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Details

Stereochemistry ACHIRAL
Molecular Formula C5H11N3O2
Molecular Weight 145.1597
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-GUANIDINOBUTYRIC ACID

SMILES

NC(=N)NCCCC(O)=O

InChI

InChIKey=TUHVEAJXIMEOSA-UHFFFAOYSA-N
InChI=1S/C5H11N3O2/c6-5(7)8-3-1-2-4(9)10/h1-3H2,(H,9,10)(H4,6,7,8)

HIDE SMILES / InChI

Molecular Formula C5H11N3O2
Molecular Weight 145.1597
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Guanidino compounds as cause of cardiovascular damage in chronic kidney disease: an in vitro evaluation.
2010
The orally active antihyperglycemic drug beta-guanidinopropionic acid is transported by the human proton-coupled amino acid transporter hPAT1.
2009-04-11
Detection of an L-amino acid dehydrogenase activity in Synechocystis sp. PCC 6803.
2009
Neurotransmitter alterations in embryonic succinate semialdehyde dehydrogenase (SSADH) deficiency suggest a heightened excitatory state during development.
2008-11-28
Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803.
2007-11-28
Anisoin: a useful pre-chromatographic derivatization fluorogenic reagent for LC analysis of guanidino compounds.
2006-09-11
Biodegradability of end-groups of the biocide polyhexamethylene biguanide (PHMB) assessed using model compounds.
2006-08
Increased guanidino species in murine and human succinate semialdehyde dehydrogenase (SSADH) deficiency.
2006-04
On the role of arginine-glutamic acid ion pair in the ATP hydrolysis.
2006-01-01
Pseudomonas aeruginosa PAO1 genes for 3-guanidinopropionate and 4-guanidinobutyrate utilization may be derived from a common ancestor.
2005-12
Influence of 4-guanidinobutyric acid as coadsorbent in reducing recombination in dye-sensitized solar cells.
2005-11-24
A role for guanidino compounds in the brain.
2003-02
Dehydration modifies guanidino compound concentrations in the different zones of the rat kidney.
2002-05
The effect of high protein diet on urea and guanidino compound levels in renal insufficient mice.
2001-12
Long-term effect of partial nephrectomy on biological parameters, kidney histology, and guanidino compound levels in mice.
2001-12
Influence of 72% injury in one kidney on several organs involved in guanidino compound metabolism: a time course study.
2001-07
Transport and metabolism of agmatine in rat hepatocyte cultures.
2001-02
Guanidino compounds in serum and urine of cirrhotic patients.
1995-05
Guanidino compounds in hyperargininemia.
1987-11
Guanidino compounds in serum and cerebrospinal fluid of non-dialyzed patients with renal insufficiency.
1987-07-30
Guanidino compounds in plasma, urine and cerebrospinal fluid of hyperargininemic patients during therapy.
1985-02-28
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:17:00 GMT 2025
Edited
by admin
on Mon Mar 31 19:17:00 GMT 2025
Record UNII
15ADP48O8Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-GUANIDINOBUTYRIC ACID
Systematic Name English
HL 6450
Preferred Name English
BUTANOIC ACID, 4-((AMINOIMINOMETHYL)AMINO)-
Common Name English
NSC-521717
Code English
N-(4-BUTANOIC ACID)GUANIDINE
Common Name English
.GAMMA.-GUANIDINEBUTYRIC ACID
Common Name English
.GAMMA.-GUANIDINOBUTYRATE
Systematic Name English
Code System Code Type Description
FDA UNII
15ADP48O8Q
Created by admin on Mon Mar 31 19:17:00 GMT 2025 , Edited by admin on Mon Mar 31 19:17:00 GMT 2025
PRIMARY
PUBCHEM
500
Created by admin on Mon Mar 31 19:17:00 GMT 2025 , Edited by admin on Mon Mar 31 19:17:00 GMT 2025
PRIMARY
CAS
463-00-3
Created by admin on Mon Mar 31 19:17:00 GMT 2025 , Edited by admin on Mon Mar 31 19:17:00 GMT 2025
PRIMARY
CHEBI
15728
Created by admin on Mon Mar 31 19:17:00 GMT 2025 , Edited by admin on Mon Mar 31 19:17:00 GMT 2025
PRIMARY
MESH
C001317
Created by admin on Mon Mar 31 19:17:00 GMT 2025 , Edited by admin on Mon Mar 31 19:17:00 GMT 2025
PRIMARY
EPA CompTox
DTXSID50196785
Created by admin on Mon Mar 31 19:17:00 GMT 2025 , Edited by admin on Mon Mar 31 19:17:00 GMT 2025
PRIMARY
NSC
521717
Created by admin on Mon Mar 31 19:17:00 GMT 2025 , Edited by admin on Mon Mar 31 19:17:00 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-331-1
Created by admin on Mon Mar 31 19:17:00 GMT 2025 , Edited by admin on Mon Mar 31 19:17:00 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT