NP-MRD: Showing NP-Card for 4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone (NP0200249)

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Record Information

Version

2.0

Created at

2022-09-04 19:02:54 UTC

Updated at

2022-09-04 19:02:54 UTC

NP-MRD ID

NP0200249

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone

Description

[1,1'-Binaphthalene]-5,5',8,8'-tetrone, 6,7-dihydro-4,4'-dihydroxy-7,7'-dimethyl- belongs to the class of organic compounds known as biphenols. These are organic compounds containing two phenol groups linked together by a C-C bond. 4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone is found in Diospyros maritima and Plumbago zeylanica. Based on a literature review very few articles have been published on [1,1'-Binaphthalene]-5,5',8,8'-tetrone, 6,7-dihydro-4,4'-dihydroxy-7,7'-dimethyl-.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042221022D          

 28 31  0  0  0  0            999 V2000
   -4.2868   -1.6500    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
   -3.5724   -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
   -2.8579    0.8250    0.0000 O   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
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 O   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
   -0.7145   -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 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 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
   -0.7145   -3.7125    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
    0.0000   -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
    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
    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 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
   -2.1434   -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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  2  0  0  0  0
 11 26  2  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
   -3.6671   -1.2767    2.8525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5149   -0.8516    1.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4701   -1.0042    0.5348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2305   -0.5645   -0.8442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1814   -0.7279   -1.6849 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9799    0.0312   -1.2548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7850    0.4056   -2.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8234    0.2199   -3.4551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5759    0.9445   -2.9250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5674    1.1145   -2.0056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7518    0.7422   -0.6835 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2966    1.0428    0.2600 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0749    1.9955    1.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1072    2.3446    2.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3570    1.7735    1.9833 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4189    2.1085    2.8220 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5940    0.8290    1.0082 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5669    0.4642    0.1479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8633   -0.5393   -0.8440 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8936   -1.0797   -1.4457 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2136   -1.0115   -1.2364 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2992   -2.5223   -1.1346 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3243   -0.4083   -0.4468 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8732    0.1747    0.8368 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6267    0.1151    1.8681 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9507    0.2033   -0.3201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2286   -0.2505    1.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3267   -0.1172    1.9075 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1746   -2.2924    2.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7112   -1.3128    3.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0803   -0.6078    3.4901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4118   -1.4451    0.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7665    0.4662   -4.4242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4469    1.2311   -3.9632 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3759    1.5405   -2.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8781    2.4947    1.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9538    3.0965    2.8878 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2534    2.8010    3.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3720   -0.7464   -2.3149 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4144   -2.7549   -0.0395 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4265   -3.0168   -1.5568 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2495   -2.8215   -1.5961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8707    0.4021   -0.9819 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0969   -1.1902   -0.2160 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 23  1  0
 23 24  1  0
 24 25  2  0
 24 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 18 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 12 11  1  0
 11 26  2  0
 26 27  1  0
 27 28  2  0
 27  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 19 21  1  0
 10 11  1  0
 15 17  1  0
  6 26  1  0
 22 40  1  0
 22 41  1  0
 22 42  1  0
 21 39  1  6
 23 43  1  0
 23 44  1  0
 13 36  1  0
 14 37  1  0
 16 38  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
M  END


  Mrv1652309042221022D          

 28 31  0  0  0  0            999 V2000
   -4.2868   -1.6500    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
   -3.5724   -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
   -2.8579    0.8250    0.0000 O   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
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 O   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
   -0.7145   -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 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 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
   -0.7145   -3.7125    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
    0.0000   -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
    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
    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 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
   -2.1434   -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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  2  0  0  0  0
 11 26  2  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0200249

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(=O)C2=C(C1=O)C(=CC=C2O)C1=C2C(=O)C(C)=CC(=O)C2=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H16O6/c1-9-7-15(25)19-13(23)5-3-11(17(19)21(9)27)12-4-6-14(24)20-16(26)8-10(2)22(28)18(12)20/h3-7,10,23-24H,8H2,1-2H3

> <INCHI_KEY>
YJYNIQQTZMGISK-UHFFFAOYSA-N

> <FORMULA>
C22H16O6

> <MOLECULAR_WEIGHT>
376.364

> <EXACT_MASS>
376.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
37.606306719830044

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,4'-dihydroxy-7,7'-dimethyl-7,8-dihydro-5H,5'H,6H,8'H-[1,1'-binaphthalene]-5,5',8,8'-tetrone

> <JCHEM_LOGP>
3.936452935666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.178299771413858

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.495074462597822

> <JCHEM_PKA_STRONGEST_BASIC>
-6.032469877431864

> <JCHEM_POLAR_SURFACE_AREA>
108.74

> <JCHEM_REFRACTIVITY>
103.26799999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.335   1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.667   1.540   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.000  -9.240   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   26                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   26                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   24                                                  
CONECT   18   17   12   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   17   25                                                  
CONECT   25   24                                                            
CONECT   26   11    6   27                                                  
CONECT   27   26    2   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₁₆O₆

Average Mass

376.3640 Da

Monoisotopic Mass

376.09469 Da

IUPAC Name

4,4'-dihydroxy-7,7'-dimethyl-7,8-dihydro-5H,5'H,6H,8'H-[1,1'-binaphthalene]-5,5',8,8'-tetrone

Traditional Name

4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone

CAS Registry Number

Not Available

SMILES

CC1CC(=O)C2=C(C1=O)C(=CC=C2O)C1=C2C(=O)C(C)=CC(=O)C2=C(O)C=C1

InChI Identifier

InChI=1S/C22H16O6/c1-9-7-15(25)19-13(23)5-3-11(17(19)21(9)27)12-4-6-14(24)20-16(26)8-10(2)22(28)18(12)20/h3-7,10,23-24H,8H2,1-2H3

InChI Key

YJYNIQQTZMGISK-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
Diospyros maritima	LOTUS Database	35616633
Plumbago zeylanica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biphenols. These are organic compounds containing two phenol groups linked together by a C-C bond.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Biphenols

Direct Parent

Biphenols

Alternative Parents

Substituents

Biphenol
Naphthoquinone
Naphthalene
Tetralin
Aryl alkyl ketone
Aryl ketone
Quinone
1-hydroxy-2-unsubstituted benzenoid
Phenol
Vinylogous acid
Ketone
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
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	3.94	ChemAxon
pKa (Strongest Acidic)	7.5	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	108.74 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	103.27 m³·mol⁻¹	ChemAxon
Polarizability	37.61 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

4440577

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5276617

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone (NP0200249)

MOL for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

3D MOL for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

3D SDF for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

3D-SDF for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

PDB for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

3D PDB for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

SMILES for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

INCHI for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

Structure for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)

3D Structure for NP0200249 (4,4'-dihydroxy-7,7'-dimethyl-6,7-dihydro-[1,1'-binaphthalene]-5,5',8,8'-tetrone)