MiMeDB: Showing metabocard for Pheofungin A (MMDBc0015591)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:23:08 UTC

Update Date

2022-08-31 06:39:32 UTC

Metabolite ID

MMDBc0015591

Metabolite Identification

Common Name

Pheofungin A

Description

Pheofungin A belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). Based on a literature review very few articles have been published on Pheofungin A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108232D          

 23 26  0  0  0  0            999 V2000
    5.5753    1.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    3.0434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    2.1079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444    2.1079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    3.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    2.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    2.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    2.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    3.6671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    3.6671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    2.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    3.0434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    3.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    3.9789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    3.1993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    4.6025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    4.1348    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9058    2.5757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    4.4466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    5.3821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    4.4466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    2.5757    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
  7  3  2  0  0  0  0
  7  4  1  0  0  0  0
  8  2  1  0  0  0  0
  8  5  2  0  0  0  0
  9  5  1  0  0  0  0
  9  6  2  0  0  0  0
 10  3  1  0  0  0  0
 11  6  1  0  0  0  0
 12  4  2  0  0  0  0
 13  8  1  0  0  0  0
 13 11  2  0  0  0  0
 14 10  2  0  0  0  0
 14 12  1  0  0  0  0
 16 13  1  0  0  0  0
 16 15  2  0  0  0  0
 17 15  1  0  0  0  0
 18 14  1  0  0  0  0
 18 15  1  0  0  0  0
 19  9  1  0  0  0  0
 20 10  1  0  0  0  0
 21 17  2  0  0  0  0
 22 11  1  0  0  0  0
 22 17  1  0  0  0  0
 23 12  1  0  0  0  0
 23 16  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015591

> <DATABASE_NAME>
MIME

> <SMILES>
CC1=CC(O)=C2NC3=C(SC2=C1)C1=C(OC3=O)C=C(O)C=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C17H13NO4S/c1-7-3-10(20)14-12(4-7)23-16-13-8(2)5-9(19)6-11(13)22-17(21)15(16)18-14/h3-6,18-20H,1-2H3

> <INCHI_KEY>
UTPHJLRPCMSHGB-UHFFFAOYSA-N

> <FORMULA>
C17H13NO4S

> <MOLECULAR_WEIGHT>
327.35

> <EXACT_MASS>
327.056529077

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
33.87808169646872

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,8-dihydroxy-1,10-dimethyl-6,7-dihydro-5-oxa-12-thia-7-azatetraphen-6-one

> <ALOGPS_LOGP>
3.28

> <JCHEM_LOGP>
2.9421636009999994

> <ALOGPS_LOGS>
-3.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.81748766719121

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.633290659396593

> <JCHEM_PKA_STRONGEST_BASIC>
-5.797761877575936

> <JCHEM_POLAR_SURFACE_AREA>
78.79

> <JCHEM_REFRACTIVITY>
92.0882

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.73e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,8-dihydroxy-1,10-dimethyl-7H-5-oxa-12-thia-7-azatetraphen-6-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      10.407   3.062   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.350   3.062   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.903   5.681   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.887   3.935   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.830   3.935   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.326   6.554   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.399   4.226   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.342   4.226   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.179   5.099   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.895   6.845   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.838   6.845   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.879   5.099   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.846   5.681   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.383   6.554   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.862   7.427   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.358   5.972   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.854   8.591   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       6.375   7.718   0.000  0.00  0.00           N+0
HETATM   19  O   UNK     0      -1.691   4.808   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       9.399   8.300   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       4.358  10.047   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       2.342   8.300   0.000  0.00  0.00           O+0
HETATM   23  S   UNK     0       5.366   4.808   0.000  0.00  0.00           S+0
CONECT    1    7                                                            
CONECT    2    8                                                            
CONECT    3    7   10                                                       
CONECT    4    7   12                                                       
CONECT    5    8    9                                                       
CONECT    6    9   11                                                       
CONECT    7    1    3    4                                                  
CONECT    8    2    5   13                                                  
CONECT    9    5    6   19                                                  
CONECT   10    3   14   20                                                  
CONECT   11    6   13   22                                                  
CONECT   12    4   14   23                                                  
CONECT   13    8   11   16                                                  
CONECT   14   10   12   18                                                  
CONECT   15   16   17   18                                                  
CONECT   16   13   15   23                                                  
CONECT   17   15   21   22                                                  
CONECT   18   14   15                                                       
CONECT   19    9                                                            
CONECT   20   10                                                            
CONECT   21   17                                                            
CONECT   22   11   17                                                       
CONECT   23   12   16                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

Synonyms

Not Available

Molecular Formula

C₁₇H₁₃NO₄S

Average Mass

327.35

Monoisotopic Mass

327.056529077

IUPAC Name

3,8-dihydroxy-1,10-dimethyl-6,7-dihydro-5-oxa-12-thia-7-azatetraphen-6-one

Traditional Name

3,8-dihydroxy-1,10-dimethyl-7H-5-oxa-12-thia-7-azatetraphen-6-one

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=C2NC3=C(SC2=C1)C1=C(OC3=O)C=C(O)C=C1C

InChI Identifier

InChI=1S/C17H13NO4S/c1-7-3-10(20)14-12(4-7)23-16-13-8(2)5-9(19)6-11(13)22-17(21)15(16)18-14/h3-6,18-20H,1-2H3

InChI Key

UTPHJLRPCMSHGB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Not Available

Direct Parent

Coumarins and derivatives

Alternative Parents

Substituents

Coumarin
Diarylthioether
Benzopyran
Benzothiazine
1-benzopyran
Aryl thioether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Para-thiazine
Primary aromatic amine
Vinylogous thioester
Pyran
Benzenoid
Heteroaromatic compound
Lactone
Secondary amine
Organoheterocyclic compound
Azacycle
Oxacycle
Thioether
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Amine
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	0.087 g/L	ALOGPS
logP	3.28	ALOGPS
logP	2.94	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	7.63	ChemAxon
pKa (Strongest Basic)	-5.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	78.79 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	92.09 m³·mol⁻¹	ChemAxon
Polarizability	33.88 Å³	ChemAxon
Number of Rings	4	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

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

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

78435014

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

56641605

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 Pheofungin A (MMDBc0015591)

MOL for #<Metabolite:0x00005645c9286580>

3D MOL for #<Metabolite:0x00005645c9286580>

3D SDF for #<Metabolite:0x00005645c9286580>

3D-SDF for #<Metabolite:0x00005645c9286580>

PDB for #<Metabolite:0x00005645c9286580>

3D PDB for #<Metabolite:0x00005645c9286580>

SMILES for #<Metabolite:0x00005645c9286580>

INCHI for #<Metabolite:0x00005645c9286580>

Structure for #<Metabolite:0x00005645c9286580>

3D Structure for #<Metabolite:0x00005645c9286580>