CHEBI:143076 - Nπ-methyl-L-histidine zwitterion

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
This entity has been annotated by a third party. If you would like more information added to this entry, please contact ChEBI via email or GitHub.
ChEBI Name Nπ-methyl-L-histidine zwitterion
ChEBI ID CHEBI:143076
ChEBI ASCII Name N(pros)-methyl-L-histidine zwitterion
Definition A L-histidine derivative that is L-histidine substituted by a methyl group at position 3 on the imidazole ring; major species at pH 7.3.
Stars This entity has been manually annotated by a third party.
Submitter Anne Morgat
Supplier Information
Download Molfile XML SDF
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 )
Related Structures
Nπ-methyl-L-histidine zwitterion 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 zwitterion is a Tautomer of
N(pros)-methyl-L-histidine
Mass : 169.18126
Formula : C7H11N3O2
27596
Graph View Tree View
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
Checked
Unchecked