NP-MRD: Showing NP-Card for 1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate (NP0240333)

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Record Information

Version

2.0

Created at

2022-09-07 00:07:44 UTC

Updated at

2022-09-07 00:07:44 UTC

NP-MRD ID

NP0240333

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate

Description

MADERONE belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone). Based on a literature review very few articles have been published on MADERONE.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202072D          

 26 27  0  0  0  0            999 V2000
   -4.2868    2.4750    0.0000 C   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
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    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
   -2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 O   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
   -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 O   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
    0.7145    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    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
    3.5724    2.8875    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
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 O   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
  6  7  1  0  0  0  0
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  8 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
   -5.9111   -1.0833   -0.1440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5751   -1.4600   -0.0872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5251   -0.5622    0.1535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7337    0.7863    0.3566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6701    1.6343    0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8577    2.9891    0.7963 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1815    3.4839    0.7601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3627    1.1693    0.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1308   -0.1756    0.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2254   -1.0107    0.1952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0077   -2.3617   -0.0074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7957   -2.7847   -1.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2298   -0.6991    0.4644 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3821   -2.0642    0.2535 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3121    0.0290    0.6801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6803   -0.5677    0.7060 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5337    0.0359   -0.3592 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8797   -0.2414   -1.7052 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8048   -0.5889   -0.2984 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9703    0.1320   -0.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2742   -0.5784   -0.0360 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9166    1.3746    0.0506 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1513    1.4611    0.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1373    2.2234    1.1143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2138    2.0323    0.8739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829    3.2451    1.0582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2310   -0.8899   -1.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1891   -0.2647    0.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5223   -1.9707    0.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7575    1.1718    0.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5784    3.4985   -0.2739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2031    4.5370    1.1175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8521    2.9143    1.4602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8148   -2.8966   -1.8010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2299   -3.7271   -1.4126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3132   -1.9514   -1.9230 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7834   -2.6762    0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6096   -1.6699    0.6048 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0792   -0.3642    1.7266 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6790    1.1043   -0.2180 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9414    0.3416   -1.7705 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5981   -1.3031   -1.8069 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5686    0.0844   -2.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1184    0.1193   -0.0960 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3406   -1.1100    0.9423 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2742   -1.3662   -0.8107 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
  6  7  1  0
  5  8  2  0
  8 25  1  0
 25 26  2  0
 25 23  1  0
 23 24  2  0
 23 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 15 13  2  0
 13 14  1  0
 13  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 10  3  1  0
  9  8  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
 16 38  1  0
 16 39  1  0
 17 40  1  1
 18 41  1  0
 18 42  1  0
 18 43  1  0
 21 44  1  0
 21 45  1  0
 21 46  1  0
 14 37  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
M  END


  Mrv1652309072202072D          

 26 27  0  0  0  0            999 V2000
   -4.2868    2.4750    0.0000 C   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
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    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
   -2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 O   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
   -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 O   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
    0.7145    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    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
    3.5724    2.8875    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
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 O   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
  6  7  1  0  0  0  0
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  8 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0240333

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C2C(=O)C(=O)C(CC(C)OC(C)=O)=C(O)C2=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C18H20O8/c1-8(26-9(2)19)6-10-15(20)14-13(17(22)16(10)21)11(23-3)7-12(24-4)18(14)25-5/h7-8,20H,6H2,1-5H3

> <INCHI_KEY>
BBMJALGKCLSLAE-UHFFFAOYSA-N

> <FORMULA>
C18H20O8

> <MOLECULAR_WEIGHT>
364.35

> <EXACT_MASS>
364.115817604

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
35.98450212350877

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxo-3,4-dihydronaphthalen-2-yl)propan-2-yl acetate

> <JCHEM_LOGP>
1.2408794373333327

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.837535617502504

> <JCHEM_PKA_STRONGEST_BASIC>
-4.432385589168734

> <JCHEM_POLAR_SURFACE_AREA>
108.35999999999999

> <JCHEM_REFRACTIVITY>
91.90399999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate

> <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      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.668   5.390   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335   3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -4.001   0.770   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001   5.390   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001   6.930   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -5.335   7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   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  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.001   5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668   5.390   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.335   3.080   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.334   0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9   25                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9    3   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13    9   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   15   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    8   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₀O₈

Average Mass

364.3500 Da

Monoisotopic Mass

364.11582 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C2C(=O)C(=O)C(CC(C)OC(C)=O)=C(O)C2=C1OC

InChI Identifier

InChI=1S/C18H20O8/c1-8(26-9(2)19)6-10-15(20)14-13(17(22)16(10)21)11(23-3)7-12(24-4)18(14)25-5/h7-8,20H,6H2,1-5H3

InChI Key

BBMJALGKCLSLAE-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, 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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone).

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Naphthoquinone
1-naphthol
Aryl ketone
Quinone
Anisole
Alkyl aryl ether
Vinylogous acid
Cyclic ketone
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Enol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source

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

35797879

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90477921

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate (NP0240333)

MOL for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

3D MOL for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

3D SDF for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

3D-SDF for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

PDB for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

3D PDB for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

SMILES for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

INCHI for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

Structure for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)

3D Structure for NP0240333 (1-(1-hydroxy-5,7,8-trimethoxy-3,4-dioxonaphthalen-2-yl)propan-2-yl acetate)