Interesting facts
Interesting Facts about 2-(2-Sulfanylpropanoylamino)acetic acid
2-(2-Sulfanylpropanoylamino)acetic acid, often referred to in the context of its intriguing properties and applications, is a compound that showcases the intricate intersection of biochemistry and synthetic chemistry. Here are some engaging aspects of this remarkable compound:
- Biological Significance: This compound can play crucial roles in various biological systems, particularly in relation to sulfur amino acids, which are vital for protein synthesis and metabolic processes.
- Research Applications: Due to its unique structure, it has potential applications in medicinal chemistry, where it may serve as a lead compound for developing new pharmaceuticals.
- Functional Groups: The presence of both amine and carboxylic acid functional groups makes this compound a prime candidate for interesting reactivity and the formation of various derivatives.
- Peptide Synthesis: Being an amino acid derivative, it can be used in peptide synthesis, which is crucial for developing biomolecules with potential therapeutic effects.
- Sulfur Chemistry: The inclusion of sulfur in its structure opens up avenues for research into this element's unique properties, especially in the context of enzyme catalysis and redox reactions.
In the words of famous chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This compound embodies the spirit of innovative thinking and encourages exploration of new chemical landscapes. Its diverse properties and potential functionalities make it an intriguing topic for both students and professionals in the field of chemistry.
Synonyms
tiopronin
1953-02-2
N-(2-Mercaptopropionyl)glycine
Acadione
Thiopronine
Captimer
Mucolysin
Tiopronine
Capen
Thiopronin
Epatiol
Thiola
Sutilan
Thiosol
Glycine, N-(2-mercapto-1-oxopropyl)-
Thiolpropionamidoacetic acid
Tioglis
Vincol
2-(2-sulfanylpropanoylamino)acetic acid
Tiopronin (Thiola)
Meprin (detoxicant)
N-(2-Mercapto-1-oxopropyl)glycine
tiopronina
Tiopronino
Tioproninum
(2-Mercaptopropionyl)glycine
NSC-760416
C5W04GO61S
CCRIS 1935
DTXSID4023678
THIOLA EC
EINECS 217-778-4
Tiopronine [INN-French]
Tioproninum [INN-Latin]
2-(2-sulfanylpropanamido)acetic acid
2-(2-Mercaptopropanamido)acetic acid
Tiopronino [INN-Spanish]
BRN 1859822
CHEMBL1314
UNII-C5W04GO61S
alpha-mercaptopropionyl glycine
GLYCINE, N-(2-MERCAPTOPROPIONYL)-
DTXCID803678
N-(2-mercaptopropanoyl)glycine
MERCAPTOPROPIONYLGLYCINE-
CHEBI:32229
NSC 760416
NCGC00159422-02
NCGC00159422-04
Tiopronine (INN-French)
Tioproninum (INN-Latin)
Tiopronino (INN-Spanish)
TIOPRONIN (MART.)
TIOPRONIN [MART.]
Glycine, N-(2-mercapto-1-oxopropyl)- (9CI)
alpha-Mercaptopropionylglycine
CAS-1953-02-2
A-MERCAPTOPROPIONYL GLYCINE
Tiopronin; 2-(2-Sulfanylpropanoylamino)acetic acid
2 Mercaptopropionylglycine
2-Mercaptopropionylglycine
Tiopronin [INN:DCF:JAN]
alpha Mercaptopropionylglycine
2 Thiolpropionamidoacetic Acid
2-Thiolpropionamidoacetic Acid
Tiopronin Base
Acid, 2-Thiolpropionamidoacetic
2 Thiol propionamido acetic Acid
2-Thiol-propionamido-acetic Acid
Acid, 2-Thiol-propionamido-acetic
(S)-2-(2-Mercaptopropanamido)acetic Acid
MFCD00004861
Thiola (TN)
Tiopronin (JAN/INN)
TIOPRONIN [INN]
TIOPRONIN [JAN]
TIOPRONIN [MI]
TIOPRONIN [VANDF]
2-mercapto-propionylglycine
TIOPRONIN [WHO-DD]
(2-mercaptopropanoyl)glycine
SCHEMBL19989
MLS006010632
N-(2-Sulfanylpropanoyl)glycine
TIOPRONIN [ORANGE BOOK]
n-(2-mercaptopropionyl) glycine
N-(2-mercaptopropanoyl) glycine
G04BX16
Acadione; Capen; Epatiol; Vincol
(+)-(2-Mercaptopropanoyl)glycine
(-)-(2-Mercaptopropanoyl)glycine
HMS3264B11
HMS3655L15
Pharmakon1600-01506190
BCP13354
HY-B0373
2-(2-Mercaptopropanamido)aceticacid
Tox21_111654
BDBM50020805
MFCD30157366
NSC760416
s2062
(2-Mercaptopropionylamino)acetic acid
AKOS015895408
N-(2-Mercaptopropionyl)glycine, 99%
Tox21_111654_1
AC-2087
CCG-214007
DB06823
FM28287
(2-Mercapto-propionylamino)-acetic acid
NCGC00159422-03
AS-12522
SMR001550282
SY262996
DB-352240
NS00005173
SW219206-1
T2614
Tiopronin, VETRANAL(TM), analytical standard
C73708
D01430
SBI-0653504.0001
AB00376096_02
EN300-7408657
Q414456
SR-01000942263
SR-01000942263-1
BRD-A85295731-001-02-3
BRD-A85295731-001-03-1
BRD-A85295731-001-04-9
BRD-A85295731-001-05-6
BRD-A85295731-001-06-4
Z2681891170
N-(2-Mercaptopropionyl)glycine;alpha-Mercaptopropionyl glycine
TIOPRONIN, Dextiopronin, Tiopronin (n-2-mercaptopropionyl glycine)
1939-02-2
217-778-4
2254742-22-6
2254742-23-7
Solubility of 2-(2-sulfanylpropanoylamino)acetic acid
The compound 2-(2-sulfanylpropanoylamino)acetic acid, with the formula C3H7NO2S, exhibits unique solubility properties that are influenced by its molecular structure. Understanding its solubility is essential for applications in pharmacology and biochemistry.
In general, the solubility of this compound can be characterized as follows:
However, solubility can also be affected by various factors:
In conclusion, while 2-(2-sulfanylpropanoylamino)acetic acid is predicted to have reasonable solubility in polar solvents, specific conditions such as temperature and pH must be considered for optimal solubility outcomes.