Interesting facts
Interesting Facts about 2,6-Diaminoheptanedioic Acid
2,6-Diaminoheptanedioic acid, also known as homospermidine, is a fascinating compound with a variety of applications and significance in the world of biochemistry and pharmaceuticals. Here are some intriguing insights:
- Composition and Structure: This compound features two amino groups (–NH2) located at the 2nd and 6th positions of a heptanedioic acid structure, making it a crucial player in various biochemical pathways.
- Biological Role: As a polyamine derivative, 2,6-diaminoheptanedioic acid plays an essential role in cellular growth, differentiation, and function. It is involved in the biosynthesis of important biomolecules.
- Medical Applications: Research has shown that compounds structurally related to 2,6-diaminoheptanedioic acid may have potential therapeutic applications, especially in addressing certain neurological disorders.
- Research Interest: The study of homospermidine has attracted attention in the fields of cancer research and regenerative medicine due to its properties that promote cell proliferation and survival.
- Genetic Engineering: In the context of genetic engineering, this compound can be utilized in developing new methods for gene delivery, revealing its importance in modern biotechnology.
In conclusion, 2,6-diaminoheptanedioic acid is more than just a chemical formula; it represents a bridge between chemistry and biological sciences, offering insights into cell biology and potential therapeutic strategies. As research advances, compounds like this may lead to impactful discoveries in both medicine and biotechnology.
Synonyms
2,6-Diaminopimelic acid
583-93-7
2,6-Diaminoheptanedioic acid
Heptanedioic acid, 2,6-diamino-
DIAMINOPIMELIC ACID
MFCD00002637
dl-2,6-Diaminoheptanedioic acid
M-DAP
EINECS 209-524-6
NSC 45225
CHEBI:23673
meso-A2pm
(2R,6S)-rel-2,6-Diaminoheptanedioic acid
DL-2,6-Diaminopimelic acid
ll-diaminopimelate
D,L-diaminopimelate
DL-alpha,epsilon-Diaminopimelic acid
LL-A2pm
1,5-Diaminoheptanedioic Acid
a,a'-Diaminopimelic acid
D,L-meso-diaminoheptanedioate
L,L-A2pm
D,L-DAP
L,L-DAP
meso-1-alpha,epsilon-diaminopimelate
NSC-45225
NSC-206278
NSC-206289
Acid, Diaminopimelic
2,6diaminopimelic acid
starbld0009699
2,6 Diaminopimelic Acid
bmse000401
Acid, 2,6-Diaminopimelic
2,6Diaminoheptanedioic acid
SCHEMBL29289
Heptanedioic acid,6-diamino-
D1377_SIGMA
Heptanedioic acid, 2,6diamino
2,6-Diaminoheptanedioic acid #
alpha,epsilon-diaminopimelic acid
alpha, epsilonDiaminopimelic acid
DTXSID10862237
(+/-)-2,6-Diaminopimelic acid
ALBB-025755
NSC45225
PAA28934
NSC206278
NSC206289
STL377919
AKOS005256777
MS-20162
PD025037
(2R,6R)-rel-2,6-Diaminoheptanedioic acid
2,6-Diaminopimelic acid, >=98% (TLC)
HY-128746
2,6-Diaminopimelic acid, >=97.0% (NT)
CS-0102540
D0112
NS00015080
D89595
Q30126674
A9A6073C-7593-463C-B690-B39C960915E7
209-524-6
629-070-6
Solubility of 2,6-Diaminoheptanedioic Acid
2,6-Diaminoheptanedioic acid, with the chemical formula C7H14N2O4, exhibits interesting solubility characteristics that are influenced by its molecular structure and functional groups. Here are some key points to consider:
In conclusion, the solubility of 2,6-diaminoheptanedioic acid can be described as good in water, primarily due to the presence of functional groups that favor strong solute-solvent interactions. This makes it a versatile compound for various applications in biochemical contexts.