Interesting facts
Interesting Facts about Pyrrolidine-2-Carboxylic Acid
Pyrrolidine-2-carboxylic acid, often referred to as proline, is an intriguing compound with significant roles in both chemistry and biology. This amino acid is notable not only for its structural features but also for its diverse applications:
- Biological Importance: Proline is classified as a non-essential amino acid, which means that the human body can synthesize it. It plays a key role in protein synthesis and is crucial for the respiration process in cells.
- Structural Role: The cyclic structure of pyrrolidine allows it to adopt unique conformations, making it an important element in the stability and function of proteins. Proline often introduces bends and turns in protein structures, impacting their overall three-dimensional conformation.
- Medical Applications: Proline has garnered attention in the field of medicine. Its derivatives are studied for their potential antiviral activities and may support the healing of wounds through their roles in collagen synthesis.
- Conditions for Synthesis: In laboratory settings, the synthesis of pyrrolidine-2-carboxylic acid can be achieved through various methods, including ring-opening reactions and the Strecker synthesis, showcasing the compound's versatility in organic chemistry.
- Food Industry Use: This compound is also found in some food products, contributing to flavors and serving as a flavor enhancer, showcasing the connection between chemistry and culinary practices.
"To understand the chemistry of life, one must study the building blocks," and pyrrolidine-2-carboxylic acid is undoubtedly one of them. With its unique properties and functional roles, it remains a focus of excitement for both chemical and biological research.
In addition, proline's engaging structure makes it a favorite subject of study for students and researchers alike, driving deeper inquiry into the fascinating world of amino acids and proteins.
Synonyms
DL-Proline
609-36-9
pyrrolidine-2-carboxylic acid
H-DL-Pro-OH
Proline, DL-
Proline DL-form
D-Pyrrolidine-2-carboxylic acid
MFCD00005250
2-Pyrrolidine carboxylic acid
Prolin
Hpro
UNII-DCS9E77JPQ
DCS9E77JPQ
(+/-)-Pyrrolidine-2-carboxylic acid
CCRIS 8602
25191-13-3
(+/-)-proline
NSC97923
EINECS 210-189-3
NSC 97923
NSC-97923
PROLINE DL-FORM [MI]
DTXSID9041104
2-PYRROLIDINYLCARBOXYLIC ACID
NSC46703
DL proline
D,L-proline
d,1-proline
Proline #
10-proline
CCCu
DL-Proline,(S)
PROLINE,(L)
SCHEMBL2939
7005-20-1
L-Proline, non-animal origin
CHEMBL72275
DL-2-Pyrrolidinecarboxylic acid
DTXCID7021104
CHEBI:26271
DL-Pyrrolidine-2-carboxylic acid
BCP26673
2-Pyrralidinecarboxylic acid, (S)-
Tox21_110042
BDBM50000105
DL-Proline, ReagentPlus(R), 99%
STK410971
(R,S)-Pyrrolidine-2-carboxylic acid
AKOS000119715
AKOS016182584
AB02582
AB87033
CS-W013624
FP15447
HY-W012908
NCGC00014017-01
NCGC00166223-01
NCGC00166223-02
AC-24084
AS-10782
BP-13283
CAS-609-36-9
NCI60_042190
SY001305
SY001352
SY006205
DB-053748
DL-Proline, Vetec(TM) reagent grade, 98%
NS00014010
P0480
EN300-20112
M02942
SBI-0053882.0001
D-(+)-Proline; D-Pyrrolidine-2-carboxylic acid
Q484583
AD91343D-BC4F-4A8C-AC31-D9888F4607B8
F3157-0002
Z104476886
210-189-3
2PC
Solubility of Pyrrolidine-2-carboxylic Acid
Pyrrolidine-2-carboxylic acid, with the chemical formula C5H9NO2, is known for its interesting solubility properties.
Key Features of Solubility
The solubility characteristics make pyrrolidine-2-carboxylic acid an interesting compound for various applications, especially in biological and chemical research. Overall, its solubility in a range of solvents is a notable aspect to consider in experimental settings.