CHEBI:136680 - β-guanidino-L-alanine

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ChEBI Name β-guanidino-L-alanine
ChEBI ID CHEBI:136680
ChEBI ASCII Name beta-guanidino-L-alanine
Definition A L-alanine derivative in which one of the methyl hydrogens of L-alanine has been replaced by a guanidino group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C4H10N4O2
Net Charge 0
Average Mass 146.148
Monoisotopic Mass 146.08038
InChI InChI=1S/C4H10N4O2/c5-2(3(9)10)1-8-4(6)7/h2H,1,5H2,(H,9,10)(H4,6,7,8)/t2-/m0/s1
InChIKey XNBJHKABANTVCP-REOHCLBHSA-N
SMILES OC(=O)[C@@H](N)CNC(N)=N
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): Brassica napus metabolite
Any plant metabolite that is produced by rapeseed (Brassica napus).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-guanidino-L-alanine (CHEBI:136680) has role Brassica napus metabolite (CHEBI:140165)
β-guanidino-L-alanine (CHEBI:136680) is a L-alanine derivative (CHEBI:83943)
β-guanidino-L-alanine (CHEBI:136680) is a guanidines (CHEBI:24436)
β-guanidino-L-alanine (CHEBI:136680) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
IUPAC Name
3-carbamimidamido-L-alanine
Synonyms Sources
3-((Aminoiminomethyl)amino)-L-alanine ChemIDplus
3-guanidino-L-alanine ChEBI
dinor-L-arginine ChEBI
L-2-amino-3-guanidinopropionic acid ChEBI
L-α-amino-β-guanidinopropionic acid ChEBI
Registry Numbers Types Sources
14191-91-4 CAS Registry Number ChemIDplus
2413421 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
22869115 PubMed citation Europe PMC
23434137 PubMed citation Europe PMC
237904 PubMed citation Europe PMC
6520174 PubMed citation Europe PMC
IND92015176 Agricola citation Europe PMC
Last Modified
16 February 2018