NP-MRD: Showing NP-Card for Naphterpin B (NP0005924)

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Record Information

Version

2.0

Created at

2020-12-09 03:02:20 UTC

Updated at

2021-07-15 16:53:21 UTC

NP-MRD ID

NP0005924

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Naphterpin B

Provided By

NPAtlas

Description

Naphterpin B is found in Streptomyces sp. CL190. Based on a literature review very few articles have been published on Naphterpin B.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118243D          

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M  END

     RDKit          3D

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 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
  8  2  1  0  0  0  0
 27 12  1  0  0  0  0
 14  6  1  0  0  0  0
 23 16  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  4 31  1  0  0  0  0
  5 32  1  0  0  0  0
  9 33  1  0  0  0  0
 17 34  1  0  0  0  0
 19 35  1  0  0  0  0
 19 36  1  0  0  0  0
 19 37  1  0  0  0  0
 20 38  1  0  0  0  0
 21 39  1  0  0  0  0
 21 40  1  0  0  0  0
 22 41  1  0  0  0  0
 22 42  1  0  0  0  0
 23 43  1  6  0  0  0
 25 44  1  0  0  0  0
 25 45  1  0  0  0  0
 25 46  1  0  0  0  0
 26 47  1  0  0  0  0
 26 48  1  0  0  0  0
 26 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005924

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C(O[H])=C2C(=O)C3=C(C(=O)C2=C1[H])C1=C([H])[C@@](O[H])(C([H])([H])[H])C([H])([H])C([H])([H])[C@]1([H])C(O3)(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O6/c1-9-13(22)7-10-14(16(9)23)18(25)19-15(17(10)24)11-8-21(4,26)6-5-12(11)20(2,3)27-19/h7-8,12,22-23,26H,5-6H2,1-4H3/t12-,21+/m0/s1

> <INCHI_KEY>
IENVNCRRTRCLFH-LAJNKCICSA-N

> <FORMULA>
C21H22O6

> <MOLECULAR_WEIGHT>
370.401

> <EXACT_MASS>
370.141638428

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
39.28367913178883

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4aS)-2,8,10-trihydroxy-2,5,5,9-tetramethyl-3,4,4a,5,7,12-hexahydro-2H-6-oxatetraphene-7,12-dione

> <ALOGPS_LOGP>
3.06

> <JCHEM_LOGP>
2.4301058390000003

> <ALOGPS_LOGS>
-3.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.15261611986297

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.647593142249848

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2761261853383772

> <JCHEM_POLAR_SURFACE_AREA>
104.06

> <JCHEM_REFRACTIVITY>
101.61200000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4aS)-2,8,10-trihydroxy-2,5,5,9-tetramethyl-4,4a-dihydro-3H-6-oxatetraphene-7,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 49 52  0  0  0  0  0  0  0  0999 V2000
    6.5651    0.0274    0.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1260    0.3270    0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7147    1.6278    0.1899 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6409    2.6873    0.2049 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3705    1.8528    0.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4301    0.8572    0.0907 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8780   -0.4731    0.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2222   -0.7595    0.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7007   -2.0178    0.3126 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8774   -1.5310    0.1411 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2070   -2.7490    0.2001 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4576   -1.2119    0.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0648    0.0579   -0.0112 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0098    1.1520    0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6349    2.3312   -0.0596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3688    0.3160   -0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8381    1.3741    0.5057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2862    1.6878    0.4583 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4473    3.1921    0.5551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9649    1.1504    1.5533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8493    1.1327   -0.8110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727   -0.3703   -0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1974   -0.6659   -0.8381 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8441   -2.0399   -0.3791 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0637   -3.0431   -1.5195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7255   -2.5009    0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5198   -2.1864    0.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8478   -0.8463   -0.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1577    0.9097    0.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8182   -0.1744    1.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2848    3.6330    0.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0130    2.8801    0.0542 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3057   -2.8846    0.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2109    2.0434    1.0564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0053    3.7339   -0.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0063    3.4832    1.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5484    3.3762    0.6714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3398    0.7520    2.2149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9039    1.4156   -0.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2601    1.5209   -1.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1710   -0.8397    0.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1692   -0.7731   -1.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9297   -0.5808   -1.9103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1967   -4.0409   -1.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9218   -2.7667   -2.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1267   -3.1258   -2.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6536   -2.9854    0.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9250   -1.6679    1.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1811   -3.2876    1.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  7 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 13 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  1  1
 18 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  6
 24 26  1  0
 24 27  1  0
  8  2  1  0
 27 12  1  0
 14  6  1  0
 23 16  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  5 32  1  0
  9 33  1  0
 17 34  1  0
 19 35  1  0
 19 36  1  0
 19 37  1  0
 20 38  1  0
 21 39  1  0
 21 40  1  0
 22 41  1  0
 22 42  1  0
 23 43  1  6
 25 44  1  0
 25 45  1  0
 25 46  1  0
 26 47  1  0
 26 48  1  0
 26 49  1  0
M  END

HEADER    PROTEIN                                 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       6.565   0.027   0.346  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.126   0.327   0.257  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.715   1.628   0.190  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.641   2.687   0.205  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.370   1.853   0.109  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.430   0.857   0.091  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.878  -0.473   0.160  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.222  -0.760   0.244  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.701  -2.018   0.313  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.877  -1.531   0.141  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.207  -2.749   0.200  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.458  -1.212   0.053  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.065   0.058  -0.011  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.010   1.152   0.003  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.635   2.331  -0.060  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.369   0.316  -0.089  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.838   1.374   0.506  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.286   1.688   0.458  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.447   3.192   0.555  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.965   1.150   1.553  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.849   1.133  -0.811  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.673  -0.370  -0.754  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.197  -0.666  -0.838  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.844  -2.040  -0.379  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.064  -3.043  -1.520  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.725  -2.501   0.781  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.520  -2.186   0.032  0.00  0.00           O+0
HETATM   28  H   UNK     0       6.848  -0.846  -0.289  0.00  0.00           H+0
HETATM   29  H   UNK     0       7.158   0.910   0.013  0.00  0.00           H+0
HETATM   30  H   UNK     0       6.818  -0.174   1.424  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.285   3.633   0.153  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.013   2.880   0.054  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.306  -2.885   0.320  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.211   2.043   1.056  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.005   3.734  -0.281  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.006   3.483   1.542  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.548   3.376   0.671  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.340   0.752   2.215  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.904   1.416  -0.988  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.260   1.521  -1.653  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.171  -0.840   0.093  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.169  -0.773  -1.678  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.930  -0.581  -1.910  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.197  -4.041  -1.022  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.922  -2.767  -2.143  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.127  -3.126  -2.110  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.654  -2.985   0.414  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.925  -1.668   1.492  0.00  0.00           H+0
HETATM   49  H   UNK     0      -2.181  -3.288   1.371  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    1    3    8                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3   31                                                       
CONECT    5    3    6   32                                                  
CONECT    6    5    7   14                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9    2                                                  
CONECT    9    8   33                                                       
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   27                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   15    6                                                  
CONECT   15   14                                                            
CONECT   16   13   17   23                                                  
CONECT   17   16   18   34                                                  
CONECT   18   17   19   20   21                                             
CONECT   19   18   35   36   37                                             
CONECT   20   18   38                                                       
CONECT   21   18   22   39   40                                             
CONECT   22   21   23   41   42                                             
CONECT   23   22   24   16   43                                             
CONECT   24   23   25   26   27                                             
CONECT   25   24   44   45   46                                             
CONECT   26   24   47   48   49                                             
CONECT   27   24   12                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    9                                                            
CONECT   34   17                                                            
CONECT   35   19                                                            
CONECT   36   19                                                            
CONECT   37   19                                                            
CONECT   38   20                                                            
CONECT   39   21                                                            
CONECT   40   21                                                            
CONECT   41   22                                                            
CONECT   42   22                                                            
CONECT   43   23                                                            
CONECT   44   25                                                            
CONECT   45   25                                                            
CONECT   46   25                                                            
CONECT   47   26                                                            
CONECT   48   26                                                            
CONECT   49   26                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  104    0
END

RDKit          3D

49 52  0  0  0  0  0  0  0  0999 V2000
    6.5651    0.0274    0.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1260    0.3270    0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7147    1.6278    0.1899 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6409    2.6873    0.2049 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3705    1.8528    0.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4301    0.8572    0.0907 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8780   -0.4731    0.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2222   -0.7595    0.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7007   -2.0178    0.3126 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8774   -1.5310    0.1411 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2070   -2.7490    0.2001 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4576   -1.2119    0.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0648    0.0579   -0.0112 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0098    1.1520    0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6349    2.3312   -0.0596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3688    0.3160   -0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8381    1.3741    0.5057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2862    1.6878    0.4583 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4473    3.1921    0.5551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9649    1.1504    1.5533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8493    1.1327   -0.8110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727   -0.3703   -0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1974   -0.6659   -0.8381 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8441   -2.0399   -0.3791 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0637   -3.0431   -1.5195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7255   -2.5009    0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5198   -2.1864    0.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8478   -0.8463   -0.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1577    0.9097    0.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8182   -0.1744    1.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2848    3.6330    0.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0130    2.8801    0.0542 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3057   -2.8846    0.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2109    2.0434    1.0564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0053    3.7339   -0.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0063    3.4832    1.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5484    3.3762    0.6714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3398    0.7520    2.2149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9039    1.4156   -0.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2601    1.5209   -1.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1710   -0.8397    0.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1692   -0.7731   -1.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9297   -0.5808   -1.9103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1967   -4.0409   -1.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9218   -2.7667   -2.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1267   -3.1258   -2.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6536   -2.9854    0.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9250   -1.6679    1.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1811   -3.2876    1.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  7 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 13 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  1  1
 18 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  6
 24 26  1  0
 24 27  1  0
  8  2  1  0
 27 12  1  0
 14  6  1  0
 23 16  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  5 32  1  0
  9 33  1  0
 17 34  1  0
 19 35  1  0
 19 36  1  0
 19 37  1  0
 20 38  1  0
 21 39  1  0
 21 40  1  0
 22 41  1  0
 22 42  1  0
 23 43  1  6
 25 44  1  0
 25 45  1  0
 25 46  1  0
 26 47  1  0
 26 48  1  0
 26 49  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Naphterpin C	MeSH

Chemical Formula

C₂₁H₂₂O₆

Average Mass

370.4010 Da

Monoisotopic Mass

370.14164 Da

IUPAC Name

(2R,4aS)-2,8,10-trihydroxy-2,5,5,9-tetramethyl-3,4,4a,5,7,12-hexahydro-2H-6-oxatetraphene-7,12-dione

Traditional Name

(2R,4aS)-2,8,10-trihydroxy-2,5,5,9-tetramethyl-4,4a-dihydro-3H-6-oxatetraphene-7,12-dione

CAS Registry Number

Not Available

SMILES

CC1=C(O)C=C2C(=O)C3=C(OC(C)(C)[C@H]4CC[C@@](C)(O)C=C34)C(=O)C2=C1O

InChI Identifier

InChI=1S/C21H22O6/c1-9-13(22)7-10-14(16(9)23)18(25)19-15(17(10)24)11-8-21(4,26)6-5-12(11)20(2,3)27-19/h7-8,12,22-23,26H,5-6H2,1-4H3/t12-,21+/m0/s1

InChI Key

IENVNCRRTRCLFH-LAJNKCICSA-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
Streptomyces sp. CL190	NPAtlas	15981415

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.06	ALOGPS
logP	2.43	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	7.65	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	101.61 m³·mol⁻¹	ChemAxon
Polarizability	39.28 Å³	ChemAxon
Number of Rings	4	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

NPA019691

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9524160

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11349223

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Naphterpin B (NP0005924)

MOL for NP0005924 (Naphterpin B)

3D MOL for NP0005924 (Naphterpin B)

3D SDF for NP0005924 (Naphterpin B)

3D-SDF for NP0005924 (Naphterpin B)

PDB for NP0005924 (Naphterpin B)

3D PDB for NP0005924 (Naphterpin B)

SMILES for NP0005924 (Naphterpin B)

INCHI for NP0005924 (Naphterpin B)

Structure for NP0005924 (Naphterpin B)

3D Structure for NP0005924 (Naphterpin B)