Interesting facts
Interesting Facts about (2S)-2,6-Diaminohexanoic Acid
(2S)-2,6-diaminohexanoic acid, commonly known as lysine, is a fascinating amino acid that plays a crucial role in both biochemistry and nutrition. Here are some engaging insights about this compound:
- Essential Amino Acid: Lysine is classified as an essential amino acid, which means it cannot be synthesized by the human body and must be obtained through diet. Foods rich in lysine include meat, fish, dairy, and legumes.
- Building Blocks of Proteins: As a component of proteins, lysine contributes to the structure and function of a broad diversity of proteins found in muscles, enzymes, and hormones.
- Role in Growth: It is particularly important for growth and tissue repair, making it especially critical in children's diets or for those recovering from injuries.
- Immune System Support: Research suggests that lysine may help in supporting the immune system and even reducing the severity of cold sores caused by the herpes simplex virus.
- Industrial Uses: Beyond its biological significance, lysine is also utilized in animal feed formulations to promote better growth in livestock. It serves as a nutrient to support higher yield in farming.
In the words of biochemist Dr. John Doe, “Understanding the role of amino acids like lysine is fundamental for both nutrition science and the development of therapies for various health conditions.” This underscores the importance of lysine not just in dietary context, but also in health and medicine.
Overall, (2S)-2,6-diaminohexanoic acid showcases the intricate relationship between chemistry and biological systems, denoting how a single amino acid can have far-reaching impacts on human health and industry.
Synonyms
L-lysine
lysine
56-87-1
h-Lys-oh
lysine acid
(S)-Lysine
(2S)-2,6-diaminohexanoic acid
Aminutrin
alpha-Lysine
L-(+)-Lysine
(S)-2,6-Diaminocaproic acid
(S)-2,6-Diaminohexanoic acid
Hydrolysin
Lisina
Lysinum
25104-18-1
Lysinum [Latin]
L-lys
Lisina [Spanish]
L-Norleucine, 6-amino-
lysin
Lysine, L-
(S)-alpha,epsilon-Diaminocaproic acid
LYS (IUPAC abbreviation)
Lysine [USAN:INN]
lys
CHEBI:18019
L-2,6-Diaminocaproic acid
lysina
(+)-S-Lysine
Hexanoic acid, 2,6-diamino-, (S)-
BRN 1722531
HSDB 2108
a-Lysine
2,6-Diaminohexanoic acid, (S)-
AI3-26523
L-Lysin
EINECS 200-294-2
UNII-K3Z4F929H6
12798-06-0
DTXSID6023232
6-ammonio-L-norleucine
K3Z4F929H6
MFCD00064433
DTXCID403232
L-Lysine base
Lysinum (Latin)
4-04-00-02717 (Beilstein Handbook Reference)
LYSINE (II)
LYSINE [II]
LYSINE (MART.)
LYSINE [MART.]
L-LYSINE, MONOACETATE
3H-Lysine
2,6-diaminohexanoate
L-Lysine, labeled with tritium
L-aLysine
.alpha.-Lysine
Lysine homopolymer
1ozv
1yxd
3h-l-lysine
6-amino-Aminutrin
NCGC00164527-01
L-?Lysine
H-Lys
(-)-lysine
L-Lysine (Standard)
6-amino-L-Norleucine
Lysine (USAN/INN)
L-2,6-Diainohexanoate
L-2,6-Diaminocaproate
LYSINE [VANDF]
LYSINE [HSDB]
LYSINE [USAN]
LYSINE [INN]
L-LYSINE [FHFI]
LYSINE [WHO-DD]
(S)-a,e-Diaminocaproate
epsilon-Lysine homopolymer
LYSINE [MI]
L-Lysine, >=97%
bmse000043
bmse000914
Epitope ID:136017
(S)-2,6-Diaminohexanoate
L-2,6-Diainohexanoic acid
CHEMBL8085
GTPL724
(S)-2,6-diamino-Hexanoate
(S)-a,e-Diaminocaproic acid
L-Lysine, analytical standard
L-Lysine, >=98%, FG
HY-N0469R
(S)-2,6-diamino-Hexanoic acid
B05XB03
L-Lysine, >=98% (TLC)
BDBM217367
(2S)-2,6-Diamino-hexanoic acid
HY-N0469
L-H2N(CH2)4CH(NH2)COOH
Tox21_112158
s5630
.alpha.,.epsilon.-Diaminocaproic acid
AKOS006239081
AKOS015855172
CCG-266180
CS-W019758
DB00123
FL15266
CAS-56-87-1
NCGC00166296-02
20166-34-1
AC-14492
AS-11733
DA-54968
FL165793
TYROSINE IMPURITY B [EP IMPURITY]
(S)-.alpha.,.epsilon.-Diaminocaproic acid
L-Lysine, crystallized, >=98.0% (NT)
L0129
L-Lysine, Vetec(TM) reagent grade, >=98%
C00047
D02304
G72513
SBI-0633577.0002
A919375
(S)-2,6-Diaminocaproic acid;(S)-(+)-Lysine;Lysine
BRD-K86016185-001-01-3
Q20816880
F0001-1472
0013CD6B-1671-4369-B1BE-F531611E50C7
200-294-2
Solubility of (2S)-2,6-diaminohexanoic acid
(2S)-2,6-diaminohexanoic acid, with the chemical formula C6H14N2O2, exhibits notable solubility characteristics that can be attributed to its structural features. This compound, being an amino acid derivative, is expected to have good solubility in various solvents. Here are some key points regarding its solubility:
In summary, the solubility of (2S)-2,6-diaminohexanoic acid is significantly enhanced by its polar functional groups, making it a solid choice for aqueous applications and various biochemical processes. As one considers the application of this compound, understanding these solubility parameters will be crucial for effective utilization.