CHEBI:65063 - cyclo(L-tyrosyl-L-tyrosyl)

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name cyclo(L-tyrosyl-L-tyrosyl)
ChEBI ID CHEBI:65063
ChEBI ASCII Name cyclo(L-tyrosyl-L-tyrosyl)
Definition A cyclo(tyrosyl-tyrosyl) in which both stereocentres have L-configuration. Synthesized by Mycobacterium tuberculosis.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C18H18N2O4
Net Charge 0
Average Mass 326.34650
Monoisotopic Mass 326.12666
InChI InChI=1S/C18H18N2O4/c21-13-5-1-11(2-6-13)9-15-17(23)20-16(18(24)19-15)10-12-3-7-14(22)8-4-12/h1-8,15-16,21-22H,9-10H2,(H,19,24)(H,20,23)/t15-,16-/m0/s1
InChIKey NGPCLOGFGKJCBP-HOTGVXAUSA-N
SMILES Oc1ccc(C[C@@H]2NC(=O)[C@H](Cc3ccc(O)cc3)NC2=O)cc1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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 cyclo(L-tyrosyl-L-tyrosyl) (CHEBI:65063) has role metabolite (CHEBI:25212)
cyclo(L-tyrosyl-L-tyrosyl) (CHEBI:65063) is a cyclo(tyrosyl-tyrosyl) (CHEBI:65048)
Incoming mycocyclosin (CHEBI:71596) has functional parent cyclo(L-tyrosyl-L-tyrosyl) (CHEBI:65063)
IUPAC Name
(3S,6S)-3,6-bis(4-hydroxybenzyl)piperazine-2,5-dione
Synonyms Sources
(3S)-cis-3,6-bis-(4-hydroxy-benzyl)-piperazine-2,5-dione ChEBI
cyclo(L-tyrosyl-L-tyrosine) ChEBI
cyclo(L-tyrosyl-L-tyrosyl) UniProt
cyclo(Tyr-Tyr) ChEBI
cyclo-(L-Tyr)2 ChEBI
cyclo-(L-Tyr-L-Tyr) ChEBI
cyclo-(L-tyrosyl-L-tyrosine) ChEBI
cyclodi-L-tyrosine ChEBI
cYY ChEBI
Registry Numbers Types Sources
10125-11-8 CAS Registry Number Reaxys
94441 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
19430487 PubMed citation Europe PMC
20852636 PubMed citation Europe PMC
21325056 PubMed citation Europe PMC
Last Modified
20 November 2014