CHEBI:53693 - 2,5-diiodo-L-histidine

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ChEBI Name 2,5-diiodo-L-histidine
ChEBI ASCII Name 2,5-diiodo-L-histidine
Definition An iodoamino acid that is L-histidine in which the imidazole ring is substituted by iodine at positions 2- and 5(4).
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H7I2N3O2
Net Charge 0
Average Mass 406.94760
Monoisotopic Mass 406.86277
InChI InChI=1S/C6H7I2N3O2/c7-4-3(10-6(8)11-4)1-2(9)5(12)13/h2H,1,9H2,(H,10,11)(H,12,13)/t2-/m0/s1
SMILES N[C@@H](Cc1nc(I)[nH]c1I)C(O)=O
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): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2,5-diiodo-L-histidine (CHEBI:53693) is a L-histidine derivative (CHEBI:84076)
2,5-diiodo-L-histidine (CHEBI:53693) is a iodoamino acid (CHEBI:24862)
2,5-diiodo-L-histidine (CHEBI:53693) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
Synonyms Sources
2,4-diiodo-L-histidine ChEBI
2,4-diiodohistidine ChEBI
2,5-diiodohistidine ChEBI
diiodohistidine ChEBI
Registry Numbers Types Sources
15249 Reaxys Registry Number Reaxys
6599014 Beilstein Registry Number Beilstein
6599014 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
15206581 PubMed citation Europe PMC
23877651 PubMed citation Europe PMC
Last Modified
11 December 2014