NP-MRD: Showing NP-Card for 1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one (NP0325182)

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Record Information

Version

2.0

Created at

2022-09-12 05:44:13 UTC

Updated at

2022-09-12 05:44:14 UTC

NP-MRD ID

NP0325182

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one

Description

1-{3-Acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. 1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one is found in Hypericum japonicum. 1-{3-Acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241501452D          

 29 29  0  0  0  0            999 V2000
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    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
    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
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   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
    0.7145   -1.2375    0.0000 O   0  0  0  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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -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
   -0.7145   -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
   -1.4289   -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
   -2.1434   -6.1875    0.0000 C   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
    0.0000    0.0000    0.0000 C   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 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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 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
 21 23  1  0  0  0  0
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 24 28  2  0  0  0  0
  7 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

     RDKit          3D

 63 63  0  0  0  0  0  0  0  0999 V2000
   -6.9130   -3.1042    0.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6397   -2.2472    1.6418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7334   -1.0604    1.3096 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5542   -0.2990    2.6185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4625   -1.5146    0.7309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2534   -2.7989    0.7251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3986   -0.7271    0.1673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2619   -1.3376   -0.2979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0933   -2.7250   -0.2189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2547   -0.5908   -0.8562 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3535    0.8039   -0.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3004    1.4600   -1.5151 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8616    1.9281   -0.8554 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6730    0.8961   -0.1973 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6058    1.4261   -1.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6924   -0.4465    0.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8711   -0.0898    0.9957 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9321    0.5809    0.2390 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1163   -0.0069    0.0863 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1658    0.7019   -0.6858 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3659   -1.3605    0.6928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4873    1.4279   -0.5107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6887    2.8347   -0.6696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7386    3.7648   -1.2910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7596    3.3787   -0.2669 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5345    0.6675    0.0693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6635    1.2180    0.5336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2450   -3.9773    0.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9936   -3.4140    0.4328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7595   -2.4965   -0.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2673   -2.8298    2.4939 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2629   -0.4196    0.6062 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2773   -3.2118   -0.5395 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4703    2.4417   -1.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2329    0.3031    0.5911 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9052    2.4358   -1.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9397    1.4569   -2.4902 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4992    0.8431   -1.9322 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9368   -1.0543    0.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0253   -1.1788   -0.6204 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3157   -1.0239    1.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5523    0.5644    1.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8016    1.5603   -0.1883 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1656    0.4050   -1.7397 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9857    1.8030   -0.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1471    0.5127   -0.1849 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2960   -1.3386    1.7937 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6349   -2.0613    0.2918 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3644   -1.6868    0.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3429    4.6381   -1.7729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0229    4.2416   -0.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1892    3.3883   -2.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0252    2.0807    0.6071 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
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  5  6  2  0
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 12 24  1  0
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 25 26  1  0
 25 27  2  0
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 28 29  1  0
 28  7  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  6
  4 36  1  0
  4 37  1  0
  4 38  1  0
  9 39  1  0
 11 40  1  0
 11 41  1  0
 11 42  1  0
 14 43  1  0
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 17 46  1  0
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 22 56  1  0
 23 57  1  0
 23 58  1  0
 23 59  1  0
 26 60  1  0
 26 61  1  0
 26 62  1  0
 29 63  1  0
M  END


  Mrv1533004241501452D          

 29 29  0  0  0  0            999 V2000
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    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
    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
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   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
    0.7145   -1.2375    0.0000 O   0  0  0  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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -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
   -0.7145   -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
   -1.4289   -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
   -2.1434   -6.1875    0.0000 C   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
    0.0000    0.0000    0.0000 C   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 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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 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
 21 23  1  0  0  0  0
 12 24  1  0  0  0  0
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 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 24 28  2  0  0  0  0
  7 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325182

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)C1=C(O)C(C)=C(OCC=C(C)CCC=C(C)C)C(C(C)=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H34O5/c1-8-16(5)21(26)20-22(27)17(6)24(19(18(7)25)23(20)28)29-13-12-15(4)11-9-10-14(2)3/h10,12,16,27-28H,8-9,11,13H2,1-7H3

> <INCHI_KEY>
SLMXSSJVARUOAM-UHFFFAOYSA-N

> <FORMULA>
C24H34O5

> <MOLECULAR_WEIGHT>
402.531

> <EXACT_MASS>
402.240624195

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.25314382291309

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one

> <ALOGPS_LOGP>
5.00

> <JCHEM_LOGP>
7.4962114886666695

> <ALOGPS_LOGS>
-4.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.930141450709375

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.014670295041093

> <JCHEM_PKA_STRONGEST_BASIC>
-3.840544573182032

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
119.053

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.01e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   28                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   24                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   12   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   24    7   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₄O₅

Average Mass

402.5310 Da

Monoisotopic Mass

402.24062 Da

IUPAC Name

1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one

Traditional Name

1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)C1=C(O)C(C)=C(OCC=C(C)CCC=C(C)C)C(C(C)=O)=C1O

InChI Identifier

InChI=1S/C24H34O5/c1-8-16(5)21(26)20-22(27)17(6)24(19(18(7)25)23(20)28)29-13-12-15(4)11-9-10-14(2)3/h10,12,16,27-28H,8-9,11,13H2,1-7H3

InChI Key

SLMXSSJVARUOAM-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, 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
Hypericum japonicum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Butyrophenone
Aromatic monoterpenoid
Monocyclic monoterpenoid
Monoterpenoid
Acetophenone
Phenylpropane
Phenoxy compound
Benzoyl
Aryl alkyl ketone
O-cresol
P-cresol
Phenol ether
Resorcinol
Alkyl aryl ether
Phenol
Toluene
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Ether
Organic oxide
Hydrocarbon derivative
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	5	ALOGPS
logP	7.5	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	8.01	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	119.05 m³·mol⁻¹	ChemAxon
Polarizability	46.25 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one (NP0325182)

MOL for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

3D MOL for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

3D SDF for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

3D-SDF for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

PDB for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

3D PDB for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

SMILES for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

INCHI for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

Structure for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)

3D Structure for NP0325182 (1-{3-acetyl-4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-2,6-dihydroxy-5-methylphenyl}-2-methylbutan-1-one)