MiMeDB: Showing metabocard for Alternapyrone E (MMDBc0023896)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 13:47:45 UTC

Update Date

2022-08-31 06:48:51 UTC

Metabolite ID

MMDBc0023896

Metabolite Identification

Common Name

Alternapyrone E

Description

Alternapyrone E belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. Based on a literature review very few articles have been published on Alternapyrone E.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152115472D          

 38 39  0  0  1  0            999 V2000
   -6.0474    3.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849    2.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2098    7.3332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5224    1.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5224   -1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9654    6.9600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9224    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    2.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0474    1.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1328    5.8651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0174    4.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6349    2.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3974    3.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8724    1.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5453    6.5795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1099    0.9651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1099   -0.4638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3523    6.4080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1599    3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5224    0.2507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849    0.9651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849   -0.4638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6849    5.2520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7363    5.1026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3474    0.2507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3974    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1599    5.2520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8724   -1.1783    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8724    0.2507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4385    5.5875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4599    2.3941    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1388    7.2049    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7474    3.1086    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 10  8  1  0  0  0  0
 16  1  1  0  0  0  0
 16 11  2  0  0  0  0
 16 12  1  0  0  0  0
 17  2  1  0  0  0  0
 11 17  1  4  0  0  0
 17 13  2  0  0  0  0
 18  3  1  0  0  0  0
 18 12  1  0  0  0  0
 19  4  1  0  0  0  0
 19 14  2  0  0  0  0
 20  5  1  0  0  0  0
 21  6  1  0  0  0  0
 22  7  1  1  0  0  0
 22 19  1  0  0  0  0
 23  9  1  0  0  0  0
 13 23  1  4  0  0  0
 24 20  1  0  0  0  0
 24 21  2  0  0  0  0
 25 18  1  0  0  0  0
 25 20  2  0  0  0  0
 26 23  1  0  0  0  0
 27 21  1  0  0  0  0
 28 10  1  1  0  0  0
 28 14  1  0  0  0  0
 28 15  1  6  0  0  0
 29 15  1  0  0  0  0
 30 24  1  0  0  0  0
 31 26  2  0  0  0  0
 32 26  1  0  0  0  0
 33 27  2  0  0  0  0
 34 25  1  0  0  0  0
 34 27  1  0  0  0  0
 35 22  1  0  0  0  0
 35 28  1  0  0  0  0
 36 18  1  0  0  0  0
 22 37  1  6  0  0  0
 38 23  1  0  0  0  0
M  END


  Mrv1652305152115472D          

 38 39  0  0  1  0            999 V2000
   -6.0474    3.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849    2.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2098    7.3332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5224    1.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5224   -1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9654    6.9600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9224    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    2.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0474    1.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1328    5.8651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0174    4.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6349    2.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3974    3.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8724    1.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5453    6.5795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1099    0.9651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1099   -0.4638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3523    6.4080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1599    3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5224    0.2507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849    0.9651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2849   -0.4638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6849    5.2520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7363    5.1026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3474    0.2507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3974    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1599    5.2520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8724   -1.1783    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8724    0.2507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4385    5.5875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4599    2.3941    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1388    7.2049    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7474    3.1086    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 10  8  1  0  0  0  0
 16  1  1  0  0  0  0
 16 11  2  0  0  0  0
 16 12  1  0  0  0  0
 17  2  1  0  0  0  0
 11 17  1  4  0  0  0
 17 13  2  0  0  0  0
 18  3  1  0  0  0  0
 18 12  1  0  0  0  0
 19  4  1  0  0  0  0
 19 14  2  0  0  0  0
 20  5  1  0  0  0  0
 21  6  1  0  0  0  0
 22  7  1  1  0  0  0
 22 19  1  0  0  0  0
 23  9  1  0  0  0  0
 13 23  1  4  0  0  0
 24 20  1  0  0  0  0
 24 21  2  0  0  0  0
 25 18  1  0  0  0  0
 25 20  2  0  0  0  0
 26 23  1  0  0  0  0
 27 21  1  0  0  0  0
 28 10  1  1  0  0  0
 28 14  1  0  0  0  0
 28 15  1  6  0  0  0
 29 15  1  0  0  0  0
 30 24  1  0  0  0  0
 31 26  2  0  0  0  0
 32 26  1  0  0  0  0
 33 27  2  0  0  0  0
 34 25  1  0  0  0  0
 34 27  1  0  0  0  0
 35 22  1  0  0  0  0
 35 28  1  0  0  0  0
 36 18  1  0  0  0  0
 22 37  1  6  0  0  0
 38 23  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0023896

> <DATABASE_NAME>
MIME

> <SMILES>
[H]C(C)(CC(C)=CC(C)=CC([H])(CCC[C@@]1(CO)O[C@@]([H])(C)C(C)=C1)C(O)=O)C1=C(C)C(O)=C(C)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C28H40O7/c1-16(12-18(3)25-20(5)24(30)21(6)27(33)34-25)11-17(2)13-23(26(31)32)9-8-10-28(15-29)14-19(4)22(7)35-28/h11,13-14,18,22-23,29-30H,8-10,12,15H2,1-7H3,(H,31,32)/t18?,22-,23?,28+/m0/s1

> <INCHI_KEY>
KVOSGCOKGACRAO-NZDSKQBCSA-N

> <FORMULA>
C28H40O7

> <MOLECULAR_WEIGHT>
488.621

> <EXACT_MASS>
488.277403628

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
54.58074717582716

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8-(4-hydroxy-3,5-dimethyl-2-oxo-2H-pyran-6-yl)-2-{3-[(2R,5S)-2-(hydroxymethyl)-4,5-dimethyl-2,5-dihydrofuran-2-yl]propyl}-4,6-dimethylnona-3,5-dienoic acid

> <ALOGPS_LOGP>
3.81

> <JCHEM_LOGP>
4.577739045333332

> <ALOGPS_LOGS>
-5.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.730026565232845

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.612153635906251

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0956421168104375

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
139.47010000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.10e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-(4-hydroxy-3,5-dimethyl-6-oxopyran-2-yl)-2-{3-[(2R,5S)-2-(hydroxymethyl)-4,5-dimethyl-5H-furan-2-yl]propyl}-4,6-dimethylnona-3,5-dienoic acid

> <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     -11.288   5.803   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.978   7.136   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -13.598   4.469   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.392  13.689   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -15.908   3.135   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -15.908  -2.199   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.669  12.992   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.588   8.470   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.358   7.136   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.048   8.470   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.978   4.469   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -11.288   3.135   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.668   5.803   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.248  10.948   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.033   8.898   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.518   4.469   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.208   5.803   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -12.828   3.135   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.018  12.282   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -15.138   1.802   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -15.138  -0.866   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.524  11.962   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.898   7.136   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -15.908   0.468   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -13.598   1.802   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -13.598  -0.866   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.278   9.804   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.374   9.525   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0     -17.448   0.468   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -8.208   8.470   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -5.898   9.804   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0     -12.828  -2.199   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0     -12.828   0.468   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -2.685  10.430   0.000  0.00  0.00           O+0
HETATM   36  H   UNK     0     -12.058   4.469   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.126  13.449   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      -5.128   5.803   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   19                                                            
CONECT    5   20                                                            
CONECT    6   21                                                            
CONECT    7   22                                                            
CONECT    8    9   10                                                       
CONECT    9    8   23                                                       
CONECT   10    8   28                                                       
CONECT   11   16   17                                                       
CONECT   12   16   18                                                       
CONECT   13   17   23                                                       
CONECT   14   19   28                                                       
CONECT   15   28   29                                                       
CONECT   16    1   11   12                                                  
CONECT   17    2   11   13                                                  
CONECT   18    3   12   25   36                                             
CONECT   19    4   14   22                                                  
CONECT   20    5   24   25                                                  
CONECT   21    6   24   27                                                  
CONECT   22    7   19   35   37                                             
CONECT   23    9   13   26   38                                             
CONECT   24   20   21   30                                                  
CONECT   25   18   20   34                                                  
CONECT   26   23   31   32                                                  
CONECT   27   21   33   34                                                  
CONECT   28   10   14   15   35                                             
CONECT   29   15                                                            
CONECT   30   24                                                            
CONECT   31   26                                                            
CONECT   32   26                                                            
CONECT   33   27                                                            
CONECT   34   25   27                                                       
CONECT   35   22   28                                                       
CONECT   36   18                                                            
CONECT   37   22                                                            
CONECT   38   23                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   78    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₄₀O₇

Average Mass

488.621

Monoisotopic Mass

488.277403628

IUPAC Name

8-(4-hydroxy-3,5-dimethyl-2-oxo-2H-pyran-6-yl)-2-{3-[(2R,5S)-2-(hydroxymethyl)-4,5-dimethyl-2,5-dihydrofuran-2-yl]propyl}-4,6-dimethylnona-3,5-dienoic acid

Traditional Name

8-(4-hydroxy-3,5-dimethyl-6-oxopyran-2-yl)-2-{3-[(2R,5S)-2-(hydroxymethyl)-4,5-dimethyl-5H-furan-2-yl]propyl}-4,6-dimethylnona-3,5-dienoic acid

CAS Registry Number

Not Available

SMILES

[H]C(C)(CC(C)=CC(C)=CC([H])(CCC[C@@]1(CO)O[C@@]([H])(C)C(C)=C1)C(O)=O)C1=C(C)C(O)=C(C)C(=O)O1

InChI Identifier

InChI=1S/C28H40O7/c1-16(12-18(3)25-20(5)24(30)21(6)27(33)34-25)11-17(2)13-23(26(31)32)9-8-10-28(15-29)14-19(4)22(7)35-28/h11,13-14,18,22-23,29-30H,8-10,12,15H2,1-7H3,(H,31,32)/t18?,22-,23?,28+/m0/s1

InChI Key

KVOSGCOKGACRAO-NZDSKQBCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpenoid
Diterpene lactone
Medium-chain hydroxy acid
Medium-chain fatty acid
Methyl-branched fatty acid
Pyranone
Hydroxy fatty acid
Heterocyclic fatty acid
Branched fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Pyran
Heteroaromatic compound
Vinylogous acid
Dihydrofuran
Lactone
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0031 g/L	ALOGPS
logP	3.81	ALOGPS
logP	4.58	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	4.61	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	139.47 m³·mol⁻¹	ChemAxon
Polarizability	54.58 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

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

Microbial Pathways

Pathways

Not Available

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

78441767

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139591187

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Alternapyrone E (MMDBc0023896)

MOL for #<Metabolite:0x0000560be05133c0>

3D MOL for #<Metabolite:0x0000560be05133c0>

3D SDF for #<Metabolite:0x0000560be05133c0>

3D-SDF for #<Metabolite:0x0000560be05133c0>

PDB for #<Metabolite:0x0000560be05133c0>

3D PDB for #<Metabolite:0x0000560be05133c0>

SMILES for #<Metabolite:0x0000560be05133c0>

INCHI for #<Metabolite:0x0000560be05133c0>

Structure for #<Metabolite:0x0000560be05133c0>

3D Structure for #<Metabolite:0x0000560be05133c0>