MiMeDB: Showing metabocard for Alternarian acid (MMDBc0015223)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:06:14 UTC

Update Date

2025-10-07 16:06:22 UTC

Metabolite ID

MMDBc0015223

Metabolite Identification

Common Name

Alternarian acid

Description

Alternarian acid is a fungal metabolite belonging to the class of organic acids. It has been identified through advanced analytical techniques such as LC-Q-TOF-MS/MS and GC-MS, which revealed its presence alongside other compounds in active extracts. The significance of alternarian acid extends beyond its chemical structure, as it has been linked to various biological activities. For instance, its role in the metabolic pathways of certain fungi suggests potential implications for plant-fungal interactions and ecological dynamics. Additionally, the detection of alternarian acid in conjunction with other metabolites indicates its potential contributions to the overall chemical profile of fungal extracts, which may possess bioactive properties relevant to pharmacology and agriculture. The exploration of alternarian acid and its associated compounds continues to be a subject of interest in the field of natural product chemistry, as researchers seek to understand their mechanisms of action and potential applications in various domains, including medicine and environmental science. For further insights into its chemical characterization, refer to the detailed analyses documented in the literature (PMID: [insert PMID here]).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004241517432D          

 23 24  0  0  0  0            999 V2000
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3789   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  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
  7 11  1  0  0  0  0
 11 12  2  0  0  0  0
  3 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  2  0  0  0  0
 17 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015223

> <DATABASE_NAME>
MIME

> <SMILES>
COC1=CC(O)=C(C(O)=O)C(=C1)C1=C(C)C=C(OC1=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H12O8/c1-6-3-10(13(17)18)23-15(21)11(6)8-4-7(22-2)5-9(16)12(8)14(19)20/h3-5,16H,1-2H3,(H,17,18)(H,19,20)

> <INCHI_KEY>
DTWGKAWUEOJXKI-UHFFFAOYSA-N

> <FORMULA>
C15H12O8

> <MOLECULAR_WEIGHT>
320.253

> <EXACT_MASS>
320.053217346

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
29.587771015095427

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(2-carboxy-3-hydroxy-5-methoxyphenyl)-4-methyl-2-oxo-2H-pyran-6-carboxylic acid

> <ALOGPS_LOGP>
2.21

> <JCHEM_LOGP>
2.1314443919999992

> <ALOGPS_LOGS>
-3.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.126948542939716

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.2711182629242748

> <JCHEM_PKA_STRONGEST_BASIC>
-4.857923731596101

> <JCHEM_POLAR_SURFACE_AREA>
130.35999999999999

> <JCHEM_REFRACTIVITY>
77.83519999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.71e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(2-carboxy-3-hydroxy-5-methoxyphenyl)-4-methyl-6-oxopyran-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.707  -8.337   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -6.668  -6.930   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12   13                                                  
CONECT   12   11    3                                                       
CONECT   13   11   14   19                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   13   20                                                  
CONECT   20   19                                                            
CONECT   21   17   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

Synonyms

Value	Source
3-(2-Carboxy-3-hydroxy-5-methoxyphenyl)-4-methyl-2-oxo-2H-pyran-6-carboxylate	Generator

Molecular Formula

C₁₅H₁₂O₈

Average Mass

320.253

Monoisotopic Mass

320.053217346

IUPAC Name

3-(2-carboxy-3-hydroxy-5-methoxyphenyl)-4-methyl-2-oxo-2H-pyran-6-carboxylic acid

Traditional Name

5-(2-carboxy-3-hydroxy-5-methoxyphenyl)-4-methyl-6-oxopyran-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C(C(O)=O)C(=C1)C1=C(C)C=C(OC1=O)C(O)=O

InChI Identifier

InChI=1S/C15H12O8/c1-6-3-10(13(17)18)23-15(21)11(6)8-4-7(22-2)5-9(16)12(8)14(19)20/h3-5,16H,1-2H3,(H,17,18)(H,19,20)

InChI Key

DTWGKAWUEOJXKI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

P-methoxybenzoic acids and derivatives

Alternative Parents

Substituents

P-methoxybenzoic acid or derivatives
Methoxyphenol
Salicylic acid or derivatives
Salicylic acid
Hydroxybenzoic acid
Benzoic acid
Phenoxy compound
Phenol ether
Anisole
Methoxybenzene
Benzoyl
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Pyranone
1-hydroxy-4-unsubstituted benzenoid
Phenol
Pyran
Vinylogous acid
Heteroaromatic compound
Lactone
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Ether
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
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	0.27 g/L	ALOGPS
logP	2.21	ALOGPS
logP	2.13	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	2.27	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.36 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	77.84 m³·mol⁻¹	ChemAxon
Polarizability	29.59 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Chromatography Type	Technique	Column	Deposition Date	Retention Time (s)
Liquid Chromatography	HILIC	Waters Acquity UPLC-BEH Amide column (void)	2025-10-23	134.1
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (void)	2025-10-23	78.9
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (eluted)	2025-10-23	303.5
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-23	315.2
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-23	326.4
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (eluted)	2025-10-23	224.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	722.4
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (void)	2025-10-23	133.3
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-23	371.8
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	181.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (void)	2025-10-23	198.9
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	158.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	99.2
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (void)	2025-10-23	285.7
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	431.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	48.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	222.4
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-23	1097.2
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-23	645.5

Retention Indices

Chromatography Type	Peak Label	SMILES	Stationary Phase	Deposition Date	Retention Index
Gas Chromatography	Alternarian acid_TMS_1	COC1=CC(O[Si](C)(C)C)=C(C(=O)O)C(C2=C(C)C=C(C(=O)O)OC2=O)=C1	standard non polar	2025-10-23	2298.63
Gas Chromatography	Alternarian acid_TMS_2	COC1=CC(O)=C(C(=O)O[Si](C)(C)C)C(C2=C(C)C=C(C(=O)O)OC2=O)=C1	standard non polar	2025-10-23	1685.69
Gas Chromatography	Alternarian acid_TMS_3	COC1=CC(O)=C(C(=O)O)C(C2=C(C)C=C(C(=O)O[Si](C)(C)C)OC2=O)=C1	standard non polar	2025-10-23	2270.6
Gas Chromatography	Alternarian acid_TMS_4	COC1=CC(O[Si](C)(C)C)=C(C(=O)O[Si](C)(C)C)C(C2=C(C)C=C(C(=O)O)OC2=O)=C1	standard non polar	2025-10-23	2554.43
Gas Chromatography	Alternarian acid_TMS_5	COC1=CC(O[Si](C)(C)C)=C(C(=O)O)C(C2=C(C)C=C(C(=O)O[Si](C)(C)C)OC2=O)=C1	standard non polar	2025-10-23	3033.52
Gas Chromatography	Alternarian acid_TMS_6	COC1=CC(O)=C(C(=O)O[Si](C)(C)C)C(C2=C(C)C=C(C(=O)O[Si](C)(C)C)OC2=O)=C1	standard non polar	2025-10-23	1987.36
Gas Chromatography	Alternarian acid_TMS_7	COC1=CC(O[Si](C)(C)C)=C(C(=O)O[Si](C)(C)C)C(C2=C(C)C=C(C(=O)O[Si](C)(C)C)OC2=O)=C1	standard non polar	2025-10-23	2602.21
Gas Chromatography	Alternarian acid_TMS_1	COC1=CC(O[Si](C)(C)C)=C(C(=O)O)C(C2=C(C)C=C(C(=O)O)OC2=O)=C1	standard polar	2025-10-23	2587.68
Gas Chromatography	Alternarian acid_TMS_2	COC1=CC(O)=C(C(=O)O[Si](C)(C)C)C(C2=C(C)C=C(C(=O)O)OC2=O)=C1	standard polar	2025-10-23	2319.72
Gas Chromatography	Alternarian acid_TMS_3	COC1=CC(O)=C(C(=O)O)C(C2=C(C)C=C(C(=O)O[Si](C)(C)C)OC2=O)=C1	standard polar	2025-10-23	1818.87
Gas Chromatography	Alternarian acid_TMS_4	COC1=CC(O[Si](C)(C)C)=C(C(=O)O[Si](C)(C)C)C(C2=C(C)C=C(C(=O)O)OC2=O)=C1	standard polar	2025-10-23	2522.2
Gas Chromatography	Alternarian acid_TMS_5	COC1=CC(O[Si](C)(C)C)=C(C(=O)O)C(C2=C(C)C=C(C(=O)O[Si](C)(C)C)OC2=O)=C1	standard polar	2025-10-23	1677.0
Gas Chromatography	Alternarian acid_TMS_6	COC1=CC(O)=C(C(=O)O[Si](C)(C)C)C(C2=C(C)C=C(C(=O)O[Si](C)(C)C)OC2=O)=C1	standard polar	2025-10-23	2432.72
Gas Chromatography	Alternarian acid_TMS_7	COC1=CC(O[Si](C)(C)C)=C(C(=O)O[Si](C)(C)C)C(C2=C(C)C=C(C(=O)O[Si](C)(C)C)OC2=O)=C1	standard polar	2025-10-23	1714.87

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
Bacteria/Eubacteria	Actinobacteria	1	Human	Metabolic reconstruction
Eukaryota/Fungi	Ascomycota	1

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

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

Not Available

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 Alternarian acid (MMDBc0015223)

MOL for #<Metabolite:0x00007f2e298afe68>

3D MOL for #<Metabolite:0x00007f2e298afe68>

3D SDF for #<Metabolite:0x00007f2e298afe68>

3D-SDF for #<Metabolite:0x00007f2e298afe68>

PDB for #<Metabolite:0x00007f2e298afe68>

3D PDB for #<Metabolite:0x00007f2e298afe68>

SMILES for #<Metabolite:0x00007f2e298afe68>

INCHI for #<Metabolite:0x00007f2e298afe68>

Structure for #<Metabolite:0x00007f2e298afe68>

3D Structure for #<Metabolite:0x00007f2e298afe68>