RefMet Compound Details
RefMet ID, RefMet name, exact mass and formula | ||
RefMet ID | RM0028125 | |
---|---|---|
RefMet name | 1-Methylhistamine | |
Systematic name | 2-(1-methyl-1H-imidazol-4-yl)ethan-1-amine | |
Synonyms | PubChem Synonyms | |
Exact mass | 125.095297 (neutral) | Calculate m/z:
View other RefMet entries with this exact (neutral) mass: +/- 0.05 amu +/- 0.1 amu +/- 0.2 amu +/- 0.5 amu |
Formula | C6H11N3 | View other entries in RefMet with this formula |
Molecular descriptors | ||
Molfile | 37490 (Download molfile/View MW Metabolite Database details) | |
InChI | InChI=1S/C6H11N3/c1-9-4-6(2-3-7)8-5-9/h4-5H,2-3,7H2,1H3 | |
InChIKey | FHQDWPCFSJMNCT-UHFFFAOYSA-N | View other enantiomers/diastereomers of this metabolite in RefMet |
SMILES | Cn1cc(CCN)nc1
Run Tanimoto similarity search (with similarity coefficient >=0.6) | |
Chemical/Biochemical Classification | ||
Super Class | Alkaloids | |
Main Class | Histidine alkaloids | |
Sub Class | Imidazole alkaloids | |
Distribution of 1-Methylhistamine in NMDR studies | ||
Species | Plot Species distribution | |
Sample source | Plot Sample source(tissue) distribution | |
Platform | Platform (MS/NMR) used for detection | |
Chromatography | Chromatography methods used for detection | |
Studies | NMDR Studies reporting 1-Methylhistamine | |
External Links | ||
Pubchem CID | 3614 | |
ChEBI ID | 29009 | |
KEGG ID | C05127 | |
HMDB ID | HMDB0000898 | |
Chemspider ID | 3488 | |
MetaCyc ID | N-METHYL-HISTAMINE | |
Spectral data for 1-Methylhistamine standards | ||
NP-MRD ID(NMR) | View NMR spectra | |
MassBank(EU) | View MS spectra | |
Structural annotation level | ||
Annotation level | 1 (1:Known structure; 2:Known regiochemistry; 3:Partial structure; 4:Sum-composition) |
Table of KEGG reactions in human pathways involving 1-Methylhistamine
Rxn ID | KEGG Reaction | Enzyme |
---|---|---|
R02155 | S-Adenosyl-L-methionine + Histamine <=> S-Adenosyl-L-homocysteine + N-Methylhistamine | S-Adenosyl-L-methionine:histamine N-tele-methyltransferase |
R04674 | N-Methylhistamine + H2O + Oxygen <=> Methylimidazole acetaldehyde + Ammonia + Hydrogen peroxide | N-methylhistamine:oxygen oxidoreductase (deaminating) |
Table of KEGG human pathways containing 1-Methylhistamine
Pathway ID | Human Pathway | # of reactions |
---|---|---|
hsa00340 | Histidine metabolism | 2 |