Skip to main content

Kynurenine

ADVERTISEMENT
Identification
Molecular formula
C10H12N2O3
CAS number
343-65-7
IUPAC name
2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid
State
State

Under standard conditions, kynurenine is found as a solid.

Melting point (Celsius)
232.00
Melting point (Kelvin)
505.15
Boiling point (Celsius)
337.80
Boiling point (Kelvin)
610.95
General information
Molecular weight
208.21g/mol
Molar mass
208.2100g/mol
Density
1.3966g/cm3
Appearence

Kynurenine is typically a crystalline solid and is often found as a colorless or slightly yellow substance. The exact appearance can vary depending on the purity of the sample.

Comment on solubility

Solubility of 2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid

2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid, with the chemical formula C10H12N2O3, presents interesting solubility characteristics. Understanding its solubility is essential for both theoretical and practical applications in biochemistry and pharmaceuticals. Here are some key points:

  • Polar Characteristics: The presence of amino groups (-NH2) and carboxylic acid (-COOH) contributes to the polarity of this compound, enhancing its solubility in polar solvents like water.
  • Aqueous Solubility: As a result of its functional groups, 2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid can be expected to have moderate solubility in aqueous solutions.
  • Solvent Interaction: The ability to form hydrogen bonds with water molecules increases its solubility further, emphasizing the importance of proper solvent selection in practical applications.

Additionally, it’s important to note that temperature and pH can significantly influence solubility:

  • Temperature Effects: Increased temperature generally enhances solubility for many organic compounds, including this acid.
  • pH Influence: The ionization of the carboxylic acid group can make it more soluble in basic conditions, affecting its overall behavior in different environments.

In conclusion, the solubility of 2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid is a critical aspect that plays a significant role in its functionality and interactions in various chemical scenarios. Harnessing this knowledge can lead to more effective applications in fields such as drug design and tailored biosystems.

Interesting facts

Interesting Facts about 2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid

2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid is a fascinating compound that exemplifies the intricate relationships between amino acids, phenyl groups, and keto acid functionalities in organic chemistry. Here are some key points that make this compound particularly interesting:

  • Structural Complexity: This molecule features a unique structure that includes both amino and carbonyl functional groups, providing a rich chemistry available for potential reactions.
  • Biological Interest: Similar compounds are often found in various biological pathways, and understanding their structure can give insights into metabolic processes and the synthesis of biomolecules.
  • Potential Applications: Research into related compounds suggests possible applications in drug development, especially as intermediates in the synthesis of pharmaceuticals.
  • Synthetic Versatility: The presence of the amino groups offers multiple sites for further functionalization, making it a versatile building block in organic synthesis.
  • Research Highlights: The examination of this compound can lead to elucidating mechanisms in therapeutic contexts, particularly concerning action mechanisms and bioactivity of designed drugs.

As chemists continue to explore the implications of compounds like 2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid, they not only enhance our understanding of chemical reactivity but also pave the way for innovations in fields such as pharmaceuticals, biochemistry, and materials science.

Quotes often reflect the curiosity and drive of scientists: "Chemistry is like a puzzle; our job is to find the missing pieces." This compound certainly adds to the puzzle!

Synonyms
kynurenine
343-65-7
dl-Kynurenine
2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid
rac Kynurenine
3-Anthraniloylalanine
3-Anthraniloyl-DL-alanine
Alanine, 3-anthraniloyl-
(+-)-Kynurenine
(+/-)-Kynurenine
Kynurenin
CHEBI:28683
298M20B2AU
Benzenebutanoic acid, alpha,2-diamino-gamma-oxo-
Benzenebutanoic acid, .alpha.,2-diamino-.gamma.-oxo-
alpha-2-Diamino-gamma-oxobenzenebutyric acid
Quinurenine
UNII-298M20B2AU
Alanine, 3-anthraniloyl-, DL-
a,2-Diamino-?-oxobenzenebutanoic Acid; 3-Anthraniloylalanine; DL-Kynurenine; Kynurenin; dl-Kynurenine;
EINECS 206-445-9
MFCD00025194
Spectrum_001162
KYNURENINE [MI]
KYNURENINE, DL-
SpecPlus_000330
2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid #
Spectrum2_001380
Spectrum3_000781
Spectrum4_001916
Spectrum5_000632
alpha,2-Diamino-gamma-oxobenzenebutanoic acid
DL-Kynurenine, free base
2-Amino-4-(2-aminophenyl)-4-oxobutanoicacid
SCHEMBL20874
BSPBio_002482
KBioGR_002539
KBioSS_001642
DivK1c_006426
SPECTRUM1500879
SPBio_001340
CHEMBL1377927
BDBM31880
KBio1_001370
KBio2_001642
KBio2_004210
KBio2_006778
KBio3_001702
KYNURENINE, (+/-)-
DTXSID90861884
Alanine, 3-anthraniloyl- (8CI)
CCG-38856
DL-Kynurenine, >=95.0% (NT)
STL453545
AKOS015894416
CS-W015220
HY-W014504
SDCCGMLS-0066734.P001
NCGC00017339-02
NCGC00017339-03
NCGC00095648-01
NCGC00095648-02
3039-10-9
AS-12298
FK172296
2-Amino-3-(2-aminobenzoyl)propionic acid
DB-006353
DB-050656
NS00074151
2-Amino-4-(2-aminophenyl)-4-oxobutyric acid
C01718
D86788
.alpha.-2-diamino-.gamma.-oxobenzenebutyric acid
SR-05000002450
SR-05000002450-1
Q32908783
Benzenebutanoic acid, alpha,2-diamino-gamma-oxo- (9CI)
AD0899CA-9379-461E-BD7D-45908947C589