NP-MRD: Showing NP-Card for 7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione (NP0171332)

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Record Information

Version

2.0

Created at

2022-09-03 07:48:34 UTC

Updated at

2022-09-03 07:48:34 UTC

NP-MRD ID

NP0171332

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione

Description

Imbricatonol 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). 7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione is found in Stypandra glauca. Imbricatonol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251523522D          

 33 36  0  0  0  0            999 V2000
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   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
   -2.1434   -3.7125    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
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -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
    0.0000   -1.6500    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
    0.7145   -2.8875    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
    0.0000   -4.1250    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 C   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
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    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
    2.8579   -2.4750    0.0000 O   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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  2  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 25 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 21 31  1  0  0  0  0
 31 32  2  0  0  0  0
 18 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
   -6.6888    2.6975   -0.0427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8415    1.2377   -0.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9985    0.7509   -0.0742 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6964    0.3202   -0.1276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8947   -1.0388   -0.1620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2453   -1.6580   -0.1554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7842   -1.8458   -0.2043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4808   -1.3553   -0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3015    0.0256   -0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3957    0.8791   -0.1351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2500    2.2245   -0.1002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9193    0.4958   -0.1905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6892    1.7124   -0.1558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7578   -0.4130   -0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6102    0.0926   -0.2372 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8020    1.2476   -1.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0899    1.7014   -1.2063 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1787    1.0299   -0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4629    1.4691   -0.8574 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5613    0.7859   -0.3054 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9226    1.3283   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3910   -0.3489    0.4512 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4552   -1.0977    1.0416 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9065   -0.8512    0.9797 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1365   -2.1436    1.7322 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0687   -0.8158    0.6630 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8098   -1.9037    1.3813 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0127   -0.0898    0.0856 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6985   -0.5589    0.2990 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5831   -1.6748    1.0679 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9967   -1.7140   -0.2675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3471   -2.2638   -0.2587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5044   -3.5101   -0.2900 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1860    3.0109    0.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2107    3.1394   -0.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7118    3.1727    0.0213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8233   -1.4063    0.7576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8649   -1.3547   -1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1160   -2.7692   -0.2553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8664   -2.9398   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4759    2.7877   -0.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0098    1.7970   -1.4661 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2761    2.5881   -1.7916 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6359    2.3543   -1.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5180    1.4937    0.3403 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7415    2.4050   -0.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4323    0.8769   -1.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2358   -0.1248    1.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3195   -0.6615   -0.0218 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4657   -1.8239    1.2725 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0450   -2.6345    1.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8434   -2.1836    1.4328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1658   -2.4423   -0.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 25  2  0
 23 22  1  0
 22 26  2  0
 26 27  1  0
 26 28  1  0
 28 29  2  0
 29 30  1  0
 29 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 15 14  1  0
 14 31  2  0
 31 32  1  0
 32 33  2  0
 32  8  1  0
  8  7  2  0
  7  5  1  0
  5  6  1  0
  5  4  2  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  4 10  1  0
 10 11  1  0
 10  9  2  0
  9 12  1  0
 12 13  2  0
 20 22  1  0
 12 14  1  0
 18 28  1  0
  9  8  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
 27 51  1  0
 30 52  1  0
 16 42  1  0
 17 43  1  0
 19 44  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 31 53  1  0
  7 40  1  0
  6 37  1  0
  6 38  1  0
  6 39  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
 11 41  1  0
M  END


  Mrv1533004251523522D          

 33 36  0  0  0  0            999 V2000
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   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
   -2.1434   -3.7125    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
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -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
    0.0000   -1.6500    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
    0.7145   -2.8875    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
    0.0000   -4.1250    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 C   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
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    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
    2.8579   -2.4750    0.0000 O   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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  2  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 25 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 21 31  1  0  0  0  0
 31 32  2  0  0  0  0
 18 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171332

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)C1=C(O)C2=C(O)C(=CC=C2C=C1C)C1=CC(=O)C2=CC(C)=C(C(C)=O)C(O)=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H20O7/c1-10-7-14-5-6-15(23(30)21(14)25(32)19(10)12(3)27)16-9-18(29)17-8-11(2)20(13(4)28)26(33)22(17)24(16)31/h5-9,30,32-33H,1-4H3

> <INCHI_KEY>
CAENAFFQDWSJRV-UHFFFAOYSA-N

> <FORMULA>
C26H20O7

> <MOLECULAR_WEIGHT>
444.439

> <EXACT_MASS>
444.120902984

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
47.14702407571323

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-acetyl-2-(7-acetyl-1,8-dihydroxy-6-methylnaphthalen-2-yl)-8-hydroxy-6-methyl-1,4-dihydronaphthalene-1,4-dione

> <ALOGPS_LOGP>
4.07

> <JCHEM_LOGP>
5.333324353666667

> <ALOGPS_LOGS>
-5.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.028044944423316

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.1089769226806405

> <JCHEM_PKA_STRONGEST_BASIC>
-4.885142551008362

> <JCHEM_POLAR_SURFACE_AREA>
128.97

> <JCHEM_REFRACTIVITY>
123.91619999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-acetyl-2-(7-acetyl-1,8-dihydroxy-6-methylnaphthalen-2-yl)-8-hydroxy-6-methylnaphthalene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.334 -10.010   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   16                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    8   16                                                  
CONECT   16   15    4   17                                                  
CONECT   17   16                                                            
CONECT   18   12   19   32                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   31                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   29                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   25   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   21   32                                                  
CONECT   32   31   18   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₀O₇

Average Mass

444.4390 Da

Monoisotopic Mass

444.12090 Da

IUPAC Name

7-acetyl-2-(7-acetyl-1,8-dihydroxy-6-methylnaphthalen-2-yl)-8-hydroxy-6-methyl-1,4-dihydronaphthalene-1,4-dione

Traditional Name

7-acetyl-2-(7-acetyl-1,8-dihydroxy-6-methylnaphthalen-2-yl)-8-hydroxy-6-methylnaphthalene-1,4-dione

CAS Registry Number

Not Available

SMILES

CC(=O)C1=C(O)C2=C(O)C(=CC=C2C=C1C)C1=CC(=O)C2=CC(C)=C(C(C)=O)C(O)=C2C1=O

InChI Identifier

InChI=1S/C26H20O7/c1-10-7-14-5-6-15(23(30)21(14)25(32)19(10)12(3)27)16-9-18(29)17-8-11(2)20(13(4)28)26(33)22(17)24(16)31/h5-9,30,32-33H,1-4H3

InChI Key

CAENAFFQDWSJRV-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

Species Name	Source	Reference
Stypandra glauca	LOTUS Database	35616633

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
Acetophenone
Aryl alkyl ketone
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
Vinylogous acid
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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
logP	4.07	ALOGPS
logP	5.33	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	7.11	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	128.97 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	123.92 m³·mol⁻¹	ChemAxon
Polarizability	47.15 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

188769

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione (NP0171332)

MOL for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

3D MOL for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

3D SDF for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

3D-SDF for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

PDB for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

3D PDB for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

SMILES for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

INCHI for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

Structure for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)

3D Structure for NP0171332 (7,7'-diacetyl-1',8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,4-dione)