MiMeDB: Showing metabocard for Terretrione C (MMDBc0019895)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 09:54:49 UTC

Update Date

2025-10-07 16:07:02 UTC

Metabolite ID

MMDBc0019895

Metabolite Identification

Common Name

Terretrione C

Description

Terretrione C is a member of the chemical class of metabolites derived from fungal sources, specifically isolated from Penicillium sp. Its chemical structure features a unique arrangement that contributes to its classification within the broader category of secondary metabolites. While the precise details of its structure are not provided, it is known to be associated with a variety of biochemical pathways. Terretrione C is involved in the metabolic processes of the producing organism, potentially influencing secondary metabolite synthesis and interaction with other compounds such as tryptamine and indole derivatives, which are known for their roles in various biological functions. The compound's isolation alongside other metabolites, such as terretrione D and methyl-2-([2-(1H-indol-3-yl)ethyl]carbamoyl)acetate, suggests it may play a role in the ecological interactions of fungi, possibly affecting their growth or defense mechanisms (PMID:25815893 ). Further studies could elucidate its specific functions and applications in biochemistry and pharmacology.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152111542D          

 23 24  0  0  0  0            999 V2000
   -5.9321    5.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    5.3198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1210    4.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8522    1.8077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4674    4.5149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1066   -0.2535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3921    0.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8211    0.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3921    0.9840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8211    0.9840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1066    2.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6447    4.5765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1066    1.3965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8211    2.6340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1800    3.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7594    3.4567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5027    2.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5925    3.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3642    4.0179    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2911    2.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9914    3.7581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3798    1.3535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4152    3.2421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  2  0  0  0  0
 12  2  1  0  0  0  0
 12  5  1  0  0  0  0
 13  9  2  0  0  0  0
 13 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 14  1  0  0  0  0
 17 14  1  0  0  0  0
 18 15  1  0  0  0  0
 19  3  1  0  0  0  0
 19 15  1  0  0  0  0
 19 16  1  0  0  0  0
 20  4  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 16  2  0  0  0  0
 22 17  2  0  0  0  0
 23 18  2  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0019895

> <DATABASE_NAME>
MIME

> <SMILES>
CCC(C)C1N(C)C(=O)C(CC2=CC=CC=C2)C(=O)N(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H24N2O3/c1-5-12(2)15-18(23)20(4)17(22)14(16(21)19(15)3)11-13-9-7-6-8-10-13/h6-10,12,14-15H,5,11H2,1-4H3

> <INCHI_KEY>
ZJQJAOQHQVJSFD-UHFFFAOYSA-N

> <FORMULA>
C18H24N2O3

> <MOLECULAR_WEIGHT>
316.401

> <EXACT_MASS>
316.178692641

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.54145386969585

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-benzyl-3-(butan-2-yl)-1,4-dimethyl-1,4-diazepane-2,5,7-trione

> <ALOGPS_LOGP>
1.96

> <JCHEM_LOGP>
2.438150074333333

> <ALOGPS_LOGS>
-2.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.545469872935165

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.03142200036499

> <JCHEM_PKA_STRONGEST_BASIC>
-4.262986668417139

> <JCHEM_POLAR_SURFACE_AREA>
57.690000000000005

> <JCHEM_REFRACTIVITY>
87.69010000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.03e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-benzyl-1,4-dimethyl-3-(sec-butyl)-1,4-diazepane-2,5,7-trione

> <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     -11.073   9.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.002   9.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.826   8.972   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.057   3.374   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.206   8.428   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.932  -0.473   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.599   0.297   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.266   0.297   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.599   1.837   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.266   1.837   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.932   4.147   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.670   8.543   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.932   2.607   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.266   4.917   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -7.803   7.270   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.151   6.453   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.538   4.049   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -8.573   5.937   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      -6.280   7.500   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0      -8.010   4.503   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0      -3.717   7.015   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -6.309   2.527   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0     -10.108   6.052   0.000  0.00  0.00           O+0
CONECT    1    5                                                            
CONECT    2   12                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5    1   12                                                       
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   13                                                       
CONECT   10    8   13                                                       
CONECT   11   13   14                                                       
CONECT   12    2    5   15                                                  
CONECT   13    9   10   11                                                  
CONECT   14   11   16   17                                                  
CONECT   15   12   18   19                                                  
CONECT   16   14   19   21                                                  
CONECT   17   14   20   22                                                  
CONECT   18   15   20   23                                                  
CONECT   19    3   15   16                                                  
CONECT   20    4   17   18                                                  
CONECT   21   16                                                            
CONECT   22   17                                                            
CONECT   23   18                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

Synonyms

Not Available

Molecular Formula

C₁₈H₂₄N₂O₃

Average Mass

316.401

Monoisotopic Mass

316.178692641

IUPAC Name

6-benzyl-3-(butan-2-yl)-1,4-dimethyl-1,4-diazepane-2,5,7-trione

Traditional Name

6-benzyl-1,4-dimethyl-3-(sec-butyl)-1,4-diazepane-2,5,7-trione

CAS Registry Number

Not Available

SMILES

CCC(C)C1N(C)C(=O)C(CC2=CC=CC=C2)C(=O)N(C)C1=O

InChI Identifier

InChI=1S/C18H24N2O3/c1-5-12(2)15-18(23)20(4)17(22)14(16(21)19(15)3)11-13-9-7-6-8-10-13/h6-10,12,14-15H,5,11H2,1-4H3

InChI Key

ZJQJAOQHQVJSFD-UHFFFAOYSA-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
1,4-diazepane
Diazepane
Monocyclic benzene moiety
Benzenoid
1,3-dicarbonyl compound
Carboxylic acid imide, n-substituted
Carboxylic acid imide
Tertiary carboxylic acid amide
Dicarboximide
Carboxamide group
Lactam
Azacycle
Organoheterocyclic compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organooxygen compound
Organonitrogen 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	0.6 g/L	ALOGPS
logP	1.96	ALOGPS
logP	2.44	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	12.03	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.69 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	87.69 m³·mol⁻¹	ChemAxon
Polarizability	34.54 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

Spectrum Type	Description	Splash Key	Deposition Date	View
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	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

29215053

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71480634

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 Terretrione C (MMDBc0019895)

MOL for #<Metabolite:0x00007f8de965a288>

3D MOL for #<Metabolite:0x00007f8de965a288>

3D SDF for #<Metabolite:0x00007f8de965a288>

3D-SDF for #<Metabolite:0x00007f8de965a288>

PDB for #<Metabolite:0x00007f8de965a288>

3D PDB for #<Metabolite:0x00007f8de965a288>

SMILES for #<Metabolite:0x00007f8de965a288>

INCHI for #<Metabolite:0x00007f8de965a288>

Structure for #<Metabolite:0x00007f8de965a288>

3D Structure for #<Metabolite:0x00007f8de965a288>