NP-MRD: Showing NP-Card for 6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol (NP0200515)

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Record Information

Version

2.0

Created at

2022-09-04 19:22:33 UTC

Updated at

2022-09-04 19:22:33 UTC

NP-MRD ID

NP0200515

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol

Description

6-[(2S,3S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol belongs to the class of organic compounds known as cinnamylphenols. These are organic compounds containing the 1,3-diphenylpropene moiety with one benzene ring bearing one or more hydroxyl groups. Based on a literature review very few articles have been published on 6-[(2S,3S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042221222D          

 31 33  0  0  1  0            999 V2000
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 O   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
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -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
   -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  2  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
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  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 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
   -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 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    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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
   -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 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
   -0.7145   -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
  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
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
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 10  9  1  6  0  0  0
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 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
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 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 23  1  0  0  0  0
  8 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
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 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
    5.2894   -1.3765   -0.2373 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4063   -1.2833    0.8653 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1134   -1.8243    0.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8706   -3.1080    1.1861 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8765   -3.9317    1.6464 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5673   -3.5815    1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5700   -2.7512    0.6407 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8169   -1.4271    0.2471 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8641    0.3114    0.8540 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3421   -0.5318    1.9847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3356   -1.4468    1.6560 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3720    2.2108    1.3410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0576    1.6104    2.3588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8794    0.7521   -0.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6898    0.7276   -1.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6577    0.2348   -2.7782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4306    0.2244   -4.1657 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8351   -0.2414   -2.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0546   -0.2298   -0.8819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2471   -0.7136   -0.3614 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0473    0.2797   -0.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0957   -0.9684    0.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4403    0.3729   -0.0980 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5498    0.6946   -1.4328 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9121    1.9674   -1.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1718    2.9437   -0.9176 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5385    4.2321   -1.3264 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0696    2.6483    0.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7543    1.1061   -2.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1683   -0.1463   -4.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6151   -0.6382   -2.9030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4132   -0.7062    0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2968    0.2622    0.9975 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3562   -0.0345   -2.2039 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9932    2.2027   -2.8889 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8348    4.9477   -1.4912 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2797    3.4364    1.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6392    1.1840    1.8635 H   0  0  0  0  0  0  0  0  0  0  0  0
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 29 55  1  0
 30 56  1  0
 31 57  1  0
M  END


  Mrv1652309042221222D          

 31 33  0  0  1  0            999 V2000
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 O   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
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -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
   -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  2  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
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  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 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
   -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 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    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -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 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
   -0.7145   -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
  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
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
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 18 20  2  0  0  0  0
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 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 23  1  0  0  0  0
  8 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0200515

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=CC(C[C@H](CO)[C@H](CO)C2=CC(O)=CC(O)=C2)=C1C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H26O7/c1-31-24-22(30)7-4-15(23(24)14-2-5-18(27)6-3-14)8-17(12-25)21(13-26)16-9-19(28)11-20(29)10-16/h2-7,9-11,17,21,25-30H,8,12-13H2,1H3/t17-,21-/m1/s1

> <INCHI_KEY>
AAJUUUMILGODNM-DYESRHJHSA-N

> <FORMULA>
C24H26O7

> <MOLECULAR_WEIGHT>
426.465

> <EXACT_MASS>
426.167853177

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
44.03052974584192

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[(2S,3S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol

> <JCHEM_LOGP>
3.086058402

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.69640608058765

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.100162801959074

> <JCHEM_PKA_STRONGEST_BASIC>
-2.607887623506067

> <JCHEM_POLAR_SURFACE_AREA>
130.61

> <JCHEM_REFRACTIVITY>
117.32079999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
6-[(2S,3S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol

> <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      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.335  -9.240   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -8.002  -7.700   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   24                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   16                                                       
CONECT   24    8    3   25                                                  
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   25                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₆O₇

Average Mass

426.4650 Da

Monoisotopic Mass

426.16785 Da

IUPAC Name

6-[(2S,3S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol

Traditional Name

6-[(2S,3S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=CC(C[C@H](CO)[C@H](CO)C2=CC(O)=CC(O)=C2)=C1C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C24H26O7/c1-31-24-22(30)7-4-15(23(24)14-2-5-18(27)6-3-14)8-17(12-25)21(13-26)16-9-19(28)11-20(29)10-16/h2-7,9-11,17,21,25-30H,8,12-13H2,1H3/t17-,21-/m1/s1

InChI Key

AAJUUUMILGODNM-DYESRHJHSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cinnamylphenols. These are organic compounds containing the 1,3-diphenylpropene moiety with one benzene ring bearing one or more hydroxyl groups.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Cinnamylphenols

Direct Parent

Cinnamylphenols

Alternative Parents

Substituents

Cinnamylphenol
Biphenyl
Methoxyphenol
Anisole
Phenoxy compound
Phenol ether
Resorcinol
Methoxybenzene
Phenol
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Ether
Primary alcohol
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	3.09	ChemAxon
pKa (Strongest Acidic)	9.1	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	130.61 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	117.32 m³·mol⁻¹	ChemAxon
Polarizability	44.03 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162869840

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol (NP0200515)

MOL for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

3D MOL for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

3D SDF for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

3D-SDF for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

PDB for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

3D PDB for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

SMILES for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

INCHI for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

Structure for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)

3D Structure for NP0200515 (6-[(2s,3s)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(hydroxymethyl)butyl]-2-methoxy-[1,1'-biphenyl]-3,4'-diol)