MiMeDB: Showing metabocard for Bis(dethio)-10a-methylthio-3a-deoxy-3,3a-didehydrogliotoxin (MMDBc0001638)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 19:50:45 UTC

Update Date

2025-10-07 16:04:30 UTC

Metabolite ID

MMDBc0001638

Metabolite Identification

Common Name

Bis(dethio)-10a-methylthio-3a-deoxy-3,3a-didehydrogliotoxin

Description

Bis(dethio)-10a-methylthio-3a-deoxy-3,3a-didehydrogliotoxin is a novel metabolite belonging to the class of didehydrogliotoxins, which are structurally related to various alkaloids. This compound has been identified in recent studies, but there is limited literature available regarding its biological activity and pharmacological properties. Specifically, a study highlighted the presence of bis(dethio)-10a-methylthio-3a-deoxy-3,3a-didehydrogliotoxin alongside another new metabolite, 6-deoxy-5a,6-didehydrogliotoxin, and five known metabolites (PMID:22148349 ). Further research is needed to elucidate its potential effects and mechanisms of action within biological systems.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142121502D          

 22 24  0  0  1  0            999 V2000
   -0.3896   -0.8137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995    0.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7081    2.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7054   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985   -0.3721    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3464    0.2410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9694   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    1.0256    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0925    0.5840    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.2410    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6435   -1.1567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2243   -1.1567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2046    1.9817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0950    1.8326    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.0915   -0.5436    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1534    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  6  4  2  0  0  0  0
  8  1  2  0  0  0  0
  9  5  2  0  0  0  0
  9  7  1  0  0  0  0
 10  6  1  0  0  0  0
 11  9  1  0  0  0  0
 11 10  1  0  0  0  0
 12  8  1  0  0  0  0
 14  7  1  0  0  0  0
 14 13  1  0  0  0  0
 15  2  1  0  0  0  0
 15  8  1  0  0  0  0
 15 13  1  0  0  0  0
 16 11  1  0  0  0  0
 16 12  1  0  0  0  0
 16 14  1  0  0  0  0
 10 17  1  6  0  0  0
 18 12  2  0  0  0  0
 19 13  2  0  0  0  0
 20  3  1  0  0  0  0
 14 20  1  1  0  0  0
 10 21  1  1  0  0  0
 11 22  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0001638

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12N3C(=O)C(=C)N(C)C(=O)[C@@]3(CC1=CC=C[C@]2([H])O)SC

> <INCHI_IDENTIFIER>
InChI=1S/C14H16N2O3S/c1-8-12(18)16-11-9(5-4-6-10(11)17)7-14(16,20-3)13(19)15(8)2/h4-6,10-11,17H,1,7H2,2-3H3/t10-,11-,14+/m0/s1

> <INCHI_KEY>
OXNWZASJHXTGNL-COPLHBTASA-N

> <FORMULA>
C14H16N2O3S

> <MOLECULAR_WEIGHT>
292.35

> <EXACT_MASS>
292.088163557

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
29.399487786421602

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5aS,6S,10aR)-6-hydroxy-2-methyl-3-methylidene-10a-(methylsulfanyl)-1H,2H,3H,4H,5aH,6H,10H,10aH-pyrazino[1,2-a]indole-1,4-dione

> <ALOGPS_LOGP>
0.56

> <JCHEM_LOGP>
0.22011950433333363

> <ALOGPS_LOGS>
-1.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.124491613538869

> <JCHEM_PKA_STRONGEST_BASIC>
-0.238939152290354

> <JCHEM_POLAR_SURFACE_AREA>
60.85

> <JCHEM_REFRACTIVITY>
79.3407

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.17e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5aS,6S,10aR)-6-hydroxy-2-methyl-3-methylidene-10a-(methylsulfanyl)-5aH,6H,10H-pyrazino[1,2-a]indole-1,4-dione

> <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      -0.727  -1.519   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.679   1.410   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.188   4.451   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.393   1.090   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.362   2.235   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.917  -0.374   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.610   2.820   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.303  -0.374   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.856   1.914   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.410  -0.695   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.380   0.450   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.810  -0.695   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.858   2.235   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.364   1.914   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -0.173   1.090   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0       2.840   0.450   0.000  0.00  0.00           N+0
HETATM   17  O   UNK     0       4.935  -2.159   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       2.285  -2.159   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.382   3.699   0.000  0.00  0.00           O+0
HETATM   20  S   UNK     0       2.044   3.421   0.000  0.00  0.00           S+0
HETATM   21  H   UNK     0       3.904  -1.015   0.000  0.00  0.00           H+0
HETATM   22  H   UNK     0       5.886   0.770   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2   15                                                            
CONECT    3   20                                                            
CONECT    4    5    6                                                       
CONECT    5    4    9                                                       
CONECT    6    4   10                                                       
CONECT    7    9   14                                                       
CONECT    8    1   12   15                                                  
CONECT    9    5    7   11                                                  
CONECT   10    6   11   17   21                                             
CONECT   11    9   10   16   22                                             
CONECT   12    8   16   18                                                  
CONECT   13   14   15   19                                                  
CONECT   14    7   13   16   20                                             
CONECT   15    2    8   13                                                  
CONECT   16   11   12   14                                                  
CONECT   17   10                                                            
CONECT   18   12                                                            
CONECT   19   13                                                            
CONECT   20    3   14                                                       
CONECT   21   10                                                            
CONECT   22   11                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

Synonyms

Not Available

Molecular Formula

C₁₄H₁₆N₂O₃S

Average Mass

292.35

Monoisotopic Mass

292.088163557

IUPAC Name

(5aS,6S,10aR)-6-hydroxy-2-methyl-3-methylidene-10a-(methylsulfanyl)-1H,2H,3H,4H,5aH,6H,10H,10aH-pyrazino[1,2-a]indole-1,4-dione

Traditional Name

(5aS,6S,10aR)-6-hydroxy-2-methyl-3-methylidene-10a-(methylsulfanyl)-5aH,6H,10H-pyrazino[1,2-a]indole-1,4-dione

CAS Registry Number

Not Available

SMILES

[H][C@]12N3C(=O)C(=C)N(C)C(=O)[C@@]3(CC1=CC=C[C@]2([H])O)SC

InChI Identifier

InChI=1S/C14H16N2O3S/c1-8-12(18)16-11-9(5-4-6-10(11)17)7-14(16,20-3)13(19)15(8)2/h4-6,10-11,17H,1,7H2,2-3H3/t10-,11-,14+/m0/s1

InChI Key

OXNWZASJHXTGNL-COPLHBTASA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Indole or derivatives
Thiodioxopiperazine
Dioxopiperazine
2,5-dioxopiperazine
N-methylpiperazine
N-alkylpiperazine
1,4-diazinane
Piperazine
Pyrrolidine
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Secondary alcohol
Tertiary amine
Hemithioaminal
Thioether
Organoheterocyclic compound
Azacycle
Sulfenyl compound
Dialkylthioether
Amine
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organosulfur compound
Organic oxide
Organic nitrogen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	5.17 g/L	ALOGPS
logP	0.56	ALOGPS
logP	0.22	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	14.12	ChemAxon
pKa (Strongest Basic)	-0.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	60.85 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	79.34 m³·mol⁻¹	ChemAxon
Polarizability	29.4 Å³	ChemAxon
Number of Rings	3	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

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	Species

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	2	Human feces; Human sputum; Human	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

28289594

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

57333568

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Bis(dethio)-10a-methylthio-3a-deoxy-3,3a-didehydrogliotoxin (MMDBc0001638)

MOL for #<Metabolite:0x00007fb4d0a8de78>

3D MOL for #<Metabolite:0x00007fb4d0a8de78>

3D SDF for #<Metabolite:0x00007fb4d0a8de78>

3D-SDF for #<Metabolite:0x00007fb4d0a8de78>

PDB for #<Metabolite:0x00007fb4d0a8de78>

3D PDB for #<Metabolite:0x00007fb4d0a8de78>

SMILES for #<Metabolite:0x00007fb4d0a8de78>

INCHI for #<Metabolite:0x00007fb4d0a8de78>

Structure for #<Metabolite:0x00007fb4d0a8de78>

3D Structure for #<Metabolite:0x00007fb4d0a8de78>