NP-MRD: Showing NP-Card for (3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate (NP0317647)

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Record Information

Version

2.0

Created at

2022-09-11 17:39:07 UTC

Updated at

2022-09-11 17:39:08 UTC

NP-MRD ID

NP0317647

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate

Description

(3,8-Dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-3,4-dihydro-1H-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate 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. (3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate is found in Aspergillus banksianus. Based on a literature review very few articles have been published on (3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-3,4-dihydro-1H-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112219392D          

 31 33  0  0  0  0            999 V2000
   -2.1434   -0.4125    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
   -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 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
    1.4289   -0.0000    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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256    0.3627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2380   -1.3310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505   -1.4743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5808   -0.8423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3327   -2.2495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1451   -2.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6754   -1.7608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4273   -3.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1792   -4.5753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0845   -3.6567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5542   -4.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8024   -2.8815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9899   -2.7382    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   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  0  0  0  0
 13 29  1  0  0  0  0
 29 30  1  0  0  0  0
  7 30  1  0  0  0  0
 30 31  2  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
   -7.7093   -0.9028   -0.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5879   -0.4715   -0.7329 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3324   -0.2844   -0.1241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2480   -0.5455    1.2171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0062   -0.3660    1.8453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9762   -0.6380    3.1737 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9157    0.0594    1.1248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0107    0.3241   -0.2464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2460    0.1395   -0.8428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4425    0.3961   -2.2964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8439    0.7846   -1.0383 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7967    2.2920   -1.1230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5392    0.2466   -0.4178 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6370   -1.1309   -0.5190 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6119    0.7537   -1.2051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8797    0.4484   -0.7745 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5069   -0.7600   -0.6192 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8204   -1.7671   -0.9203 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8761   -0.8897   -0.1388 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4471   -2.1409   -0.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8339   -3.3169   -0.2904 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7785   -2.2515    0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4847   -1.1099    0.7774 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8009   -1.2269    1.2394 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9227    0.1444    0.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6734    1.3200    0.9812 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6263    0.2342    0.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0502    1.5486    0.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5375    0.6961    0.9263 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6046    0.2606    1.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4271    0.0464    2.9583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8332   -0.2522    0.8778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6237   -1.9500    0.3423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5939   -0.8091   -0.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1212   -0.8849    1.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2469   -0.5871    3.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4166    0.9594   -2.3694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6766    1.0464   -2.7270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6038   -0.5479   -2.8299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8572    0.3911   -2.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1826    2.7355   -0.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8004    2.7538   -1.0710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3415    2.6433   -2.0909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8828   -1.5399    0.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    0.5208   -2.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5306    1.8848   -1.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9540   -3.5555   -0.6171 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2079   -3.2380    0.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2237   -2.1384    1.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3562    1.9024    1.8497 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7463    1.0669    1.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6905    2.0494    0.1180 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6982    2.3882    0.3911 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1429    1.6313    0.6929 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7398    1.7313   -0.9895 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
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7 30  1  0
 30 31  2  0
 30 29  1  0
 29 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  2  0
 27 28  1  0
 13 11  1  0
 11 12  1  0
 11  8  1  0
  8  9  2  0
  9 10  1  0
  9  3  1  0
  8  7  1  0
 27 19  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  6 36  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 21 47  1  0
 22 48  1  0
 24 49  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
 28 53  1  0
 28 54  1  0
 28 55  1  0
 11 40  1  6
 12 41  1  0
 12 42  1  0
 12 43  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
M  END


  Mrv1652309112219392D          

 31 33  0  0  0  0            999 V2000
   -2.1434   -0.4125    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
   -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 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
    1.4289   -0.0000    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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256    0.3627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2380   -1.3310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505   -1.4743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5808   -0.8423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3327   -2.2495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1451   -2.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6754   -1.7608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4273   -3.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1792   -4.5753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0845   -3.6567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5542   -4.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8024   -2.8815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9899   -2.7382    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   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  0  0  0  0
 13 29  1  0  0  0  0
 29 30  1  0  0  0  0
  7 30  1  0  0  0  0
 30 31  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0317647

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(=O)OC(O)(COC(=O)C3=C(O)C=C(O)C(C)=C3C)C(C)C2=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C22H24O9/c1-9-10(2)18(14(24)6-13(9)23)20(26)30-8-22(28)12(4)17-11(3)16(29-5)7-15(25)19(17)21(27)31-22/h6-7,12,23-25,28H,8H2,1-5H3

> <INCHI_KEY>
REUACJUQRKZNRP-UHFFFAOYSA-N

> <FORMULA>
C22H24O9

> <MOLECULAR_WEIGHT>
432.425

> <EXACT_MASS>
432.142032353

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
43.36072168983331

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-3,4-dihydro-1H-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate

> <JCHEM_LOGP>
5.514411181999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.896774153362912

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.952429430260338

> <JCHEM_PKA_STRONGEST_BASIC>
-3.953080736972237

> <JCHEM_POLAR_SURFACE_AREA>
142.75000000000003

> <JCHEM_REFRACTIVITY>
110.70099999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4H-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.001  -0.770   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      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.528   0.677   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.518  -1.037   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.044  -2.485   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.561  -2.752   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.551  -1.572   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.088  -4.199   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.604  -4.467   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.594  -3.287   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.131  -5.914   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.141  -7.093   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.668  -8.540   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.624  -6.826   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.635  -8.006   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.098  -5.379   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.581  -5.111   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   30                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   29                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   27                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   19   28                                                  
CONECT   28   27                                                            
CONECT   29   13   30                                                       
CONECT   30   29    7   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
(3,8-Dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-3,4-dihydro-1H-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoic acid	Generator

Chemical Formula

C₂₂H₂₄O₉

Average Mass

432.4250 Da

Monoisotopic Mass

432.14203 Da

IUPAC Name

(3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-3,4-dihydro-1H-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate

Traditional Name

(3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4H-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=O)OC(O)(COC(=O)C3=C(O)C=C(O)C(C)=C3C)C(C)C2=C1C

InChI Identifier

InChI=1S/C22H24O9/c1-9-10(2)18(14(24)6-13(9)23)20(26)30-8-22(28)12(4)17-11(3)16(29-5)7-15(25)19(17)21(27)31-22/h6-7,12,23-25,28H,8H2,1-5H3

InChI Key

REUACJUQRKZNRP-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
Aspergillus banksianus	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
2-benzopyran
Salicylic acid or derivatives
Isochromane
Benzopyran
O-xylene
Xylene
Resorcinol
P-cresol
O-cresol
M-cresol
Benzoyl
Anisole
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Dicarboxylic acid or derivatives
Vinylogous acid
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	5.51	ChemAxon
pKa (Strongest Acidic)	8.95	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	142.75 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	110.7 m³·mol⁻¹	ChemAxon
Polarizability	43.36 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

162815657

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate (NP0317647)

MOL for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

3D MOL for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

3D SDF for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

3D-SDF for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

PDB for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

3D PDB for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

SMILES for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

INCHI for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

Structure for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)

3D Structure for NP0317647 ((3,8-dihydroxy-6-methoxy-4,5-dimethyl-1-oxo-4h-2-benzopyran-3-yl)methyl 4,6-dihydroxy-2,3-dimethylbenzoate)