NP-MRD: Showing NP-Card for methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate (NP0150142)

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Record Information

Version

2.0

Created at

2022-09-02 06:10:07 UTC

Updated at

2022-09-02 06:10:07 UTC

NP-MRD ID

NP0150142

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate

Description

Methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group. methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate is found in Ononis natrix and Ononis viscosa. Methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171512522D          

 27 27  0  0  0  0            999 V2000
   -7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   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
   -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
   -0.7145   -1.2375    0.0000 C   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 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
    0.7145   -0.4125    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
    0.0000    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
   -1.4289    0.8250    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    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
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  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
  7  8  1  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  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 61 61  0  0  0  0  0  0  0  0999 V2000
   -8.0042    0.2644   -1.1411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9910   -0.6489   -0.5308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7403    0.1447   -0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1201    0.8392   -1.1955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9896    1.7396   -1.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6876    1.3639   -0.4754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7039    0.9803    0.9636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3117    0.6594    1.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7368   -0.4853    0.7838 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6374   -0.8869    1.3026 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6384    0.2367    1.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8281    0.6828   -0.1949 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0527    1.4626   -0.6793 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9538    0.2118   -1.0571 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9322   -0.6265   -0.3373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9200   -2.0003   -0.5152 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8066   -2.8192    0.1333 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7971   -4.2070   -0.0440 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8464   -4.7892   -0.9168 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7049   -2.2241    0.9642 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7408   -0.8156    1.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6916   -0.3469    2.0260 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510    0.0051    0.5154 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8386    1.4456    0.6804 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6564    2.0030    1.4385 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9579    2.3122    0.0426 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9990    3.7164    0.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9007    0.2072   -2.2566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8703    1.3031   -0.8061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0571   -0.0192   -0.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4136   -1.0923    0.3876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7014   -1.4504   -1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1085   -0.7017    0.3310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1026    0.8032    0.7493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9186    0.0424   -2.0094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9982    1.3898   -1.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3545    2.6977   -0.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7973    2.2035   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2618    0.5215   -1.1021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9721    2.2114   -0.6724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1471    1.8336    1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3714    0.1372    1.1254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6819    1.5907    1.4499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4567    0.4909    2.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6835   -0.2489   -0.3018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4030   -1.3608    0.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9826   -1.7402    0.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5225   -1.2567    2.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2885    1.0871    1.8276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5817   -0.1178    1.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3974    0.9904   -1.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4367   -0.4803   -1.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1869   -2.4521   -1.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0410   -4.5401   -1.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8322   -4.3921   -0.6752 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8683   -5.8952   -0.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4184   -2.8428    1.4902 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8702    0.5585    2.2861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3732    4.2578   -0.4622 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7625    4.0116    1.2734 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0703    4.0352    0.0820 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 23 15  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 14 51  1  0
 14 52  1  0
 16 53  1  0
 19 54  1  0
 19 55  1  0
 19 56  1  0
 20 57  1  0
 22 58  1  0
 27 59  1  0
 27 60  1  0
 27 61  1  0
M  END


  Mrv1533004171512522D          

 27 27  0  0  0  0            999 V2000
   -7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   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
   -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
   -0.7145   -1.2375    0.0000 C   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 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
    0.7145   -0.4125    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
    0.0000    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
   -1.4289    0.8250    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    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
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  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
  7  8  1  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  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0150142

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC(=O)CC1=CC(OC)=CC(O)=C1C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-18(23)14-17-15-19(26-2)16-20(24)21(17)22(25)27-3/h15-16,24H,4-14H2,1-3H3

> <INCHI_KEY>
MWVQQAPWKBGDKG-UHFFFAOYSA-N

> <FORMULA>
C22H34O5

> <MOLECULAR_WEIGHT>
378.509

> <EXACT_MASS>
378.240624195

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
43.73561697054397

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate

> <ALOGPS_LOGP>
5.91

> <JCHEM_LOGP>
6.834513836666667

> <ALOGPS_LOGS>
-5.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.688777569047858

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.551418970192236

> <JCHEM_PKA_STRONGEST_BASIC>
-4.062328997644484

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
107.42199999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.93e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0     -14.670  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -13.337  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.003  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   15   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoic acid	Generator
2-(2-Oxotridecyl)-6-hydroxy-4-methoxybenzoate methyl ester	Generator

Chemical Formula

C₂₂H₃₄O₅

Average Mass

378.5090 Da

Monoisotopic Mass

378.24062 Da

IUPAC Name

methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate

Traditional Name

methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC(=O)CC1=CC(OC)=CC(O)=C1C(=O)OC

InChI Identifier

InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-18(23)14-17-15-19(26-2)16-20(24)21(17)22(25)27-3/h15-16,24H,4-14H2,1-3H3

InChI Key

MWVQQAPWKBGDKG-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
Ononis natrix	LOTUS Database	35616633
Ononis viscosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

P-methoxybenzoic acids and derivatives

Alternative Parents

Substituents

O-hydroxybenzoic acid ester
P-methoxybenzoic acid or derivatives
Benzoate ester
Methoxyphenol
Salicylic acid or derivatives
Anisole
Phenoxy compound
Benzoyl
Phenol ether
Methoxybenzene
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Vinylogous acid
Methyl ester
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Carbonyl group
Organooxygen compound
Organic oxygen compound
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	5.91	ALOGPS
logP	6.83	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	9.55	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	107.42 m³·mol⁻¹	ChemAxon
Polarizability	43.74 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	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

14539295

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate (NP0150142)

MOL for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

3D MOL for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

3D SDF for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

3D-SDF for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

PDB for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

3D PDB for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

SMILES for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

INCHI for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

Structure for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)

3D Structure for NP0150142 (methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate)