NP-MRD: Showing NP-Card for methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate (NP0237812)

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Record Information

Version

2.0

Created at

2022-09-06 21:03:42 UTC

Updated at

2022-09-06 21:03:42 UTC

NP-MRD ID

NP0237812

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate

Description

[3,5-Dihydroxy-2-(methoxycarbonyl)-4-methylphenyl]methyl 3-formyl-2,4-dihydroxy-6-methylbenzoate belongs to the class of organic compounds known as p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group. methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate is found in Gowardia nigricans. [3,5-Dihydroxy-2-(methoxycarbonyl)-4-methylphenyl]methyl 3-formyl-2,4-dihydroxy-6-methylbenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171520132D          

 28 29  0  0  0  0            999 V2000
   -1.4289    0.8250    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
   -2.1434   -0.4125    0.0000 C   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
   -2.1434   -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 O   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   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -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
   -3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    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
   -5.7158   -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
   -7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.8250    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  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  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
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 24 27  2  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
   -4.9724   -3.3710    1.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6631   -2.1871    0.3047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3980   -1.6650    0.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5248   -2.3173    0.8849 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0751   -0.4585   -0.5066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7432   -0.0071   -0.5087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7205   -0.7629    0.2433 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5663   -0.1539    0.1207 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6268   -0.7879    0.7979 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3369   -1.8260    1.4428 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9847   -0.2811    0.7616 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9794   -0.9463    1.4453 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6576   -2.1755    2.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2779   -0.5017    1.4381 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6428    0.6593    0.7263 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9505    1.0506    0.7577 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6464    1.3180    0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9475    2.5155   -0.7050 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0559    3.0772   -0.8359 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3282    0.8627    0.0566 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3070    1.4843   -0.6033 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3596    1.1261   -1.1929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2690    1.8709   -1.9091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8745    3.0110   -2.5955 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5722    1.4616   -1.9289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6141    2.2089   -2.6771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9709    0.2947   -1.2252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2970   -0.0583   -1.2887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8309   -3.8606    0.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3250   -3.0989    2.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0869   -4.0384    1.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9440   -0.7635    1.3094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5923   -1.7726   -0.1595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3133   -3.0136    1.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6181   -2.5320    2.6698 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9749   -2.0142    3.0606 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0785   -0.9977    1.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3281    1.8254    0.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1271    3.0277   -1.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573    2.2883   -1.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3433    1.4922   -1.2093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5327    3.5666   -3.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5322    1.5951   -2.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2566    2.6029   -3.6401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9100    3.0740   -2.0137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6967   -0.8217   -0.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5 27  2  0
 27 28  1  0
 27 25  1  0
 25 26  1  0
 25 23  2  0
 23 24  1  0
 23 22  1  0
 22  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
 17 20  2  0
 20 21  1  0
  6  5  1  0
 20 11  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 28 46  1  0
 26 43  1  0
 26 44  1  0
 26 45  1  0
 24 42  1  0
 22 41  1  0
  7 32  1  0
  7 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  0
 16 38  1  0
 18 39  1  0
 21 40  1  0
M  END


  Mrv1533004171520132D          

 28 29  0  0  0  0            999 V2000
   -1.4289    0.8250    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
   -2.1434   -0.4125    0.0000 C   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
   -2.1434   -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 O   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   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -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
   -3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    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
   -5.7158   -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
   -7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.8250    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  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  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
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 24 27  2  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237812

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C(O)C(C)=C(O)C=C1COC(=O)C1=C(C)C=C(O)C(C=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O9/c1-8-4-13(22)11(6-20)17(24)14(8)19(26)28-7-10-5-12(21)9(2)16(23)15(10)18(25)27-3/h4-6,21-24H,7H2,1-3H3

> <INCHI_KEY>
FHELLTXVIACUDU-UHFFFAOYSA-N

> <FORMULA>
C19H18O9

> <MOLECULAR_WEIGHT>
390.344

> <EXACT_MASS>
390.09508216

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
37.74933444687855

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate

> <ALOGPS_LOGP>
2.28

> <JCHEM_LOGP>
5.829756698000001

> <ALOGPS_LOGS>
-3.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.801966430429685

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.681568105227501

> <JCHEM_PKA_STRONGEST_BASIC>
-3.993489208986783

> <JCHEM_POLAR_SURFACE_AREA>
150.59

> <JCHEM_REFRACTIVITY>
99.3112

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.80e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate

> <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      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.667  -0.000   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -5.335   0.000   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.334  -2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -8.002   1.540   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0     -13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0     -12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -13.337  -0.000   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -13.337   1.540   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0     -10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -10.669   1.540   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   13                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12    5   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   27                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   18   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Value	Source
[3,5-Dihydroxy-2-(methoxycarbonyl)-4-methylphenyl]methyl 3-formyl-2,4-dihydroxy-6-methylbenzoic acid	Generator

Chemical Formula

C₁₉H₁₈O₉

Average Mass

390.3440 Da

Monoisotopic Mass

390.09508 Da

IUPAC Name

methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate

Traditional Name

methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C(O)C(C)=C(O)C=C1COC(=O)C1=C(C)C=C(O)C(C=O)=C1O

InChI Identifier

InChI=1S/C19H18O9/c1-8-4-13(22)11(6-20)17(24)14(8)19(26)28-7-10-5-12(21)9(2)16(23)15(10)18(25)27-3/h4-6,21-24H,7H2,1-3H3

InChI Key

FHELLTXVIACUDU-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
Gowardia nigricans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

p-Hydroxybenzoic acid alkyl esters

Alternative Parents

Substituents

P-hydroxybenzoic acid alkyl ester
O-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Benzyloxycarbonyl
Salicylic acid or derivatives
Hydroxybenzaldehyde
Benzaldehyde
Benzoyl
M-cresol
O-cresol
Resorcinol
Toluene
1-hydroxy-4-unsubstituted benzenoid
Phenol
1-hydroxy-2-unsubstituted benzenoid
Aryl-aldehyde
Dicarboxylic acid or derivatives
Methyl ester
Vinylogous acid
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Aldehyde
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	2.28	ALOGPS
logP	5.83	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	7.68	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	150.59 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	99.31 m³·mol⁻¹	ChemAxon
Polarizability	37.75 Å³	ChemAxon
Number of Rings	2	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

13963329

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate (NP0237812)

MOL for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

3D MOL for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

3D SDF for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

3D-SDF for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

PDB for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

3D PDB for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

SMILES for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

INCHI for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

Structure for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)

3D Structure for NP0237812 (methyl 6-[(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)methyl]-2,4-dihydroxy-3-methylbenzoate)