NP-MRD: Showing NP-Card for 10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione (NP0191402)

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Record Information

Version

2.0

Created at

2022-09-04 08:21:03 UTC

Updated at

2022-09-04 08:21:04 UTC

NP-MRD ID

NP0191402

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione

Description

10-(3,5-Dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3. Based on a literature review very few articles have been published on 10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042210212D          

 26 27  0  0  0  0            999 V2000
    0.7145    7.0125    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
    1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    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    3.3000    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 O   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
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 O   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
   -0.2475    4.7025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2475    5.5275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   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    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 O   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
   -0.7145    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
  7 14  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  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
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
   -4.2353   -0.3171    1.2004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3624   -0.0663    0.0168 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3693   -1.1313   -0.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4289   -1.8142   -1.2485 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2458   -1.4214    0.7190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7975   -2.3981    1.7721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0746   -2.0584    0.0847 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5501   -2.8618   -0.9809 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0029   -1.1734   -0.4400 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8501   -0.9146   -1.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1882    0.1202    0.2659 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6799    0.3725    0.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3485    0.8474   -0.7839 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7179    1.0952   -0.7824 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2667    1.5705   -1.9624 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4089    0.8559    0.3626 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7860    0.3814    1.4980 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5245    0.1419    2.6705 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4269    0.1490    1.4536 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530    1.2021   -0.3658 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3895    2.0313   -0.2631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4309    3.1909    0.2773 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6941    1.5960   -0.8364 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3309    2.6872   -1.6814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6715    1.2826    0.2705 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6927    2.2276    0.3639 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5320   -1.3736    1.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2048    0.2353    1.0215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7966    0.1447    2.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9914    0.0586   -0.8701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0700   -0.4871    1.2701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9980   -3.0931    2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1773   -1.8823    2.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5621   -3.0629    1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3594   -2.8199    0.8015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0229   -3.6267   -0.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9638   -1.7584   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992   -1.6433   -2.3158 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7935   -1.1700   -2.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5987    0.1218   -2.1659 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9022   -0.0403    1.3218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581    1.0293   -1.6894 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6300    0.9338   -2.6852 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4881    1.0573    0.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9277   -0.7864    2.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9332   -0.2222    2.3383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6134    0.7125   -1.4926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0576    3.6635   -1.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9015    2.6731   -2.7064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4178    2.6179   -1.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2017    1.2091    1.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4863    1.9139   -0.1380 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  7  1  0
  7  8  1  0
  7  5  1  0
  5  6  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  1  0
  2 25  1  0
 25 26  1  0
 25 23  1  0
 23 24  1  0
 23 21  1  0
 21 22  2  0
 21 20  1  0
 20 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 11  9  1  0
 19 12  1  0
 10 38  1  0
 10 39  1  0
 10 40  1  0
  9 37  1  6
  7 35  1  1
  8 36  1  0
  5 31  1  1
  6 32  1  0
  6 33  1  0
  6 34  1  0
  2 30  1  6
  1 27  1  0
  1 28  1  0
  1 29  1  0
 25 51  1  1
 26 52  1  0
 23 47  1  6
 24 48  1  0
 24 49  1  0
 24 50  1  0
 11 41  1  1
 13 42  1  0
 15 43  1  0
 16 44  1  0
 18 45  1  0
 19 46  1  0
M  END


  Mrv1652309042210212D          

 26 27  0  0  0  0            999 V2000
    0.7145    7.0125    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
    1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    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    3.3000    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 O   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
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 O   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
   -0.2475    4.7025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2475    5.5275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   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    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 O   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
   -0.7145    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
  7 14  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  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
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0191402

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(O)C(C)C(=O)C(C)C(O)C(C)C(=O)OC1C1=CC(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O7/c1-8-15(22)9(2)17(24)11(4)19(25)26-18(10(3)16(8)23)12-5-13(20)7-14(21)6-12/h5-11,16-18,20-21,23-24H,1-4H3

> <INCHI_KEY>
FILCWWHFFXLICK-UHFFFAOYSA-N

> <FORMULA>
C19H26O7

> <MOLECULAR_WEIGHT>
366.41

> <EXACT_MASS>
366.167853177

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.74290561512294

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione

> <JCHEM_LOGP>
2.100060163666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.553308051867551

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.091135327614428

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0428508769781892

> <JCHEM_POLAR_SURFACE_AREA>
124.29

> <JCHEM_REFRACTIVITY>
93.17239999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334  13.090   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  11.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  10.780   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.001  11.550   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       2.667   9.240   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.000   6.160   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.462   8.778   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.462  10.318   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.001   8.470   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -4.001  11.550   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.334  11.550   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334  13.090   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000  10.780   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.000   9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8   14                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    7                                                       
CONECT   15    6   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    2   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₇

Average Mass

366.4100 Da

Monoisotopic Mass

366.16785 Da

IUPAC Name

10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione

Traditional Name

10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione

CAS Registry Number

Not Available

SMILES

CC1C(O)C(C)C(=O)C(C)C(O)C(C)C(=O)OC1C1=CC(O)=CC(O)=C1

InChI Identifier

InChI=1S/C19H26O7/c1-8-15(22)9(2)17(24)11(4)19(25)26-18(10(3)16(8)23)12-5-13(20)7-14(21)6-12/h5-11,16-18,20-21,23-24H,1-4H3

InChI Key

FILCWWHFFXLICK-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Cyclic ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	2.1	ChemAxon
pKa (Strongest Acidic)	9.09	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	124.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	93.17 m³·mol⁻¹	ChemAxon
Polarizability	37.74 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

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

163062621

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione (NP0191402)

MOL for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

3D MOL for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

3D SDF for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

3D-SDF for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

PDB for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

3D PDB for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

SMILES for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

INCHI for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

Structure for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)

3D Structure for NP0191402 (10-(3,5-dihydroxyphenyl)-4,8-dihydroxy-3,5,7,9-tetramethyloxecane-2,6-dione)