CHEBI:39866 - 2-hydroxy-5-[(1E)-(2-phenylethylidene)amino]-L-tyrosine

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ChEBI Name 2-hydroxy-5-[(1E)-(2-phenylethylidene)amino]-L-tyrosine
ChEBI ID CHEBI:39866
ChEBI ASCII Name 2-hydroxy-5-[(1E)-(2-phenylethylidene)amino]-L-tyrosine
Definition An imine that is L-tyrosine bearing an additional hydroxy substituent at position 2 as well as a (2-phenylethylidene)amino substituent at position 5.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C17H18N2O4
Net Charge 0
Average Mass 314.33580
Monoisotopic Mass 314.12666
InChI InChI=1S/C17H18N2O4/c18-13(17(22)23)8-12-9-14(16(21)10-15(12)20)19-7-6-11-4-2-1-3-5-11/h1-5,7,9-10,13,20-21H,6,8,18H2,(H,22,23)/b19-7+/t13-/m0/s1
InChIKey BSKROLLIUIDPDT-KUJOXMSCSA-N
SMILES N[C@@H](Cc1cc(\N=C\Cc2ccccc2)c(O)cc1O)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): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-hydroxy-5-[(1E)-(2-phenylethylidene)amino]-L-tyrosine (CHEBI:39866) has functional parent 2-phenylethylamine (CHEBI:18397)
2-hydroxy-5-[(1E)-(2-phenylethylidene)amino]-L-tyrosine (CHEBI:39866) has role metabolite (CHEBI:25212)
2-hydroxy-5-[(1E)-(2-phenylethylidene)amino]-L-tyrosine (CHEBI:39866) is a L-tyrosine derivative (CHEBI:27177)
2-hydroxy-5-[(1E)-(2-phenylethylidene)amino]-L-tyrosine (CHEBI:39866) is a imine (CHEBI:24783)
2-hydroxy-5-[(1E)-(2-phenylethylidene)amino]-L-tyrosine (CHEBI:39866) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
IUPAC Name
2-hydroxy-5-[(E)-(2-phenylethylidene)amino]-L-tyrosine
Manual Xref Database
2TY PDBeChem
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Citation Waiting for Citations Type Source
22882828 PubMed citation Europe PMC
Last Modified
17 December 2014