NP-MRD: Showing NP-Card for 8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol (NP0269347)

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Record Information

Version

2.0

Created at

2022-09-08 14:46:54 UTC

Updated at

2022-09-08 14:46:54 UTC

NP-MRD ID

NP0269347

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

Description

8-(4-Hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol belongs to the class of organic compounds known as hydrophenanthrenes. These are a phenanthrene derivative where at least one ring CC bond is substituted by hydrogenation. 8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol is found in Monomeria barbata. Based on a literature review very few articles have been published on 8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082216462D          

 27 30  0  0  0  0            999 V2000
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    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
  9 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
 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
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 21 27  1  0  0  0  0
  7 27  1  0  0  0  0
M  END

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
   -1.8485   -3.9882   -1.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6955   -2.9081   -0.8628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5709   -2.1040   -0.7740 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5607   -2.2304   -1.5378 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6540   -1.4049   -1.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7205   -1.6265   -2.2461 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5950   -0.4045   -0.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4605   -0.2585    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6070   -1.0953    0.1721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7845   -0.8509    1.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8940   -1.3501    2.1630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8679   -0.0084    0.5397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1703   -0.1458    1.0089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2214    0.6340    0.6058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9555    1.6064   -0.3186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9730    2.4521   -0.7931 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6626    1.7862   -0.8205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6510    0.9897   -0.3955 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3760    0.8918    1.2829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6823    1.0805    1.9617 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7986    1.2137    1.0052 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8504    2.0487    1.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9327    2.0369    0.4054 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0318    2.8869    0.6618 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9277    1.2193   -0.6673 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8616    0.3539   -0.9627 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7856    0.3638   -0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9525   -4.2277   -1.8023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3167   -4.8966   -1.4092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4932   -3.6571   -2.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5061   -3.0537   -2.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8269   -2.5801   -2.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3547   -0.9434    1.7490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2227    0.5155    0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7992    3.1808   -1.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4808    2.5739   -1.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6400    1.1148   -0.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1215    1.7825    0.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4454    0.7161    2.0169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6285    1.9082    2.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8962    0.1043    2.5126 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8942    2.7163    2.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8075    2.6109    1.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7708    1.2039   -1.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9180   -0.2569   -1.8205 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  8  1  0
  8 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 25 26  1  0
 26 27  2  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
  9  3  1  0
 18 12  1  0
 27  7  1  0
 27 21  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  6 32  1  0
 19 38  1  0
 19 39  1  0
 20 40  1  0
 20 41  1  0
 22 42  1  0
 24 43  1  0
 25 44  1  0
 26 45  1  0
 13 33  1  0
 14 34  1  0
 16 35  1  0
 17 36  1  0
 18 37  1  0
M  END


  Mrv1652309082216462D          

 27 30  0  0  0  0            999 V2000
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    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
  9 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
 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
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 21 27  1  0  0  0  0
  7 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0269347

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(CCC3=CC(O)=CC=C23)=C1C(=O)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H18O5/c1-27-19-11-18(25)20-16-9-7-15(24)10-13(16)4-8-17(20)21(19)22(26)12-2-5-14(23)6-3-12/h2-3,5-7,9-11,23-25H,4,8H2,1H3

> <INCHI_KEY>
JWFYTGBXGKZYFE-UHFFFAOYSA-N

> <FORMULA>
C22H18O5

> <MOLECULAR_WEIGHT>
362.381

> <EXACT_MASS>
362.11542368

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
38.493556664819316

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

> <JCHEM_LOGP>
4.574573860666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.072618224949373

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.461286697321765

> <JCHEM_PKA_STRONGEST_BASIC>
-4.8846111602860445

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
102.4558

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.034   0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.414   3.437   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.494  -1.897   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.724  -3.231   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.034  -1.897   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.114  -1.897   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.654  -1.897   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.344  -3.231   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.804  -3.231   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.874   0.770   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   27                                                  
CONECT    8    7    9   19                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   12                                                       
CONECT   19    8   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   21    7                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₁₈O₅

Average Mass

362.3810 Da

Monoisotopic Mass

362.11542 Da

IUPAC Name

8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

Traditional Name

8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(CCC3=CC(O)=CC=C23)=C1C(=O)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C22H18O5/c1-27-19-11-18(25)20-16-9-7-15(24)10-13(16)4-8-17(20)21(19)22(26)12-2-5-14(23)6-3-12/h2-3,5-7,9-11,23-25H,4,8H2,1H3

InChI Key

JWFYTGBXGKZYFE-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
Monomeria barbata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrophenanthrenes. These are a phenanthrene derivative where at least one ring CC bond is substituted by hydrogenation.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Hydrophenanthrenes

Direct Parent

Hydrophenanthrenes

Alternative Parents

Substituents

Benzophenone
Hydrophenanthrene
1-naphthalenecarboxylic acid or derivatives
Aryl-phenylketone
1-naphthol
Naphthalene
Anisole
Benzoyl
Aryl ketone
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Ketone
Ether
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	4.57	ChemAxon
pKa (Strongest Acidic)	7.46	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	102.46 m³·mol⁻¹	ChemAxon
Polarizability	38.49 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

162944579

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol (NP0269347)

MOL for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

3D MOL for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

3D SDF for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

3D-SDF for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

PDB for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

3D PDB for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

SMILES for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

INCHI for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

Structure for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)

3D Structure for NP0269347 (8-(4-hydroxybenzoyl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol)