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

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ChEBI Name	(2S,3R)-capreomycidine

ChEBI ID	CHEBI:75851

ChEBI ASCII Name	(2S,3R)-capreomycidine

Definition	An L-α-amino acid obtained by enzyme-mediated intramolecular cyclisation of L-arginine.

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information

Download	Molfile XML SDF

Formula

C6H12N4O2

Net Charge

Average Mass

172.18510

Monoisotopic Mass

172.09603

InChI

InChI=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

InChIKey

XHNWDEHKMJLKGG-DMTCNVIQSA-N

SMILES

N[C@@H]([C@H]1CCNC(=N)N1)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.

ChEBI Ontology
Outgoing	(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	(2S,3R)-capreomycidine(1+) (CHEBI:75665) is conjugate acid of (2S,3R)-capreomycidine (CHEBI:75851)

Registry Number	Type	Source
881957	Reaxys Registry Number	Reaxys

Last Modified

08 January 2015