NP-MRD: Showing NP-Card for 1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate (NP0263881)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 07:12:45 UTC

Updated at

2022-09-08 07:12:45 UTC

NP-MRD ID

NP0263881

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate

Description

1-(3,4-Dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl acetate belongs to the class of organic compounds known as dibenzylbutane lignans. These are lignan compounds containing a 2,3-dibenzylbutane moiety. 1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate is found in Magnolia ovata. 1-(3,4-Dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251505482D          

 29 30  0  0  0  0            999 V2000
    2.0329    1.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204    1.0974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    1.0974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5941   -3.2955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704   -4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -3.9039    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 11 16  1  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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 21 29  1  0  0  0  0
M  END

     RDKit          3D

 59 60  0  0  0  0  0  0  0  0999 V2000
    5.8662   -1.2057    1.9935 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3593   -0.7195    0.7786 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5773   -0.0944   -0.1584 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2053    0.1109    0.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4104    0.7377   -0.9098 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9906    0.9600   -0.7065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0623   -0.0624   -1.2615 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4865   -1.4374   -0.8192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3755    0.2280   -1.0222 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1867   -0.6755   -1.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8783    0.1814    0.3600 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7773   -1.1308    0.8764 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1494   -1.4453    2.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1031   -2.8598    2.5185 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3647   -0.5217    2.7498 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3142    0.6440    0.4188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6198    1.9273    0.8178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9120    2.4098    0.8979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9541    1.5807    0.5666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2706    2.0466    0.6399 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6028    3.3398    1.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6706    0.2925    0.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7623   -0.5097   -0.1606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6475   -1.8364   -0.5850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3722   -0.1737    0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0224    1.1772   -2.0809 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3712    0.9945   -2.3009 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1317    0.3600   -1.3351 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5070    0.1820   -1.5769 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1810   -2.0574    1.7633 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7255   -1.5504    2.6002 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2715   -0.4349    2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8066   -0.2574    0.9788 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6499    1.9629   -1.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8176    0.9672    0.4122 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1495   -0.0987   -2.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9813   -1.4794    0.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1932   -1.9129   -1.5385 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6091   -2.1377   -0.7533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6122    1.2685   -1.4192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1734   -0.2763   -2.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2797   -1.6999   -1.5550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6258   -0.8014   -2.9202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3554    0.8276    1.0809 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8402   -3.3526    2.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1770   -2.8465    3.6402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9194   -3.4610    2.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7871    2.5780    1.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1036    3.4277    1.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2950    4.1210    0.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6531    3.4210    1.3463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9965    3.5618    1.9621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4421   -2.4982    0.2944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8719   -1.9412   -1.3641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6354   -2.1527   -0.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1968   -1.1904   -0.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3760    1.6639   -2.7939 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8441    1.3367   -3.2111 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9204    0.5126   -2.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 25  1  0
 25 22  2  0
 22 23  1  0
 23 24  1  0
 16 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 11  9  1  0
  9 10  1  0
  9  7  1  0
  7  8  1  0
  7  6  1  0
  6  5  1  0
  5 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28  3  1  0
  3  2  1  0
  2  1  1  0
  3  4  2  0
 22 19  1  0
  4  5  1  0
 21 50  1  0
 21 51  1  0
 21 52  1  0
 18 49  1  0
 17 48  1  0
 25 56  1  0
 24 53  1  0
 24 54  1  0
 24 55  1  0
 11 44  1  1
 14 45  1  0
 14 46  1  0
 14 47  1  0
  9 40  1  6
 10 41  1  0
 10 42  1  0
 10 43  1  0
  7 36  1  6
  8 37  1  0
  8 38  1  0
  8 39  1  0
  6 34  1  0
  6 35  1  0
 26 57  1  0
 27 58  1  0
 29 59  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
M  END


  Mrv1533004251505482D          

 29 30  0  0  0  0            999 V2000
    2.0329    1.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204    1.0974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    1.0974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5941   -3.2955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704   -4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -3.9039    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 11 16  1  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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 21 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0263881

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1OC)C(OC(C)=O)C(C)C(C)CC1=CC=C(O)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O6/c1-14(11-17-7-9-19(25)21(12-17)27-5)15(2)23(29-16(3)24)18-8-10-20(26-4)22(13-18)28-6/h7-10,12-15,23,25H,11H2,1-6H3

> <INCHI_KEY>
VUUHIXIUHGVFKO-UHFFFAOYSA-N

> <FORMULA>
C23H30O6

> <MOLECULAR_WEIGHT>
402.487

> <EXACT_MASS>
402.204238686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
44.127494499887916

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(3,4-dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl acetate

> <ALOGPS_LOGP>
4.76

> <JCHEM_LOGP>
4.484472985333333

> <ALOGPS_LOGS>
-4.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.275005893679285

> <JCHEM_PKA_STRONGEST_BASIC>
-4.415026253750364

> <JCHEM_POLAR_SURFACE_AREA>
74.22000000000001

> <JCHEM_REFRACTIVITY>
110.65589999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.68e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(3,4-dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       3.795   3.382   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.025   2.048   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.795   0.715   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.025  -0.619   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.795  -1.953   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -1.953   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.105  -0.619   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   0.715   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.105   2.048   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.335   3.382   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.105  -3.286   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.105  -5.954   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.645  -5.954   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.335  -7.287   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.645  -3.286   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.415  -1.953   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.415  -4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.576  -6.152   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.955  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.725  -5.954   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.265  -5.954   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.035  -7.287   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.265  -8.621   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.035  -9.955   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.725  -8.621   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.955  -9.955   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.415  -9.955   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.955  -7.287   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    6   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   11   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   21                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Value	Source
1-(3,4-Dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl acetic acid	Generator

Chemical Formula

C₂₃H₃₀O₆

Average Mass

402.4870 Da

Monoisotopic Mass

402.20424 Da

IUPAC Name

1-(3,4-dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl acetate

Traditional Name

1-(3,4-dimethoxyphenyl)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1OC)C(OC(C)=O)C(C)C(C)CC1=CC=C(O)C(OC)=C1

InChI Identifier

InChI=1S/C23H30O6/c1-14(11-17-7-9-19(25)21(12-17)27-5)15(2)23(29-16(3)24)18-8-10-20(26-4)22(13-18)28-6/h7-10,12-15,23,25H,11H2,1-6H3

InChI Key

VUUHIXIUHGVFKO-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
Magnolia ovata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzylbutane lignans. These are lignan compounds containing a 2,3-dibenzylbutane moiety.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Dibenzylbutane lignans

Sub Class

Not Available

Direct Parent

Dibenzylbutane lignans

Alternative Parents

Substituents

Dibenzylbutane lignan skeleton
O-dimethoxybenzene
Dimethoxybenzene
Benzyloxycarbonyl
Methoxyphenol
Phenylpropane
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Carboxylic acid ester
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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	4.76	ALOGPS
logP	4.48	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	10.28	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	74.22 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	110.66 m³·mol⁻¹	ChemAxon
Polarizability	44.13 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

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-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate (NP0263881)

MOL for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

3D MOL for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

3D SDF for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

3D-SDF for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

PDB for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

3D PDB for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

SMILES for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

INCHI for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

Structure for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)

3D Structure for NP0263881 (1-(3,4-dimethoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-methylbutyl acetate)