Interesting facts
Interesting Facts about (2S)-azetidine-2-carboxylic acid
(2S)-azetidine-2-carboxylic acid, commonly referred to as proline, is a fascinating amino acid characterized by its unique cyclic structure. Here are some intriguing points about this compound:
- Structural Uniqueness: Unlike most amino acids, which have a linear structure, proline features a five-membered ring. This cyclic nature contributes to its unique properties and role in protein structure.
- Biological Importance: Proline plays a critical role in protein synthesis and is vital for the stability of collagen, a key protein in connective tissues. Its presence in proteins influences their folding and overall stability.
- Metabolic Pathway: Proline can be synthesized in the human body from another amino acid, glutamate, which highlights its significance in metabolism. It can also be converted into other derivatives used in various biological processes.
- Role in Plant Physiology: In plants, proline accumulates as a response to stress conditions, such as drought and salinity. It acts as an osmoprotectant, helping to stabilize proteins and cell structures under extreme conditions.
- Health Benefits: Some studies suggest that proline may have potential health benefits, including wound healing and immune support. It also serves as a precursor for the synthesis of neurotransmitters.
As a scientist or chemistry student, understanding the multifaceted role of (2S)-azetidine-2-carboxylic acid in biological systems can deepen one’s appreciation for the complexity of life at the molecular level. Its unique structure and diverse functions underscore the beauty of biochemical pathways and the intricate relationships within living organisms.
Synonyms
(S)-Azetidine-2-carboxylic acid
(2S)-azetidine-2-carboxylic acid
(S)-2-Azetidinecarboxylic acid
2-Azetidinecarboxylic acid, (S)-
2-Azetidinecarboxylic acid, (2S)-
CHEBI:6198
(S)-(-)-2-azetidine carboxylic acid
218-362-5
2133-34-8
L-Azetidine-2-carboxylic acid
(S)-(-)-2-Azetidinecarboxylic acid
Azetidyl-2-carboxylic acid
(S)-(-)-Azetidine-2-carboxylic acid
L-Azetidine 2-carboxylic acid
Azetidine-2-carboxylic acid, L-
(L)-AZETIDINE-2-CARBOXYLIC ACID
Azetidinecarboxylic acid
2-Azetidinecarboxylic acid, L-
(S)-L-Azetidine-2-carboxylic acid
MFCD00005166
5GZ3E0L9ZU
L-2-Azetidinecarboxylic acid
Acide L-azetidine-2-carboxylic
CHEMBL1165239
L-azetidine-2-carboxylate
C4H7NO2
azetidine-2-carboxylate
(S)-Azetidine-2-carboxylicacid
(2s)-2-azetidinecarboxylic acid
HSDB 3465
(2S)azetidine-2-carboxylic acid
AzeOH
(2S)-(-)-Azetidine-2-carboxylic acid
02A
(S)-2-Azetidinecarboxylic acid;H-Aze-OH
EINECS 218-362-5
L-AzeOH
L-Trimethyleneimine-2-carboxylic Acid
(S)-(-) Azetidine-2-carboxylic acid
Acide L-azetidine-2-carboxylic [French]
ST059592
H-Aze(2)-OH
UNII-5GZ3E0L9ZU
L-azetidine-2caboxylic acid
(S)-Azetidin-2-carbonsaure
L-azetidine-2carboxylic acid
Lopac0_000023
SCHEMBL20296
(S)-2-azetidinecarboxyic acid
GTPL4686
2-(S)-azetidinecarboxylic acid
azetidine-2(S)-carboxylic acid
L--Azetidine-2-carboxylic acid
DTXSID0044020
(S)-2-azetidine carboxylic acid
azetidine-2-(S)-carboxylic acid
HMS3260E07
Tox21_500023
(-)-AZETIDINECARBOXYLIC ACID
BDBM50357225
AKOS005254687
AKOS006239010
(S)-(-)-2-azetidine-carboxylic acid
AC-5699
CCG-204119
FA14215
HY-W050044
LP00023
SDCCGSBI-0050012.P002
L-Azetidine-2-carboxylic acid, >=99%
NCGC00093546-01
NCGC00093546-02
NCGC00093546-03
NCGC00093546-04
NCGC00260708-01
DS-16309
AZETIDYL-2-CARBOXYLIC ACID [HSDB]
A1043
CS-0031389
EU-0100023
NS00048671
EN300-85821
A 0760
C08267
AN-584/43509810
Q793715
SR-01000075656
SR-01000075656-1
L-Azetidine-2-carboxylic acid is known as a proline analog.
Solubility of (2S)-azetidine-2-carboxylic acid
(2S)-azetidine-2-carboxylic acid, a cyclic amino acid, exhibits specific solubility characteristics that are of notable interest in chemical and biological contexts. This compound is generally considered to be soluble in polar solvents such as water and methanol, which is facilitated by its carboxylic acid functional group. The solubility behavior can be summarized as follows:
To summarize, the solubility of (2S)-azetidine-2-carboxylic acid is strongly influenced by the solvent's polarity, providing essential insights into its behavior in various chemical environments. As a general rule, “like dissolves like”—the more polar the solvent, the better the solubility of this compound tends to be.