NP-MRD: Showing NP-Card for 6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate (NP0254486)

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Record Information

Version

1.0

Created at

2022-09-07 18:39:36 UTC

Updated at

2022-09-07 18:39:37 UTC

NP-MRD ID

NP0254486

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate

Description

6-Hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6,7,8-tetrahydro-1H-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate belongs to the class of organic compounds known as azaphilones. These are a structurally variable family of fungal polyketide metabolites possessing a highly oxygenated pyranoquinone bicyclic core, usually known as isochromene, and a quaternary carbon center. 6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate is found in Penicillium commune. Based on a literature review very few articles have been published on 6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6,7,8-tetrahydro-1H-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072220392D          

 30 32  0  0  0  0            999 V2000
   -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
    0.7145   -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
   -0.7145   -0.4125    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
    1.4289    0.8250    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
    2.4256    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -0.5558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4862    0.0762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2040    0.8515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2986   -0.0670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8289    0.5650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5468    1.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6414    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9236   -0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7360   -0.4968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3933   -0.9855    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
    4.5808   -0.8423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505   -1.4743    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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    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  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
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  7  8  1  0  0  0  0
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  4  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
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 12 13  1  0  0  0  0
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 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
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 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
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 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 12 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
  6 30  1  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
    6.0648    0.4662   -3.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8364   -0.1271   -2.5485 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3102   -0.5311   -1.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8845   -0.4242   -1.1317 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3786   -0.8366    0.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9596   -0.7245    0.2836 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1585   -0.2073   -0.6282 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7678    0.5879   -1.7219 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0309    0.1156   -2.0769 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7044   -0.4121   -0.5561 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0322   -0.1838   -1.5722 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0590   -2.3644    0.8097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1774   -0.2897    0.9335 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1449   -1.3831   -0.7948 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5879    0.0316    0.4198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6772   -0.2762   -0.3584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5574   -1.2335   -1.4942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9276    0.2832   -0.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0991    1.1739    0.9132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3684    1.7075    1.1084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0284    1.4934    1.6988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1950    2.3816    2.7351 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7721    0.9223    1.4523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6822    1.2397    2.2418 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9019    2.3677    1.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0523   -0.4581    1.8104 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3109    0.9100    1.7691 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3555   -1.1786    1.5578 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7309    0.7179   -4.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9384   -0.9593   -0.6429 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0747   -1.2606    0.7534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0964    0.6355   -2.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8133    1.6446   -1.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1425   -2.6821    0.8242 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4195   -2.9278   -0.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8793   -0.7988   -2.2287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2678   -2.2566   -1.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5645   -1.3991   -1.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7572    0.0033   -0.7728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1452    1.4559    0.5140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4589    2.6575    3.3455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9344    2.3699    2.3595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4733    3.2736    2.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7322    2.3877    0.7360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6526   -0.7171    2.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8570    1.3436    0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2517   -2.2766    1.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0374   -1.0051    2.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
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  6  7  2  0
  7  8  1  0
  8  9  1  0
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  4  3  1  0
  3  2  2  0
  2  1  1  0
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  7 10  1  0
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 17 25  1  0
 10 12  1  0
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 27 48  1  0
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 13 39  1  0
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 30 53  1  0
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  8 37  1  0
  8 38  1  0
  3 35  1  0
  2 34  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 36  1  0
M  END


  Mrv1652309072220392D          

 30 32  0  0  0  0            999 V2000
   -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
    0.7145   -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
   -0.7145   -0.4125    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
    1.4289    0.8250    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
    2.4256    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -0.5558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4862    0.0762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2040    0.8515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2986   -0.0670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8289    0.5650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5468    1.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6414    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9236   -0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7360   -0.4968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3933   -0.9855    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
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  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  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
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 17 25  1  0  0  0  0
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 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
  6 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0254486

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C(O)=CC(C)=C1C(=O)OC1(C)C(O)CC2=C(COC(C=CC)=C2)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H24O8/c1-5-6-13-8-12-9-16(24)22(3,20(26)14(12)10-29-13)30-21(27)17-11(2)7-15(23)18(25)19(17)28-4/h5-8,16,23-25H,9-10H2,1-4H3

> <INCHI_KEY>
BVPLOPDDUJTCFL-UHFFFAOYSA-N

> <FORMULA>
C22H24O8

> <MOLECULAR_WEIGHT>
416.426

> <EXACT_MASS>
416.147117733

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.661002357627034

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6,7,8-tetrahydro-1H-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate

> <JCHEM_LOGP>
2.589862951666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.057557527593978

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.85173939519425

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3630917078768148

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000001

> <JCHEM_REFRACTIVITY>
111.62909999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1H-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -3.080   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  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.528   0.677   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.518  -1.037   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.508   0.142   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.981   1.589   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.024  -0.125   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.014   1.055   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.487   2.502   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.531   0.787   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.057  -0.660   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      12.574  -0.927   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.067  -1.840   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.594  -3.287   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.551  -1.572   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.561  -2.752   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.088  -4.199   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.335  -3.080   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
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   30                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4                                                       
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14   28                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   25                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   17   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   12   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    6                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
6-Hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6,7,8-tetrahydro-1H-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoic acid	Generator

Chemical Formula

C₂₂H₂₄O₈

Average Mass

416.4260 Da

Monoisotopic Mass

416.14712 Da

IUPAC Name

6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6,7,8-tetrahydro-1H-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate

Traditional Name

6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1H-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate

CAS Registry Number

Not Available

SMILES

COC1=C(O)C(O)=CC(C)=C1C(=O)OC1(C)C(O)CC2=C(COC(C=CC)=C2)C1=O

InChI Identifier

InChI=1S/C22H24O8/c1-5-6-13-8-12-9-16(24)22(3,20(26)14(12)10-29-13)30-21(27)17-11(2)7-15(23)18(25)19(17)28-4/h5-8,16,23-25H,9-10H2,1-4H3

InChI Key

BVPLOPDDUJTCFL-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
Penicillium commune	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azaphilones. These are a structurally variable family of fungal polyketide metabolites possessing a highly oxygenated pyranoquinone bicyclic core, usually known as isochromene, and a quaternary carbon center.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azaphilones

Sub Class

Not Available

Direct Parent

Azaphilones

Alternative Parents

Substituents

Azaphilone
Dihydroxybenzoic acid
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
O-methoxybenzoic acid or derivatives
Methoxyphenol
Benzoate ester
Benzoic acid or derivatives
Catechol
Benzoyl
Phenoxy compound
M-cresol
Anisole
P-cresol
Phenol ether
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Phenol
Toluene
Cyclohexenone
Alkyl aryl ether
Pyran
Benzenoid
Monocyclic benzene moiety
Carboxylic acid ester
Ketone
Secondary alcohol
Oxacycle
Ether
Carboxylic acid derivative
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
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	2.59	ChemAxon
pKa (Strongest Acidic)	8.85	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	122.52 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	111.63 m³·mol⁻¹	ChemAxon
Polarizability	42.66 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

75604878

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate (NP0254486)

MOL for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

3D MOL for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

3D SDF for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

3D-SDF for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

PDB for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

3D PDB for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

SMILES for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

INCHI for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

Structure for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)

3D Structure for NP0254486 (6-hydroxy-7-methyl-8-oxo-3-(prop-1-en-1-yl)-5,6-dihydro-1h-isochromen-7-yl 3,4-dihydroxy-2-methoxy-6-methylbenzoate)