| Identification | More | [Name]
L-3-Cyanophenylalanine | [CAS]
57213-48-6 | [Synonyms]
3-CYANO-L-PHENYLALANINE
H-M-CYANO-L-PHE-OH
H-PHE(3-CN)-OH
H-PHE(M-CN)-OH
L-3-CYANOPHE
L-3-CYANOPHENYLALANINE
(M-CN)PHE-OH
M-CYANO-L-PHENYLALANINE
RARECHEM BK PT 0151
(S)-2-AMINO-3-(3-CYANOPHENYL)PROPANOIC ACID
(S)-3-CYANOPHENYLALANINE
(S)-N-3-CYANOPHENYLALANINE
(S)-N-3-Cyanophenylalanine(e.e.)
(2R)-2-amino-3-(3-cyanophenyl)propanoic acid
L-3-CN-Phe-OH
3-(3-Cyanophenyl)-L-alanine
(S)-N-3-CYANOPHENYLALANINE 95%, (98% E.E.)
(S)-N-3-Cyanophenylalanine, 98% ee
L-3-Cyano-phe-OH | [Molecular Formula]
C10H10N2O2 | [MDL Number]
MFCD01860885 | [Molecular Weight]
190.2 | [MOL File]
57213-48-6.mol |
| Chemical Properties | Back Directory | [Appearance]
white to slightly yellow powder | [Boiling point ]
325.7°C (rough estimate) | [density ]
1.2167 (rough estimate) | [refractive index ]
1.6300 (estimate) | [storage temp. ]
Store at 0°C | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [form ]
Powder | [pka]
2.14±0.10(Predicted) | [color ]
White to slightly yellow | [CAS DataBase Reference]
57213-48-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN3439 | [HazardClass ]
6.1 | [PackingGroup ]
III | [HS Code ]
29225090 |
| Hazard Information | Back Directory | [Chemical Properties]
white to slightly yellow powder | [Antimicrobial activity]
L-3-Cyanophenylalanine (3CP) is a β-amino acid that has been shown to
have an interaction with serine protease. 3CP is an antibacterial agent
that is used in the treatment of bacterial infections. It has been shown
to inhibit the growth of bacteria by inhibiting the acid transporter,
which leads to a decrease in intracellular pH. 3CP binds to the basic
group of the enzyme and forms a covalent bond, inhibiting its function.
The synthesis of 3CP can be achieved through synthetic chemistry or by
enzymatic conversion from L-serine. This compound can also be obtained
as an enantiomer, meaning it has two different forms: one that is active
and one that is inactive. |
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