MiMeDB: Showing metabocard for Asperpyrone E (MMDBc0002634)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 20:55:00 UTC

Update Date

2025-10-07 16:04:37 UTC

Metabolite ID

MMDBc0002634

Metabolite Identification

Common Name

Asperpyrone E

Description

Asperpyrone E is a naphtho-γ-pyrone, a chemical class known for its diverse biological activities and potential applications in pharmacology. This metabolite has been identified in various studies focusing on secondary metabolites produced by fungi. Specifically, Aspergillus tubingensis G131, a non-toxigenic strain, has been reported to yield several naphtho-γ-pyrones, including asperpyrone E, alongside other compounds such as aurasperone A and fonsecin (PMID:31878243 ). Additionally, bioactivity-guided fractionation of extracts from Aspergillus niger, an endophytic fungus associated with the Chinese liverwort Heteroscyphus tener, has led to the isolation of asperpyrone E among other naphtho-γ-pyrones, indicating its potential cytotoxic properties (PMID:31878243 ). The presence of such metabolites suggests a role in the ecological interactions of these fungi, possibly contributing to their competitive advantage in various environments. Further research into the biochemical pathways and biological functions of asperpyrone E may reveal insights into its mechanisms of action and potential therapeutic uses.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142122552D          

 41 46  0  0  0  0            999 V2000
    8.6329   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6329   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2204   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2204   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6329   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 13  1  1  0  0  0  0
 13  6  1  0  0  0  0
 13  7  2  0  0  0  0
 14  2  1  0  0  0  0
 14  8  2  0  0  0  0
 15  9  1  0  0  0  0
 15 10  2  0  0  0  0
 16 11  2  0  0  0  0
 16 12  1  0  0  0  0
 17  6  1  0  0  0  0
 18 11  1  0  0  0  0
 19  7  1  0  0  0  0
 20  8  1  0  0  0  0
 21  9  2  0  0  0  0
 22 10  1  0  0  0  0
 23 12  2  0  0  0  0
 24 15  1  0  0  0  0
 25 17  2  0  0  0  0
 25 18  1  0  0  0  0
 25 23  1  0  0  0  0
 26 17  1  0  0  0  0
 26 19  1  0  0  0  0
 27 18  2  0  0  0  0
 28 20  2  0  0  0  0
 28 21  1  0  0  0  0
 29 22  1  0  0  0  0
 29 27  1  0  0  0  0
 30 26  2  0  0  0  0
 30 27  1  0  0  0  0
 31 24  1  0  0  0  0
 31 29  2  0  0  0  0
 32 24  2  0  0  0  0
 32 28  1  0  0  0  0
 33 19  2  0  0  0  0
 34 20  1  0  0  0  0
 35 21  1  0  0  0  0
 36 22  2  0  0  0  0
 37 30  1  0  0  0  0
 38  3  1  0  0  0  0
 38 16  1  0  0  0  0
 39  4  1  0  0  0  0
 39 23  1  0  0  0  0
 40  5  1  0  0  0  0
 40 31  1  0  0  0  0
 41 14  1  0  0  0  0
 41 32  1  0  0  0  0
M  END


  Mrv1652305142122552D          

 41 46  0  0  0  0            999 V2000
    8.6329   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6329   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2204   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2204   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6329   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 13  1  1  0  0  0  0
 13  6  1  0  0  0  0
 13  7  2  0  0  0  0
 14  2  1  0  0  0  0
 14  8  2  0  0  0  0
 15  9  1  0  0  0  0
 15 10  2  0  0  0  0
 16 11  2  0  0  0  0
 16 12  1  0  0  0  0
 17  6  1  0  0  0  0
 18 11  1  0  0  0  0
 19  7  1  0  0  0  0
 20  8  1  0  0  0  0
 21  9  2  0  0  0  0
 22 10  1  0  0  0  0
 23 12  2  0  0  0  0
 24 15  1  0  0  0  0
 25 17  2  0  0  0  0
 25 18  1  0  0  0  0
 25 23  1  0  0  0  0
 26 17  1  0  0  0  0
 26 19  1  0  0  0  0
 27 18  2  0  0  0  0
 28 20  2  0  0  0  0
 28 21  1  0  0  0  0
 29 22  1  0  0  0  0
 29 27  1  0  0  0  0
 30 26  2  0  0  0  0
 30 27  1  0  0  0  0
 31 24  1  0  0  0  0
 31 29  2  0  0  0  0
 32 24  2  0  0  0  0
 32 28  1  0  0  0  0
 33 19  2  0  0  0  0
 34 20  1  0  0  0  0
 35 21  1  0  0  0  0
 36 22  2  0  0  0  0
 37 30  1  0  0  0  0
 38  3  1  0  0  0  0
 38 16  1  0  0  0  0
 39  4  1  0  0  0  0
 39 23  1  0  0  0  0
 40  5  1  0  0  0  0
 40 31  1  0  0  0  0
 41 14  1  0  0  0  0
 41 32  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0002634

> <DATABASE_NAME>
MIME

> <SMILES>
COC1=CC2=C(C(O)=C3C(=O)C=C(C)CC3=C2C(OC)=C1)C1=C(OC)C2=C3OC(C)=CC(O)=C3C(O)=CC2=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H26O9/c1-13-6-17-25-18(11-16(38-3)12-23(25)39-4)27(30(37)26(17)19(33)7-13)29-22(36)10-15-9-21(35)28-20(34)8-14(2)41-32(28)24(15)31(29)40-5/h7-12,34-35,37H,6H2,1-5H3

> <INCHI_KEY>
KVCRJELRKNDEHT-UHFFFAOYSA-N

> <FORMULA>
C32H26O9

> <MOLECULAR_WEIGHT>
554.551

> <EXACT_MASS>
554.157682417

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
58.11956384848966

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5-dihydroxy-9-(10-hydroxy-5,7-dimethoxy-3-methyl-1-oxo-1,4-dihydrophenanthren-9-yl)-10-methoxy-2-methyl-8H-cyclohexa[h]chromen-8-one

> <ALOGPS_LOGP>
2.99

> <JCHEM_LOGP>
3.515913215333332

> <ALOGPS_LOGS>
-5.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.358969207417543

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.248020576143403

> <JCHEM_PKA_STRONGEST_BASIC>
2.644088047564457

> <JCHEM_POLAR_SURFACE_AREA>
131.75000000000003

> <JCHEM_REFRACTIVITY>
159.3364

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.56e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5-dihydroxy-9-(10-hydroxy-5,7-dimethoxy-3-methyl-1-oxo-4H-phenanthren-9-yl)-10-methoxy-2-methylcyclohexa[h]chromen-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAY-21         0                                  
HETATM    1  C   UNK     0      16.115  -9.542   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.795  -4.207   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.105  -8.208   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.035  -9.542   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.875  -4.207   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.805  -8.208   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.115  -6.875   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.185  -5.541   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.185  -8.208   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.345  -8.208   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.415  -6.875   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.035  -6.875   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.725  -5.541   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      15.345  -5.541   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.725  -8.208   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.495  -6.875   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.805  -5.541   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.495  -4.207   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.035  -4.207   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      16.115  -4.207   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       3.795   1.127   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       6.105   2.461   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      13.035  -1.540   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      13.805  -2.874   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       6.875  -6.875   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      11.495  -9.542   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       8.415  -4.207   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       6.105  -2.874   0.000  0.00  0.00           O+0
CONECT    1   13                                                            
CONECT    2   14                                                            
CONECT    3   38                                                            
CONECT    4   39                                                            
CONECT    5   40                                                            
CONECT    6   13   17                                                       
CONECT    7   13   19                                                       
CONECT    8   14   20                                                       
CONECT    9   15   21                                                       
CONECT   10   15   22                                                       
CONECT   11   16   18                                                       
CONECT   12   16   23                                                       
CONECT   13    1    6    7                                                  
CONECT   14    2    8   41                                                  
CONECT   15    9   10   24                                                  
CONECT   16   11   12   38                                                  
CONECT   17    6   25   26                                                  
CONECT   18   11   25   27                                                  
CONECT   19    7   26   33                                                  
CONECT   20    8   28   34                                                  
CONECT   21    9   28   35                                                  
CONECT   22   10   29   36                                                  
CONECT   23   12   25   39                                                  
CONECT   24   15   31   32                                                  
CONECT   25   17   18   23                                                  
CONECT   26   17   19   30                                                  
CONECT   27   18   29   30                                                  
CONECT   28   20   21   32                                                  
CONECT   29   22   27   31                                                  
CONECT   30   26   27   37                                                  
CONECT   31   24   29   40                                                  
CONECT   32   24   28   41                                                  
CONECT   33   19                                                            
CONECT   34   20                                                            
CONECT   35   21                                                            
CONECT   36   22                                                            
CONECT   37   30                                                            
CONECT   38    3   16                                                       
CONECT   39    4   23                                                       
CONECT   40    5   31                                                       
CONECT   41   14   32                                                       
MASTER        0    0    0    0    0    0    0    0   41    0   92    0
END

Synonyms

Not Available

Molecular Formula

C₃₂H₂₆O₉

Average Mass

554.551

Monoisotopic Mass

554.157682417

IUPAC Name

4,5-dihydroxy-9-(10-hydroxy-5,7-dimethoxy-3-methyl-1-oxo-1,4-dihydrophenanthren-9-yl)-10-methoxy-2-methyl-8H-cyclohexa[h]chromen-8-one

Traditional Name

4,5-dihydroxy-9-(10-hydroxy-5,7-dimethoxy-3-methyl-1-oxo-4H-phenanthren-9-yl)-10-methoxy-2-methylcyclohexa[h]chromen-8-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C(O)=C3C(=O)C=C(C)CC3=C2C(OC)=C1)C1=C(OC)C2=C3OC(C)=CC(O)=C3C(O)=CC2=CC1=O

InChI Identifier

InChI=1S/C32H26O9/c1-13-6-17-25-18(11-16(38-3)12-23(25)39-4)27(30(37)26(17)19(33)7-13)29-22(36)10-15-9-21(35)28-20(34)8-14(2)41-32(28)24(15)31(29)40-5/h7-12,34-35,37H,6H2,1-5H3

InChI Key

KVCRJELRKNDEHT-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrols. Phenanthrols are compounds containing a phenanthrene (or its hydrogenated derivative) to which a hydroxyl group is attached.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Phenanthrols

Direct Parent

Phenanthrols

Alternative Parents

Substituents

Phenanthrol
Naphthopyran
Hydrophenanthrene
2-naphthol
1-benzopyran
Naphthalene
Benzopyran
Aryl ketone
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyran
Heteroaromatic compound
Vinylogous ester
Vinylogous acid
Cyclic ketone
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	0.0026 g/L	ALOGPS
logP	2.99	ALOGPS
logP	3.52	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	7.25	ChemAxon
pKa (Strongest Basic)	2.64	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	131.75 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	159.34 m³·mol⁻¹	ChemAxon
Polarizability	58.12 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

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

Microbial Pathways

Pathways

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

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

Other Exposures

Source Type	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

78435574

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583607

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

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 Asperpyrone E (MMDBc0002634)

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