NP-MRD: Showing NP-Card for candidachalcone (NP0035827)

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Record Information

Version

2.0

Created at

2021-06-20 19:09:55 UTC

Updated at

2021-06-30 00:07:04 UTC

NP-MRD ID

NP0035827

Secondary Accession Numbers

None

Natural Product Identification

Common Name

candidachalcone

Provided By

JEOL Database JEOL Logo

Description

Candidachalcone belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position. Candidachalcone 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. candidachalcone is found in Tephrosia candida. candidachalcone was first documented in 2011 (PMID: 21510635). Based on a literature review very few articles have been published on candidachalcone.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121093D          

 49 50  0  0  0  0            999 V2000
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   -1.7063    1.2499   -0.4835 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5045    1.1940   -1.1400 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2183    2.6568   -3.9898 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0744    1.0899   -2.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3977    0.9522   -2.9674 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3563    1.8819   -3.1260 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3834    3.3305   -2.7094 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306202121093D          

 49 50  0  0  0  0            999 V2000
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 21 22  2  0  0  0  0
  3 16  1  0  0  0  0
 22 23  1  0  0  0  0
  9 10  1  0  0  0  0
 23 24  2  0  0  0  0
 10 12  1  0  0  0  0
 24 26  1  0  0  0  0
  8  9  2  0  0  0  0
 26 27  2  0  0  0  0
 27 21  1  0  0  0  0
 16 14  2  0  0  0  0
 24 25  1  0  0  0  0
 10 13  1  0  0  0  0
  2  1  1  0  0  0  0
  7  8  1  0  0  0  0
  8 33  1  0  0  0  0
  9 34  1  0  0  0  0
 13 41  1  0  0  0  0
 11 35  1  0  0  0  0
 11 36  1  0  0  0  0
 11 37  1  0  0  0  0
 12 38  1  0  0  0  0
 12 39  1  0  0  0  0
 12 40  1  0  0  0  0
  4 31  1  0  0  0  0
 19 43  1  0  0  0  0
 20 44  1  0  0  0  0
 15 42  1  0  0  0  0
  6 32  1  0  0  0  0
 22 45  1  0  0  0  0
 23 46  1  0  0  0  0
 26 48  1  0  0  0  0
 27 49  1  0  0  0  0
 25 47  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0035827

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(\C([H])=C(/[H])C(=O)C2=C(O[H])C(\C([H])=C(\[H])C(O[H])(C([H])([H])[H])C([H])([H])[H])=C(O[H])C([H])=C2OC([H])([H])[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O6/c1-21(2,26)11-10-15-17(24)12-18(27-3)19(20(15)25)16(23)9-6-13-4-7-14(22)8-5-13/h4-12,22,24-26H,1-3H3/b9-6+,11-10-

> <INCHI_KEY>
KOWOOXVTWKELMT-RQDFUGDESA-N

> <FORMULA>
C21H22O6

> <MOLECULAR_WEIGHT>
370.401

> <EXACT_MASS>
370.141638428

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
40.02843530564677

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-1-{2,4-dihydroxy-3-[(1Z)-3-hydroxy-3-methylbut-1-en-1-yl]-6-methoxyphenyl}-3-(4-hydroxyphenyl)prop-2-en-1-one

> <ALOGPS_LOGP>
3.25

> <JCHEM_LOGP>
4.011675677333333

> <ALOGPS_LOGS>
-4.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.433804986092433

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.099386959937233

> <JCHEM_PKA_STRONGEST_BASIC>
-2.795376767787382

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
105.47439999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.10e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-1-{2,4-dihydroxy-3-[(1Z)-3-hydroxy-3-methylbut-1-en-1-yl]-6-methoxyphenyl}-3-(4-hydroxyphenyl)prop-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 49 50  0  0  0  0  0  0  0  0999 V2000
   -2.6865    2.1638   -0.9634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7063    1.2499   -0.4835 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5045    1.1940   -1.1400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2144    1.9378   -2.2874 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0536    1.8840   -2.8717 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2183    2.6568   -3.9898 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0744    1.0899   -2.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3977    0.9522   -2.9674 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3563    1.8819   -3.1260 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3834    3.3305   -2.7094 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0003    3.5708   -1.2461 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7712    3.9309   -2.9747 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4525    4.0047   -3.5610 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7789    0.3338   -1.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7916   -0.4385   -0.6569 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4933    0.3586   -0.6030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2622   -0.5054    0.5847 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -0.6763    1.3796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0305   -1.2277    0.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3025   -1.9091    1.8380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5442   -2.6630    2.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7895   -2.1955    1.6112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9514   -2.9304    1.8601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8732   -4.1273    2.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0313   -4.8115    2.7808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6510   -4.6021    3.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4894   -3.8651    2.7729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0173    1.8917   -1.9709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3179    3.1943   -0.9289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5545    2.0987   -0.3002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9489    2.5846   -2.7569 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1630    2.9307   -4.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6001   -0.0605   -3.3165 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2573    1.5338   -3.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6111    2.9695   -0.5643 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9449    3.3576   -1.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1346    4.6264   -0.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7835    5.0037   -2.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0457    3.8408   -4.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5456    3.4434   -2.3724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4664    4.9461   -3.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5413   -0.6825    0.2624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7156   -1.2034   -0.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5781   -1.9418    2.6501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8736   -1.2508    1.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9141   -2.5656    1.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8236   -5.6196    3.2778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5795   -5.5333    3.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5366   -4.2427    3.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
 14  7  1  0
  3  2  1  0
 16 17  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
  7  5  2  0
 17 18  2  0
 10 11  1  0
 14 15  1  0
  5  6  1  0
  5  4  1  0
  4  3  2  0
 21 22  2  0
  3 16  1  0
 22 23  1  0
  9 10  1  0
 23 24  2  0
 10 12  1  0
 24 26  1  0
  8  9  2  0
 26 27  2  0
 27 21  1  0
 16 14  2  0
 24 25  1  0
 10 13  1  0
  2  1  1  0
  7  8  1  0
  8 33  1  0
  9 34  1  0
 13 41  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 12 40  1  0
  4 31  1  0
 19 43  1  0
 20 44  1  0
 15 42  1  0
  6 32  1  0
 22 45  1  0
 23 46  1  0
 26 48  1  0
 27 49  1  0
 25 47  1  0
  1 28  1  0
  1 29  1  0
  1 30  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  C   UNK     0      -2.687   2.164  -0.963  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.706   1.250  -0.484  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.504   1.194  -1.140  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.214   1.938  -2.287  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.054   1.884  -2.872  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.218   2.657  -3.990  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.074   1.090  -2.337  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.398   0.952  -2.967  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.356   1.882  -3.126  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.383   3.330  -2.709  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.000   3.571  -1.246  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.771   3.931  -2.975  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.453   4.005  -3.561  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.779   0.334  -1.189  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.792  -0.439  -0.657  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.493   0.359  -0.603  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.262  -0.505   0.585  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.187  -0.676   1.380  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.030  -1.228   0.715  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.303  -1.909   1.838  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.544  -2.663   2.054  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.789  -2.196   1.611  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.951  -2.930   1.860  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.873  -4.127   2.560  0.00  0.00           C+0
HETATM   25  O   UNK     0      -6.031  -4.811   2.781  0.00  0.00           O+0
HETATM   26  C   UNK     0      -3.651  -4.602   3.022  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.489  -3.865   2.773  0.00  0.00           C+0
HETATM   28  H   UNK     0      -3.017   1.892  -1.971  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.318   3.194  -0.929  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.555   2.099  -0.300  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.949   2.585  -2.757  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.163   2.931  -4.027  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.600  -0.061  -3.317  0.00  0.00           H+0
HETATM   34  H   UNK     0       5.257   1.534  -3.632  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.611   2.970  -0.564  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.945   3.358  -1.055  0.00  0.00           H+0
HETATM   37  H   UNK     0       4.135   4.626  -0.981  0.00  0.00           H+0
HETATM   38  H   UNK     0       5.784   5.004  -2.749  0.00  0.00           H+0
HETATM   39  H   UNK     0       6.046   3.841  -4.033  0.00  0.00           H+0
HETATM   40  H   UNK     0       6.546   3.443  -2.372  0.00  0.00           H+0
HETATM   41  H   UNK     0       3.466   4.946  -3.310  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.541  -0.683   0.262  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.716  -1.203  -0.123  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.578  -1.942   2.650  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.874  -1.251   1.080  0.00  0.00           H+0
HETATM   46  H   UNK     0      -5.914  -2.566   1.514  0.00  0.00           H+0
HETATM   47  H   UNK     0      -5.824  -5.620   3.278  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.579  -5.533   3.575  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.537  -4.243   3.139  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    3    1                                                       
CONECT    3    2    4   16                                                  
CONECT    4    5    3   31                                                  
CONECT    5    7    6    4                                                  
CONECT    6    5   32                                                       
CONECT    7   14    5    8                                                  
CONECT    8    9    7   33                                                  
CONECT    9   10    8   34                                                  
CONECT   10   11    9   12   13                                             
CONECT   11   10   35   36   37                                             
CONECT   12   10   38   39   40                                             
CONECT   13   10   41                                                       
CONECT   14    7   15   16                                                  
CONECT   15   14   42                                                       
CONECT   16   17    3   14                                                  
CONECT   17   16   19   18                                                  
CONECT   18   17                                                            
CONECT   19   17   20   43                                                  
CONECT   20   19   21   44                                                  
CONECT   21   20   22   27                                                  
CONECT   22   21   23   45                                                  
CONECT   23   22   24   46                                                  
CONECT   24   23   26   25                                                  
CONECT   25   24   47                                                       
CONECT   26   24   27   48                                                  
CONECT   27   26   21   49                                                  
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    4                                                            
CONECT   32    6                                                            
CONECT   33    8                                                            
CONECT   34    9                                                            
CONECT   35   11                                                            
CONECT   36   11                                                            
CONECT   37   11                                                            
CONECT   38   12                                                            
CONECT   39   12                                                            
CONECT   40   12                                                            
CONECT   41   13                                                            
CONECT   42   15                                                            
CONECT   43   19                                                            
CONECT   44   20                                                            
CONECT   45   22                                                            
CONECT   46   23                                                            
CONECT   47   25                                                            
CONECT   48   26                                                            
CONECT   49   27                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  100    0
END

RDKit          3D

49 50  0  0  0  0  0  0  0  0999 V2000
   -2.6865    2.1638   -0.9634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7063    1.2499   -0.4835 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5045    1.1940   -1.1400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2144    1.9378   -2.2874 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0536    1.8840   -2.8717 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2183    2.6568   -3.9898 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0744    1.0899   -2.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3977    0.9522   -2.9674 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3563    1.8819   -3.1260 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3834    3.3305   -2.7094 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0003    3.5708   -1.2461 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7712    3.9309   -2.9747 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4525    4.0047   -3.5610 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7789    0.3338   -1.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7916   -0.4385   -0.6569 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4933    0.3586   -0.6030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2622   -0.5054    0.5847 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -0.6763    1.3796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0305   -1.2277    0.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3025   -1.9091    1.8380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5442   -2.6630    2.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7895   -2.1955    1.6112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9514   -2.9304    1.8601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8732   -4.1273    2.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0313   -4.8115    2.7808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6510   -4.6021    3.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4894   -3.8651    2.7729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0173    1.8917   -1.9709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3179    3.1943   -0.9289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5545    2.0987   -0.3002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9489    2.5846   -2.7569 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1630    2.9307   -4.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6001   -0.0605   -3.3165 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2573    1.5338   -3.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6111    2.9695   -0.5643 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9449    3.3576   -1.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1346    4.6264   -0.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7835    5.0037   -2.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0457    3.8408   -4.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5456    3.4434   -2.3724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4664    4.9461   -3.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5413   -0.6825    0.2624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7156   -1.2034   -0.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5781   -1.9418    2.6501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8736   -1.2508    1.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9141   -2.5656    1.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8236   -5.6196    3.2778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5795   -5.5333    3.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5366   -4.2427    3.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
 14  7  1  0
  3  2  1  0
 16 17  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
  7  5  2  0
 17 18  2  0
 10 11  1  0
 14 15  1  0
  5  6  1  0
  5  4  1  0
  4  3  2  0
 21 22  2  0
  3 16  1  0
 22 23  1  0
  9 10  1  0
 23 24  2  0
 10 12  1  0
 24 26  1  0
  8  9  2  0
 26 27  2  0
 27 21  1  0
 16 14  2  0
 24 25  1  0
 10 13  1  0
  2  1  1  0
  7  8  1  0
  8 33  1  0
  9 34  1  0
 13 41  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 12 40  1  0
  4 31  1  0
 19 43  1  0
 20 44  1  0
 15 42  1  0
  6 32  1  0
 22 45  1  0
 23 46  1  0
 26 48  1  0
 27 49  1  0
 25 47  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
M  END

View in JSmol

Synonyms

Value	Source
(2E)-1-(2,4-Dihydroxy)-3-((e)-3-hydroxy-3-methylbut-1-enyl)-6-methoxyphenyl-3-(4-hydroxyphenyl)prop-2-en-1-one	MeSH

Chemical Formula

C₂₁H₂₂O₆

Average Mass

370.4010 Da

Monoisotopic Mass

370.14164 Da

IUPAC Name

(2E)-1-{2,4-dihydroxy-3-[(1Z)-3-hydroxy-3-methylbut-1-en-1-yl]-6-methoxyphenyl}-3-(4-hydroxyphenyl)prop-2-en-1-one

Traditional Name

(2E)-1-{2,4-dihydroxy-3-[(1Z)-3-hydroxy-3-methylbut-1-en-1-yl]-6-methoxyphenyl}-3-(4-hydroxyphenyl)prop-2-en-1-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(\C([H])=C(/[H])C(=O)C2=C(O[H])C(\C([H])=C(\[H])C(O[H])(C([H])([H])[H])C([H])([H])[H])=C(O[H])C([H])=C2OC([H])([H])[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C21H22O6/c1-21(2,26)11-10-15-17(24)12-18(27-3)19(20(15)25)16(23)9-6-13-4-7-14(22)8-5-13/h4-12,22,24-26H,1-3H3/b9-6+,11-10-

InChI Key

KOWOOXVTWKELMT-RQDFUGDESA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, 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
Tephrosia candida	JEOL database	Hegazy, M. -E. F., et al, J. Nat. Prod. 74, 937 (2011)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

2'-Hydroxychalcones

Alternative Parents

Substituents

2'-hydroxychalcone
Cinnamylphenol
Hydroxycinnamic acid or derivatives
Methoxyphenol
Cinnamyl alcohol
Phenoxy compound
Phenol ether
Resorcinol
Styrene
Aryl ketone
Anisole
Methoxybenzene
Benzoyl
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Acryloyl-group
Vinylogous acid
Alpha,beta-unsaturated ketone
Enone
Tertiary alcohol
Ketone
Ether
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

tertiary alcohol (CHEBI:67345 )
resorcinols (CHEBI:67345 )
monomethoxybenzene (CHEBI:67345 )
chalcones (CHEBI:67345 )

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	3.25	ALOGPS
logP	4.01	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	7.1	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	105.47 m³·mol⁻¹	ChemAxon
Polarizability	40.03 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

26334170

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

67345

Good Scents ID

Not Available

References

General References

Hegazy ME, El-Hamd H Mohamed A, El-Halawany AM, Djemgou PC, Shahat AA, Pare PW: Estrogenic activity of chemical constituents from Tephrosia candida. J Nat Prod. 2011 May 27;74(5):937-42. doi: 10.1021/np100378d. Epub 2011 Apr 21. [PubMed:21510635 ]
Hegazy, M. -E. F., et al. (2011). Hegazy, M. -E. F., et al, J. Nat. Prod. 74, 937 (2011). J. Nat. Prod..

Showing NP-Card for candidachalcone (NP0035827)

MOL for NP0035827 (candidachalcone)

3D MOL for NP0035827 (candidachalcone)

3D SDF for NP0035827 (candidachalcone)

3D-SDF for NP0035827 (candidachalcone)

PDB for NP0035827 (candidachalcone)

3D PDB for NP0035827 (candidachalcone)

SMILES for NP0035827 (candidachalcone)

INCHI for NP0035827 (candidachalcone)

Structure for NP0035827 (candidachalcone)

3D Structure for NP0035827 (candidachalcone)