NP-MRD: Showing NP-Card for 1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol (NP0035549)

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Record Information

Version

2.0

Created at

2021-06-20 18:57:52 UTC

Updated at

2021-06-30 00:06:35 UTC

NP-MRD ID

NP0035549

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol

Provided By

JEOL Database JEOL Logo

Description

(-)-(3S)-1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol belongs to the class of organic compounds known as linear diarylheptanoids. These are diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain (-)-(3S)-1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. 1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol is found in Curcuma kwangsiensis. 1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol was first documented in 2010 (Li, J., et al.). Based on a literature review very few articles have been published on (-)-(3S)-1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202120573D          

 44 45  0  0  0  0            999 V2000
   -4.9199    2.5764    3.5613 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2216    2.1338    2.4779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1609    2.8630    1.9547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4537    2.3576    0.8600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8104    1.1321    0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0295    0.5307   -0.8100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4349    1.2220   -1.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5969    1.0160   -1.4763 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9021    1.5816   -1.6385 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7632   -0.4227   -0.9692 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4135   -0.5037    0.4211 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5428    0.0633    1.5185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8734    1.2808    2.1303 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0436    1.8286    3.1102 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9264    1.7499    4.4079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4556   -0.0550    2.8975 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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   -4.2216    2.1338    2.4779 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306202120573D          

 44 45  0  0  0  0            999 V2000
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   -4.2216    2.1338    2.4779 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0035549

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(\C([H])=C(/[H])C([H])([H])C([H])([H])[C@]([H])(O[H])C([H])([H])C([H])([H])C2=C([H])C([H])=C(O[H])C([H])=C2[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H22O3/c20-17(10-7-16-8-13-19(22)14-9-16)4-2-1-3-15-5-11-18(21)12-6-15/h1,3,5-6,8-9,11-14,17,20-22H,2,4,7,10H2/b3-1+/t17-/m0/s1

> <INCHI_KEY>
HLWUXTFOZZSNLD-DUXHTMCSSA-N

> <FORMULA>
C19H22O3

> <MOLECULAR_WEIGHT>
298.382

> <EXACT_MASS>
298.156894568

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
32.3300857389013

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(1E,5S)-5-hydroxy-7-(4-hydroxyphenyl)hept-1-en-1-yl]phenol

> <ALOGPS_LOGP>
4.11

> <JCHEM_LOGP>
4.459381005999999

> <ALOGPS_LOGS>
-3.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.366229237051613

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.469900303842966

> <JCHEM_PKA_STRONGEST_BASIC>
-2.693679042837984

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
90.14910000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(1E,5S)-5-hydroxy-7-(4-hydroxyphenyl)hept-1-en-1-yl]phenol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 44 45  0  0  0  0  0  0  0  0999 V2000
   -4.9199    2.5764    3.5613 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2216    2.1338    2.4779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1609    2.8630    1.9547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4537    2.3576    0.8600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8104    1.1321    0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0295    0.5307   -0.8100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4349    1.2220   -1.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5696    0.5809   -2.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8702    1.1062   -2.8279 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5969    1.0160   -1.4763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9021    1.5816   -1.6385 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7632   -0.4227   -0.9692 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4135   -0.5037    0.4211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5428    0.0633    1.5185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8734    1.2808    2.1303 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0436    1.8286    3.1102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1192    1.1635    3.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9264    1.7499    4.4079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4556   -0.0550    2.8975 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3772   -0.6048    1.9207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8822    0.4136    0.8256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5897    0.9159    1.9207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5919    3.4600    3.7992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8491    3.8050    2.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5958    2.9149    0.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9261   -0.5513   -0.7668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5523    2.3015   -1.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0092    0.7889   -3.8268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5671   -0.5102   -2.7383 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4533    0.5729   -3.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8712    2.1554   -3.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0722    1.6274   -0.7354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7837    2.5193   -1.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4071   -0.9728   -1.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984   -0.9392   -0.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -1.5554    0.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3906   -0.0055    0.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7734    1.8160    1.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2979    2.7762    3.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7604    1.2496    4.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3621   -0.5805    3.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1039   -1.5527    1.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1746   -0.5456    0.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4208    0.3551    2.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
 14 15  2  0
  8  7  1  0
 15 16  1  0
  7  6  2  0
 16 17  2  0
  6  5  1  0
 14 13  1  0
 17 18  1  0
 19 20  2  0
 10 11  1  0
 13 12  1  0
  5  4  2  0
  4  3  1  0
 12 10  1  0
  3  2  2  0
 20 14  1  0
  2 22  1  0
 10  9  1  0
 22 21  2  0
 21  5  1  0
 17 19  1  0
  2  1  1  0
 16 39  1  0
 19 41  1  0
 20 42  1  0
 15 38  1  0
 13 36  1  0
 13 37  1  0
 12 34  1  0
 12 35  1  0
 10 32  1  0
  9 30  1  0
  9 31  1  0
  8 28  1  0
  8 29  1  0
  7 27  1  0
  6 26  1  0
 18 40  1  0
 11 33  1  0
  4 25  1  0
  3 24  1  0
 22 44  1  0
 21 43  1  0
  1 23  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  O   UNK     0      -4.920   2.576   3.561  0.00  0.00           O+0
HETATM    2  C   UNK     0      -4.222   2.134   2.478  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.161   2.863   1.955  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.454   2.358   0.860  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.810   1.132   0.279  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.030   0.531  -0.810  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.435   1.222  -1.796  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.570   0.581  -2.844  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.870   1.106  -2.828  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.597   1.016  -1.476  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.902   1.582  -1.639  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.763  -0.423  -0.969  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.414  -0.504   0.421  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.543   0.063   1.519  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.873   1.281   2.130  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.044   1.829   3.110  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.119   1.163   3.477  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.926   1.750   4.408  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.456  -0.055   2.898  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.377  -0.605   1.921  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.882   0.414   0.826  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.590   0.916   1.921  0.00  0.00           C+0
HETATM   23  H   UNK     0      -4.592   3.460   3.799  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.849   3.805   2.395  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.596   2.915   0.492  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.926  -0.551  -0.767  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.552   2.301  -1.861  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.009   0.789  -3.827  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.567  -0.510  -2.738  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.453   0.573  -3.590  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.871   2.155  -3.154  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.072   1.627  -0.735  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.784   2.519  -1.869  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.407  -0.973  -1.667  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.798  -0.939  -0.947  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.619  -1.555   0.659  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.391  -0.006   0.414  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.773   1.816   1.836  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.298   2.776   3.575  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.760   1.250   4.435  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.362  -0.581   3.180  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.104  -1.553   1.464  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.175  -0.546   0.405  0.00  0.00           H+0
HETATM   44  H   UNK     0      -5.421   0.355   2.339  0.00  0.00           H+0
CONECT    1    2   23                                                       
CONECT    2    3   22    1                                                  
CONECT    3    4    2   24                                                  
CONECT    4    5    3   25                                                  
CONECT    5    6    4   21                                                  
CONECT    6    7    5   26                                                  
CONECT    7    8    6   27                                                  
CONECT    8    9    7   28   29                                             
CONECT    9    8   10   30   31                                             
CONECT   10   11   12    9   32                                             
CONECT   11   10   33                                                       
CONECT   12   13   10   34   35                                             
CONECT   13   14   12   36   37                                             
CONECT   14   15   13   20                                                  
CONECT   15   14   16   38                                                  
CONECT   16   15   17   39                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   40                                                       
CONECT   19   20   17   41                                                  
CONECT   20   19   14   42                                                  
CONECT   21   22    5   43                                                  
CONECT   22    2   21   44                                                  
CONECT   23    1                                                            
CONECT   24    3                                                            
CONECT   25    4                                                            
CONECT   26    6                                                            
CONECT   27    7                                                            
CONECT   28    8                                                            
CONECT   29    8                                                            
CONECT   30    9                                                            
CONECT   31    9                                                            
CONECT   32   10                                                            
CONECT   33   11                                                            
CONECT   34   12                                                            
CONECT   35   12                                                            
CONECT   36   13                                                            
CONECT   37   13                                                            
CONECT   38   15                                                            
CONECT   39   16                                                            
CONECT   40   18                                                            
CONECT   41   19                                                            
CONECT   42   20                                                            
CONECT   43   21                                                            
CONECT   44   22                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   90    0
END

RDKit          3D

44 45  0  0  0  0  0  0  0  0999 V2000
   -4.9199    2.5764    3.5613 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2216    2.1338    2.4779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1609    2.8630    1.9547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4537    2.3576    0.8600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8104    1.1321    0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0295    0.5307   -0.8100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4349    1.2220   -1.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5696    0.5809   -2.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8702    1.1062   -2.8279 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5969    1.0160   -1.4763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9021    1.5816   -1.6385 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7632   -0.4227   -0.9692 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4135   -0.5037    0.4211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5428    0.0633    1.5185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8734    1.2808    2.1303 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0436    1.8286    3.1102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1192    1.1635    3.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9264    1.7499    4.4079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4556   -0.0550    2.8975 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3772   -0.6048    1.9207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8822    0.4136    0.8256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5897    0.9159    1.9207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5919    3.4600    3.7992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8491    3.8050    2.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5958    2.9149    0.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9261   -0.5513   -0.7668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5523    2.3015   -1.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0092    0.7889   -3.8268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5671   -0.5102   -2.7383 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4533    0.5729   -3.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8712    2.1554   -3.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0722    1.6274   -0.7354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7837    2.5193   -1.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4071   -0.9728   -1.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984   -0.9392   -0.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -1.5554    0.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3906   -0.0055    0.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7734    1.8160    1.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2979    2.7762    3.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7604    1.2496    4.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3621   -0.5805    3.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1039   -1.5527    1.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1746   -0.5456    0.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4208    0.3551    2.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
 14 15  2  0
  8  7  1  0
 15 16  1  0
  7  6  2  0
 16 17  2  0
  6  5  1  0
 14 13  1  0
 17 18  1  0
 19 20  2  0
 10 11  1  0
 13 12  1  0
  5  4  2  0
  4  3  1  0
 12 10  1  0
  3  2  2  0
 20 14  1  0
  2 22  1  0
 10  9  1  0
 22 21  2  0
 21  5  1  0
 17 19  1  0
  2  1  1  0
 16 39  1  0
 19 41  1  0
 20 42  1  0
 15 38  1  0
 13 36  1  0
 13 37  1  0
 12 34  1  0
 12 35  1  0
 10 32  1  0
  9 30  1  0
  9 31  1  0
  8 28  1  0
  8 29  1  0
  7 27  1  0
  6 26  1  0
 18 40  1  0
 11 33  1  0
  4 25  1  0
  3 24  1  0
 22 44  1  0
 21 43  1  0
  1 23  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂O₃

Average Mass

298.3820 Da

Monoisotopic Mass

298.15689 Da

IUPAC Name

4-[(1E,5S)-5-hydroxy-7-(4-hydroxyphenyl)hept-1-en-1-yl]phenol

Traditional Name

4-[(1E,5S)-5-hydroxy-7-(4-hydroxyphenyl)hept-1-en-1-yl]phenol

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(\C([H])=C(/[H])C([H])([H])C([H])([H])[C@]([H])(O[H])C([H])([H])C([H])([H])C2=C([H])C([H])=C(O[H])C([H])=C2[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C19H22O3/c20-17(10-7-16-8-13-19(22)14-9-16)4-2-1-3-15-5-11-18(21)12-6-15/h1,3,5-6,8-9,11-14,17,20-22H,2,4,7,10H2/b3-1+/t17-/m0/s1

InChI Key

HLWUXTFOZZSNLD-DUXHTMCSSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Curcuma kwangsiensis	JEOL database	Li, J., et al, J. Nat. Prod. 73, 1667 (2010)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear diarylheptanoids. These are diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Diarylheptanoids

Sub Class

Linear diarylheptanoids

Direct Parent

Linear diarylheptanoids

Alternative Parents

Substituents

Linear 1,7-diphenylheptane skeleton
Fatty alcohol
Styrene
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

secondary alcohol (CHEBI:70686 )
phenols (CHEBI:70686 )
diarylheptanoid (CHEBI:70686 )

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	4.11	ALOGPS
logP	4.46	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	9.47	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	90.15 m³·mol⁻¹	ChemAxon
Polarizability	32.33 Å³	ChemAxon
Number of Rings	2	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

26363430

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

70686

Good Scents ID

Not Available

References

General References

Li, J., et al. (2010). Li, J., et al, J. Nat. Prod. 73, 1667 (2010). J. Nat. Prod..

Showing NP-Card for 1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol (NP0035549)

MOL for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

3D MOL for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

3D SDF for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

3D-SDF for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

PDB for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

3D PDB for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

SMILES for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

INCHI for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

Structure for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)

3D Structure for NP0035549 (1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol)