CHEBI:75851 - (2S,3R)-capreomycidine

ChEBI IDCHEBI:75851
ChEBI Name(2S,3R)-capreomycidine
Stars
ASCII Name(2S,3R)-capreomycidine
DefinitionAn L-α-amino acid obtained by enzyme-mediated intramolecular cyclisation of L-arginine.
Last Modified8 January 2015
SubmitterSteve
DownloadsMolfile
FormulaC6H12N4O2
Net Charge0
Average Mass172.188
Monoisotopic Mass172.09603
SMILES[H][C@]1([C@H](N)C(=O)O)CCNC(=N)N1
InChIInChI=1S/C6H12N4O2/c7-4(5(11)12)3-1-2-9-6(8)10-3/h3-4H,1-2,7H2,(H,11,12)(H3,8,9,10)/t3-,4+/m1/s1
InChIKeyXHNWDEHKMJLKGG-DMTCNVIQSA-N
Roles Classification
Chemical Roles:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
ChEBI Ontology
Outgoing Relation(s)
(2S,3R)-capreomycidine (CHEBI:75851) has role metabolite (CHEBI:25212)
(2S,3R)-capreomycidine (CHEBI:75851) is a L-arginine derivative (CHEBI:83965)
(2S,3R)-capreomycidine (CHEBI:75851) is a guanidines (CHEBI:24436)
(2S,3R)-capreomycidine (CHEBI:75851) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
(2S,3R)-capreomycidine (CHEBI:75851) is a pyrimidines (CHEBI:39447)
(2S,3R)-capreomycidine (CHEBI:75851) is conjugate base of (2S,3R)-capreomycidine(1+) (CHEBI:75665)
Incoming Relation(s)
(2S,3R)-capreomycidine(1+) (CHEBI:75665) is conjugate acid of (2S,3R)-capreomycidine (CHEBI:75851)
Synonyms  Source
L-CapreomycidineKEGG COMPOUND
(2S,3R)-CapreomycidineKEGG COMPOUND
Manual XrefsDatabases
C18472KEGG COMPOUND
MYNPDBeChem
CPD-15414MetaCyc
CSIPDBeChem
Registry NumbersSources
Reaxys:881957Reaxys
Citations