CHEBI:27596 - Nπ-methyl-L-histidine

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ChEBI Name Nπ-methyl-L-histidine
ChEBI ID CHEBI:27596
ChEBI ASCII Name N(pros)-methyl-L-histidine
Definition A L-histidine derivative that is L-histidine substituted by a methyl group at position 3 on the imidazole ring.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:7067, CHEBI:21445, CHEBI:19854
Supplier Information
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Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Related Structures
Nπ-methyl-L-histidine has Substituent Group(s)
N(pros)-methyl-L-histidine residue
Mass : 151.16598
Formula : C7H9N3O
43903
Nπ-methyl-L-histidine is a Structural Derivative of
L-histidine
Mass : 155.15468
Formula : C6H9N3O2
15971 		histidine
Mass : 155.15468
Formula : C6H9N3O2
27570 		proteinogenic amino acid
Definition : Any of the 23 alpha-amino acids that are precursors to proteins, and are incorporated into proteins during translation. The group includes the 20 amino acids encoded by the nuclear genes of eukaryotes together with selenocysteine, pyrrolysine, and N-formylmethionine. Apart from glycine, which is non-chiral, all have L configuration.
 ammonia
Mass : 17.03056
Formula : H3N
16134
Nπ-methyl-L-histidine is a Tautomer of
N(pros)-methyl-L-histidine zwitterion
Mass : 169.181
143076
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Relationship Types
is a
has part
is conjugate base of
is conjugate acid of
is tautomer of
is enantiomer of
has functional parent
has parent hydride
is substituent group from
has role
Status
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