NP-MRD: Showing NP-Card for 6'-hydroxy-3'-methoxy-mitorubrin (NP0009262)

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Record Information

Version

2.0

Created at

2020-12-09 06:40:11 UTC

Updated at

2021-07-15 17:02:46 UTC

NP-MRD ID

NP0009262

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6'-hydroxy-3'-methoxy-mitorubrin

Provided By

NPAtlas

Description

(7S)-7-methyl-6,8-dioxo-3-[(1E)-prop-1-en-1-yl]-7,8-dihydro-6H-isochromen-7-yl 3,4-dihydroxy-6-methoxy-2-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-3'-methoxy-mitorubrin is found in Penicillium and Talaromyces radicus. 6'-hydroxy-3'-methoxy-mitorubrin was first documented in 2010 (PMID: 20522994). Based on a literature review very few articles have been published on (7S)-7-methyl-6,8-dioxo-3-[(1E)-prop-1-en-1-yl]-7,8-dihydro-6H-isochromen-7-yl 3,4-dihydroxy-6-methoxy-2-methylbenzoate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106343D          

 50 52  0  0  0  0            999 V2000
    8.8578   -1.9755   -0.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3839   -1.9415   -0.5537 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5987   -1.1930    0.1930 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1567   -1.1316   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4410   -0.3596    0.7540 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0045   -0.2710    0.5589 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2117    0.4779    1.3055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7642    0.5770    1.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0225    0.8981    2.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2067    0.2898   -0.2266 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6567    1.4163   -1.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1643    0.0864   -0.2268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1345    0.9595    0.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7666    2.0893    0.5777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5566    0.6891    0.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4923    1.6140    0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8012    3.8933    1.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8449    1.3354    0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2950    0.1103    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3589   -1.8992   -1.2631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3642   -1.0397   -0.5134 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1783   -1.7788   -1.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5390   -1.8458   -1.0371 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4217   -2.3689   -1.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0828   -2.5834    0.6150 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.8760    0.2267    1.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.7811   -2.2550   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548   -1.8979    0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5774   -2.4725   -1.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4524   -1.2400   -1.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6800   -2.3499   -2.0438 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  7 37  1  0  0  0  0
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 25 49  1  0  0  0  0
 29 50  1  0  0  0  0
M  END

     RDKit          3D

 50 52  0  0  0  0  0  0  0  0999 V2000
    8.8578   -1.9755   -0.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3839   -1.9415   -0.5537 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2067    0.2898   -0.2266 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -4.4923    1.6140    0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8012    3.8933    1.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8449    1.3354    0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2950    0.1103    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.7892   -2.0701   -0.7890 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3589   -1.8992   -1.2631 O   0  0  0  0  0  0  0  0  0  0  0  0
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  3  4  1  0
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M  END


  Mrv1652306242106343D          

 50 52  0  0  0  0            999 V2000
    8.8578   -1.9755   -0.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3839   -1.9415   -0.5537 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5987   -1.1930    0.1930 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1567   -1.1316   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7642    0.5770    1.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0225    0.8981    2.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2067    0.2898   -0.2266 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6567    1.4163   -1.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3548   -1.8979    0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5774   -2.4725   -1.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4524   -1.2400   -1.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6800   -2.3499   -2.0438 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  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  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 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  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30  4  1  0  0  0  0
 28  6  1  0  0  0  0
 24 15  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  2 34  1  0  0  0  0
  3 35  1  0  0  0  0
  5 36  1  0  0  0  0
  7 37  1  0  0  0  0
 11 38  1  0  0  0  0
 11 39  1  0  0  0  0
 11 40  1  0  0  0  0
 18 41  1  0  0  0  0
 18 42  1  0  0  0  0
 18 43  1  0  0  0  0
 19 44  1  0  0  0  0
 21 45  1  0  0  0  0
 23 46  1  0  0  0  0
 25 47  1  0  0  0  0
 25 48  1  0  0  0  0
 25 49  1  0  0  0  0
 29 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0009262

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(OC([H])([H])[H])=C(C(=O)O[C@]2(C(=O)C([H])=C3C([H])=C(OC([H])=C3C2=O)C(\[H])=C(/[H])C([H])([H])[H])C([H])([H])[H])C(=C1O[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H20O8/c1-5-6-13-7-12-8-17(24)22(3,20(26)14(12)10-29-13)30-21(27)18-11(2)19(25)15(23)9-16(18)28-4/h5-10,23,25H,1-4H3/b6-5+/t22-/m0/s1

> <INCHI_KEY>
FZBGUENQZXUQSN-BDNZGDGKSA-N

> <FORMULA>
C22H20O8

> <MOLECULAR_WEIGHT>
412.394

> <EXACT_MASS>
412.115817604

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
41.67517081889973

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(7S)-7-methyl-6,8-dioxo-3-[(1E)-prop-1-en-1-yl]-7,8-dihydro-6H-isochromen-7-yl 3,4-dihydroxy-6-methoxy-2-methylbenzoate

> <ALOGPS_LOGP>
3.21

> <JCHEM_LOGP>
3.3692073886666667

> <ALOGPS_LOGS>
-4.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.020515360020333

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.77093330302054

> <JCHEM_PKA_STRONGEST_BASIC>
-4.728235439434383

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000003

> <JCHEM_REFRACTIVITY>
111.03059999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(7S)-7-methyl-6,8-dioxo-3-[(1E)-prop-1-en-1-yl]isochromen-7-yl 3,4-dihydroxy-6-methoxy-2-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 50 52  0  0  0  0  0  0  0  0999 V2000
    8.8578   -1.9755   -0.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3839   -1.9415   -0.5537 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5987   -1.1930    0.1930 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1567   -1.1316   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4410   -0.3596    0.7540 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0045   -0.2710    0.5589 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2117    0.4779    1.3055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7642    0.5770    1.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0225    0.8981    2.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2067    0.2898   -0.2266 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6567    1.4163   -1.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1643    0.0864   -0.2268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1345    0.9595    0.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7666    2.0893    0.5777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5566    0.6891    0.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4923    1.6140    0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9915    2.8432    0.9954 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8012    3.8933    1.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8449    1.3354    0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2950    0.1103    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6543   -0.2052    0.0351 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3703   -0.8282   -0.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7892   -2.0701   -0.7890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0022   -0.5368   -0.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0350   -1.5467   -0.7465 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9255   -0.9450   -0.7062 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3589   -1.8992   -1.2631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3642   -1.0397   -0.5134 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1783   -1.7788   -1.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5390   -1.8458   -1.0371 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4217   -2.3689   -1.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0828   -2.5834    0.6150 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2119   -0.9466   -0.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9345   -2.5230   -1.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0212   -0.6146    0.9872 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8760    0.2267    1.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6971    1.0517    2.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1169    2.2039   -1.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6480    1.8149   -0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7892    0.9786   -2.1417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0139    3.8197    2.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2262    4.8409    1.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7414    4.0026    0.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5584    2.0804    0.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3124    0.5202    0.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7811   -2.2550   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548   -1.8979    0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5774   -2.4725   -1.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4524   -1.2400   -1.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6800   -2.3499   -2.0438 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  1  1
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 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  2  0
 26 28  1  0
 28 29  2  0
 29 30  1  0
 30  4  1  0
 28  6  1  0
 24 15  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  3 35  1  0
  5 36  1  0
  7 37  1  0
 11 38  1  0
 11 39  1  0
 11 40  1  0
 18 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 21 45  1  0
 23 46  1  0
 25 47  1  0
 25 48  1  0
 25 49  1  0
 29 50  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       8.858  -1.976  -0.284  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.384  -1.942  -0.554  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.599  -1.193   0.193  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.157  -1.132  -0.036  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.441  -0.360   0.754  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.005  -0.271   0.559  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.212   0.478   1.306  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.764   0.577   1.121  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.023   0.898   2.089  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.207   0.290  -0.227  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.657   1.416  -1.130  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.164   0.086  -0.227  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.135   0.960   0.165  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.767   2.089   0.578  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.557   0.689   0.143  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.492   1.614   0.552  0.00  0.00           C+0
HETATM   17  O   UNK     0      -3.991   2.843   0.995  0.00  0.00           O+0
HETATM   18  C   UNK     0      -4.801   3.893   1.446  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.845   1.335   0.523  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.295   0.110   0.078  0.00  0.00           C+0
HETATM   21  O   UNK     0      -7.654  -0.205   0.035  0.00  0.00           O+0
HETATM   22  C   UNK     0      -5.370  -0.828  -0.336  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.789  -2.070  -0.789  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.002  -0.537  -0.303  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.035  -1.547  -0.747  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.926  -0.945  -0.706  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.359  -1.899  -1.263  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.364  -1.040  -0.513  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.178  -1.779  -1.243  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.539  -1.846  -1.037  0.00  0.00           O+0
HETATM   31  H   UNK     0       9.422  -2.369  -1.133  0.00  0.00           H+0
HETATM   32  H   UNK     0       9.083  -2.583   0.615  0.00  0.00           H+0
HETATM   33  H   UNK     0       9.212  -0.947  -0.079  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.934  -2.523  -1.357  0.00  0.00           H+0
HETATM   35  H   UNK     0       7.021  -0.615   0.987  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.876   0.227   1.560  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.697   1.052   2.107  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.117   2.204  -1.236  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.648   1.815  -0.832  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.789   0.979  -2.142  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.014   3.820   2.534  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.226   4.841   1.267  0.00  0.00           H+0
HETATM   43  H   UNK     0      -5.741   4.003   0.851  0.00  0.00           H+0
HETATM   44  H   UNK     0      -6.558   2.080   0.850  0.00  0.00           H+0
HETATM   45  H   UNK     0      -8.312   0.520   0.352  0.00  0.00           H+0
HETATM   46  H   UNK     0      -6.781  -2.255  -0.803  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.355  -1.898   0.080  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.577  -2.473  -1.067  0.00  0.00           H+0
HETATM   49  H   UNK     0      -2.452  -1.240  -1.652  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.680  -2.350  -2.044  0.00  0.00           H+0
CONECT    1    2   31   32   33                                             
CONECT    2    1    3   34                                                  
CONECT    3    2    4   35                                                  
CONECT    4    3    5   30                                                  
CONECT    5    4    6   36                                                  
CONECT    6    5    7   28                                                  
CONECT    7    6    8   37                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12   26                                             
CONECT   11   10   38   39   40                                             
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   24                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17   41   42   43                                             
CONECT   19   16   20   44                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20   45                                                       
CONECT   22   20   23   24                                                  
CONECT   23   22   46                                                       
CONECT   24   22   25   15                                                  
CONECT   25   24   47   48   49                                             
CONECT   26   10   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29    6                                                  
CONECT   29   28   30   50                                                  
CONECT   30   29    4                                                       
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    1                                                            
CONECT   34    2                                                            
CONECT   35    3                                                            
CONECT   36    5                                                            
CONECT   37    7                                                            
CONECT   38   11                                                            
CONECT   39   11                                                            
CONECT   40   11                                                            
CONECT   41   18                                                            
CONECT   42   18                                                            
CONECT   43   18                                                            
CONECT   44   19                                                            
CONECT   45   21                                                            
CONECT   46   23                                                            
CONECT   47   25                                                            
CONECT   48   25                                                            
CONECT   49   25                                                            
CONECT   50   29                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  104    0
END

RDKit          3D

50 52  0  0  0  0  0  0  0  0999 V2000
    8.8578   -1.9755   -0.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3839   -1.9415   -0.5537 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5987   -1.1930    0.1930 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1567   -1.1316   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4410   -0.3596    0.7540 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0045   -0.2710    0.5589 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2117    0.4779    1.3055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7642    0.5770    1.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0225    0.8981    2.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2067    0.2898   -0.2266 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6567    1.4163   -1.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1643    0.0864   -0.2268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1345    0.9595    0.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7666    2.0893    0.5777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5566    0.6891    0.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4923    1.6140    0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9915    2.8432    0.9954 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8012    3.8933    1.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8449    1.3354    0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2950    0.1103    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6543   -0.2052    0.0351 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3703   -0.8282   -0.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7892   -2.0701   -0.7890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0022   -0.5368   -0.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0350   -1.5467   -0.7465 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9255   -0.9450   -0.7062 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3589   -1.8992   -1.2631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3642   -1.0397   -0.5134 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1783   -1.7788   -1.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5390   -1.8458   -1.0371 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4217   -2.3689   -1.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0828   -2.5834    0.6150 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2119   -0.9466   -0.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9345   -2.5230   -1.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0212   -0.6146    0.9872 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8760    0.2267    1.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6971    1.0517    2.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1169    2.2039   -1.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6480    1.8149   -0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7892    0.9786   -2.1417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0139    3.8197    2.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2262    4.8409    1.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7414    4.0026    0.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5584    2.0804    0.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3124    0.5202    0.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7811   -2.2550   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548   -1.8979    0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5774   -2.4725   -1.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4524   -1.2400   -1.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6800   -2.3499   -2.0438 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  1  1
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 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  2  0
 26 28  1  0
 28 29  2  0
 29 30  1  0
 30  4  1  0
 28  6  1  0
 24 15  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  3 35  1  0
  5 36  1  0
  7 37  1  0
 11 38  1  0
 11 39  1  0
 11 40  1  0
 18 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 21 45  1  0
 23 46  1  0
 25 47  1  0
 25 48  1  0
 25 49  1  0
 29 50  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(7S)-7-Methyl-6,8-dioxo-3-[(1E)-prop-1-en-1-yl]-7,8-dihydro-6H-isochromen-7-yl 3,4-dihydroxy-6-methoxy-2-methylbenzoic acid	Generator

Chemical Formula

C₂₂H₂₀O₈

Average Mass

412.3940 Da

Monoisotopic Mass

412.11582 Da

IUPAC Name

(7S)-7-methyl-6,8-dioxo-3-[(1E)-prop-1-en-1-yl]-7,8-dihydro-6H-isochromen-7-yl 3,4-dihydroxy-6-methoxy-2-methylbenzoate

Traditional Name

(7S)-7-methyl-6,8-dioxo-3-[(1E)-prop-1-en-1-yl]isochromen-7-yl 3,4-dihydroxy-6-methoxy-2-methylbenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C(O)C(C)=C1C(=O)O[C@@]1(C)C(=O)C=C2C=C(OC=C2C1=O)\C=C\C

InChI Identifier

InChI=1S/C22H20O8/c1-5-6-13-7-12-8-17(24)22(3,20(26)14(12)10-29-13)30-21(27)18-11(2)19(25)15(23)9-16(18)28-4/h5-10,23,25H,1-4H3/b6-5+/t22-/m0/s1

InChI Key

FZBGUENQZXUQSN-BDNZGDGKSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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	NPAtlas	20522994
Talaromyces radicus	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
4-alkoxyphenol
Benzoic acid or derivatives
Phenoxy compound
Catechol
M-cresol
Benzoyl
O-cresol
Phenol ether
Anisole
Methoxybenzene
Phenol
Toluene
Alkyl aryl ether
Cyclohexenone
1-hydroxy-2-unsubstituted benzenoid
Pyran
Benzenoid
Monocyclic benzene moiety
Vinylogous ester
Cyclic ketone
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Oxacycle
Ether
Carbonyl group
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
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	3.21	ALOGPS
logP	3.37	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	8.77	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	111.03 m³·mol⁻¹	ChemAxon
Polarizability	41.68 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

NPAtlas ID

NPA013678

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28287553

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46833664

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yamazaki H, Omura S, Tomoda H: 6'-Hydroxy-3'-methoxy-mitorubrin, a new potentiator of antifungal miconazole activity, produced by Penicillium radicum FKI-3765-2. Chem Pharm Bull (Tokyo). 2010 Jun;58(6):829-32. doi: 10.1248/cpb.58.829. [PubMed:20522994 ]

Showing NP-Card for 6'-hydroxy-3'-methoxy-mitorubrin (NP0009262)

MOL for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

3D MOL for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

3D SDF for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

3D-SDF for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

PDB for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

3D PDB for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

SMILES for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

INCHI for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

Structure for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)

3D Structure for NP0009262 (6'-hydroxy-3'-methoxy-mitorubrin)