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Key Documents

P1883

Sigma-Aldrich

L-Phenylalaninamide

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About This Item

Empirical Formula (Hill Notation):
C9H12N2O
CAS Number:
Molecular Weight:
164.20
Beilstein:
6270941
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.26

Assay

≥98%

form

powder

color

white to off-white

mp

92.8 °C

application(s)

detection

SMILES string

N[C@@H](Cc1ccccc1)C(N)=O

InChI

1S/C9H12N2O/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H2,11,12)/t8-/m0/s1

InChI key

OBSIQMZKFXFYLV-QMMMGPOBSA-N

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Biochem/physiol Actions

L-Phenylalaninamide is a chiral selector.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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A V Chetkauskaĭte et al.
Zhurnal evoliutsionnoi biokhimii i fiziologii, 24(4), 465-470 (1988-07-01)
Synthesis of peptides during polymerization of GlyNH2 and PheNH2 has been demonstrated by means of gel-chromatography and thin-layer chromatography. The optima of pH and temperature have been estimated for the reaction. Grem's salt, tripolyphosphate and pyrophosphate were shown to cause
Rebecca Fransson et al.
Journal of medicinal chemistry, 53(6), 2383-2389 (2010-02-25)
Substance P 1-7 (SP(1-7), H-Arg-Pro-Lys-Pro-Gln-Gln-Phe-OH) is the major bioactive metabolite of substance P. The interest in this heptapeptide originates from the observation that it modulates, and in certain cases opposes the effects of the parent peptide, e.g., the nociceptive effect.
A routine method for alkaline phosphatase assay in pregnancy serum.
D R Pledger et al.
Clinica chimica acta; international journal of clinical chemistry, 122(1), 71-74 (1982-06-16)
Seiji Okazaki et al.
Acta crystallographica. Section D, Biological crystallography, 64(Pt 3), 331-334 (2008-03-08)
The crystal structures of D-amino-acid amidase (DAA) from Ochrobactrum anthropi SV3 in complex with L-phenylalanine and with L-phenylalanine amide were determined at 2.3 and 2.2 A resolution, respectively. Comparison of the L-phenylalanine amide complex with the D-phenylalanine complex reveals that
C Carles et al.
FEBS letters, 212(1), 163-167 (1987-02-09)
This paper is the first to report specific labelling of a native protein at its C-terminal end by carboxypeptidase Y-catalyzed transpeptidation between beta-casein and tritiated Phe amide. A tryptic digest of the radiolabelled protein was resolved by reversed-phase HPLC and

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