NP-MRD: Showing NP-Card for (3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione (NP0244582)

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Record Information

Version

2.0

Created at

2022-09-07 05:25:27 UTC

Updated at

2022-09-07 05:25:27 UTC

NP-MRD ID

NP0244582

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione

Description

(3R)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4,6,11-tetrahydro-1H-2-oxatetracene-1,6,11-trione belongs to the class of organic compounds known as isochromanequinones. These are polycyclic compounds containing an isochromanequinone, which is structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton. (3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione is found in Dermocybe sanguinea. Based on a literature review very few articles have been published on (3R)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4,6,11-tetrahydro-1H-2-oxatetracene-1,6,11-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072207252D          

 27 30  0  0  1  0            999 V2000
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   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
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 15 27  1  0  0  0  0
M  END

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
    6.8322   -1.2381    1.2583 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6672   -1.7297    0.6047 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4850   -0.9693    0.6437 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4268    0.2296    1.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2754    1.0318    1.3658 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2982    2.2121    2.0317 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1342    0.5826    0.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1755   -0.6266    0.0822 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3395   -1.4050    0.0274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616   -1.1039   -0.5795 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0281   -2.2205   -1.1808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2992   -0.3785   -0.5858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4177   -0.8648   -1.2218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3831   -2.0620   -1.8789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6059   -0.1248   -1.1962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6654    1.0771   -0.5443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5077    1.5567    0.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6427    2.7545    0.7247 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3127    0.8414    0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8814    1.3383    0.7568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8569    2.4299    1.3577 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8899    1.8592   -0.4879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0033    2.9526    0.0850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0182    1.3259   -1.1333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0920   -0.0912   -1.3215 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3660   -0.7303    0.0253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8122   -0.6325   -1.8918 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9454   -0.1739    0.8972 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -1.8253    0.9751 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6997   -1.2262    2.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3011    0.6246    1.7990 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7467    2.9424    2.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3154   -2.3490   -0.5071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0979   -2.5315   -2.3752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0286    3.2848    1.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9336   -0.2644   -1.9956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5287   -0.4823    0.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3188   -0.3106    0.4316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5034   -1.8019   -0.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8843   -1.7406   -1.8251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7860   -0.3202   -2.9740 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 20  1  0
 20 21  2  0
 20 19  1  0
 19 17  2  0
 17 18  1  0
 17 16  1  0
 16 15  2  0
 15 27  1  0
 27 25  1  0
 25 26  1  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
 15 13  1  0
 13 14  1  0
 13 12  2  0
 12 10  1  0
 10 11  2  0
 10  8  1  0
  8  9  2  0
  9  3  1  0
  8  7  1  0
 12 19  1  0
 22 16  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  6 32  1  0
 18 35  1  0
 27 40  1  0
 27 41  1  0
 25 36  1  6
 26 37  1  0
 26 38  1  0
 26 39  1  0
 14 34  1  0
  9 33  1  0
M  END


  Mrv1652309072207252D          

 27 30  0  0  1  0            999 V2000
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   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
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 15 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0244582

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(=O)C3=C(O)C4=C(C[C@@H](C)OC4=O)C(O)=C3C(=O)C2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H14O8/c1-6-3-8-12(19(25)27-6)18(24)14-13(15(8)21)16(22)9-4-7(26-2)5-10(20)11(9)17(14)23/h4-6,20-21,24H,3H2,1-2H3/t6-/m1/s1

> <INCHI_KEY>
NWKXJUHARHFAFD-ZCFIWIBFSA-N

> <FORMULA>
C19H14O8

> <MOLECULAR_WEIGHT>
370.313

> <EXACT_MASS>
370.068867411

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
36.10649912452644

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4,6,11-tetrahydro-1H-2-oxatetracene-1,6,11-trione

> <JCHEM_LOGP>
4.710279338999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.29567362956676

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.641117484518217

> <JCHEM_PKA_STRONGEST_BASIC>
-3.914234571200258

> <JCHEM_POLAR_SURFACE_AREA>
130.35999999999999

> <JCHEM_REFRACTIVITY>
93.3106

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.335  -7.700   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.000  -9.240   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   20                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    3                                                       
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   19                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   27                                                  
CONECT   16   15   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12   20                                                  
CONECT   20   19    7   21                                                  
CONECT   21   20                                                            
CONECT   22   16   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   15                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₄O₈

Average Mass

370.3130 Da

Monoisotopic Mass

370.06887 Da

IUPAC Name

(3R)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4,6,11-tetrahydro-1H-2-oxatetracene-1,6,11-trione

Traditional Name

(3R)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=O)C3=C(O)C4=C(C[C@@H](C)OC4=O)C(O)=C3C(=O)C2=C1

InChI Identifier

InChI=1S/C19H14O8/c1-6-3-8-12(19(25)27-6)18(24)14-13(15(8)21)16(22)9-4-7(26-2)5-10(20)11(9)17(14)23/h4-6,20-21,24H,3H2,1-2H3/t6-/m1/s1

InChI Key

NWKXJUHARHFAFD-ZCFIWIBFSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Dermocybe sanguinea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isochromanequinones. These are polycyclic compounds containing an isochromanequinone, which is structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isochromanequinones

Sub Class

Not Available

Direct Parent

Isochromanequinones

Alternative Parents

Substituents

9,10-anthraquinone
Anthraquinone
Isochromanequinone
Naphthopyranone
Anthracene
Naphthopyran
Dihydroxybenzoic acid
Benzopyran
Isochromane
2-benzopyran
Anisole
Aryl ketone
Pyranone
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Pyran
Vinylogous acid
Lactone
Ketone
Carboxylic acid ester
Polyol
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Ether
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	4.71	ChemAxon
pKa (Strongest Acidic)	7.64	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.36 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	93.31 m³·mol⁻¹	ChemAxon
Polarizability	36.11 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162961229

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione (NP0244582)

MOL for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

3D MOL for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

3D SDF for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

3D-SDF for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

PDB for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

3D PDB for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

SMILES for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

INCHI for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

Structure for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)

3D Structure for NP0244582 ((3r)-5,10,12-trihydroxy-8-methoxy-3-methyl-3,4-dihydro-2-oxatetracene-1,6,11-trione)