NP-MRD: Showing NP-Card for methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate (NP0207573)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 04:14:25 UTC

Updated at

2022-09-05 04:14:25 UTC

NP-MRD ID

NP0207573

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate

Description

Methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate is found in Podostictina pickeringii. Methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241507112D          

 29 30  0  0  0  0            999 V2000
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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   -2.4750    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
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   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
    0.0000   -4.1250    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
    0.0000   -2.4750    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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  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
 18 19  2  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

     RDKit          3D

 51 52  0  0  0  0  0  0  0  0999 V2000
    7.4456   -0.7875    0.8669 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0610   -0.7727    0.5774 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2839    0.3534    0.5489 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8407    1.4544    0.7980 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8606    0.3667    0.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1953   -0.8040   -0.0294 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9219   -2.1016   -0.0318 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8284   -0.8024   -0.3169 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1340   -2.0937   -0.6181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1268    0.3806   -0.3226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2374    0.3144   -0.6177 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2151    0.1428    0.3535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7339    0.0530    1.5363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6224    0.0639    0.1504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1417    0.1620   -1.1360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2100    0.3435   -2.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4947    0.0894   -1.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0934    0.1850   -2.6760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3688    0.1045   -2.7728 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3703   -0.0857   -0.2866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7629   -0.1612   -0.5114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8749   -0.1835    0.9807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8238   -0.3722    2.1345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4935   -0.1084    1.2009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1283   -0.2204    2.5152 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7722    1.5511   -0.0464 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9999    2.8222   -0.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1273    1.5370    0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7759    2.7079    0.5140 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9495    0.1548    0.5806 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9656   -1.6421    0.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5536   -0.8919    1.9673 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2030   -2.9380   -0.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7009   -2.0627   -0.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3448   -2.2945    0.9903 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1099   -1.8724   -0.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6459   -2.6110   -1.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0726   -2.7477    0.2646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6253    1.3083   -2.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7458    0.4031   -3.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4719   -0.4822   -2.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5592    0.3194   -3.5935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3616   -0.2868    0.2790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3975    0.5495    2.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2682   -0.6168    3.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4557   -1.2517    1.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3124   -0.2148    3.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0115    2.6682   -0.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9836    3.2209    0.9818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5897    3.5726   -0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2643    3.5772    0.5106 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  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  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
 20 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 10 26  1  0
 26 27  1  0
 26 28  2  0
 28 29  1  0
 28  5  1  0
 24 14  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 18 42  1  0
 21 43  1  0
 23 44  1  0
 23 45  1  0
 23 46  1  0
 25 47  1  0
 27 48  1  0
 27 49  1  0
 27 50  1  0
 29 51  1  0
M  END


  Mrv1533004241507112D          

 29 30  0  0  0  0            999 V2000
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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   -2.4750    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
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   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
    0.0000   -4.1250    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
    0.0000   -2.4750    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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  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
 18 19  2  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207573

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C(C)C(C)=C(OC(=O)C2=C(C)C(C=O)=C(O)C(C)=C2O)C(C)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O8/c1-8-9(2)19(12(5)18(25)14(8)20(26)28-6)29-21(27)15-10(3)13(7-22)16(23)11(4)17(15)24/h7,23-25H,1-6H3

> <INCHI_KEY>
MUKMJPYYNNZPRS-UHFFFAOYSA-N

> <FORMULA>
C21H22O8

> <MOLECULAR_WEIGHT>
402.399

> <EXACT_MASS>
402.131467668

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
40.90867399918939

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate

> <ALOGPS_LOGP>
2.75

> <JCHEM_LOGP>
6.957071518999999

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.841257976469988

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.739994393374726

> <JCHEM_PKA_STRONGEST_BASIC>
-4.686450401189409

> <JCHEM_POLAR_SURFACE_AREA>
130.36

> <JCHEM_REFRACTIVITY>
107.61889999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.17e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.002 -13.860   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.001 -16.170   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.000  -4.620   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   28                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   26                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   24                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   14   25                                                  
CONECT   25   24                                                            
CONECT   26   10   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26    5   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoic acid	Generator

Chemical Formula

C₂₁H₂₂O₈

Average Mass

402.3990 Da

Monoisotopic Mass

402.13147 Da

IUPAC Name

methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate

Traditional Name

methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C(C)C(C)=C(OC(=O)C2=C(C)C(C=O)=C(O)C(C)=C2O)C(C)=C1O

InChI Identifier

InChI=1S/C21H22O8/c1-8-9(2)19(12(5)18(25)14(8)20(26)28-6)29-21(27)15-10(3)13(7-22)16(23)11(4)17(15)24/h7,23-25H,1-6H3

InChI Key

MUKMJPYYNNZPRS-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
Podostictina pickeringii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depside backbone
P-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Benzoate ester
Phenol ester
Salicylic acid or derivatives
P-xylenol
Xylenol
Benzoic acid or derivatives
Hydroxybenzaldehyde
Benzoyl
Phenoxy compound
Benzaldehyde
M-cresol
O-cresol
P-cresol
P-xylene
Xylene
Resorcinol
Phenol
Aryl-aldehyde
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Benzenoid
Methyl ester
Vinylogous acid
Carboxylic acid ester
Carboxylic acid derivative
Aldehyde
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	2.75	ALOGPS
logP	6.96	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	7.74	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.36 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	107.62 m³·mol⁻¹	ChemAxon
Polarizability	40.91 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

13964290

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate (NP0207573)

MOL for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

3D MOL for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

3D SDF for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

3D-SDF for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

PDB for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

3D PDB for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

SMILES for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

INCHI for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

Structure for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)

3D Structure for NP0207573 (methyl 4-(3-formyl-4,6-dihydroxy-2,5-dimethylbenzoyloxy)-2-hydroxy-3,5,6-trimethylbenzoate)