NP-MRD: Showing NP-Card for 1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol (NP0061073)

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Record Information

Version

2.0

Created at

2022-04-28 06:00:03 UTC

Updated at

2022-04-28 06:00:03 UTC

NP-MRD ID

NP0061073

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

Description

1-[(4-Hydroxyphenyl)methyl]-4-methoxy-9,10-dihydrophenanthrene-2,7-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. 1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol is found in Bletilla formosana, Bletilla striata , Gymnadenia conopsea, Gymnadenia conopsea R.BR. and Pleione bulbocodioides. 1-[(4-Hydroxyphenyl)methyl]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241505552D          

 26 29  0  0  0  0            999 V2000
    4.5079   -2.2539    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
    3.2704   -1.5395    0.0000 C   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
    2.4454   -0.1105    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
    1.2079    0.6039    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
   -0.0296   -0.1105    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 O   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
    0.7954    1.3184    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
    5.7454   -1.5395    0.0000 C   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
  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  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
  7 16  1  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
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
  3 26  1  0  0  0  0
 16 26  2  0  0  0  0
M  END

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -2.1407   -3.8523    1.5661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2670   -2.5754    1.0274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2741   -1.6103    1.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0836   -1.9802    1.6840 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0063   -1.1121    1.7926 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1585   -1.5370    2.4259 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8691    0.1327    1.2607 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0112    1.1113    1.3259 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0663    0.8240    0.3621 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3612    0.6252    0.7836 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    0.3335   -0.0384 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1446    0.2373   -1.3878 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1636   -0.0543   -2.2831 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8789    0.4228   -1.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8468    0.7160   -0.9901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3094    0.5610    0.6233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3593   -0.3463    0.5441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5854    0.0630   -0.1806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6880   -0.7631   -0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8809   -0.3446   -0.8397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9202    0.9029   -1.4053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0875    1.3529   -2.0296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8244    1.7147   -1.3648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6115    1.3134   -0.7455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4756    2.2254   -0.8136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4017    1.9597    0.1485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8606   -3.8400    2.6415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3320   -4.4331    1.0527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0900   -4.3895    1.4204 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0322   -2.9674    2.1083 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9531   -0.9662    2.5578 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4079    0.9604    2.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6933    2.1516    1.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6087    0.6967    1.8562 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4346    0.1857    0.3603 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3720   -1.0303   -2.5149 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883    0.3423   -2.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8823    0.8385   -1.4475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6690   -1.7266    0.2189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6939   -1.0478   -0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8119    1.8611   -1.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8629    2.6873   -1.8085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0174    2.1011   -1.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8107    3.2991   -0.7569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5104    2.6277    1.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    2.3290   -0.2764 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  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
  7 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 17  3  1  0
 24 18  1  0
 15  9  1  0
 26 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  6 31  1  0
  8 32  1  0
  8 33  1  0
 10 34  1  0
 11 35  1  0
 13 36  1  0
 14 37  1  0
 15 38  1  0
 19 39  1  0
 20 40  1  0
 22 41  1  0
 23 42  1  0
 25 43  1  0
 25 44  1  0
 26 45  1  0
 26 46  1  0
M  END


  Mrv1533004241505552D          

 26 29  0  0  0  0            999 V2000
    4.5079   -2.2539    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
    3.2704   -1.5395    0.0000 C   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
    2.4454   -0.1105    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
    1.2079    0.6039    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
   -0.0296   -0.1105    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 O   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
    0.7954    1.3184    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
    5.7454   -1.5395    0.0000 C   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
  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  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
  7 16  1  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
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
  3 26  1  0  0  0  0
 16 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0061073

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C(CC2=CC=C(O)C=C2)C2=C1C1=CC=C(O)C=C1CC2

> <INCHI_IDENTIFIER>
InChI=1S/C22H20O4/c1-26-21-12-20(25)19(10-13-2-5-15(23)6-3-13)18-8-4-14-11-16(24)7-9-17(14)22(18)21/h2-3,5-7,9,11-12,23-25H,4,8,10H2,1H3

> <INCHI_KEY>
XNPQRYUNKPQOPF-UHFFFAOYSA-N

> <FORMULA>
C22H20O4

> <MOLECULAR_WEIGHT>
348.398

> <EXACT_MASS>
348.136159124

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
37.74333585785148

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[(4-hydroxyphenyl)methyl]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

> <ALOGPS_LOGP>
3.73

> <JCHEM_LOGP>
5.2070148503333336

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.945164623500649

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.389264382126338

> <JCHEM_PKA_STRONGEST_BASIC>
-4.850924596779517

> <JCHEM_POLAR_SURFACE_AREA>
69.92

> <JCHEM_REFRACTIVITY>
101.61749999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.96e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[(4-hydroxyphenyl)methyl]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       8.415  -4.207   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.875  -4.207   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.255  -1.540   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.795   1.127   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.255   1.127   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.485  -0.206   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.055  -0.206   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.825   1.127   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.365   1.127   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.055   2.461   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.485   2.461   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      13.035  -1.540   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    9                                                       
CONECT   16    7   17   26                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   19   26                                                  
CONECT   26   25    3   16                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₀O₄

Average Mass

348.3980 Da

Monoisotopic Mass

348.13616 Da

IUPAC Name

1-[(4-hydroxyphenyl)methyl]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

Traditional Name

1-[(4-hydroxyphenyl)methyl]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C(CC2=CC=C(O)C=C2)C2=C1C1=CC=C(O)C=C1CC2

InChI Identifier

InChI=1S/C22H20O4/c1-26-21-12-20(25)19(10-13-2-5-15(23)6-3-13)18-8-4-14-11-16(24)7-9-17(14)22(18)21/h2-3,5-7,9,11-12,23-25H,4,8,10H2,1H3

InChI Key

XNPQRYUNKPQOPF-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Bletilla formosana	Plant	KNApSAcK
Bletilla striata	Plant	KNApSAcK
Gymnadenia conopsea	LOTUS Database	35616633
Gymnadenia conopsea R.BR.	Plant	KNApSAcK
Pleione bulbocodioides	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

Hydrophenanthrene
Naphthalene
Phenol ether
Anisole
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Monocyclic benzene moiety
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	3.73	ALOGPS
logP	5.21	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	9.39	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	69.92 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	101.62 m³·mol⁻¹	ChemAxon
Polarizability	37.74 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

11163864

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol (NP0061073)

MOL for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

3D MOL for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

3D SDF for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

3D-SDF for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

PDB for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

3D PDB for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

SMILES for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

INCHI for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

Structure for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)

3D Structure for NP0061073 (1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol)