CHEBI:64328 - lysidine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name lysidine
ChEBI ID CHEBI:64328
Definition Cytidine in which the 2-keto group on the cytosine ring is substituted by an ε-Llysyl residue.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C15H25N5O6
Net Charge 0
Average Mass 371.38890
Monoisotopic Mass 371.18048
InChI InChI=1S/C15H25N5O6/c16-8(14(24)25)3-1-2-5-18-15-19-10(17)4-6-20(15)13-12(23)11(22)9(7-21)26-13/h4,6,8-9,11-13,21-23H,1-3,5,7,16H2,(H,24,25)(H2,17,18,19)/t8-,9+,11+,12+,13+/m0/s1
InChIKey MDWUIKMWKDMPDE-IINAIABHSA-N
SMILES N[C@@H](CCCCNc1nc(=N)ccn1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing lysidine (CHEBI:64328) is a L-lysine derivative (CHEBI:25095)
lysidine (CHEBI:64328) is a cytidines (CHEBI:23524)
lysidine (CHEBI:64328) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
Incoming lysidine monophosphate (CHEBI:83661) has functional parent lysidine (CHEBI:64328)
IUPAC Name
N6-[4-imino-1-(β-D-ribofuranosyl)-1,4-dihydropyrimidin-2-yl]-L-lysine
Synonyms Sources
2-lysylcytidine ChEBI
k2C ChEBI
Manual Xref Database
Lysidine_(nucleoside) Wikipedia
View more database links
Registry Number Type Source
144796-96-3 CAS Registry Number Wikipedia
Citations Waiting for Citations Types Sources
14527414 PubMed citation Europe PMC
15894617 PubMed citation Europe PMC
16039592 PubMed citation Europe PMC
1698276 PubMed citation Europe PMC
17998287 PubMed citation Europe PMC
18073113 PubMed citation Europe PMC
18788046 PubMed citation Europe PMC
19233850 PubMed citation Europe PMC
19847269 PubMed citation Europe PMC
19944692 PubMed citation Europe PMC
20139989 PubMed citation Europe PMC
21435031 PubMed citation Europe PMC
3132458 PubMed citation Europe PMC
8743586 PubMed citation Europe PMC
Last Modified
21 January 2015