MiMeDB: Showing metabocard for Alternatone A (MMDBc0025402)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 15:08:02 UTC

Update Date

2025-10-07 16:07:32 UTC

Metabolite ID

MMDBc0025402

Metabolite Identification

Common Name

Alternatone A

Description

Alternatone A is a perylenequinone-related compound characterized by a unique tricyclo[6.3.1.02,7] dodecane skeleton. This metabolite was isolated from a soft-coral-derived strain of the fungus Alternaria alternata, highlighting its fungal origin (PMID:31659905 ). The chemical structure of alternatone A contributes to its notable cytotoxic properties, as demonstrated by its activity against the human hepatoma carcinoma HepG-2 cell line (PMID:34142621 ). Perylenequinones, including alternatone A, are known to participate in various biochemical pathways, often interacting with cellular components and influencing redox processes. The presence of such compounds in fungi suggests potential ecological roles, including defense mechanisms against predators or pathogens. The unique structural features of alternatone A may also allow it to engage in specific interactions with biological macromolecules, further underscoring its relevance in the study of natural products and their potential applications in cancer research.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152117082D          

 30 34  0  0  1  0            999 V2000
    3.7420   -1.6316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4813   -1.5589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9742   -1.3298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414   -1.4977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3873   -1.1176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9457   -0.8770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6066    1.1177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8517   -0.5140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6998   -0.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9614    0.6037    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2648   -0.3017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5873   -0.1339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3744    0.8159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0839   -0.2122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4970    0.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2354   -0.0727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5224   -0.8166    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2471    1.0166    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4790    0.7155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1556    0.0655    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9101    0.2123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0517    0.5480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0197    1.3300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1255    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3418    0.2011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7292    0.3019    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2670   -1.0166    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3838   -1.6299    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3092    1.8392    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4776   -0.4046    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  4  2  2  0  0  0  0
  5  1  1  0  0  0  0
  6  2  1  0  0  0  0
  8  3  1  0  0  0  0
  9  4  1  0  0  0  0
 10  7  1  0  0  0  0
 11  5  2  0  0  0  0
 12  6  2  0  0  0  0
 13  7  1  0  0  0  0
 14  8  1  0  0  0  0
 14 10  1  0  0  0  0
 15  8  2  0  0  0  0
 15 11  1  0  0  0  0
 15 13  1  0  0  0  0
 16  9  2  0  0  0  0
 16 12  1  0  0  0  0
 17  9  1  0  0  0  0
 17 14  1  0  0  0  0
 18 10  1  0  0  0  0
 19 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 11  1  0  0  0  0
 22 12  1  0  0  0  0
 23 13  2  0  0  0  0
 24 19  2  0  0  0  0
 25 20  1  0  0  0  0
 10 26  1  6  0  0  0
 14 27  1  6  0  0  0
 17 28  1  6  0  0  0
 18 29  1  6  0  0  0
 20 30  1  1  0  0  0
M  END


  Mrv1652305152117082D          

 30 34  0  0  1  0            999 V2000
    3.7420   -1.6316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4813   -1.5589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9742   -1.3298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414   -1.4977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3873   -1.1176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9457   -0.8770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6066    1.1177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8517   -0.5140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6998   -0.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9614    0.6037    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2648   -0.3017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5873   -0.1339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3744    0.8159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0839   -0.2122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4970    0.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2354   -0.0727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5224   -0.8166    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2471    1.0166    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4790    0.7155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1556    0.0655    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9101    0.2123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0517    0.5480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0197    1.3300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1255    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3418    0.2011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7292    0.3019    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2670   -1.0166    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3838   -1.6299    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3092    1.8392    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4776   -0.4046    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  4  2  2  0  0  0  0
  5  1  1  0  0  0  0
  6  2  1  0  0  0  0
  8  3  1  0  0  0  0
  9  4  1  0  0  0  0
 10  7  1  0  0  0  0
 11  5  2  0  0  0  0
 12  6  2  0  0  0  0
 13  7  1  0  0  0  0
 14  8  1  0  0  0  0
 14 10  1  0  0  0  0
 15  8  2  0  0  0  0
 15 11  1  0  0  0  0
 15 13  1  0  0  0  0
 16  9  2  0  0  0  0
 16 12  1  0  0  0  0
 17  9  1  0  0  0  0
 17 14  1  0  0  0  0
 18 10  1  0  0  0  0
 19 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 11  1  0  0  0  0
 22 12  1  0  0  0  0
 23 13  2  0  0  0  0
 24 19  2  0  0  0  0
 25 20  1  0  0  0  0
 10 26  1  6  0  0  0
 14 27  1  6  0  0  0
 17 28  1  6  0  0  0
 18 29  1  6  0  0  0
 20 30  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0025402

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(O)[C@@]2([H])C(=O)C3=C(C=CC=C3O)[C@]1([H])[C@]1([H])C3=C(C(=O)C[C@]21[H])C(O)=CC=C3

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O5/c21-11-5-1-3-8-14-10(7-13(23)15(8)11)18-19(24)16-9(17(14)20(18)25)4-2-6-12(16)22/h1-6,10,14,17-18,20-22,25H,7H2/t10-,14+,17+,18+,20-/m0/s1

> <INCHI_KEY>
JGTRUZSFUZQJBG-NEUAYCJXSA-N

> <FORMULA>
C20H16O5

> <MOLECULAR_WEIGHT>
336.343

> <EXACT_MASS>
336.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
32.51426323365695

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,11S,12S,20S)-7,15,20-trihydroxypentacyclo[10.7.1.0^{2,11}.0^{3,8}.0^{14,19}]icosa-3(8),4,6,14(19),15,17-hexaene-9,13-dione

> <ALOGPS_LOGP>
2.21

> <JCHEM_LOGP>
2.8005784583333333

> <ALOGPS_LOGS>
-2.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.952766667385465

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.350288469608792

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0970894284682924

> <JCHEM_POLAR_SURFACE_AREA>
94.83

> <JCHEM_REFRACTIVITY>
90.2656

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.58e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,11S,12S,20S)-7,15,20-trihydroxypentacyclo[10.7.1.0^{2,11}.0^{3,8}.0^{14,19}]icosa-3(8),4,6,14(19),15,17-hexaene-9,13-dione

> <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       6.985  -3.046   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.898  -2.910   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.552  -2.482   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.637  -2.796   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.190  -2.086   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.765  -1.637   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.866   2.086   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.323  -0.959   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.306  -1.409   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.661   1.127   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.961  -0.563   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.096  -0.250   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.299   1.523   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.890  -0.396   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.528   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.439  -0.136   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.842  -1.524   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.328   1.898   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.894   1.336   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.157   0.122   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.165   0.396   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -1.963   1.023   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       7.503   2.483   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -0.234   2.384   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.638   0.375   0.000  0.00  0.00           O+0
HETATM   26  H   UNK     0       5.094   0.563   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.232  -1.898   0.000  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.583  -3.043   0.000  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.444   3.433   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.892  -0.755   0.000  0.00  0.00           H+0
CONECT    1    3    5                                                       
CONECT    2    4    6                                                       
CONECT    3    1    8                                                       
CONECT    4    2    9                                                       
CONECT    5    1   11                                                       
CONECT    6    2   12                                                       
CONECT    7   10   13                                                       
CONECT    8    3   14   15                                                  
CONECT    9    4   16   17                                                  
CONECT   10    7   14   18   26                                             
CONECT   11    5   15   21                                                  
CONECT   12    6   16   22                                                  
CONECT   13    7   15   23                                                  
CONECT   14    8   10   17   27                                             
CONECT   15    8   11   13                                                  
CONECT   16    9   12   19                                                  
CONECT   17    9   14   20   28                                             
CONECT   18   10   19   20   29                                             
CONECT   19   16   18   24                                                  
CONECT   20   17   18   25   30                                             
CONECT   21   11                                                            
CONECT   22   12                                                            
CONECT   23   13                                                            
CONECT   24   19                                                            
CONECT   25   20                                                            
CONECT   26   10                                                            
CONECT   27   14                                                            
CONECT   28   17                                                            
CONECT   29   18                                                            
CONECT   30   20                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

Synonyms

Not Available

Molecular Formula

C₂₀H₁₆O₅

Average Mass

336.343

Monoisotopic Mass

336.099773615

IUPAC Name

(1S,2R,11S,12S,20S)-7,15,20-trihydroxypentacyclo[10.7.1.0^{2,11}.0^{3,8}.0^{14,19}]icosa-3(8),4,6,14(19),15,17-hexaene-9,13-dione

Traditional Name

(1S,2R,11S,12S,20S)-7,15,20-trihydroxypentacyclo[10.7.1.0^{2,11}.0^{3,8}.0^{14,19}]icosa-3(8),4,6,14(19),15,17-hexaene-9,13-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]1(O)[C@@]2([H])C(=O)C3=C(C=CC=C3O)[C@]1([H])[C@]1([H])C3=C(C(=O)C[C@]21[H])C(O)=CC=C3

InChI Identifier

InChI=1S/C20H16O5/c21-11-5-1-3-8-14-10(7-13(23)15(8)11)18-19(24)16-9(17(14)20(18)25)4-2-6-12(16)22/h1-6,10,14,17-18,20-22,25H,7H2/t10-,14+,17+,18+,20-/m0/s1

InChI Key

JGTRUZSFUZQJBG-NEUAYCJXSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Tetralins

Sub Class

Not Available

Direct Parent

Tetralins

Alternative Parents

Substituents

Tetralin
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Vinylogous acid
Cyclic alcohol
Secondary alcohol
Ketone
Polyol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.46 g/L	ALOGPS
logP	2.21	ALOGPS
logP	2.8	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	8.35	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	90.27 m³·mol⁻¹	ChemAxon
Polarizability	32.51 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	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

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; Human supragingival plaque	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

81360793

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

145721284

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 Alternatone A (MMDBc0025402)

MOL for #<Metabolite:0x00007f8dc4452c58>

3D MOL for #<Metabolite:0x00007f8dc4452c58>

3D SDF for #<Metabolite:0x00007f8dc4452c58>

3D-SDF for #<Metabolite:0x00007f8dc4452c58>

PDB for #<Metabolite:0x00007f8dc4452c58>

3D PDB for #<Metabolite:0x00007f8dc4452c58>

SMILES for #<Metabolite:0x00007f8dc4452c58>

INCHI for #<Metabolite:0x00007f8dc4452c58>

Structure for #<Metabolite:0x00007f8dc4452c58>

3D Structure for #<Metabolite:0x00007f8dc4452c58>