Interesting facts
Interesting Facts About 2-(4-Aminobutyl)guanidine
2-(4-aminobutyl)guanidine is an intriguing compound that plays a significant role in various biological and chemical processes. Here are some fascinating insights into this molecule:
- Biological Relevance: This compound is known for its potential as a nitric oxide (NO) donor. Nitric oxide itself is a signaling molecule with crucial roles in cardiovascular health, neuronal function, and immune response.
- Applications in Research: Researchers are exploring its use in pharmacological studies, particularly in developing treatments for conditions related to vasodilation and inflammation.
- Structure and Function: The presence of an amino group in its structure suggests that the compound may interact with biological systems in ways similar to amino acids, potentially influencing protein behavior.
- Historical Uses: Compounds with similar structural motifs have been utilized in various therapeutic applications, showcasing the importance of molecular structure in dictating biological activity.
As a compound that bridges chemistry and biology, 2-(4-aminobutyl)guanidine exemplifies how a simple change in molecular structure can lead to significant effects in living organisms. Scientists continue to unravel its complexities, positioning it as a potentially valuable tool in medicinal chemistry and pharmacotherapy.
Synonyms
agmatine
1-(4-Aminobutyl)guanidine
306-60-5
(4-Aminobutyl)guanidine
Argmatine
1-Amino-4-guanidobutane
N-(4-aminobutyl)guanidine
N-4-Aminobutylguanidine
guanidine, (4-aminobutyl)-
2-(4-aminobutyl)guanidine
(4-Aminobutyl) guanidine
1,4-Butanediamine, N-(aminoiminomethyl)-
agmatinium
4-Guanidino-1-butanamine
1-Amino-4-guanidinobutane
EINECS 206-187-7
NSC 56332
UNII-70J407ZL5Q
CHEBI:17431
70J407ZL5Q
AGMATINE [MI]
(4-aminobutyl)-Guanidine
NSC-56332
AGMATINE [WHO-DD]
CHEMBL58343
AGMATINE SULFATE ENDOGENOUS AGONIST AT
DTXSID0040961
N-(aminoiminomethyl)-1,4-Butanediamine
AG2
Guanidine, (4-aminobutyl)- (8CI)(9CI)
1 Amino 4 guanidinobutane
.Agmatin
Spectrum_001656
Tocris-0842
SpecPlus_000500
Spectrum2_001608
Spectrum4_001905
Spectrum5_000590
Lopac-A-7127
bmse000063
bmse000812
bmse000936
1, N-(aminoiminomethyl)-
Lopac0_000060
SCHEMBL19647
US8633208, Agmatine
KBioGR_002496
KBioGR_002550
KBioSS_002136
KBioSS_002559
DivK1c_006596
SPBio_001615
CS-WAA0304
GTPL4127
DTXCID8020961
BDBM85213
KBio1_001540
KBio2_002136
KBio2_002550
KBio2_004704
KBio2_005118
KBio2_007272
KBio2_007686
KBio3_003028
NSC_199
cMAP_000079
Guanidine, (4-aminobutyl)-(8CI)
NSC56332
AKOS006230062
AKOS015894488
CCG-204155
DB08838
SDCCGMLS-0066765.P001
SDCCGSBI-0050048.P003
NCGC00015083-01
NCGC00015083-02
NCGC00015083-03
NCGC00015083-04
NCGC00015083-05
NCGC00015083-06
NCGC00015083-10
NCGC00024820-01
NCGC00024820-02
NCGC00024820-03
NCGC00024820-04
CAS_306-60-5
Guanidine, (4-aminobutyl)-(8CI)(9CI)
DB-068320
NS00000073
C00179
EN300-150993
Q394317
BRD-K49738308-065-04-9
C4D19DE1-F243-434B-9E72-720B42C5AD40
Solubility of 2-(4-aminobutyl)guanidine
2-(4-aminobutyl)guanidine, with the chemical formula C5H14N4, exhibits noteworthy solubility characteristics that are essential to understanding its behavior in various chemical environments.
This compound is primarily soluble in water due to its ability to form hydrogen bonds, thanks to the amino groups present in its structure. Here are some key points to consider:
In practical applications, understanding the solubility of this compound is crucial for its use in fields such as biochemistry and pharmaceuticals. To summarize:
As a result, the solubility profile of 2-(4-aminobutyl)guanidine makes it a versatile compound in both laboratory and industrial settings.