MiMeDB: Showing metabocard for Methyl penicyrone (MMDBc0027583)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 17:17:26 UTC

Update Date

2022-08-31 06:52:50 UTC

Metabolite ID

MMDBc0027583

Metabolite Identification

Common Name

Methyl penicyrone

Description

Methyl penicyrone belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone. Based on a literature review very few articles have been published on Methyl penicyrone.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152119172D          

 37 39  0  0  1  0            999 V2000
    4.3859   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -2.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5281   -5.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -7.7411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975    1.3909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1320   -4.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9070   -1.4823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224    1.1050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -1.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5281   -7.7411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -1.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -3.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -1.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -5.6786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -6.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425    0.6062    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6715   -2.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -6.5036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -5.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -6.5036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4579   -0.4737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9570   -4.4411    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2425   -0.7286    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4579    0.3513    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3859   -6.9161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7820   -4.4411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -1.9661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5281   -6.9161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -5.6786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275   -0.0612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7434   -0.0612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -3.2036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -0.7286    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592    1.1896    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -2.7911    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224   -1.2274    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 13  1  1  0  0  0  0
 13 11  2  0  0  0  0
 14  2  1  0  0  0  0
 14 12  2  0  0  0  0
 15  3  1  0  0  0  0
 16  4  1  0  0  0  0
 17  5  1  1  0  0  0
 18 13  1  0  0  0  0
 18 14  1  0  0  0  0
 19 15  1  0  0  0  0
 19 16  2  0  0  0  0
 20 15  2  0  0  0  0
 21 16  1  0  0  0  0
 23  6  1  1  0  0  0
 23 11  1  0  0  0  0
 23 20  1  0  0  0  0
 24  7  1  6  0  0  0
 24 12  1  1  0  0  0
 24 22  1  0  0  0  0
 25  8  1  1  0  0  0
 25 17  1  0  0  0  0
 25 22  1  0  0  0  0
 26 21  2  0  0  0  0
 23 27  1  1  0  0  0
 28  9  1  0  0  0  0
 28 18  1  0  0  0  0
 29 10  1  0  0  0  0
 29 19  1  0  0  0  0
 30 20  1  0  0  0  0
 30 21  1  0  0  0  0
 31 17  1  0  0  0  0
 31 24  1  0  0  0  0
 32 22  1  0  0  0  0
 32 25  1  0  0  0  0
 33 11  1  0  0  0  0
 34 12  1  0  0  0  0
 17 35  1  6  0  0  0
 36 18  1  0  0  0  0
 22 37  1  1  0  0  0
M  END


  Mrv1652305152119172D          

 37 39  0  0  1  0            999 V2000
    4.3859   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -2.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5281   -5.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -7.7411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975    1.3909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1320   -4.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9070   -1.4823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224    1.1050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -1.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5281   -7.7411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -1.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -3.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -1.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -5.6786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -6.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425    0.6062    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6715   -2.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -6.5036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -5.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -6.5036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4579   -0.4737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9570   -4.4411    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2425   -0.7286    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4579    0.3513    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3859   -6.9161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7820   -4.4411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -1.9661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5281   -6.9161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -5.6786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275   -0.0612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7434   -0.0612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -3.2036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -0.7286    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592    1.1896    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -2.7911    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224   -1.2274    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 13  1  1  0  0  0  0
 13 11  2  0  0  0  0
 14  2  1  0  0  0  0
 14 12  2  0  0  0  0
 15  3  1  0  0  0  0
 16  4  1  0  0  0  0
 17  5  1  1  0  0  0
 18 13  1  0  0  0  0
 18 14  1  0  0  0  0
 19 15  1  0  0  0  0
 19 16  2  0  0  0  0
 20 15  2  0  0  0  0
 21 16  1  0  0  0  0
 23  6  1  1  0  0  0
 23 11  1  0  0  0  0
 23 20  1  0  0  0  0
 24  7  1  6  0  0  0
 24 12  1  1  0  0  0
 24 22  1  0  0  0  0
 25  8  1  1  0  0  0
 25 17  1  0  0  0  0
 25 22  1  0  0  0  0
 26 21  2  0  0  0  0
 23 27  1  1  0  0  0
 28  9  1  0  0  0  0
 28 18  1  0  0  0  0
 29 10  1  0  0  0  0
 29 19  1  0  0  0  0
 30 20  1  0  0  0  0
 30 21  1  0  0  0  0
 31 17  1  0  0  0  0
 31 24  1  0  0  0  0
 32 22  1  0  0  0  0
 32 25  1  0  0  0  0
 33 11  1  0  0  0  0
 34 12  1  0  0  0  0
 17 35  1  6  0  0  0
 36 18  1  0  0  0  0
 22 37  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0027583

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(=C(\C)C([H])(OC)C(\C)=C(/[H])[C@]1(C)O[C@]([H])(C)[C@@]2(C)O[C@@]12[H])[C@](C)(O)C1=C(C)C(OC)=C(C)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O7/c1-13(11-23(6,27)20-15(3)19(29-10)16(4)21(26)30-20)18(28-9)14(2)12-24(7)22-25(8,32-22)17(5)31-24/h11-12,17-18,22,27H,1-10H3/b13-11+,14-12+/t17-,18?,22+,23+,24+,25-/m1/s1

> <INCHI_KEY>
HNPREDVUCQUXRJ-HSUPQFAFSA-N

> <FORMULA>
C25H36O7

> <MOLECULAR_WEIGHT>
448.556

> <EXACT_MASS>
448.246103499

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
48.21741023223152

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[(2S,3E,6E)-2-hydroxy-5-methoxy-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-3,6-dien-2-yl]-4-methoxy-3,5-dimethyl-2H-pyran-2-one

> <ALOGPS_LOGP>
3.92

> <JCHEM_LOGP>
2.868228691333335

> <ALOGPS_LOGS>
-4.64

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.300928837887927

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5419737263078215

> <JCHEM_POLAR_SURFACE_AREA>
86.75000000000001

> <JCHEM_REFRACTIVITY>
123.81899999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.04e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[(2S,3E,6E)-2-hydroxy-5-methoxy-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-3,6-dien-2-yl]-4-methoxy-3,5-dimethylpyran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       8.187  -6.750   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.186  -4.440   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.852  -9.830   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.520 -14.450   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.662   2.596   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.980  -8.290   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.560  -2.767   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.095   2.063   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.187  -2.130   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.852 -14.450   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.520  -6.750   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.520  -2.130   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.853  -5.980   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.520  -3.670   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.186 -10.600   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.520 -12.910   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.186   1.132   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.853  -4.440   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.186 -12.140   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.520  -9.830   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.853 -12.140   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.721  -0.884   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.520  -8.290   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.186  -1.360   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.721   0.656   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.187 -12.910   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       7.060  -8.290   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       8.187  -3.670   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.852 -12.910   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       6.853 -10.600   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.091  -0.114   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       1.388  -0.114   0.000  0.00  0.00           O+0
HETATM   33  H   UNK     0       4.186  -5.980   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.853  -1.360   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.097   2.221   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.520  -5.210   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.095  -2.291   0.000  0.00  0.00           H+0
CONECT    1   13                                                            
CONECT    2   14                                                            
CONECT    3   15                                                            
CONECT    4   16                                                            
CONECT    5   17                                                            
CONECT    6   23                                                            
CONECT    7   24                                                            
CONECT    8   25                                                            
CONECT    9   28                                                            
CONECT   10   29                                                            
CONECT   11   13   23   33                                                  
CONECT   12   14   24   34                                                  
CONECT   13    1   11   18                                                  
CONECT   14    2   12   18                                                  
CONECT   15    3   19   20                                                  
CONECT   16    4   19   21                                                  
CONECT   17    5   25   31   35                                             
CONECT   18   13   14   28   36                                             
CONECT   19   15   16   29                                                  
CONECT   20   15   23   30                                                  
CONECT   21   16   26   30                                                  
CONECT   22   24   25   32   37                                             
CONECT   23    6   11   20   27                                             
CONECT   24    7   12   22   31                                             
CONECT   25    8   17   22   32                                             
CONECT   26   21                                                            
CONECT   27   23                                                            
CONECT   28    9   18                                                       
CONECT   29   10   19                                                       
CONECT   30   20   21                                                       
CONECT   31   17   24                                                       
CONECT   32   22   25                                                       
CONECT   33   11                                                            
CONECT   34   12                                                            
CONECT   35   17                                                            
CONECT   36   18                                                            
CONECT   37   22                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   78    0
END

Synonyms

Not Available

Molecular Formula

C₂₅H₃₆O₇

Average Mass

448.556

Monoisotopic Mass

448.246103499

IUPAC Name

6-[(2S,3E,6E)-2-hydroxy-5-methoxy-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-3,6-dien-2-yl]-4-methoxy-3,5-dimethyl-2H-pyran-2-one

Traditional Name

6-[(2S,3E,6E)-2-hydroxy-5-methoxy-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-3,6-dien-2-yl]-4-methoxy-3,5-dimethylpyran-2-one

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\C)C([H])(OC)C(\C)=C(/[H])[C@]1(C)O[C@]([H])(C)[C@@]2(C)O[C@@]12[H])[C@](C)(O)C1=C(C)C(OC)=C(C)C(=O)O1

InChI Identifier

InChI=1S/C25H36O7/c1-13(11-23(6,27)20-15(3)19(29-10)16(4)21(26)30-20)18(28-9)14(2)12-24(7)22-25(8,32-22)17(5)31-24/h11-12,17-18,22,27H,1-10H3/b13-11+,14-12+/t17-,18?,22+,23+,24+,25-/m1/s1

InChI Key

HNPREDVUCQUXRJ-HSUPQFAFSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Pyranones and derivatives

Direct Parent

Pyranones and derivatives

Alternative Parents

Substituents

Pyranone
Alkyl aryl ether
Para-dioxane
Heteroaromatic compound
Vinylogous ester
Tetrahydrofuran
Tertiary alcohol
Lactone
Oxacycle
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Organooxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.01 g/L	ALOGPS
logP	3.92	ALOGPS
logP	2.87	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	13.3	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	86.75 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	123.82 m³·mol⁻¹	ChemAxon
Polarizability	48.22 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	Yes	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB 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

146684051

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Methyl penicyrone (MMDBc0027583)

MOL for #<Metabolite:0x00007f469acd0360>

3D MOL for #<Metabolite:0x00007f469acd0360>

3D SDF for #<Metabolite:0x00007f469acd0360>

3D-SDF for #<Metabolite:0x00007f469acd0360>

PDB for #<Metabolite:0x00007f469acd0360>

3D PDB for #<Metabolite:0x00007f469acd0360>

SMILES for #<Metabolite:0x00007f469acd0360>

INCHI for #<Metabolite:0x00007f469acd0360>

Structure for #<Metabolite:0x00007f469acd0360>

3D Structure for #<Metabolite:0x00007f469acd0360>