NP-MRD: Showing NP-Card for Microsphaerol (NP0013813)

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Record Information

Version

2.0

Created at

2021-01-05 23:07:38 UTC

Updated at

2021-07-15 17:15:32 UTC

NP-MRD ID

NP0013813

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Microsphaerol

Provided By

NPAtlas

Description

Microsphaerol is found in Microsphaeropsis sp. Microsphaerol was first documented in 2015 (PMID: 25676510). Based on a literature review very few articles have been published on 4-chloro-5-[2-chloro-4-(2-chloro-6-methylphenoxy)-3,5,6-trimethylphenoxy]-3-methoxybenzene-1,2-diol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119503D          

 52 54  0  0  0  0            999 V2000
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   -6.6862    0.9438   -1.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3437   -2.1770    1.5969 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242119503D          

 52 54  0  0  0  0            999 V2000
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    4.4772    1.7957    1.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0013    0.9817   -0.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0445   -1.2322   -0.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7347   -3.2217   -0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5479   -3.2241   -1.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2720   -2.2528   -2.7356 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8378   -2.0622   -1.9644 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  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  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
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 28 29  1  0  0  0  0
  9 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30  3  1  0  0  0  0
 28 11  1  0  0  0  0
 24 18  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  5 35  1  0  0  0  0
  7 36  1  0  0  0  0
  8 37  1  0  0  0  0
 13 38  1  0  0  0  0
 13 39  1  0  0  0  0
 13 40  1  0  0  0  0
 15 41  1  0  0  0  0
 15 42  1  0  0  0  0
 15 43  1  0  0  0  0
 20 44  1  0  0  0  0
 20 45  1  0  0  0  0
 20 46  1  0  0  0  0
 21 47  1  0  0  0  0
 22 48  1  0  0  0  0
 23 49  1  0  0  0  0
 27 50  1  0  0  0  0
 27 51  1  0  0  0  0
 27 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0013813

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(OC2=C(C(=C(OC3=C(C([H])=C([H])C([H])=C3Cl)C([H])([H])[H])C(=C2Cl)C([H])([H])[H])C([H])([H])[H])C([H])([H])[H])=C(Cl)C(OC([H])([H])[H])=C1O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H21Cl3O5/c1-10-7-6-8-14(24)20(10)31-21-11(2)12(3)22(17(25)13(21)4)30-16-9-15(27)19(28)23(29-5)18(16)26/h6-9,27-28H,1-5H3

> <INCHI_KEY>
NEHFAEVGPMAOKI-UHFFFAOYSA-N

> <FORMULA>
C23H21Cl3O5

> <MOLECULAR_WEIGHT>
483.77

> <EXACT_MASS>
482.0454569

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
48.54730079819135

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-chloro-5-[2-chloro-4-(2-chloro-6-methylphenoxy)-3,5,6-trimethylphenoxy]-3-methoxybenzene-1,2-diol

> <ALOGPS_LOGP>
6.85

> <JCHEM_LOGP>
8.074837859333334

> <ALOGPS_LOGS>
-6.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.45953509645658

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.812863805982813

> <JCHEM_PKA_STRONGEST_BASIC>
-3.41692348093857

> <JCHEM_POLAR_SURFACE_AREA>
68.15

> <JCHEM_REFRACTIVITY>
123.54379999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.28e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-chloro-5-[2-chloro-4-(2-chloro-6-methylphenoxy)-3,5,6-trimethylphenoxy]-3-methoxybenzene-1,2-diol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
   -7.3347    2.0413   -0.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6862    0.9438   -1.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4896    0.4108   -0.7678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5056   -0.6001    0.1556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6914   -1.1427    0.6504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3366   -1.1558    0.6641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3437   -2.1770    1.5969 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1562   -0.6321    0.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1219    0.3776   -0.7358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9118    0.8720   -1.1865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6861    0.3937   -0.7488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0615    0.9357    0.3350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7096    2.0781    1.0772 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1558    0.4736    0.7844 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7406    1.1199    2.0158 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8081   -0.5833    0.1369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9867   -0.9713    0.6272 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2752   -0.9558    0.2631 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0606    0.1667    0.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5315    1.5346    0.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4057    0.0781   -0.2691 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0011   -1.1357   -0.5077 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2508   -2.2569   -0.3649 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9304   -2.1666    0.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0853   -3.6857    0.2194 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.1730   -1.1248   -0.9545 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7501   -2.2275   -1.7353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0657   -0.6457   -1.4005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8662   -1.3446   -2.7928 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -4.2924    0.9026   -1.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2603    2.2164   -2.4163 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -8.0390    2.4822   -1.3927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9040    1.7612    0.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6299    2.8564   -0.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5949   -0.8220    0.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1759   -2.5761    1.9609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2274   -1.0585    0.5768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6292    1.7448    1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8588    2.8722    0.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0325    2.4680    1.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6523    0.5471    2.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0794    2.1508    1.7990 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0457    1.0579    2.8708 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2084    2.2958   -0.1344 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5552    1.6963   -0.2180 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4772    1.7957    1.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0013    0.9817   -0.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0445   -1.2322   -0.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7347   -3.2217   -0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5479   -3.2241   -1.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2720   -2.2528   -2.7356 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8378   -2.0622   -1.9644 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
  4  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 16 26  1  0
 26 27  1  0
 26 28  2  0
 28 29  1  0
  9 30  2  0
 30 31  1  0
 30  3  1  0
 28 11  1  0
 24 18  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  5 35  1  0
  7 36  1  0
  8 37  1  0
 13 38  1  0
 13 39  1  0
 13 40  1  0
 15 41  1  0
 15 42  1  0
 15 43  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
 27 50  1  0
 27 51  1  0
 27 52  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      -7.335   2.041  -0.634  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.686   0.944  -1.256  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.490   0.411  -0.768  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.506  -0.600   0.156  0.00  0.00           C+0
HETATM    5  O   UNK     0      -6.691  -1.143   0.650  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.337  -1.156   0.664  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.344  -2.177   1.597  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.156  -0.632   0.187  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.122   0.378  -0.736  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.912   0.872  -1.187  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.686   0.394  -0.749  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.062   0.936   0.335  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.710   2.078   1.077  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.156   0.474   0.784  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.741   1.120   2.016  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.808  -0.583   0.137  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.987  -0.971   0.627  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.275  -0.956   0.263  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.061   0.167   0.111  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.532   1.535   0.327  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.406   0.078  -0.269  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.001  -1.136  -0.508  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.251  -2.257  -0.365  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.930  -2.167   0.010  0.00  0.00           C+0
HETATM   25 Cl   UNK     0       4.085  -3.686   0.219  0.00  0.00          Cl+0
HETATM   26  C   UNK     0       1.173  -1.125  -0.955  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.750  -2.228  -1.735  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.066  -0.646  -1.401  0.00  0.00           C+0
HETATM   29 Cl   UNK     0      -0.866  -1.345  -2.793  0.00  0.00          Cl+0
HETATM   30  C   UNK     0      -4.292   0.903  -1.216  0.00  0.00           C+0
HETATM   31 Cl   UNK     0      -4.260   2.216  -2.416  0.00  0.00          Cl+0
HETATM   32  H   UNK     0      -8.039   2.482  -1.393  0.00  0.00           H+0
HETATM   33  H   UNK     0      -7.904   1.761   0.258  0.00  0.00           H+0
HETATM   34  H   UNK     0      -6.630   2.856  -0.382  0.00  0.00           H+0
HETATM   35  H   UNK     0      -7.595  -0.822   0.357  0.00  0.00           H+0
HETATM   36  H   UNK     0      -5.176  -2.576   1.961  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.227  -1.059   0.577  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.629   1.745   1.577  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.859   2.872   0.327  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.033   2.468   1.852  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.652   0.547   2.319  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.079   2.151   1.799  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.046   1.058   2.871  0.00  0.00           H+0
HETATM   44  H   UNK     0       5.208   2.296  -0.134  0.00  0.00           H+0
HETATM   45  H   UNK     0       3.555   1.696  -0.218  0.00  0.00           H+0
HETATM   46  H   UNK     0       4.477   1.796   1.386  0.00  0.00           H+0
HETATM   47  H   UNK     0       7.001   0.982  -0.381  0.00  0.00           H+0
HETATM   48  H   UNK     0       8.044  -1.232  -0.805  0.00  0.00           H+0
HETATM   49  H   UNK     0       6.735  -3.222  -0.558  0.00  0.00           H+0
HETATM   50  H   UNK     0       1.548  -3.224  -1.291  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.272  -2.253  -2.736  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.838  -2.062  -1.964  0.00  0.00           H+0
CONECT    1    2   32   33   34                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   30                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4   35                                                       
CONECT    6    4    7    8                                                  
CONECT    7    6   36                                                       
CONECT    8    6    9   37                                                  
CONECT    9    8   10   30                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   28                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   38   39   40                                             
CONECT   14   12   15   16                                                  
CONECT   15   14   41   42   43                                             
CONECT   16   14   17   26                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   24                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19   44   45   46                                             
CONECT   21   19   22   47                                                  
CONECT   22   21   23   48                                                  
CONECT   23   22   24   49                                                  
CONECT   24   23   25   18                                                  
CONECT   25   24                                                            
CONECT   26   16   27   28                                                  
CONECT   27   26   50   51   52                                             
CONECT   28   26   29   11                                                  
CONECT   29   28                                                            
CONECT   30    9   31    3                                                  
CONECT   31   30                                                            
CONECT   32    1                                                            
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    5                                                            
CONECT   36    7                                                            
CONECT   37    8                                                            
CONECT   38   13                                                            
CONECT   39   13                                                            
CONECT   40   13                                                            
CONECT   41   15                                                            
CONECT   42   15                                                            
CONECT   43   15                                                            
CONECT   44   20                                                            
CONECT   45   20                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
CONECT   48   22                                                            
CONECT   49   23                                                            
CONECT   50   27                                                            
CONECT   51   27                                                            
CONECT   52   27                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  108    0
END

RDKit          3D

52 54  0  0  0  0  0  0  0  0999 V2000
   -7.3347    2.0413   -0.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6862    0.9438   -1.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4896    0.4108   -0.7678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5056   -0.6001    0.1556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6914   -1.1427    0.6504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3366   -1.1558    0.6641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3437   -2.1770    1.5969 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1562   -0.6321    0.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1219    0.3776   -0.7358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9118    0.8720   -1.1865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6861    0.3937   -0.7488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0615    0.9357    0.3350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7096    2.0781    1.0772 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1558    0.4736    0.7844 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7406    1.1199    2.0158 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8081   -0.5833    0.1369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9867   -0.9713    0.6272 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2752   -0.9558    0.2631 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0606    0.1667    0.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5315    1.5346    0.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4057    0.0781   -0.2691 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0011   -1.1357   -0.5077 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2508   -2.2569   -0.3649 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9304   -2.1666    0.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0853   -3.6857    0.2194 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.1730   -1.1248   -0.9545 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7501   -2.2275   -1.7353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0657   -0.6457   -1.4005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8662   -1.3446   -2.7928 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -4.2924    0.9026   -1.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2603    2.2164   -2.4163 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -8.0390    2.4822   -1.3927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9040    1.7612    0.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6299    2.8564   -0.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5949   -0.8220    0.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1759   -2.5761    1.9609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2274   -1.0585    0.5768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6292    1.7448    1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8588    2.8722    0.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0325    2.4680    1.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6523    0.5471    2.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0794    2.1508    1.7990 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0457    1.0579    2.8708 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2084    2.2958   -0.1344 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5552    1.6963   -0.2180 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4772    1.7957    1.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0013    0.9817   -0.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0445   -1.2322   -0.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7347   -3.2217   -0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5479   -3.2241   -1.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2720   -2.2528   -2.7356 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8378   -2.0622   -1.9644 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
  4  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 16 26  1  0
 26 27  1  0
 26 28  2  0
 28 29  1  0
  9 30  2  0
 30 31  1  0
 30  3  1  0
 28 11  1  0
 24 18  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  5 35  1  0
  7 36  1  0
  8 37  1  0
 13 38  1  0
 13 39  1  0
 13 40  1  0
 15 41  1  0
 15 42  1  0
 15 43  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
 27 50  1  0
 27 51  1  0
 27 52  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₃H₂₁Cl₃O₅

Average Mass

483.7700 Da

Monoisotopic Mass

482.04546 Da

IUPAC Name

4-chloro-5-[2-chloro-4-(2-chloro-6-methylphenoxy)-3,5,6-trimethylphenoxy]-3-methoxybenzene-1,2-diol

Traditional Name

4-chloro-5-[2-chloro-4-(2-chloro-6-methylphenoxy)-3,5,6-trimethylphenoxy]-3-methoxybenzene-1,2-diol

CAS Registry Number

Not Available

SMILES

COC1=C(O)C(O)=CC(OC2=C(Cl)C(C)=C(OC3=C(C)C=CC=C3Cl)C(C)=C2C)=C1Cl

InChI Identifier

InChI=1S/C23H21Cl3O5/c1-10-7-6-8-14(24)20(10)31-21-11(2)12(3)22(17(25)13(21)4)30-16-9-15(27)19(28)23(29-5)18(16)26/h6-9,27-28H,1-5H3

InChI Key

NEHFAEVGPMAOKI-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
Microsphaeropsis sp.	NPAtlas	25676510

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	6.85	ALOGPS
logP	8.07	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	8.81	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	68.15 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	123.54 m³·mol⁻¹	ChemAxon
Polarizability	48.55 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

NPA014292

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78434983

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587066

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hussain H, Root N, Jabeen F, Al-Harrasi A, Ahmad M, Mabood F, Hassan Z, Shah A, Green IR, Schulz B, Krohn K: Microsphaerol and seimatorone: two new compounds isolated from the endophytic fungi, Microsphaeropsis sp. and Seimatosporium sp. Chem Biodivers. 2015 Feb;12(2):289-94. doi: 10.1002/cbdv.201400098. [PubMed:25676510 ]

Showing NP-Card for Microsphaerol (NP0013813)

MOL for NP0013813 (Microsphaerol)

3D MOL for NP0013813 (Microsphaerol)

3D SDF for NP0013813 (Microsphaerol)

3D-SDF for NP0013813 (Microsphaerol)

PDB for NP0013813 (Microsphaerol)

3D PDB for NP0013813 (Microsphaerol)

SMILES for NP0013813 (Microsphaerol)

INCHI for NP0013813 (Microsphaerol)

Structure for NP0013813 (Microsphaerol)

3D Structure for NP0013813 (Microsphaerol)