Interesting facts
Interesting Facts about 2-Amino-3-(4-fluorophenyl)propanoic Acid
2-Amino-3-(4-fluorophenyl)propanoic acid, often referred to in the scientific community as a derivative of phenylalanine, is noteworthy for its unique structural characteristics and potential applications. Here are several fascinating aspects of this compound:
- Fluorination Significance: The presence of a fluorine atom in the structure often enhances the compound's biological activity and lipophilicity. Fluorinated compounds can exhibit improved metabolic stability and bioavailability, making them valuable in medicinal chemistry.
- Neurotransmitter Influence: As an amino acid derivative, this compound can play a role in the synthesis of neurotransmitters. Compounds like this one are studied for their impact on neural signaling pathways, particularly in the context of diseases like depression and anxiety.
- Potential Therapeutic Uses: Research into compounds like 2-amino-3-(4-fluorophenyl)propanoic acid may unveil their potential as therapeutic agents in treating a variety of conditions, including but not limited to neurological disorders and metabolic syndromes.
- Emerging Research: Several studies focus on the derivative's capabilities, particularly in pharmaceuticals. Understanding its interaction with biological systems could lead to the development of new drugs or treatments.
- Chirality: The chiral nature of this compound contributes to its biological activity. Chirality can significantly influence the pharmacodynamics and pharmacokinetics, resulting in varied effects from its enantiomers.
In summary, 2-amino-3-(4-fluorophenyl)propanoic acid represents a compelling area of study in contemporary chemistry and pharmacology. Its unique properties and potential therapeutic applications make it a subject of ongoing research and discovery.
Synonyms
51-65-0
4-FLUORO-DL-PHENYLALANINE
4-Fluorophenylalanine
p-fluorophenylalanine
p-Fluoro-dl-phenylalanine
2-amino-3-(4-fluorophenyl)propanoic acid
Alnasid
DL-p-Fluorophenylalanine
dl-4-Fluorophenylalanine
DL-3-(4-Fluorophenyl)alanine
D,L-Fluorophenylalanine
D,L-p-Fluorophenylalanine
4-Fluoro-dl-para-phenylalanine
CCRIS 4819
60-17-3
EINECS 200-113-7
EINECS 200-459-9
MFCD00002600
NSC 71433
DL-Phenylalanine, 4-fluoro-
Alanine, 3-(p-fluorophenyl)-
DTXSID3025332
HSDB 7748
NSC-71433
42T8578M1E
DTXCID805332
CHEBI:84060
H-D-Phe(4-F)-OH
P-FLUOROPHENYLALANINE, DL-
4-Fluoro-DL-.beta.-phenylalanine
4-FLUOROPHENYLALANINE, DL-
P-FLUOROPHENYLALANINE [HSDB]
Alanine, 3-(p-fluorophenyl)-, dl-
PHENYLALANINE, 4-FLUORO-, DL-
3-(P-FLUOROPHENYL)ALANINE, DL-
4-FLUOROPHENYLALANINE, (+/-)-
D-4-FLUOROPHE
h-dl-phe(4-f)-oh
MFCD00063064
UNII-42T8578M1E
DL-p-phenylalanine
4fluorophenylalanine
p Fluorophenylalanine
DLpFluorophenylalanine
pFluoroDLphenylalanine
4FluoroDLphenylalanine
D,LFluorophenylalanine
DL-Fluorophenylalanine
DL4Fluorophenylalanine
Fluorophenylalanine, p
rho-Fluorophenylalanine
D,LpFluorophenylalanine
pFluoroD,Lphenylalanine
Phenylalanine, 4fluoro
4FluoroD,Lphenylalanine
para Fluorophenylalanine
Para-Fluorophenylalanine
Spectrum_001970
2-Amino-3-(4-fluorophenyl)propanoicacid
4-Fluorophenylalanine #
DLPhenylalanine, 4fluoro
Spectrum2_000902
Spectrum3_001878
Spectrum4_001253
Spectrum5_000766
4FluoroDLparaphenylalanine
DL3(4Fluorophenyl)alanine
Alanine, 3(pfluorophenyl)
dl-(4-Fluorophenyl)alanine
H-D-PHE(P-F)-OH
SCHEMBL44070
BSPBio_003356
H-P-FLUORO-D-PHE-OH
KBioGR_001806
KBioSS_002534
DivK1c_000957
L-3-(4-Fluorophenyl)alanine
SPBio_000744
dl-.beta.-p-Fluorophenylalanine
Alanine, 3(pfluorophenyl), DL
CHEMBL3185250
HMS502P19
KBio1_000957
KBio2_002526
KBio2_005094
KBio2_007662
KBio3_002858
NINDS_000957
P-FLUORO-D,L-PHENYLALANINE
4-FLUORO-D,L-PHENYLALANINE
BCP11609
NSC71433
Alanine, 3-(p-fluorophenyl)-, dl
Tox21_202890
CCG-39903
STK410968
DL-3-(P-FLUOROPHENYL)ALANINE
AKOS000196918
AKOS016050376
AB00239
AB02498
AC-9899
CS-W017056
HY-W016340
CAS-51-65-0
IDI1_000957
NCGC00015435-02
NCGC00015435-04
NCGC00260436-01
AS-13556
SY009526
SY030990
SY044822
2-Amino-3-(4-fluorophenyl)propionic Acid
DB-006815
F0106
NS00015563
EN300-61659
AB00052275-04
BRD-A12490356-001-03-0
Q27105098
Z57969728
(R)-2-AMINO-3-(4-FLUORO-PHENYL)-PROPIONIC ACID
D-4-Fluorophenylalanine;(S)-2-amino-3-(4-fluorophenyl)propanoic acid
200-113-7
Solubility of 2-amino-3-(4-fluorophenyl)propanoic acid (C9H10FNO2)
2-amino-3-(4-fluorophenyl)propanoic acid is an intriguing compound when it comes to its solubility characteristics. This molecule belongs to a class of amino acids known for their diverse functionalities, which contribute significantly to their solubility profiles. Key points to consider about the solubility of this compound include:
In conclusion, the solubility of 2-amino-3-(4-fluorophenyl)propanoic acid is notably influenced by its functional groups and molecular structure. This results in favorable solubility traits primarily in polar solvents. Understanding these properties not only aids in the utilization of this compound in various applications but also sets the stage for further exploration in biochemical processes where solubility plays a crucial role.