NP-MRD: Showing NP-Card for 3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione (NP0005907)

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Record Information

Version

2.0

Created at

2020-12-09 03:01:42 UTC

Updated at

2021-07-15 16:53:18 UTC

NP-MRD ID

NP0005907

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione

Provided By

NPAtlas

Description

3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione is found in Unknown-fungus sp. Based on a literature review very few articles have been published on CHEMBL457364.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118233D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306242118233D          

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   -1.7023   -1.4366    3.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2768   -1.4772    2.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6218   -3.7759    2.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  3  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 14 17  1  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
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
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 25 26  2  0  0  0  0
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 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  2  0  0  0  0
 10  2  1  0  0  0  0
 20 12  1  0  0  0  0
 30 23  1  0  0  0  0
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  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  3 36  1  0  0  0  0
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 29 60  1  0  0  0  0
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 31 63  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005907

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C2=C(C(=O)C3=C([H])[C@@]([H])(Cl)C(O[C@]3(C2=O)C([H])([H])[C@]2([H])C(=C([H])[H])C([H])([H])C([H])([H])[C@]([H])(Cl)C2(C([H])([H])[H])C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C(O[H])=C1C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C26H30Cl2O5/c1-12-7-8-18(27)24(3,4)16(12)11-26-15(10-19(28)25(5,6)33-26)22(31)20-14(23(26)32)9-17(29)13(2)21(20)30/h9-10,16,18-19,29-30H,1,7-8,11H2,2-6H3/t16-,18+,19-,26-/m1/s1

> <INCHI_KEY>
FSXIFSYEMGCEFU-ZBTFPREESA-N

> <FORMULA>
C26H30Cl2O5

> <MOLECULAR_WEIGHT>
493.42

> <EXACT_MASS>
492.1470295

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
50.71270428432213

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,10aR)-3-chloro-10a-{[(1R,3S)-3-chloro-2,2-dimethyl-6-methylidenecyclohexyl]methyl}-6,8-dihydroxy-2,2,7-trimethyl-2H,3H,5H,10H,10aH-naphtho[2,3-b]pyran-5,10-dione

> <ALOGPS_LOGP>
5.27

> <JCHEM_LOGP>
6.3252416920000005

> <ALOGPS_LOGS>
-5.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.28805122414747

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.773655274661713

> <JCHEM_PKA_STRONGEST_BASIC>
-4.306633758293326

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
130.1449

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.80e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,10aR)-3-chloro-10a-{[(1R,3S)-3-chloro-2,2-dimethyl-6-methylidenecyclohexyl]methyl}-6,8-dihydroxy-2,2,7-trimethyl-3H-naphtho[2,3-b]pyran-5,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 63 66  0  0  0  0  0  0  0  0999 V2000
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  1  2  2  3
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  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
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 13 14  1  0
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 10  2  1  0
 20 12  1  0
 30 23  1  0
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  3 36  1  0
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 29 60  1  0
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 29 62  1  0
 31 63  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      -2.926   1.547  -0.482  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.625   0.297  -0.227  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.517  -0.829  -0.722  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.943  -1.674   0.462  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.928  -1.873   1.516  0.00  0.00           C+0
HETATM    6 Cl   UNK     0      -3.769  -2.317   3.043  0.00  0.00          Cl+0
HETATM    7  C   UNK     0      -2.099  -0.640   1.848  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.110   0.424   2.291  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.161  -0.860   2.968  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.471  -0.190   0.570  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.289   0.677   0.646  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.413   0.949  -0.697  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.309   1.544  -1.637  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.051   2.773  -2.111  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.247   3.565  -2.572  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.807   2.589  -3.375  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.750   3.664  -1.194  0.00  0.00           C+0
HETATM   18 Cl   UNK     0       1.535   4.972  -2.111  0.00  0.00          Cl+0
HETATM   19  C   UNK     0       1.820   2.899  -0.518  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.669   1.641  -0.287  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.708   0.818   0.372  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.534   1.429   1.096  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.748  -0.620   0.174  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.821  -1.212  -0.623  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.891  -2.592  -0.790  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.857  -3.361  -0.180  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.865  -4.751  -0.395  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.794  -2.756   0.627  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.828  -3.603   1.275  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.732  -1.391   0.797  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.678  -0.793   1.610  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.798  -0.411  -1.270  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.249  -0.846  -2.283  0.00  0.00           O+0
HETATM   34  H   UNK     0      -3.831   1.750  -1.060  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.298   2.335  -0.106  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.906  -1.395  -1.446  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.412  -0.417  -1.220  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.901  -1.297   0.891  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.194  -2.683   0.034  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.240  -2.736   1.310  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.919   0.549   1.543  0.00  0.00           H+0
HETATM   42  H   UNK     0      -2.634   1.407   2.430  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.612   0.061   3.229  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.702  -1.437   3.767  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.277  -1.477   2.715  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.889   0.105   3.438  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.182  -1.187   0.048  0.00  0.00           H+0
HETATM   48  H   UNK     0       0.461   0.409   1.386  0.00  0.00           H+0
HETATM   49  H   UNK     0      -0.651   1.706   0.954  0.00  0.00           H+0
HETATM   50  H   UNK     0      -1.738   4.056  -1.704  0.00  0.00           H+0
HETATM   51  H   UNK     0      -1.995   2.817  -2.961  0.00  0.00           H+0
HETATM   52  H   UNK     0      -1.003   4.323  -3.334  0.00  0.00           H+0
HETATM   53  H   UNK     0       1.023   3.584  -3.812  0.00  0.00           H+0
HETATM   54  H   UNK     0       0.192   1.970  -4.064  0.00  0.00           H+0
HETATM   55  H   UNK     0       1.719   2.031  -3.150  0.00  0.00           H+0
HETATM   56  H   UNK     0       0.136   4.143  -0.404  0.00  0.00           H+0
HETATM   57  H   UNK     0       2.720   3.411  -0.226  0.00  0.00           H+0
HETATM   58  H   UNK     0       1.154  -3.072  -1.425  0.00  0.00           H+0
HETATM   59  H   UNK     0       2.178  -5.170  -0.983  0.00  0.00           H+0
HETATM   60  H   UNK     0       4.914  -4.593   0.794  0.00  0.00           H+0
HETATM   61  H   UNK     0       4.622  -3.776   2.346  0.00  0.00           H+0
HETATM   62  H   UNK     0       5.837  -3.125   1.138  0.00  0.00           H+0
HETATM   63  H   UNK     0       5.380  -1.362   2.052  0.00  0.00           H+0
CONECT    1    2   34   35                                                  
CONECT    2    1    3   10                                                  
CONECT    3    2    4   36   37                                             
CONECT    4    3    5   38   39                                             
CONECT    5    4    6    7   40                                             
CONECT    6    5                                                            
CONECT    7    5    8    9   10                                             
CONECT    8    7   41   42   43                                             
CONECT    9    7   44   45   46                                             
CONECT   10    7   11    2   47                                             
CONECT   11   10   12   48   49                                             
CONECT   12   11   13   20   32                                             
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14   50   51   52                                             
CONECT   16   14   53   54   55                                             
CONECT   17   14   18   19   56                                             
CONECT   18   17                                                            
CONECT   19   17   20   57                                                  
CONECT   20   19   21   12                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   30                                                  
CONECT   24   23   25   32                                                  
CONECT   25   24   26   58                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26   59                                                       
CONECT   28   26   29   30                                                  
CONECT   29   28   60   61   62                                             
CONECT   30   28   31   23                                                  
CONECT   31   30   63                                                       
CONECT   32   24   33   12                                                  
CONECT   33   32                                                            
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    3                                                            
CONECT   37    3                                                            
CONECT   38    4                                                            
CONECT   39    4                                                            
CONECT   40    5                                                            
CONECT   41    8                                                            
CONECT   42    8                                                            
CONECT   43    8                                                            
CONECT   44    9                                                            
CONECT   45    9                                                            
CONECT   46    9                                                            
CONECT   47   10                                                            
CONECT   48   11                                                            
CONECT   49   11                                                            
CONECT   50   15                                                            
CONECT   51   15                                                            
CONECT   52   15                                                            
CONECT   53   16                                                            
CONECT   54   16                                                            
CONECT   55   16                                                            
CONECT   56   17                                                            
CONECT   57   19                                                            
CONECT   58   25                                                            
CONECT   59   27                                                            
CONECT   60   29                                                            
CONECT   61   29                                                            
CONECT   62   29                                                            
CONECT   63   31                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  132    0
END

RDKit          3D

63 66  0  0  0  0  0  0  0  0999 V2000
   -2.9262    1.5465   -0.4819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6254    0.2967   -0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5170   -0.8286   -0.7220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9433   -1.6735    0.4621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9282   -1.8725    1.5160 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7690   -2.3172    3.0429 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.0986   -0.6399    1.8480 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1099    0.4242    2.2911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1606   -0.8598    2.9680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4706   -0.1904    0.5697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2894    0.6773    0.6460 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4132    0.9490   -0.6970 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3088    1.5439   -1.6365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0514    2.7728   -2.1113 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2469    3.5648   -2.5718 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8073    2.5892   -3.3749 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7504    3.6644   -1.1939 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5345    4.9722   -2.1115 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.8200    2.8986   -0.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6687    1.6409   -0.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    0.8181    0.3718 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5340    1.4285    1.0964 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7475   -0.6197    0.1740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8208   -1.2116   -0.6227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8906   -2.5925   -0.7900 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8571   -3.3612   -0.1798 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8650   -4.7510   -0.3953 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7937   -2.7557    0.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8278   -3.6029    1.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7320   -1.3913    0.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6776   -0.7925    1.6096 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7979   -0.4113   -1.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2487   -0.8462   -2.2831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8308    1.7495   -1.0599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2977    2.3349   -0.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9055   -1.3945   -1.4455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4116   -0.4169   -1.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9011   -1.2967    0.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1943   -2.6827    0.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2403   -2.7364    1.3104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9186    0.5488    1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6339    1.4072    2.4301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6120    0.0610    3.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7023   -1.4366    3.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2768   -1.4772    2.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8888    0.1048    3.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1822   -1.1873    0.0475 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4612    0.4094    1.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6510    1.7058    0.9536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7380    4.0558   -1.7036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9952    2.8169   -2.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0031    4.3233   -3.3337 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0229    3.5844   -3.8118 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1922    1.9703   -4.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7186    2.0306   -3.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1358    4.1431   -0.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7196    3.4113   -0.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1536   -3.0724   -1.4253 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1775   -5.1697   -0.9831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9142   -4.5932    0.7944 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6218   -3.7759    2.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8370   -3.1247    1.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3798   -1.3620    2.0516 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  1
  7  9  1  0
  7 10  1  0
 10 11  1  0
 12 11  1  1
 12 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  2  0
 30 31  1  0
 24 32  1  0
 32 33  2  0
 10  2  1  0
 20 12  1  0
 30 23  1  0
 32 12  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  6
  8 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  6
 11 48  1  0
 11 49  1  0
 15 50  1  0
 15 51  1  0
 15 52  1  0
 16 53  1  0
 16 54  1  0
 16 55  1  0
 17 56  1  1
 19 57  1  0
 25 58  1  0
 27 59  1  0
 29 60  1  0
 29 61  1  0
 29 62  1  0
 31 63  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₆H₃₀Cl₂O₅

Average Mass

493.4200 Da

Monoisotopic Mass

492.14703 Da

IUPAC Name

(3R,10aR)-3-chloro-10a-{[(1R,3S)-3-chloro-2,2-dimethyl-6-methylidenecyclohexyl]methyl}-6,8-dihydroxy-2,2,7-trimethyl-2H,3H,5H,10H,10aH-naphtho[2,3-b]pyran-5,10-dione

Traditional Name

(3R,10aR)-3-chloro-10a-{[(1R,3S)-3-chloro-2,2-dimethyl-6-methylidenecyclohexyl]methyl}-6,8-dihydroxy-2,2,7-trimethyl-3H-naphtho[2,3-b]pyran-5,10-dione

CAS Registry Number

Not Available

SMILES

CC1=C(O)C=C2C(=O)[C@]3(C[C@@H]4C(=C)CC[C@H](Cl)C4(C)C)OC(C)(C)[C@H](Cl)C=C3C(=O)C2=C1O

InChI Identifier

InChI=1S/C26H30Cl2O5/c1-12-7-8-18(27)24(3,4)16(12)11-26-15(10-19(28)25(5,6)33-26)22(31)20-14(23(26)32)9-17(29)13(2)21(20)30/h9-10,16,18-19,29-30H,1,7-8,11H2,2-6H3/t16-,18+,19-,26-/m1/s1

InChI Key

FSXIFSYEMGCEFU-ZBTFPREESA-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
Unknown-fungus sp.	NPAtlas	15974616

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	5.27	ALOGPS
logP	6.33	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	7.77	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	130.14 m³·mol⁻¹	ChemAxon
Polarizability	50.71 Å³	ChemAxon
Number of Rings	4	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

NPA007936

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9458288

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11283291

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione (NP0005907)

MOL for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

3D MOL for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

3D SDF for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

3D-SDF for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

PDB for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

3D PDB for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

SMILES for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

INCHI for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

Structure for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)

3D Structure for NP0005907 (3-chloro-10a-(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexylmethyl)-6,8-dihydroxy-2,2,7-trimethyl-3,4,4a,10a-tetrahydro-2H-benzo[g]-chromene-5,10-dione)