Interesting facts
Interesting Facts about (2S)-2-amino-6-guanidino-hexanoic acid
(2S)-2-amino-6-guanidino-hexanoic acid, commonly known as arginine, is an essential amino acid that plays a crucial role in many biochemical processes. Here are some compelling aspects of this remarkable compound:
- Biological Importance: Arginine is a precursor to nitric oxide, a vital signaling molecule involved in regulating blood flow, thus impacting cardiovascular health.
- Protein Synthesis: As one of the building blocks of proteins, arginine is integral in various physiological functions, aiding in muscle growth and repair.
- Wound Healing: Studies have shown that arginine may enhance healing processes by promoting collagen formation, crucial for skin and tissue repair.
- Immune Function: This amino acid plays a crucial role in immune response, supporting the activity of T-cells, which are essential for fighting infections.
- Hormonal Regulation: Arginine stimulates the release of growth hormone and insulin, highlighting its role in metabolism and endocrine functions.
As a nutrient, arginine is commonly found in foods such as:
- Meats
- Dairy products
- Nuts and seeds
- Legumes
Furthermore, arginine's ability to generate nitric oxide has led to its exploration in various therapeutic applications, including:
- Atherosclerosis treatment
- Erectile dysfunction management
- Improving exercise performance
As a fascinating compound, (2S)-2-amino-6-guanidino-hexanoic acid continues to be a subject of extensive research, underscoring its significant biological and medical relevance in the field of biochemistry.
Synonyms
L-Homoarginine
homoarginine
156-86-5
H-HoArg-OH
homo-l-arginine
H-HomoArg-OH
n6-amidino-lysine
L-N(sup 6)-Amidinolysine
N6-amidino-L-Lysine
N6-(Aminoiminomethyl)-L-lysine
L-Lysine, N(sup 6)-(aminoiminomethyl)-
L-Lysine, N6-(aminoiminomethyl)-
NSC 27429
LYSINE, N(sup 6)-AMIDINO-, L-
CHEBI:27747
(2S)-2-amino-6-(diaminomethylideneamino)hexanoic acid
L-N(6)-amidinolysine
L-Lysine, N(6)-(aminoiminomethyl)-
(S)-2-Amino-6-guanidinohexanoic acid
CHEMBL589752
JF751CK38I
DTXSID70926980
Homoarginine, L-
N6-carbamimidoyl-L-lysine
UNII-JF751CK38I
LHomoarginine
h-Homoarginine
MFCD00237108
NSC-27429
NSC-88868
HRG
L-HomoArg-OH
LN(sup 6)Amidinolysine
bmse000745
SCHEMBL43287
LYSINE, N6-AMIDINO-
N(6)-carbamimidoyl-L-lysine
N~6~-carbamimidoyl-L-lysine
Lysine, N(sup 6)amidino, L
LLysine, N6(aminoiminomethyl)
SCHEMBL21802133
DTXCID001355785
LYSINE, N6-AMIDINO-, L-
AC2507
BDBM50309588
s6109
LLysine, N(sup 6)(aminoiminomethyl)
AKOS006282043
AKOS015894481
LLysine, N6(aminoiminomethyl) (9CI)
CS-W008385
DB03974
HY-W008385
13094-78-5
DS-15039
L-Lysine, N6-(aminoiminomethyl)- (9CI)
(2S)-2-amino-6-carbamimidamidohexanoic acid
NS00068514
C01924
(S)-2-Amino-6-guanidinohexanoic acid (H-L-hArg-OH)
Q57828472
Solubility of (2S)-2-amino-6-guanidino-hexanoic acid
(2S)-2-amino-6-guanidino-hexanoic acid, commonly known as L-arginine, exhibits notable solubility characteristics essential for its biochemical interactions. The solubility of this compound can be summarized as follows:
The polar functionality of the guanidino group and amino groups in the structure leads to strong hydrogen bonding with water, enhancing solubility. Overall, the solubility of (2S)-2-amino-6-guanidino-hexanoic acid is a critical factor that underpins its biological functions, especially in metabolic pathways and nitrogen metabolism.