NP-MRD: Showing NP-Card for 1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one (NP0154191)

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Record Information

Version

2.0

Created at

2022-09-02 10:57:56 UTC

Updated at

2022-09-02 10:57:56 UTC

NP-MRD ID

NP0154191

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one

Description

Alpha,4,2'-Trihydroxy-4-O-geranyldihydrochalcone belongs to the class of organic compounds known as 2'-hydroxy-dihydrochalcones. These are organic compounds containing dihydrochalcone skeleton that carries a hydroxyl group at the 2'-position. Thus, alpha,4,2'-trihydroxy-4-O-geranyldihydrochalcone is considered to be a flavonoid. 1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one is found in Millettia usaramensis. Based on a literature review very few articles have been published on alpha,4,2'-Trihydroxy-4-O-geranyldihydrochalcone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022212572D          

 29 30  0  0  0  0            999 V2000
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   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
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  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
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    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
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    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
   -2.1434   -2.8875    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 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 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -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
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    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
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  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
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 20 26  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 11 29  1  0  0  0  0
M  END

     RDKit          3D

 57 58  0  0  0  0  0  0  0  0999 V2000
   -5.7357   -1.3162   -1.7696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3479   -0.9168   -0.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3018   -1.8208    0.2087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0252    0.2555    0.0416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0682    1.1593   -0.6505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9178    1.3525    0.3299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1994    0.1974    0.8655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6759    2.5758    0.7179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6628    3.0613    1.6171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7218    2.2812    2.2117 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6490    1.6522    1.5931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3790    1.7694    0.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6999    1.1311   -0.3433 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5584    0.3428    0.3852 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6893   -0.3180   -0.2350 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4521   -1.0291    0.5314 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1110   -0.3033   -1.6315 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2944    0.2903   -2.5517 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4888    0.3439   -1.8151 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5582   -0.3329   -1.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2693   -1.4069   -1.6117 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2734   -1.9912   -0.8779 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6174   -1.5568    0.3823 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6540   -2.1877    1.0959 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9222   -0.4964    0.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9142    0.0952    0.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2986    0.2129    1.7477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0699   -0.5335    2.5655 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1921    0.8738    2.3340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6140   -1.3530   -1.6941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0254   -0.5713   -2.5431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0669   -2.3162   -2.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2552   -2.8185   -0.2658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0418   -1.9745    1.2768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3223   -1.3992    0.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4350    0.6121    0.9836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6899    0.7217   -1.5905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5980    2.1124   -0.8062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9749   -0.6596    0.8211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0041    0.2309    1.9671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3815   -0.2047    0.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3367    3.4089    0.3096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0721    3.8524    1.0125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1740    3.7559    2.3716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0317    2.3807   -0.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8330    1.2867   -1.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2084   -1.3839   -1.9523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9513   -0.3198   -3.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3692    1.3782   -1.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6981    0.5026   -2.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0058   -1.7562   -2.6033 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8492   -2.8416   -1.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3534   -2.9670    1.6817 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1463   -0.1106    1.9016 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3446    0.9424    0.5835 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8396   -1.0803    2.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0457    0.7341    3.3872 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 14 27  1  0
 27 28  1  0
 27 29  2  0
 29 11  1  0
 26 20  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  7 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 12 45  1  0
 13 46  1  0
 17 47  1  6
 18 48  1  0
 19 49  1  0
 19 50  1  0
 21 51  1  0
 22 52  1  0
 24 53  1  0
 25 54  1  0
 26 55  1  0
 28 56  1  0
 29 57  1  0
M  END


  Mrv1652309022212572D          

 29 30  0  0  0  0            999 V2000
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   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
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  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
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    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
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    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
   -2.1434   -2.8875    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 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 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -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
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    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
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  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
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 20 26  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 11 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154191

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC\C(C)=C\COC1=CC=C(C(=O)C(O)CC2=CC=C(O)C=C2)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O5/c1-16(2)4-5-17(3)12-13-29-20-10-11-21(22(26)15-20)24(28)23(27)14-18-6-8-19(25)9-7-18/h4,6-12,15,23,25-27H,5,13-14H2,1-3H3/b17-12+

> <INCHI_KEY>
VDTQLOASZLCFCY-SFQUDFHCSA-N

> <FORMULA>
C24H28O5

> <MOLECULAR_WEIGHT>
396.483

> <EXACT_MASS>
396.193674002

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
44.27082276453092

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(4-{[(2E)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one

> <ALOGPS_LOGP>
3.91

> <JCHEM_LOGP>
5.400325689333334

> <ALOGPS_LOGS>
-5.03

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.602173672606362

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.812787312170311

> <JCHEM_PKA_STRONGEST_BASIC>
-3.57160167500071

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
116.0207

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.68e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(4-{[(2E)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.000 -12.320   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   29                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   20                                                       
CONECT   27   14   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   11                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Value	Source
a,4,2'-Trihydroxy-4-O-geranyldihydrochalcone	Generator
Α,4,2'-trihydroxy-4-O-geranyldihydrochalcone	Generator

Chemical Formula

C₂₄H₂₈O₅

Average Mass

396.4830 Da

Monoisotopic Mass

396.19367 Da

IUPAC Name

1-(4-{[(2E)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one

Traditional Name

1-(4-{[(2E)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one

CAS Registry Number

Not Available

SMILES

CC(C)=CC\C(C)=C\COC1=CC=C(C(=O)C(O)CC2=CC=C(O)C=C2)C(O)=C1

InChI Identifier

InChI=1S/C24H28O5/c1-16(2)4-5-17(3)12-13-29-20-10-11-21(22(26)15-20)24(28)23(27)14-18-6-8-19(25)9-7-18/h4,6-12,15,23,25-27H,5,13-14H2,1-3H3/b17-12+

InChI Key

VDTQLOASZLCFCY-SFQUDFHCSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Millettia usaramensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-hydroxy-dihydrochalcones. These are organic compounds containing dihydrochalcone 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'-Hydroxy-dihydrochalcones

Alternative Parents

Substituents

2'-hydroxy-dihydrochalcone
Cinnamylphenol
Alkyl-phenylketone
Butyrophenone
Phenylketone
Benzoyl
Phenol ether
Phenoxy compound
Aryl ketone
Aryl alkyl ketone
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Acyloin
Alpha-hydroxy ketone
Vinylogous acid
Secondary alcohol
Ketone
Ether
Organic oxygen compound
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120572 )

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	3.91	ALOGPS
logP	5.4	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	8.81	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	116.02 m³·mol⁻¹	ChemAxon
Polarizability	44.27 Å³	ChemAxon
Number of Rings	2	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

24846124

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

42607723

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one (NP0154191)

MOL for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

3D MOL for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

3D SDF for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

3D-SDF for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

PDB for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

3D PDB for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

SMILES for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

INCHI for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

Structure for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)

3D Structure for NP0154191 (1-(4-{[(2e)-3,6-dimethylhepta-2,5-dien-1-yl]oxy}-2-hydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one)