MiMeDB: Showing metabocard for Ergotryptamine (MMDBc0010368)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 02:34:44 UTC

Update Date

2025-10-07 16:05:44 UTC

Metabolite ID

MMDBc0010368

Metabolite Identification

Common Name

Ergotryptamine

Description

Ergotryptamine is a member of the ergot alkaloid chemical class, which encompasses a diverse group of compounds derived from the ergot fungus. This metabolite has been identified in various species, including the endophytic fungus Epichloë typhina × festucae, where it occurs alongside other early pathway metabolites like chanoclavine-I and the end-product ergovaline (PMID:27248330 ). Research utilizing an RNAi-based approach has demonstrated that reducing the mRNA levels of the easA gene, which encodes an enzyme crucial for the biosynthetic pathway, leads to decreased ergovaline levels and increased concentrations of both ergotryptamine and chanoclavine-I (PMID:27248330 ). Structural elucidation studies have shown that ergotryptamine differs from N-methyl-4-dimethylallyltryptophan by the absence of a carboxyl group, the presence of a hydroxyl group, and a shift in a carbon–carbon double bond (PMID:25491167 ). Additionally, feeding studies with Aspergillus mutants indicate that ergotryptamine may function as a byproduct rather than a key intermediate in the biosynthetic pathway (PMID:25491167 ). Its equivalency with a provisional Epichloë-derived ergot alkaloid, 6,7-secolysergine, has also been established (PMID:25491167 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152104342D          

 21 22  0  0  0  0            999 V2000
    3.3523    5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5273    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851    4.1027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768    3.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781    3.9312    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1773    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.5854    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    3.1729    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  2  0  0  0  0
  6  4  1  0  0  0  0
  9  7  2  0  0  0  0
 10  8  1  0  0  0  0
 12  5  1  0  0  0  0
 12  7  1  0  0  0  0
 13  8  1  0  0  0  0
 13 11  2  0  0  0  0
 14  6  2  0  0  0  0
 15 12  2  0  0  0  0
 15 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16  1  1  0  0  0  0
 16  2  1  0  0  0  0
 16  9  1  0  0  0  0
 17  3  1  0  0  0  0
 17 10  1  0  0  0  0
 18 11  1  0  0  0  0
 18 14  1  0  0  0  0
 19 16  1  0  0  0  0
 20  7  1  0  0  0  0
 21  9  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0010368

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(=C(\[H])C(C)(C)O)C1=C2C(CCNC)=CNC2=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H22N2O/c1-16(2,19)9-7-12-5-4-6-14-15(12)13(11-18-14)8-10-17-3/h4-7,9,11,17-19H,8,10H2,1-3H3/b9-7+

> <INCHI_KEY>
QCWMNSFZHYEJJO-VQHVLOKHSA-N

> <FORMULA>
C16H22N2O

> <MOLECULAR_WEIGHT>
258.365

> <EXACT_MASS>
258.173213336

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
30.45789755293056

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E)-2-methyl-4-{3-[2-(methylamino)ethyl]-1H-indol-4-yl}but-3-en-2-ol

> <ALOGPS_LOGP>
2.71

> <JCHEM_LOGP>
2.4587354426666663

> <ALOGPS_LOGS>
-4.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
17.242638123731442

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.009872117087564

> <JCHEM_PKA_STRONGEST_BASIC>
10.308395849772037

> <JCHEM_POLAR_SURFACE_AREA>
48.05

> <JCHEM_REFRACTIVITY>
81.33899999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.52e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E)-2-methyl-4-{3-[2-(methylamino)ethyl]-1H-indol-4-yl}but-3-en-2-ol

> <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       6.258   9.773   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.718   8.233   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.839   7.658   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.924   5.923   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.650   5.553   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.258   6.693   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.143   5.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.258   8.233   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0      -0.333   7.338   0.000  0.00  0.00           N+0
HETATM   18  N   UNK     0       2.126   1.597   0.000  0.00  0.00           N+0
HETATM   19  O   UNK     0       7.798   8.233   0.000  0.00  0.00           O+0
HETATM   20  H   UNK     0       3.590   6.693   0.000  0.00  0.00           H+0
HETATM   21  H   UNK     0       7.591   5.923   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   16                                                            
CONECT    3   17                                                            
CONECT    4    5    6                                                       
CONECT    5    4   12                                                       
CONECT    6    4   14                                                       
CONECT    7    9   12   20                                                  
CONECT    8   10   13                                                       
CONECT    9    7   16   21                                                  
CONECT   10    8   17                                                       
CONECT   11   13   18                                                       
CONECT   12    5    7   15                                                  
CONECT   13    8   11   15                                                  
CONECT   14    6   15   18                                                  
CONECT   15   12   13   14                                                  
CONECT   16    1    2    9   19                                             
CONECT   17    3   10                                                       
CONECT   18   11   14                                                       
CONECT   19   16                                                            
CONECT   20    7                                                            
CONECT   21    9                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

Synonyms

Not Available

Molecular Formula

C₁₆H₂₂N₂O

Average Mass

258.365

Monoisotopic Mass

258.173213336

IUPAC Name

(3E)-2-methyl-4-{3-[2-(methylamino)ethyl]-1H-indol-4-yl}but-3-en-2-ol

Traditional Name

(3E)-2-methyl-4-{3-[2-(methylamino)ethyl]-1H-indol-4-yl}but-3-en-2-ol

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])C(C)(C)O)C1=C2C(CCNC)=CNC2=CC=C1

InChI Identifier

InChI=1S/C16H22N2O/c1-16(2,19)9-7-12-5-4-6-14-15(12)13(11-18-14)8-10-17-3/h4-7,9,11,17-19H,8,10H2,1-3H3/b9-7+

InChI Key

QCWMNSFZHYEJJO-VQHVLOKHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tryptamines and derivatives. Tryptamines and derivatives are compounds containing the tryptamine backbone, which is structurally characterized by an indole ring substituted at the 3-position by an ethanamine.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Tryptamines and derivatives

Direct Parent

Tryptamines and derivatives

Alternative Parents

Substituents

Tryptamine
3-alkylindole
Indole
Styrene
Aralkylamine
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Tertiary alcohol
Pyrrole
Azacycle
Secondary amine
Secondary aliphatic amine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
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	0.025 g/L	ALOGPS
logP	2.71	ALOGPS
logP	2.46	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	15.01	ChemAxon
pKa (Strongest Basic)	10.31	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	48.05 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	81.34 m³·mol⁻¹	ChemAxon
Polarizability	30.46 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 GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	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

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	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

78435476

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585842

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 Ergotryptamine (MMDBc0010368)

MOL for #<Metabolite:0x00007f2ad05c5920>

3D MOL for #<Metabolite:0x00007f2ad05c5920>

3D SDF for #<Metabolite:0x00007f2ad05c5920>

3D-SDF for #<Metabolite:0x00007f2ad05c5920>

PDB for #<Metabolite:0x00007f2ad05c5920>

3D PDB for #<Metabolite:0x00007f2ad05c5920>

SMILES for #<Metabolite:0x00007f2ad05c5920>

INCHI for #<Metabolite:0x00007f2ad05c5920>

Structure for #<Metabolite:0x00007f2ad05c5920>

3D Structure for #<Metabolite:0x00007f2ad05c5920>