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.3449   -0.5546 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2361    0.8490   -1.0550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2504    0.5056   -0.0091 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6214    0.8881   -0.5792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0447    1.4028    1.0649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2194   -0.8866    0.4745 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1628   -0.8959    1.8873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1718   -1.7701   -0.0609 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6664   -2.5138   -1.1488 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8799   -1.1278   -0.4286 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2035   -1.3977    0.5888 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0650   -2.1083    1.5860 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0938    1.4153   -0.3468 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1720    0.6325    0.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5757   -0.2784   -0.5631 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7655   -0.8615    1.0246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4216   -2.4338    2.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1218    2.3158   -2.4413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2191    0.3780   -2.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4456    2.4853   -2.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7982    0.7834    0.4803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1771    1.9577   -1.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4913    0.4915   -2.0661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8854    0.0835   -1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4806    1.8649   -1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3586    1.0303    0.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9014    1.6996    1.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2227   -1.3531    0.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7214   -1.6339    2.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9352   -2.5488    0.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8928   -1.8669   -1.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5077   -1.5709   -1.3728 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  1
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
  9  3  1  0
 22 13  1  0
 23  7  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  6 29  1  0
 10 30  1  0
 11 31  1  6
 12 32  1  0
 13 33  1  1
 14 34  1  0
 14 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  1
 19 41  1  0
 20 42  1  1
 21 43  1  0
 22 44  1  6
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       6.268   0.691  -0.113  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.084   1.125  -0.738  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.894   0.485  -0.378  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.845  -0.522   0.536  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.634  -1.104   0.838  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.574  -2.129   1.765  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.462  -0.704   0.247  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.507   0.329  -0.689  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.734   0.929  -1.007  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.846   1.940  -1.920  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.256   0.835  -1.343  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.240   2.244  -1.406  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.910   0.345  -0.555  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.236   0.849  -1.055  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.250   0.506  -0.009  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.621   0.888  -0.579  0.00  0.00           C+0
HETATM   17  O   UNK     0      -3.045   1.403   1.065  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.219  -0.887   0.475  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.163  -0.896   1.887  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.172  -1.770  -0.061  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.666  -2.514  -1.149  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.880  -1.128  -0.429  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.204  -1.398   0.589  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.065  -2.108   1.586  0.00  0.00           O+0
HETATM   25  H   UNK     0       7.094   1.415  -0.347  0.00  0.00           H+0
HETATM   26  H   UNK     0       6.172   0.633   0.985  0.00  0.00           H+0
HETATM   27  H   UNK     0       6.576  -0.278  -0.563  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.766  -0.862   1.025  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.422  -2.434   2.206  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.122   2.316  -2.441  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.219   0.378  -2.353  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.446   2.485  -2.068  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.798   0.783   0.480  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.177   1.958  -1.117  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.491   0.492  -2.066  0.00  0.00           H+0
HETATM   36  H   UNK     0      -4.885   0.084  -1.289  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.481   1.865  -1.073  0.00  0.00           H+0
HETATM   38  H   UNK     0      -5.359   1.030   0.229  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.901   1.700   1.452  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.223  -1.353   0.241  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.721  -1.634   2.259  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.935  -2.549   0.724  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.893  -1.867  -1.862  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.508  -1.571  -1.373  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   28                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   29                                                       
CONECT    7    5    8   23                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10    3                                                  
CONECT   10    9   30                                                       
CONECT   11    8   12   13   31                                             
CONECT   12   11   32                                                       
CONECT   13   11   14   22   33                                             
CONECT   14   13   15   34   35                                             
CONECT   15   14   16   17   18                                             
CONECT   16   15   36   37   38                                             
CONECT   17   15   39                                                       
CONECT   18   15   19   20   40                                             
CONECT   19   18   41                                                       
CONECT   20   18   21   22   42                                             
CONECT   21   20   43                                                       
CONECT   22   20   23   13   44                                             
CONECT   23   22   24    7                                                  
CONECT   24   23                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    4                                                            
CONECT   29    6                                                            
CONECT   30   10                                                            
CONECT   31   11                                                            
CONECT   32   12                                                            
CONECT   33   13                                                            
CONECT   34   14                                                            
CONECT   35   14                                                            
CONECT   36   16                                                            
CONECT   37   16                                                            
CONECT   38   16                                                            
CONECT   39   17                                                            
CONECT   40   18                                                            
CONECT   41   19                                                            
CONECT   42   20                                                            
CONECT   43   21                                                            
CONECT   44   22                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

RDKit          3D

44 46  0  0  0  0  0  0  0  0999 V2000
    6.2676    0.6907   -0.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0838    1.1255   -0.7377 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8943    0.4851   -0.3779 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8449   -0.5216    0.5360 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6342   -1.1040    0.8375 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5740   -2.1290    1.7649 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4622   -0.7039    0.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5069    0.3289   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7337    0.9288   -1.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8456    1.9402   -1.9200 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2560    0.8351   -1.3435 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2395    2.2436   -1.4056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.3449   -0.5546 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2361    0.8490   -1.0550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2504    0.5056   -0.0091 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6214    0.8881   -0.5792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0447    1.4028    1.0649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2194   -0.8866    0.4745 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1628   -0.8959    1.8873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1718   -1.7701   -0.0609 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6664   -2.5138   -1.1488 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8799   -1.1278   -0.4286 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2035   -1.3977    0.5888 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0650   -2.1083    1.5860 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0938    1.4153   -0.3468 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1720    0.6325    0.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5757   -0.2784   -0.5631 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7655   -0.8615    1.0246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4216   -2.4338    2.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1218    2.3158   -2.4413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2191    0.3780   -2.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4456    2.4853   -2.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7982    0.7834    0.4803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1771    1.9577   -1.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4913    0.4915   -2.0661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8854    0.0835   -1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4806    1.8649   -1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3586    1.0303    0.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9014    1.6996    1.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2227   -1.3531    0.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7214   -1.6339    2.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9352   -2.5488    0.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8928   -1.8669   -1.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5077   -1.5709   -1.3728 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  1
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
  9  3  1  0
 22 13  1  0
 23  7  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  6 29  1  0
 10 30  1  0
 11 31  1  6
 12 32  1  0
 13 33  1  1
 14 34  1  0
 14 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  1
 19 41  1  0
 20 42  1  1
 21 43  1  0
 22 44  1  6
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₆H₂₀O₈

Average Mass

340.3280 Da

Monoisotopic Mass

340.11582 Da

IUPAC Name

(1S,2R,3S,4aS,9aR,10R)-1,2,3,5,8,10-hexahydroxy-6-methoxy-3-methyl-1,2,3,4,4a,9,9a,10-octahydroanthracen-9-one

Traditional Name

(1S,2R,3S,4aS,9aR,10R)-1,2,3,5,8,10-hexahydroxy-6-methoxy-3-methyl-1,2,4,4a,9a,10-hexahydroanthracen-9-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C2=C(C(O)=C1)C(=O)[C@H]1[C@H](O)[C@@H](O)[C@@](C)(O)C[C@@H]1[C@H]2O

InChI Identifier

InChI=1S/C16H20O8/c1-16(23)4-5-8(14(21)15(16)22)13(20)9-6(17)3-7(24-2)12(19)10(9)11(5)18/h3,5,8,11,14-15,17-19,21-23H,4H2,1-2H3/t5-,8-,11+,14-,15+,16-/m0/s1

InChI Key

BECCUNGYVJUQCO-BJVFMSSPSA-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
Aspergillus sp.	NPAtlas	18776653

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Not Available

Direct Parent

Anthracenes

Alternative Parents

Substituents

Anthracene
Tetralin
Anisole
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Cyclitol or derivatives
Vinylogous acid
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Ketone
Polyol
Ether
Alcohol
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	-0.43	ALOGPS
logP	-0.83	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	8.97	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	147.68 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	81.59 m³·mol⁻¹	ChemAxon
Polarizability	33.59 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

NPAtlas ID

NPA017653

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00048582

Chemspider ID

25056232

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25014989

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Xu J, Nakazawa T, Ukai K, Kobayashi H, Mangindaan RE, Wewengkang DS, Rotinsulu H, Namikoshi M: Tetrahydrobostrycin and 1-deoxytetrahydrobostrycin, two new hexahydroanthrone derivatives, from a marine-derived fungus Aspergillus sp. J Antibiot (Tokyo). 2008 Jul;61(7):415-9. doi: 10.1038/ja.2008.57. [PubMed:18776653 ]

Showing NP-Card for Tetrahydrobostrycin (NP0007978)

MOL for NP0007978 (Tetrahydrobostrycin)

3D MOL for NP0007978 (Tetrahydrobostrycin)

3D SDF for NP0007978 (Tetrahydrobostrycin)

3D-SDF for NP0007978 (Tetrahydrobostrycin)

PDB for NP0007978 (Tetrahydrobostrycin)

3D PDB for NP0007978 (Tetrahydrobostrycin)

SMILES for NP0007978 (Tetrahydrobostrycin)

INCHI for NP0007978 (Tetrahydrobostrycin)

Structure for NP0007978 (Tetrahydrobostrycin)

3D Structure for NP0007978 (Tetrahydrobostrycin)