NP-MRD: Showing NP-Card for 2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol (NP0333565)

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Record Information

Version

2.0

Created at

2024-07-05 09:08:48 UTC

Updated at

2024-09-03 04:22:56 UTC

NP-MRD ID

NP0333565

Natural Product DOI

https://doi.org/10.57994/3034

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol

Description

CHEMBL4073402 belongs to the class of organic compounds known as phenanthrols. Phenanthrols are compounds containing a phenanthrene (or its hydrogenated derivative) to which a hydroxyl group is attached. 2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol was first documented in 2024 (PMID: 38945493). Based on a literature review very few articles have been published on CHEMBL4073402.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 03192311432D          

 40 45  0  0  0  0            999 V2000
   -1.6796    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2671    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4421    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0296    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4421    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2671    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6796    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5046    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9171    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0296   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -1.5395    0.0000 C   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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  4 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 25 33  2  0  0  0  0
 33 34  1  0  0  0  0
 22 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 37 38  1  0  0  0  0
 21 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END


  Mrv2104 03192311432D          

 40 45  0  0  0  0            999 V2000
   -1.6796    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2671    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4421    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0296    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4421    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2671    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6796    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5046    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9171    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0296   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -1.5395    0.0000 C   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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  4 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 25 33  2  0  0  0  0
 33 34  1  0  0  0  0
 22 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 37 38  1  0  0  0  0
 21 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0333565

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1O)C1=C(C=C2)C(=C(OC)C=C1O)C1=C(OC)C=C(O)C2=C1C=CC1=C2C=C(O)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H26O8/c1-37-25-9-15-5-7-17-29(19(15)11-21(25)33)23(35)13-27(39-3)31(17)32-18-8-6-16-10-26(38-2)22(34)12-20(16)30(18)24(36)14-28(32)40-4/h5-14,33-36H,1-4H3

> <INCHI_KEY>
XHGHYXJLVZUZSE-UHFFFAOYSA-N

> <FORMULA>
C32H26O8

> <MOLECULAR_WEIGHT>
538.552

> <EXACT_MASS>
538.162767797

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
57.64755622969757

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,2',7,7'-tetramethoxy-[1,1'-biphenanthrene]-4,4',6,6'-tetrol

> <JCHEM_LOGP>
5.733431855333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.045324891653339

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.475739605969999

> <JCHEM_PKA_STRONGEST_BASIC>
-4.277779287094313

> <JCHEM_POLAR_SURFACE_AREA>
117.84000000000002

> <JCHEM_REFRACTIVITY>
150.77139999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2,2',7,7'-tetramethoxy-[1,1'-biphenanthrene]-4,4',6,6'-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-MAR-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-MAR-23         0                                  
HETATM    1  O   UNK     0      -3.135   5.128   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -2.365   3.795   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.825   3.795   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.055   2.461   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.825   1.127   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.365   1.127   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.135   2.461   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.675   2.461   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -5.445   3.795   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.055  -0.206   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.485  -0.206   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.255   1.127   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.485   2.461   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.255   3.795   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.485   5.128   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.795   3.795   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.565   2.461   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.105   2.461   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.875   3.795   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.795   1.127   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.035  -1.540   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.805  -2.874   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      11.495  -4.207   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       6.875  -4.207   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       2.255  -1.540   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       1.485  -2.874   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   13                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    5   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12    4   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   12   21                                                  
CONECT   21   20   22   38                                                  
CONECT   22   21   23   34                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   33                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   25   34                                                  
CONECT   34   33   22   35                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   21   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₂₆O₈

Average Mass

538.5520 Da

Monoisotopic Mass

538.16277 Da

IUPAC Name

2,2',7,7'-tetramethoxy-[1,1'-biphenanthrene]-4,4',6,6'-tetrol

Traditional Name

2,2',7,7'-tetramethoxy-[1,1'-biphenanthrene]-4,4',6,6'-tetrol

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1O)C1=C(C=C2)C(=C(OC)C=C1O)C1=C(OC)C=C(O)C2=C1C=CC1=C2C=C(O)C(OC)=C1

InChI Identifier

InChI=1S/C32H26O8/c1-37-25-9-15-5-7-17-29(19(15)11-21(25)33)23(35)13-27(39-3)31(17)32-18-8-6-16-10-26(38-2)22(34)12-20(16)30(18)24(36)14-28(32)40-4/h5-14,33-36H,1-4H3

InChI Key

XHGHYXJLVZUZSE-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	[email protected]	University of Potsdam	Bernd Schmidt	2024-07-05	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	[email protected]	University of Potsdam	Bernd Schmidt	2024-07-05	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	[email protected]	University of Potsdam	Bernd Schmidt	2024-07-05	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	[email protected]	University of Potsdam	Bernd Schmidt	2024-07-05	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C2D6OS, experimental)	[email protected]	University of Potsdam	Bernd Schmidt	2024-07-05	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C2D6OS, experimental)	[email protected]	University of Potsdam	Bernd Schmidt	2024-07-05	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Dioscorea dumetorum		Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrols. Phenanthrols are compounds containing a phenanthrene (or its hydrogenated derivative) to which a hydroxyl group is attached.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Phenanthrols

Direct Parent

Phenanthrols

Alternative Parents

Substituents

Phenanthrol
Biphenol
1-naphthol
2-naphthol
Naphthalene
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Ether
Organic oxygen compound
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	5.73	ChemAxon
pKa (Strongest Acidic)	8.48	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	117.84 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	150.77 m³·mol⁻¹	ChemAxon
Polarizability	57.65 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

76748426

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

137640605

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol (NP0333565)

MOL for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

3D MOL for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

3D SDF for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

3D-SDF for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

PDB for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

3D PDB for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

SMILES for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

INCHI for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

Structure for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)

3D Structure for NP0333565 (2,2′,7,7′-tetramethoxy-[1,1′-biphenanthrene]-4,4′,6,6′-tetraol)